Skip to main content
Heliyon logoLink to Heliyon
. 2023 Jun 2;9(6):e16928. doi: 10.1016/j.heliyon.2023.e16928

The impact of silver nanoparticles on the growth of plants: The agriculture applications

Sajad Khan a, Muhammad Zahoor b,, Raham Sher Khan a, Muhammad Ikram c, Noor Ul Islam d
PMCID: PMC10279825  PMID: 37346326

Abstract

Nanotechnology is the most advanced and rapidly progressing field of science and technology. It primarily deals with developing novelty in nanomaterials by understanding and controlling matter at the nanoscale level. Silver nanoparticles (AgNPs) are the most prominent nanoparticles incorporated with wide-ranging applications, owing to their distinct characteristics. Different methods have been employed for nanoparticles synthesis like chemical method, physical method, photochemical method, top-down/bottom-up approach and biological methods. The positive impacts of silver nanoparticles have been observed in various economy-based sectors, including agriculture. The scientific curiosity about AgNPs in agriculture and plant biotechnology has shown optimum efficacy over the last few years. It not only enhances seed germination and plant growth, but also improves the quantum efficiency of the photosynthetic process. AgNPs play a vital role in agriculture by having several applications that are crucial for ensuring food security and improving crop production. Moreover, they also act as nano-pesticides, providing sufficient dose to the target plants without releasing unnecessary pesticides into the environment. Nano-fertilizers slowly release nutrients to the plants, thereby preventing excessive nutrient loss. AgNPs are utilized for effective and non-toxic pest management, making them an excellent tool for combating pests safely. They combine either edible or non-biodegradable polymers for active food packaging. In addition, AgNPs also possess diverse biological properties such as antiviral, antibacterial and antifungal activities, which protect plants from hazardous microbes. The aim of this review is to comprehensively survey and summarize recent literature regarding the positive and negative impacts of AgNPs on plant growth, as well as their agricultural applications.

Keywords: Crops protection, Food packaging, Nanotechnology, Seeds germination, Silver nanoparticles

Graphical abstract

Image 1

1. Introduction

Nanotechnology is an emerging field of science that mainly deals with nanomaterials to overcome size limitations and change the world perspective on science. It has revolutionized agriculture sectors and played essential roles in various fields like agricultural biotechnology, food security, and crop production. Nanoparticles distinct physicochemical features are extremely helpful in inducing plant metabolism. However, their interactions with plants have not been clarified and understood in detail. Several contradicting reports of nanoparticles regarding accumulation, translocation, absorption, biotransformation, and toxicity were reported in diverse plant species. AgNPs are one of the most significant nanomaterials whose impacts are still under investigation [1,2]. The synthesis of plant-based nanoparticles is an excellent approach due to their low cost, non-pathogenic factor, non-toxic phytochemical constituents, flexibility in reaction parameters, and biochemical diversity of plant extract [3]. Approximately 25% of all nanotechnology products incorporate its usage. Such particles have a large surface area in relation to their volume, and they typically measured between 1 and 100 nm in size [4,5]. AgNPs have distinct characteristics and broad range of applications, particularly in agriculture and plant biotechnology. They have been shown to enhance seed germination, plant growth, and photosynthetic efficiency, whereas also acting as safe and effective nano-pesticides and fertilizers. The antibacterial, antifungal, and antiviral properties of AgNPs have been widely utilized in various industries, including healthcare, textiles, building materials, medical devices, food services, cosmetics, and household materials. They are beneficial in these industries because of their ability to protect against harmful microorganisms and provide a safer and healthier environment [6,7]. AgNPs acts as a photochemical and good electric conductor, showing wastewater treatment and electronic device implementation. It enhances fruit ripening, plant growth, and fungicides in agriculture fields [8,9]. In general, fertilizers are essential to increase the growth and development of plants. Unfortunately, most fertilizers cannot reach plant bodies due to several factors, such as degradation by photolysis, decomposition, hydrolysis, and leaching. Thus, it is essential to reduce the loss of nutrient in fertilization and improve crop yield by manipulating novel nanomaterials and nanotechnology applications. Nano-fertilizers, also known as nano-encapsulated nutrients, have several properties, including effectiveness for crops, controlling the release of chemical fertilizers, releasing the nutrients on demand, regulating plant growth, and enhancing target activity [10,11]. Recently, nanoparticles have attracted the attention and interest in the agricultural applications that effectively minimizes the use of chemical fertilizers and enhances crop growth and yield. Metal nanoparticle phytotoxicity for plant species has recently been investigated in seed germination and root elongation tests to advocate its use in agricultural applications [12,13].

Recent studies showed that plant response to AgNPs is associated with their dosage, which can either enhance or inhibit growth. Exposure to specific and serial AgNPs enhances plant growth more than control plants, whereas low and high concentrations negatively affect plant growth [14,15]. Several reports suggest that proper concentrations of AgNPs are vital in enhancing plant growth/seed germination, improving chlorophyll content/photosynthetic efficiency, and increasing fertilizer and water efficiency [16,17].

2. Methods used to synthesize nanoparticles

There are different approaches (methods) used to synthesize nanoparticles which are discussed below.

2.1. Chemical method

The chemical method of nanoparticle synthesis is the most convenient, effective, and easy to handle. The chemical reduction technique involves the utilization of both organic and inorganic reducing agents, is the most commonly used technique for synthesizing nanoparticles. Generally, diverse types of reducing agents are typically employed for reducing silver ions (Ag+) in both aqueous and non-aqueous solutions that include: ascorbate, polyol process, sodium borohydride (NaBH4), sodium citrate, poly (ethylene glycol)-block copolymers, N-dimethylformamide (DMF), Tollens reagent, N, and elemental hydrogen. Silver nanoparticles react with these agents, reduce Ag+ and resulting in metallic silver (Ag0). Subsequently, the particles aggregate into oligomeric clusters, ultimately leading to the synthesis of silver particles [18]. Protective agents are used to stabilize dispersive NPs by protecting them during the preparation of metal nanoparticles that can be bind onto or absorbed on surfaces to avoid agglomeration. It can be possible with low-cost with high productivity compared to other methods of NPs synthesis. The chemical approaches of silver nanoparticles in true solution consist of three steps: (i) metal-based precursors, (ii) capping oxidants (iii) reducing agents. To obtain smaller size and uniformly spherical-shaped metal-based nanoparticles, it is essential to employ capping agents that help control the growth of nanoparticles during the synthesis process. The synthesis of a colloidal solution of silver nanoparticles involves two stages of growth and nucleation, which determine the morphology and size of the resulting nanoparticles. Nevertheless, the synthesis of uniformly sized and well-dispersed nanoparticles depends on achieving a consistent growth rate and size during the production process. The synthesis of single dispersed nanoparticles with regular size depends on the production of growth rate and similarity in size. The regulation of the reaction is crucial in measuring the subsequent development of primary nuclei using diverse limits such as temperature, pH, precursors, capping material (PVP), and reducing substance.

2.2. Physical method

In this technique, nanoparticles are synthesized by the process of condensation or vaporization by sustaining the furnace tube at atmospheric pressure. The physical synthesis of AgNP is possible in two techniques; evaporation–condensation and laser ablation [19]. The substances present inside the fixed vessel evaporates into the carrier gas in the furnace. In the condensation and vaporization method, nanoparticles of several materials are synthesized such as Zn, Ag, Cu, Pb, and Sn [20]. The synthesis of nanomaterial using a furnace has many drawbacks such as cylinder-shaped particles filling a massive space; a high amount of energy being consumed that causes a huge increment in the environmental heat. In addition, it also requires a prolonged period to achieve thermal constancy. There are many kilowatts of energy needed; thus, to obtain a stable temperature heating period of 10 min is required for the distinctive cylinder-based furnace. Moreover, laser ablation of bulk materials in a solution is an alternative method for synthesizing AgNPs. The laser-based technique is superior compared to the other technique, as no chemical reagent produces in the solution and resulting in pure colloids [21]. Mostly, physical synthesis consumes the physical energy to produce nanoparticles with fine-size circulation. In this type of method, a huge amount of product is fabricated in a single-step procedure and synthesizes a higher number of silver nanoparticles in ash form. When a pulsed laser is directed towards a liquid environment, it only affects the AgNPs that originate from the base metal source, without any involvement of other substances such as ions, compounds, or reducing agents. Several parameters influence the characteristics of synthesize metal NPs such as kind of base metal source, duration of irradiation, laser power, and property of liquid media. Laser ablation synthesize NPs in pure form with no contamination, as it utilizes mild surfactants in the solvent and does not involve chemical reagents [22].

2.3. Photochemical method

Photochemical processes have been a primary focus for researchers in the metallic nanoparticles fabrication due to the superior temporal and spatial control [23]. In this method, the solution containing metal precursors exposes to ultraviolet (UV) or visible light. The use of photochemical processes for creating metallic nanoparticles is highly advantageous compared to other methods because it avoids the need for toxic or harmful substances, neither require expensive equipment nor highly skilled personnel, and can be performed under normal ambient conditions i.e., atmospheric pressure and room temperature [24]. The fabrication of metallic nanoparticles in solution utilizes various reagents, including reducing agents, and metal precursors (complex or salt), but rarely use stabilizing agents [25]. The process of photochemistry is employed to begin the reduction of a metal precursor by converting the reducing agent from its n + valence state (Mn+) to a zero-valence state (Mn0) [26]. The M0 forms nuclei or nucleation centres that aggregate and grow to synthesize metallic NPs. Both capping agents and stabilizers play a vital role to control the formation of homogenous metallic NPs with respect to the desire shape and size, avoid agglomeration, and enhance colloidal stability [27]. Polymers trap and protect the NPs against coalescence and oxidation. Furthermore, due to their varying chemical compositions, polymers exhibit specific interactions with the surface of metallic materials, activating vital modification in the size and shape of the resultant nanoparticles. The process of photo-reducing layers of silver nitrate yields AgNPs, which rely on the presence of inert soil suspensions as stabilizing agents to avoid particle aggregation and act as oxidants. The process of irradiation splitting was utilized on silver nanoparticles with a distribution ratio to achieve a constant distribution ratio and absolute diameter size [28].

2.4. Top-down and bottom-up approach

The synthesis approaches of metal NPs consist of two approaches namely top-down and bottom-up. The top-down approach involves breaking down bulk materials using physical methods to produce the desired nanostructures (ball milling, ultrasonic machining, laser ablation, etc.). This technique is valuable for its ability to generate a substantial quantity of nanoparticles. However, there is certain limitation of this technique: requires costly equipment and high amount of energy, while the bottom-up approach entails the synthesis of nanoparticles utilizing chemical agents that assembles single molecules and atoms into bigger nanostructures to produce nano-sized materials using biological and chemical approaches. At present, methods for producing synthetic nanoparticles are classified into three main categories: chemical, physical, and biological green synthesis.

2.5. Biological methods

In recent times, the biological synthesis of metal nanoparticles has garnered significant attention owing to its broad relevance in diverse fields. It employs biological entities including microorganisms (bacteria or fungi) plant extracts are considered valuable alternatives compared to other synthesis routes.

2.5.1. Microorganisms mediated synthesis

The biosynthetic approach that utilizes natural reducing agents for nanoparticle syntheses such as biological microorganisms (bacteria or fungi), plant extracts, and polysaccharides is also known as green chemistry. Microbes, including bacteria and fungi, remediate the toxic materials by reducing metal ions and synthesizing metal nanoparticles in a biological way [29]. There are certain bacteria that can synthesize AgNPs intracellularly, where intracellular components perform their function as stabilizers and reducers [30]. The naturally available reducing agents that synthesize AgNPs biologically might be a promising technique that replaced the most complex physiochemical process. Green synthesis is superior to other methods due to the absence of toxic chemicals and harmful by-products but employs natural capping agents to stabilize AgNPs [31]. Bacteria generally utilize nitrate as a main source of nitrogen, in which reductase converts the nitrate into nitrite, employing the reducing power of nicotinamide adenine dinucleotide (NADH). The metabolic processes of bacteria reduce nitrate to nitrile and ammonium, which might be utilized in the bio-reduction of Ag+ ions by an intracellular electron donor. The enzyme nitrate reductase is an optimum reducer in the process of bio-reduction of silver ions. The green synthesis of AgNPs was performed by another plausible mechanism that involves the biological system of a fungus, Verticillium species. The AgNPs synthesis initiates beneath the cell wall surface, rather than the aqueous solution. Fungal cells' surface traps the Ag+ ions because of the electrostatic interaction between negatively-charged carboxylate groups of the enzyme and Ag+ ions. The formation of Ag nuclei occurs after Ag+ ions intracellularly reduce the cell wall, and further expansion occurs after Ag+ ions are reduced. Bacteria are highly capable of producing inorganic components both inside and outside the cell. As a result, they can serve as highly effective bio-factories for synthesizing nanoparticles e.g., gold, copper, silver, etc. The synthesis of silver nanoparticles is a well-known example of biologically derived nanoparticles that possess biotic characteristics.

2.5.2. Green routes for nanoparticle synthesis

Despite being in its early stages, research in the field of nanotechnology for environmentally friendly production of nanoparticles is expanding rapidly in recent years. The nanoparticles are synthesized either using plant extracts or microorganisms such as algae, bacteria, fungi, or yeast. The incorporation of this approach marks a noteworthy stride towards accomplishing the twelve principles of green chemistry established by Paul Anastas and John Warner in 1998 [32].

The synthesis of nanoparticles using microorganism is generally a highly complex and less cost-effective than utilizing plant extracts. The maintenance of cell cultures and extraction of nanoparticles from microorganisms can be challenging, making the utilization of plant extracts a more appealing option, particularly for large-scale nanoparticle production. Dried grass is generally simpler and less expensive than cultivating bacterial or fungal strains [33].

2.5.3. Plant mediated synthesis of nanoparticles

The process of collecting plants and extracting active biomolecules to synthesize silver nanoparticles is relatively straightforward process. The extract of plants contains several biomolecules, including alkaloids, terpenoids, sugars, NADH-dependent reductase, phenols, flavonoids, proteins, and tannins. Biomolecules possess the capability to reduce metal ions or stabilize particle growth after nucleation. Biomolecules such as enzymes, vitamins, proteins, lipids, and organic acids actively take part in the reduction and stabilization of nanoparticles during NPs synthesis. Generally, the active molecules hold amine, carbonyl, methoxide or hydroxyl functional groups [34].

It should be emphasized that the plant material is not the only factor that influences the production of nanoparticles with specific structures, sizes, or shapes. The conditions under which nanoparticles are synthesized, such as the pH level, exposure to sunlight, temperature, duration of mechanical stirring, and dispersion, can all have an impact on the resulting nanoparticle's size, structure, and chemical properties. One of the earliest approaches for producing metallic nanoparticles using plants involved utilized alfalfa sprouts. This method represents the first documented instance of synthesizing silver nanoparticles (AgNPs) using a living plant system. The roots of Alfalfa possess the distinctive property to assimilate Ag from agar medium and subsequently transported it to plant shoots in an identical oxidation state. After being transported to the plant shoots, the Ag atoms begin to self-organize and form nanoparticles by bonding with one another and forming a larger arrangement. When it comes to green synthesis, plants seem to be a more efficient and speedy option compared to fungi and bacteria. Initial investigations have demonstrated that these synthesis procedures are capable of rapidly producing Ag NPs. It involved extracts and plant metabolites, as well as products of biological macromolecules: lipids, carbohydrates, proteins or peptides, and nucleic acids. It is now well-proven that nanoparticle synthesis on the base of biological route saves energy and creates comparatively less harmful waste, making it a promising alternative to conventional synthesis methods. Green nanotechnology has become a driving force for both academic and industrial research, promoting the design and development of Green Nanoparticles (GNPs) with specific applications. GNPs have already been implemented in various innovative technologies, including smart electronic devices, life-saving nano-pharmaceuticals, and environmentally friendly energy production devices. This field not only fosters fundamental research but also emphasizes the importance of goal-oriented research for practical applications. Plant-based nanoparticles are tiny particles that are created from plant materials. These nanoparticles are attracting attention due to significant applications in diverse fields: medicine, agriculture, and environmental protection. The process of synthesizing these particles involves extracting active components from diverse plants part, including stems, leaves, seeds, and roots, and then treating them with various chemical or physical methods, including reduction, oxidation, and thermal treatment, to form nanoparticles. There are different methods to make plant-based nanoparticles, including bio-reduction, template-assisted synthesis, and sol-gel methods. Bio-reduction involves using plant extracts to reduce metal ions and form nanoparticles, while template-assisted synthesis uses plants as templates to grow the particles. Sol-gel methods use plant-based precursors to form nanoparticles through gelation. Compared to synthetic nanoparticles, plant-based nanoparticles have many benefits, including biocompatibility, biodegradability, and low toxicity. They can also be easily modified with biological molecules, making them useful for medical applications. The plant-based nanoparticle synthesis is a promising research area with many potential applications. With the development of science, researchers have focused on the need of developing efficient techniques that synthesized environmentally friendly and non-toxic biocompatible nanoparticles [35]. Plants harbor several bioactive chemicals such as Flavonoids, aldehydes, phenols, amino-acids, vitamins and ketones, that are present in plants, which can reduce valuable metal ions [36]. Plant-mediated synthesis is recognized as a less costly, environmentally-friendly, and easily up-scalable method of synthesizing nanoparticles. Due to their widespread availability in different climates, plant extracts are easily accessible and economical for the nanoparticles production. One of the key benefits of using plant extracts for the production of nanoparticles is the availability and ease of access to precursor materials, which can be a major benefit in the synthesis process.

Although plant extracts are a convenient source for nanoparticle synthesis, it can be more difficult to control the shape, size, and composition of the resulting nanoparticles compared to chemical methods. This is because plant extracts consist of complex mixture of organic molecules, which can make the synthesis process more challenging. Despite the difficulty in controlling nanoparticle characteristics when using plant extracts, one advantage is the ability to coat the external surface of nanoparticles with active plant molecules, allowing for functionalization. The combination of nanoparticles and plant molecules creates a synergistic effect that results from the interaction between the intrinsic properties of the nanoparticles and the specific properties of the plant molecules. This synergistic effect is particularly important in the plant-based synthesis of nanoparticles used as antimicrobials [37].

2.5.4. Algae mediated synthesis

Marine algae are a well-known functional food source that is rich in various biologically-active substances, such as minerals, vitamins, lipids, proteins, and polysaccharides, due to their enrichment with these nutrients. The medicinal potential of algae is high against allergy, oxidative stress, cancer, hypertension, lipidemia, thrombosis, and other degenerative diseases [38]. Sponges and diatoms are one of important biological entities present in marine resources. It is a nanostructure consisting of covering coral reefs and silica. Hence, algae also act as “bio-factories” in the production of silver nanoparticles. Algae are valuable compared to different types of bio-reductants due to cost-effectiveness, strong capacity of metal uptake, and macroscopic structure [39].

The novelty of this review lies in its comprehensive coverage of the multiple uses of AgNPs in agriculture and plant biotechnology, which are vital for ensuring food security and improving crop production, while also being safe and non-toxic for the environment. Additionally, it highlights the antiviral, antibacterial, and antifungal properties of these nanoparticles that protect plants from hazardous microbes, making them a promising tool for sustainable agriculture.

3. The impacts of silver nanoparticles (AgNPs) on germination of seed

The applications of AgNPs have received high focus and promotion in the medical and pharmaceutical fields. However, the utilization of AgNPs in the agricultural sector is a new research area. In contrast to AgNPs toxicity and anti-microbial properties, recent studies have explored their role in enhancing seed germination and improvement of crops. Despite remarkable significance in the agriculture field and positive effects on seed germination, their applications have also been associated with negative effects.

3.1. Positive effects on seed germination

Seed germination is one of the most vital phase for establishing plants in the agriculture and is essential for the quality of crops [40]. AgNPs can incorporate with seed coats and helps in water uptake inside seeds, promoting starch metabolism and seed germination. It is also applied as a nano-priming agent to enhance rice-aged seeds and starch metabolism. One of the priming aims of AgNPs is to regulate up the expression of aquaporin genes, thus encouraging the diffusion of H2O2 and water. AgNPs was synthesized through a green route using kaffir lime leaf extract as a nano priming agent to enhance rice-aged seed germination. The priming of rice-aged seeds with photosynthesized AgNPs (5 and 10 ppm) has remarkably enhanced the performance of seedling vigor and germination to conventional hydropriming, AgNO3 priming, and unprimed control. Nano priming is also associated with strengthening α-amylase activity and thus causes higher soluble sugar content to support seedlings' growth [41]. The extracellular AgNPs were synthesized using Bacillus subtilis spizizenni. Bajra (Pennisetum glaucum) seeds were treated with 1 mM AgNPs and found excellent for better seed germination in just 3 days. The statistical analysis by one-way analysis of variance showed a vital improvement in plumule and radicle length than control seeds of Bajra [42]. In a study, AgNPs were applied to check salinity stress in lentil seeds. Seedling growth and Lentil seed's seed germination were enhanced after exposure to AgNPs. The germination percentage was also increased for lentils at concentrations of 10 μg/mL AgNPs, enhanced the mean germination time for lentil plants, improved the germination parameters and resulted in better tolerance under drought conditions. AgNPs applied at a concentration of 10 μg/mL were found to improve lentil seed germination under conditions of drought stress [43]. Gum Arabic coated (Ga-AgNPs-6nm) and PVP-coated Ag nanoparticles (PVP-AgNPs- 20 nm) was applied to the seeds of eleven species in different concentrations such as 1, 10, and 40 mg/L. The application of GA-AgNPs reduced the rate of germination in three species and improved one species, while the application of 40 mg showed no effect on germination [44]. AgNPs were synthesized using leaf extract of Moringa oliefera and tested on seed germination and growth. The diverse AgNPs concentrations at 25 ppm, 50 ppm, 75 ppm, and 100 ppm were tested with control group to enhance wheat seed germination and seedling growth. In contrast, AgNPs concentration at 100 ppm displayed tremendous growth compared to the control. Additionally, a significant improvement in dry root weight, fresh root weight, root elongation, and root length were reported at 100 ppm AgNPs concentration [45]. In a study, thirty seeds in each Petri dish were applied with concentrations of silica (20%) and AgNPs (60%) with controlled distill water treatment. Seed germination started on the fourth day and was controlled for 14 days. The results of the analysis showed that AgNPs (20%) yielded higher values in seed germination properties [46]. In another study, AgNPs were prepared at different concentrations such as 0, 10, 20, 30, and 40 μg/mL in which 30 μg/mL significantly enhanced percent germination rate and seed germination due to higher germination potential. AgNPs with size range of 20 nm were diluted to seven concentrations: 0.05, 0.1, 0.5, 1, 1.5, 2, and 2.5 mg/L to check the seeds germination [47]. The treatments of AgNPs have improved the germination rate in watermelon (Citrullus lanatus), zucchini (Cucurbita pepo) and corn (Zea mays) [17,18]. AgNPs were synthesized using glucose (green reagent). AgNPs at concentration of 0.001–0.5 mg/L showed no effect on seed germination, while 0.06–1 mg/L and 0.03–0.1 mg/enhanced root and shoot fresh mass. AgNPs at concentrations ranging from 0.06 to 0.5 mg/L have significant applications in agriculture, including their use as an eco-friendly alternative source of fertilizer for wheat crops [49]. AgNPs and AgNO3 were used at 100, 500, and 1000 mg/L; 100 and 500 mg/L, respectively, in Brassica juncea var. The toxicity of these particles was evaluated using the Varuna mustard plant. The results indicated that AgNPs caused a minor improvement in the length of root and shoot. It increased chlorophyll as well as protein content at all concentrations compared to the control [50]. In a study, the applications of AgNPs and salt at concentrations of 0, 40, 60, and 80 ppm; 0, 30, 60, 90, and 120-mMol−1, respectively, exhibited that 80 ppm AgNPs effect was excellent (P ≤ 0.05) on percentage germination of seed. AgNPs application was essential to enhance the salinity tolerance in the S. hortensis seedling. It was crucial in activating various plants defense mechanisms against salt toxicity [51]. The economically vital crop, pearl millet (P. glaucum L.), was grown on M.S. basal medium with different concentrations of AgNPs (T1 = control, T2 = 20 ppm, T3 = 40 ppm, T4 = 60 ppm, and T5 = 80 ppm). The biochemical profile, seedling growth, and seed germination of pearl millet were highly affected (p ≤ 0.05) and found excellent in T3 treatment. Compared to the control, the T3 treatment showed the highest seedling vigour index (VI), seed germination, biomass accumulation, and root/shoot length [52]. Alnus nitida-based leaves extract was used to synthesize AgNPs, which were then applied to wheat seeds at varying concentrations (0.75 μg/mL, 1.5 μg/mL, 3 μg/mL, 6 μg/mL, and 15 μg/mL) under in vitro conditions. The study revealed that the wheat plants treated with 6 μg/mL of AgNPs exhibited significant enhancements in dry and fresh weights, as well as induced the production of secondary metabolites [53].

3.2. Negative effects on seed germination

AgNPs have been found to have several beneficial effects on plant growth, certain plants have shown toxicity in response to their application, indicating potential negative effects. The application of AgNPs at different concentrations such as 1000 μg/mL, 1600 μg/mL and 1200 μg/mL on Brassica campestris, Oryza sativa and Vigna radiata respectively. Ions inhibited roots at 4500 μg/mL and 6000 μg/mL concentrations. The roots length was retarded to 1% and 0.5% in Oryza sativa and Brassica campestris; Vigna radiata, respectively [54]. AgNPs at 10–20 mg/L reduced germination percentage in Lolium perenne [55]. In a study, three AgNPs (1–20 nm) were used for seed germination. The highest germination was observed after wheat seeds were incubated at 25 °C for 7 days in a dark environment. The result indicated that the AgNPs effect on wheat plants germination was reduced only at 10 mg/L application. At the same time, it was clarified that there was zero effect on other applications [56]. AgNPs (20 nm) exposure at 75 μg/L concentration has not shown any changes but reduced the germination rate of Arabidopsis thaliana [57].

4. The impacts of silver nanoparticles (AgNPs) on plant growth

AgNPs have shown a greater efficacy in enhancing seed germination. Several previous studies have shown their applications in plant growth parameters. The proper AgNPs concentrations have remarkably improved the growth and yield of crops. Many studies confirmed that AgNPs positively improved crops with less or no phototoxic effect on plant growth. In contrast, negative effects were also reported on several plant species.

4.1. Positive effects on plant growth

AgNPs are used as antiviral, antibacterial, and antifungal agents in agriculture application. It preserves the shelf life of fruits, foliage, flowers, and vegetables and stimulates plant growth and metabolism. The plant responses to the AgNPs applications are diverse, depending on the exposure time, types of plant species, composition, particle size, concentration, functionalization, and many other factors. In a study, AgNPs of different concentrations were used at 0, 5, 10, and 20 mg/L. The root development as novel bio stimulants enhanced upon their application at 5 mg/L. In addition, they also improved nitrogen (N), phosphorous (P), and potassium (K) concentration in leaves, which is beneficial in enhancing seedling performance during the primary developmental stages [58]. Exogenous application of AgNPs diversely affected plant growth. The treatment of Oryza sativa at 30 μg/mL of AgNPs enhanced root growth, while 60 μg/mL stopped root growth [59]. An experimental study investigated the AgNPs effect on mean germination time, rate, percentage, root length, and dry/fresh weight of seedlings for the three spices. AgNPs at different concentrations such as 0.05, 0.1, 0.5, 1, 1.5, 2, and 2.5 mg/L were used to investigate the seed germination stage. Three spices have shown varying dosage responses to AgNPs on measured growth characters and germination percentage. Germination rate values of three plants have improved in response to AgNPs [48]. Using the seed growth-mediated technique AgNPs with a size of 13 nm were synthesized on Ag seeds with a size of around 6 nm. The application of AgNPs with 50 mg/L enhanced the highest chlorophyll accumulation and lowest carotenoid accumulation in the leaves, lower GPOX activity, and fewer anthocyanins and polyphenols with 100 mg/L. AgNPs-derived seedlings showed smaller anthocyanins, carotenoids, and chlorophyll contents in kale. Still, higher GPOX activity was characterized by higher dry shoot and fresh weights and higher heterogeneous biometric parameters of the roots [[60], [61]]. Trisodium citrate salt based synthesize AgNPs (9 × 10−4 M) were sprayed at 0, 50, and 75 ppm on wheat crops of different species: Vigna sinensis, Triticum aestivum and Brassica juncea. The application of AgNPs at 50 mg/L enhanced wheat (cowpea) shoots' dry weight and length. The shoot enhancement was reported at 75 ppm in Brassica. AgNPs were synthesized and contaminated soil with AgNPs to check their impact on different plants, such as Lactuca sativa (lettuce), and Avena Raphanus sativus (radish) and byzantina (oat). It produced a higher percentage of dry mass and root growth [[30], [31], [62]]. Foliar AgNPs treatment at 20, 40, and 60 mg/L has enhanced the growth parameters of the fenugreek plant (shoot dry weight, number of plant/leaves, and shoot length). Other biochemical aspects were improved, such as the concentration of indole acetic acid (IAA) and photosynthetic pigments such as the concentration of indole acetic acid (IAA) and photosynthetic pigment such as chlorophyll a, chlorophyll b and carotenoids. It also improved the yield quantity (number of seeds/pod, seed index weight of seeds/plant, and number of pods/plant), antioxidant activity, and quality (carbohydrate%, protein%, tannins, flavonoids and phenolics contents) of the yielded seeds [10]. The application of AgNPs at different concentrations such as 0, 25, 50, 100, 200, and 400 ppm enhanced the antioxidant status and growth of 7-day-old Brassica juncea seedlings. AgNPs affected the vigor index, shoot length, root length, and fresh weight seedlings. Root length and vigor index were increased to 326% and 133% of the treated seedlings. There was evidence of increased chlorophyll concentration and photosynthetic quantum efficiency in leaves of treated seedlings [63]. The chemically synthesized AgNPs (100 nm) based on polyvinyl pyrrolidone (PVP), and biologically synthesized using leaves of Ricinus communis L were used to evaluate the growth of water plant. AgNPs (biologically and chemically) application at 1, 10 and 100 mg/L on the growth and physiology of an aquatic plant water hyacinth - Eichhornia crassipes (Mart) Solms. Chemically synthesized AgNPs have been found to reduce the growth of hyacinth, whereas biological AgNPs have not demonstrated this effect. AgNPs (10–30 nm) of 15 ml were daily supplied at different concentrations: 20, 40, 60, 80 and 100 ppm respectively. The results indicated that less concentration induced plantlets while higher concentration caused inhibition [33,34]. In a study, lotus was examined in the crops after 4 times treatments with AgNPs (4 mg/L): control, soil treatment before 5-days of planting with 4 mg/L (T1), treatments before planting with 4 mg/L (T2), and combined periodic foliar application, plant and soil treatments at 4 mg/L (T3). The different methods of AgNPs application induced leaf diameter, plant height, dry and fresh leaves weight, and some biochemical aspects [[64], [65], [66]]. AgNPs were synthesized using leaves extract of Coriandrum sativum and tested on Lupinus termis L at 0, 0.1, 0.3, and 0.5 mg/L for 10 days. The result evidenced that less concentration enhanced growth, while higher reduced the growth [67]. AgNPs at 0-, 10-, 20-, and 30-mM increased plant growth and maintained the ionic balance of cells (Na+, K+, and Na+/K+ ratio) by decreasing the uptake of Na and Cl and oxidative stress by salt-stressed plants. It also induced catalase activities, superoxide dismutase, and reduced peroxidase activity. Whereas the reduction of MDA and H2O2 contents was reported in plants under salt stress. The application of AgNPs in a dose-additive manner enhanced the yield, height, and photosynthesis pathway of the salt-stressed plants [68]. Moringa oleifera extract was employed in the production of AgNPs. The AgNPs application at 25, 50, 75, and 100 mg/L protected against heat stress, increased shoot length (22.2 and 26.1%), root length (5 and 5.4%), plant dry weight (0.36 and 0.60%), fresh plant weight (1.3 and 2%), and root number (6.6 and 7.5%) at 50 and 75 mg/L. AgNPs application at 50 and 75 mg/L have significantly induced leaf number (4 and 4.8%), leaf area (18.3 and 33.8%), dry leaf weight (0.06 and 0.18%), and fresh leaf weight (0.09 and 0.15 in over the respective value of control under heat stress [69]. The extract of pistachio seed coat waste was utilized to synthesize AgNPs. The solution of AgNPs at 75 mg/L was sprayed on egg plants which enhanced carotenoid/chlorophyll contents and plant growth. The addition of fly ash induced the plant growth. AgNPs were sprayed at 75 ppm of concentration on 20% fly ash amended soil which remarkably improved plant growth [70].

4.2. Negative effects on plant growth

The toxicity of AgNPs to plants in terrestrial ecosystems, notably crops, is concentration and size-dependent. It reduced germination and growth of seed and affected roots/shoots length and mass. Its accumulation in leaves and roots activates the defense mechanism at cellular/tissue levels and modifies proteomic expression, antioxidant activities, and metabolism. Botanical changes such as generation of reactive oxygen species, total chlorophyll, superoxide dismutase activities, increased level of H2O2, glutathione, carotenoid, ascorbate, proline contents, etc., that were either increased or decreased after exposure to AgNPs. These processes caused the suppression of photosynthesis/transition, irregular morphological modifications, and other symptoms [71]. AgNPs were synthesized using Aloe vera extract. AgNPs and AgNO3 at 40, 60-, 80-, 100-, and 120-mM reduced Brassica seedling growth due to a higher accumulation of AgNPs and AgNO3 and severely inhibited photosynthesis. Its interaction with the metabolism and growth of mustard seedlings has imposed mild stress conditions [72]. The treatment of AgNPs at 20, 200, and 2000 mg/kg on wheat (T. aestivum) resulted in less plant weight, shorter plant height, and lower biomass [73]. AgNPs were synthesized using the citrate reduction method and were stabilized with chitosan. A varied AgNPs concentration of 12.5, 25, 50, and 100 ppm was given to the Lactuca sativa L. (Asteraceae) seeds to assess the possible danger of AgNPs utilizing percentage of germinated seed and root morphological alteration as toxicity parameters. At a concentration of 100 ppm, there was a reduction in root growth compared to the positive control (distilled water) [74]. Citrate-coated AgNPs were synthesized and purified. The treatment of AgNPs at 1 mg/L reduced the biomass and height of Capsicum annuum [75]. The exogenous AgNPs application at 0.2 μg/L inhibited root hair development in Arabidopsis thaliana. AgNPs were synthesized and stabilized using PVP. The AgNPs at 100–900 μg/kg were used in the soil. The germination rate at 800 μg/kg in soil was reduced Vicia faba, R. leguminosarum bv. viciae growth and G. aggregatum [45,46]. The phototoxicity of AgNPs (10 nm) was evaluated to study hydroponic plant growth. Similarly, a higher concentration of Ag ions (2.5 mg/kg) decreased plant growth to the same extent as the AgNPs [[76], [77], [78]].

5. Applications of AgNPs in agriculture sector

Nanotechnology is the most advanced field in agriculture and is tremendous scientific interest globally. The definition of nanotechnology states that the nanoscale is the smallest particle ranging from 1 to 100 nm in size. The significance of metallic nanoparticles is very high in several fields. AgNPs have been a primary focus for researchers due to their unique biological, chemical, and physical properties. AgNPs are crucial in the bio-system that are well studied and utilized. It has a broad spectrum of anti-microbial activities and strong bactericidal/inhibitory effects. AgNPs are the most important in agriculture that involves in enhancing seeds germination and plant growth. Several applications of AgNPs including: Nano-pesticides, Nano-fertilizers, food packaging, pest management, crops, and food protection (nano-antibacterial, nano-antifungal, and nano-antiviral agents).

5.1. AgNPs as nano-pesticides

Pests are emerging threat to the agricultural sector, affecting crop yield, reducing crop quality, and applying synthetic pesticides to the soil and plants, negatively impacting the environment. Nano pesticide is a novel tool for controlling and managing pests with agricultural significance. AgNPs act as pesticides and reduce the pest burden on the crop. The most critical importance of nanocides (nanotechnology-based pesticides) is their eco-friendly relationship to the environment and minimal effect on non-targeted insects. It provides nutritional enrichment to the plants and protects against pests. Thus, constant usage of chemical fertilizer is reducing in conventional farming. It also eradicates harmful microorganisms in hydroponics systems and soil. The foliar spray application is beneficial in inhibiting rot, moulds, fungi, and numerous other microbial-associated plant diseases [79]. AgNPs were biologically synthesized from Ulva lactuca that have ability to reduce silver nitrate into AgNPs, and the formation of brown color confirms their presence in the solution. The anti-microbial activity of biologically synthesized pesticides showed their fight against fungi and bacteria, causing various crop diseases [80]. AgNPs of 50–100 nm was synthesized using Solanum lycopersicum. AgNPs application concentrations at 200, 300, 400, and 500 ppm were applied to M. rosae, and distilled water was used as a control. The mortality rate of AgNPs showed optimum efficacy at 500 ppm concentration. The mortality rate was associated with higher concentrations [81]. In a study, three types of AgNPs (10 nm) were used to check larvicidal potential on the survival of the sixteenth larval stage Tenebrio molitor. AgNPs and silicon dioxide microparticles revealed more than 70% insecticidal effects on larval viability [82]. PVP-coated-AgNPs of different concentrations were used against two lepidopteran pests of the Ricinus communis L. (castor plant), namely castor semilooper, Achaea janata L. Larvae and Asian armyworm, Spodoptera litura F. Electron microscopic studies have demonstrated that AgNPs easily penetrate the plant, insect cell, nucleus, or mitochondria. It can also be employed as a pesticide for targeted delivery (Fig. 1) [83].

Fig. 1.

Fig. 1

Silver nanoparticles incorporate with pesticides and form AgNPs based nano fertilizers that kill and reduce pest resistance.

5.2. AgNPs as nano-fertilizers

The utilization of AgNPs as a nano fertilizer are considered the most effective approach for adequately management of plant nutrient supply. Excessive fertilizers were lost in the field, that adversely affected the environment. Nanoparticles bind to the fertilizers and release the proper number of fertilizers to the plants. Thus, in this way, the excess usage of fertilizer is reduced in the field. AgNPs have demonstrated importance across various aspects of agriculture. The synthesis of nano fertilizers from extract of onions were found effective for tomato and brinjal plants. AgNPs act as nano fertilizers that slowly and effectively release nutrients to prevent the loss of nutrients. It helps the plant to enhance nutrients absorption from the soil [84]. The nano-biofertilizer reduces farm management costs, environmental pollution, and unnecessary chemical fertilizers in the field (Fig. 2) [85]. AgNPs were synthesized using the entomopathogenic fungi, Beauveria bassiana (Bb), and Metarhizium brunneum (Mb). The efficacy of Mb-synthesized and Bb-synthesized AgNPs were tested against Tetranychus urticae Koch (Acari: Tetranychidae); a two-spotted spider mite. The results revealed that both treatments were significantly virulent toward the newly emerged adult females of T. urticae [86]. Combining AgNPs with magnetic field showed the highest fruit yield (16.420-ton/ha) in muskmelon (Cucumis melo L.). The treatment of AgNPs showed 150% more fruit yield than the control [87]. In a study, AgNPs at 0, 25, 50, 75, 100, 125, and 150 ppm were used for various seedling varieties. The growth, yield, quality of NPK uptake, and nutrient efficiency was improved in wheat. Remarkable leaf growth and yield were observed at 25 ppm, while 75 ppm showed less yield of the wheat [88]. The aqueous root bark extract of Berberis lycium Royle was used to synthesize AgNPs. The impacts of AgNPs at 0, 30, 60, and 90 ppm were used to observe carbohydrate and protein contents of Pisum sativum L. seed. The highest carbohydrate and protein contents were recorded in harvested seeds [89].

Fig. 2.

Fig. 2

The foliar spray of AgNPs as nano-fertilizers enhances nutrient uptake and plant growth.

5.3. Utilization of AgNPs in insects/pest management

The nanoparticles incorporate into insects and rapidly control their progression. AgNPs is an effective agent for pest management with numerous properties including non-toxic, safe and improved pest control method. Nano-based pesticides efficiently provide a high and proper dose to the target plants [90]. The nanoscale application of agrochemicals has changed the traditional agro-practices in nano-formulations, nano-pesticides, nano-sensors, and nano-fertilizers [91]. Inorganic-based nano pesticides have been tested for stored-based insect/pest management. The plant-based nanoparticles are significant in controlling pests in stored grains. It is ecofriendly and easy way to develop as compared to chemical-based synthesis of the nano-pesticides [92]. AgNPs are used as carriers to deliver agrochemicals to the targeted site [93]. The mortality tests, repellent activity, antifeedant tests and ovipositional deterrency confirmed that the malathion-based AgNPs determine maximum pesticidal activity against Tribolium castaneum. Tribolium castaneum is a significant beetle that infests stored grains and shows resistance to commercial synthetic insecticides. AgNPs and malathion in different concentrations were added to the disk at 50 ppm, 75 ppm, and 100 ppm. The mortality of AgNPs and malathion at 75 ppm was 75% and 95%, respectively. Therefore, AgNPs have proven effective against pests and beetles [94]. AgNPs also act as bactericidal and larvicidal. The marine bacterium Shewanella algae bangaramma were used to synthesize AgNPs. The maximum LC50 and LC90 values with a 95% confidential limit (4.529 mg/mL (2.478–5.911), 9.580 mg/mL (7.528–14.541) were reported with III- instar larvae Burmeister (Lepidiota mansueta). The mortality of the larvae was enormously enhanced in exposed groups at all concentrations (p < 0.0001). The marine bacteria-mediated synthesis of AgNPs in a culture medium provides efficient antifouling and larvicidal activities [95]. Bacillus thuringiensis kurstaki (Btk), an entomopathogenic bacteria, was used to produce Btk-AgNPs. The insecticidal activity of Btk-based synthesized AgNPs was tested against larvae of Agrotis ipsilon (Hufnagel) and A. ipsilon (Hufnagel). The application of either Btk-synthesized AgNPs using Bt pellet or Btk-synthesized AgNPs made with Bt supernatant were highly virulent toward larvae of T. ni compared to Agrotis ipsilon [96]. AgNPs of 3–25 nm size were synthesized using entomopathogenic fungus B. bassiana from both isolates. There were two groups, i.e., 50% and 51–100% of 20 isolates. The maximum mortality was 64% in 90 isolates. Its potency against mustard aphid (L. erysimi) showed the potential of AgNPs to manage insects in agriculture [97]. AgNPs were synthesized using Leonotis nepetifolia. AgNPs exhibited possible antifeedant activity against the larvae of S. litura (78.77%) and H. armigera (82.16%). S. litura and H. armigera. AgNPs also showed a high larval mortality rate and maximum pupal mortality rate (78.49 and 72.70%) and (84.66 and 77.44%), respectively. The biosynthesized AgNPs were tested on mosquito larvae and recorded LC50 values were C. quinquefasciatus 35.48 ppm and A. aegypti 47.44 ppm. The production of AgNPs using L. nepetifolia is an environmentally favorable method for management of insect pests. The histological examinations confirmed that increasing nanomaterial resulted in severe tissue damage in the goblet and epithelial cells of the larval midgut region of H. armigera, S. litura, C. quinquefasciatus, and A. aegypti [98].

5.4. Utilization of AgNPs in food packaging

Nanotechnology used the tiniest particles, measuring one billionth of a meter which have already been used in food packaging, functional food ingredients, and food supplements. One of the fields where nanotechnology is predicted to play a key role in the future is food technology. Food additives (nano inside) and food packaging are the two most common forms of nanofood applications (nano outside). For example, nanoscale food additives can be used to influence product shelf life, texture, flavor, nutritional content, identify food pathogens, and serve as food quality indicators. Nanotechnologies are regarded to be effective in the context of food packaging for enhancing product shelf life, detecting rotten components, and generally improving product quality, such as by minimizing gas flow over product packaging [99]. The essential branch of agriculture in preserving agricultural products is post-harvest management. Nanotechnological packaging applications are; reduced hydrophilic characteristics, better biodegradability, and physical-chemical properties [100]. Active packages promote a new generation of food packaging obtained by incorporating metallic nanoparticles into polymer films. AgNPs combine with edible and non-degradable polymers for active food packaging [101]. Incorporating AgNPs with hydroxypropyl methylcellulose (HPMC) matrix applications provides the best packaging materials of food. Mechanical analyses and water vapor barrier properties of the HPMC/AgNPs nanocomposites showed the best result for films containing smaller size (41 nm) AgNPs. HPMC/AgNPs nanocomposites are used in active anti-microbial internal coating in food packages [102]. A solution-based casting method was used to fabricate a hybrid nanocomposite film that consists of AgNPs, polyethylene glycol, gelatin and chitosan.

Several film series were synthesized having different concentrations of AgNPs and chitosan. AgNPs were used to increase mechanical qualities while decreasing light transmission in the visible light spectrum. By using the hybrid film for packaging red grapes, the fruit shelf life was extended further two weeks [103]. A reduction method utilized an agent NaBH4 to synthesize CNF/AgNPs composite, which is used as an anti-microbial material in active food packaging systems [104]. Low-density polyethylene films (LDPE) with AgNPs have the potential to greatly improve the safety, and quality of packaged food. In addition, it improve the antimicrobial properties and extending its shelf life [105]. CNC/AgNPs and CMC/AgNPs were developed for paper coating. This packaging of strawberries extends shelf-life to 7 days under ambient conditions [106]. Using rapid biological methods AgNPs were synthesized by utilizing leaf broth of Capparis zeylanica, that enhanced the stability of the PVA/PEG polymer. The thin-film composite displayed outstanding characteristics in every aspect, enabling it for food packaging and biomedical applications [107]. AgNPs combination with low-density polyethylene films at 1.50, 3.75, 7.50, 15.00, 30.00, 60.00, and 75.00 μg/mL have shown anti-microbial properties against microorganisms. It would be the most effective tool for improving food safety and quality [108].

5.5. Applications of AgNPs in crops and foods protection

Healthy plants are most important for animal and people health, but they often receive less emphasis and attention in health literature. Plants are the most important source of nutrition for cattle and provide more than 80% of human food. Pest infestation and plant diseases threaten plant availability and safety of human and animal consumption. Globally, losses of critical staple crops make up 30%, and billions of dollars were lost in the production of food [109]. Nanotechnology is the most effective and safe technique, providing healthier food and enhancing precision farming [110]. They can eliminate target microbes from hydroponics, soil, and plants by protecting plants in various ways, such as acting as nano-antiviral, antibacterial, and nano-antifungal.

5.5.1. AgNPs as nano-antibacterial agents

AgNPs have versatile applications such as biosensors, antioxidants, and heavy metal detection [111]. They have unique physicochemical properties, including high surface reactivity, binding capabilities with biological molecules, large surface area to volume ratio, ease of characterization, and synthesis. AgNPs can also enhance the expression of genes in redox processes. These properties allow us to use AgNPs as anti-microbial agents against the pathogenic disease of plants and other foodborne infections [112]. AgNPs affect bacterial communities in numerous agricultural soil, either harmful or advantageous to plants and the environment [113]. The antiviral and antibacterial activities of the silver ions (Ag+) could be increased to one thousand-fold when the carbonate ions concentration is less than drinking water norms [114]. AgNPs were synthesized using S. orvum based fruit extracts. The GO-Ag nanocomposite was prepared and applied to both S. aureus ATCC 6538 and E. coli ATCC 25922 by plate count and disk diffusion methods, which showed excessive antibacterial activity [115]. AgNPs were synthesized using Ziziphus joazeiro leaf extracts. Particles with less aggregation degree and smaller size were obtained in neutral conditions (pH-7) and exhibited antibacterial activities against S. aureus and E. coli [116]. AgNPs were synthesized using fruit extract of Solanum torvum which showed minimum inhibitory concentrations against bacterial plant pathogens Xanthomonas axonopodis pv. punicae (6.25 μg/mL) and Ralstonia solanacearum (12.5 μg/mL). The inhibition zones in vitro disk-diffusion assay is R. solanacearum (11.4 ± 1 mm) and X. axonopodis pv. punicae (18.1 ± 1 mm) after AgNPs application at 50 μg/mL [117]. Silver nitrate (AgNO3), sodium borohydride (NaBH4) and 1% sodium citrate dihydrate were used to synthesize AgNPs. The phytopathogenic fungi (Ralstonia solanacearum) cause severe bacterial wilt in tobacco. It has determined the bactericidal and bacteriostatic activity of surfactant-stabilized and pure AgNPs. Surfactants had varying effects on the antibacterial activity of AgNPs against R. solanacearum [118]. Fig. 3 illustrates the antibacterial mechanism of AgNPs.

Fig. 3.

Fig. 3

Antibacterial mechanism of AgNPs.

5.5.2. AgNPs as nano-antifungal agents

AgNPs are efficient and fast-acting fungicides against broad-spectrum fungal strain like Saccharomyces, Aspergillus and Candida. The extracted AgNPs using bovine mastitis with a diameter 13.5 ± 2.6 nm are considered most potent against yeast [119]. An efficient concentration of AgNPs inhibits 50% (EC50) of colony formation in B. sorokiniana than for M. grisea. Nanoparticles and silver ions stimulate the spores colony formation and plant-pathogenic fungi-related disease [120]. Stock AgNPs solution at 4000 ppm concentration was obtained from Nanocid Company. AgNPs were used with potato dextrose agar medium to grow fungal isolates in vitro. AgNPs at 6, 8, 10, 12, 14, and 16 ppm were used on five phytopathogenic fungi. The radial fungal growth was noted after 1, 2, 3, 5, and 10 days, and further calculated inhibition rates of mycelial growth. The experimental greenhouse results has revealed that treatments with fungicide and AgNPs provide a better yield than the positive control [121]. Cassia roxburghii aqueous leaf extract was used to synthesize AgNPs. The phytogenic AgNPs were utilized to combat several plant pathogenic fungus, which showed antifungal activity against Curvularia sp., Fusarium oxysporum, and Rhizoctonia solani [122]. Aldehyde-modified sodium alginate (ASA) was used to synthesize AgNPs. The antifungal activity of AgNPs primarily alters the cell membrane permeability, affects the soluble protein synthesis, destroys DNA structure, and inhibits DNA replication. It has not shown any inhibition in N. benthamiana and rice seed germination [123]. AgNPs at temperature of 95 °C were synthesized by using a chitosan-reducing agent. The chitosan-AgNPs based-composite showed remarkably higher antifungal activity against Colletotrichum gloeosporioides [124]. AgNPs were synthesized by using leaf extract of Amaranthus retroflexus. AgNPs at 50, 100, 200, and 400 μg/mL were applied to the human pathogenic fungi, mushroom, and plant growth. The minimum inhibitory concentrations (MIC50) of 50% were observed against Fusarium oxysporum (328.05 ± 13.29), Alternaria alternata (337.09 ± 19.72), and Macrophomina phaseolina (159.80 ± 14.49) μg/mL [125]. AgNPs (WA-CV-WA13B, WA-AT-WB13R, and WA-PR-WB13R) were obtained from Bio Plus Co. (Pohang, Korea). Various concentrations (10, 25, 50, and 100 ppm) were used against eighteen plant pathogenic fungi. Maximum inhibition was recorded using CV-WB13R AgNPs and at 100pm treatments [126]. AgNPs were synthesized chemically (AgNO3) and biologically (fresh plant leaves). The anti-microbial potential of AgNPs was evaluated, which showed different inhibition against three plant pathogenic fungi; Alternaria solani and Fusarium spp. (100%) and Corynespora cassiicola (85%) at 100 ppm [127].

5.5.3. AgNPs as nano-antiviral agents

Several studies exhibited that metal-based nanoparticles such as Ag, Au, Cu, Fe, etc., showed broad-spectrum antiviral activities, which enable them to use broadly in the disinfection of air/water and medicines. The metal-based nanoparticles that inactivate the virus may have an essential role before and after the entry of the virus into the host cells. The virus absorption occurs on the surface of metal and their glycoproteins moiety interact with the metal particles by making them inactive. It may also penetrate cells and interact with viral nucleic acids, inhibiting their antiviral potential [[128], [129], [130], [131]]. The adsorption effect of AgNPs is high in the virus that interacts either with the surface protein or viral envelope, affecting the virus and cell receptor interaction and preventing the virus attack on the cell. The combination of AgNPs with the virus causes the release of Ag ions. It inactivates them by reacting with a viral protein or viral nucleic acids to inhibit the replication of viruses. AgNPs surface activates the oxygen and synthesizes Reactive Oxygen Species (ROS). It oxidizes the virus by damaging its structure (Fig. 4) [[98], [99], [100]]. The bacterial strains such as Bacillus persicus, Bacillus pumilus and Bacillus licheniformis were used to synthesize AgNPs (77–92 nm). B. licheniformis has been demonstrated to be effective against both the Bean Yellow Mosaic Virus and as well as human pathogen [132]. By reducing silver nitrate; AgNPs were synthesized. AgNPs have been conducted on viricidal activities and deactivated Bean yellow mosaic virus (BYMV). The disease was inhibited at 100 mg/L, while the AgNPs ultimately arrested the virus infection at 200 mg/L [133]. AgNPs were obtained from Sigma company in a liquid form. AgNPs were sprayed on banana plants infected with BBTV (Banana bunchy top virus) at three different concentrations (40, 50, and 60 ppm). The infection rate was 36%, and the genomic DNA level changed after 50 ppm of treatment. The result showed that AgNPs could be used in the future against plant viruses [134]. Silver nitrate was used as reducing agent to synthesize AgNPs. Five different concentrations of antiviral drug (25, 50, 100, 150, and 200 ppm) were used to diminish TSWV infection on Ch. amaranticolor and potato plants. All concentrations showed inhibitory effects, but strong inhibitory effects (90.4%) at 200 ppm were recorded against Tomato spotted wilt virus. However, a similar concentration also showed an inhibitory effect of 87.5% against Tomato spotted wilt virus (TSWV) systemically infected potato seedlings [135]. AgNPs were synthesized and bio-fabricated using Pseudomonas fluorescens CZ strain fermentative broth. AgNPs of 100 μl was applied to the leaf for 24 h and mixed with tobacco mosaic virus (TMV). AgNPs were shown to be highly effective against the infection of RNA-based plant viruses [136]. AgNPs were obtained from Sigma in a liquid form. AgNPs were sprayed at concentrations such as 50, 60, and 70 ppm for 7 days period. The results indicated that 50 ppm treatment reduced the relative concentration of both viruses and the severity of diseases [137].

Fig. 4.

Fig. 4

AgNPs act as nano-antibacterial, nano-antiviral, and nano-antifungal agents.

6. Conclusions

The current review findings depicted that AgNPs have a crucial role in increasing agricultural productivity, seeds and growth of the plant. The most convenient application of AgNPs is that they act like fertilizers that reduce nutrient loss and control plant infections, similar to pesticides, which might enhance plant productivity. They also significantly improve soil quality by improving the nutrient supply and removing soil containments. AgNPs also enhance the water supply and provide essential nutrients properly to the plant. AgNPs have diverse applications in different fields, especially in agriculture. They also act as nano-fertilizers and nano-pesticides, reducing salt stress and improving the plant’s production. AgNPs protect plants against harmful bacteria, fungi, and viruses by acting as nano-bacterial, nan-fungal, and nano-antiviral. Similarly, they also provide support for food packaging, which protects food from gases (CO2, O2), light, dust, moisture, and pathogens. Therefore, it can be concluded that AgNPs should be utilized in agriculture sector to promote plant growth and increase productivity of crops.

7. Future perspective

Nanotechnology is a new field of study that investigates the unique physicochemical features of the nanoparticles and their applications in various fields such as agriculture. AgNPs are used widely for their applications in agriculture sector. They promote plant growth as they are used as nano-fertilizers, also these nanoparticles are utilized as nano-pesticides by controlling different insects and pests that attack on plants. Furthermore, they are also used as nano-bacterial, nan-fungal, and nano-antiviral agents against various microbes that cause diseases in plants. In agriculture sector low yield and crops diseases are significant issues which are under consideration, therefore researchers should work in this field to explore the efficacy of AgNPs in plant growth and agriculture. The impacts of ecofriendly and bio-based AgNPs should be tested on different plants and agriculture crops. Further research work is needed to overcome the problems of low yield and control plants diseases by the utilization of biosynthesized AgNPs and other less toxic metals.

Author contribution statement

All authors listed have significantly contributed to the development and the writing of this article.

Data availability statement

No data was used for the research described in the article.

Additional information

No additional information is available for this paper.

Declaration of competing interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper

Contributor Information

Sajad Khan, Email: dir.sajad@gmail.com.

Muhammad Zahoor, Email: mohammadzahoorus@yahoo.com.

Raham Sher Khan, Email: rahamsher@awkum.edu.pk.

Muhammad Ikram, Email: ikrambiochem2014@gmail.com.

Noor Ul Islam, Email: nooruomchem@gmail.com.

Abbreviations

AgNPs

Silver nanoparticles

Btk

Bacillus thuringiensis kurstaki

BYMV

Bean yellow mosaic virus

BBTV

Banana bunchy top virus

CNF

Cellulose nanofibril

DNA

Deoxyribonucleic acid

E.N.M. s

Engineered nanomaterials

Ga

Gum Arabic

gp

Germination percentage

GO

Graphene oxide

GPOX

Glutathione peroxidase

IAA

Indole acetic acid

LC

Lethal concentration

mL

Milliliter

mg

Milligram

nm

Nanometer

GNPs

Green Nanoparticles

NPK

Nitrogen Phosphorous Potassium

Ppm

Parts per million

PVP

Polyvinylpyrrolidone

ROS

Reactive oxygen species

SVI

Seedling vigor index

TSWV

Tomato spotted wilt virus

mg

Microgram

VI

Vigour index

LDPE

low-density polyethylene

References

  • 1.Kaegi R., Sinnet B., Zuleeg S., Hagendorfer H., Mueller E., Vonbank R., Boller M., Burkhardt M. Release of silver nanoparticles from outdoor facades. Environ. Pollut. 2010;158:2900–2905. doi: 10.1016/J.ENVPOL.2010.06.009. [DOI] [PubMed] [Google Scholar]
  • 2.Parisi C., Vigani M., Rodríguez-Cerezo E. Agricultural nanotechnologies: what are the current possibilities? Nano Today. 2015;10:124–127. doi: 10.1016/j.nantod.2014.09.009. [DOI] [Google Scholar]
  • 3.Mahakham W., Theerakulpisut P., Maensiri S., Phumying S., Sarmah A.K. Environmentally benign synthesis of phytochemicals-capped gold nanoparticles as nanopriming agent for promoting maize seed germination. Sci. Total Environ. 2016;573:1089–1102. doi: 10.1016/j.scitotenv.2016.08.120. [DOI] [PubMed] [Google Scholar]
  • 4.Khan M.M., Kalathil S., Lee J., Cho M.H. Synthesis of cysteine capped silver nanoparticles by electrochemically active biofilm and their antibacterial activities. Bull. Kor. Chem. Soc. 2012;33:2592–2596. doi: 10.5012/bkcs.2012.33.8.2592. [DOI] [Google Scholar]
  • 5.Khan A.U., Malik N., Khan M., Cho M.H., Khan M.M. Fungi-assisted silver nanoparticle synthesis and their applications. Bioproc. Biosyst. Eng. 2018;41:1–20. doi: 10.1007/s00449-017-1846-3. [DOI] [PubMed] [Google Scholar]
  • 6.Khan A.U., Khan M., Khan M.M. Antifungal and antibacterial assay by silver nanoparticles synthesized from aqueous leaf extract of Trigonella foenum-graecum. Bionanoscience. 2019;9:597–602. doi: 10.1007/s12668-019-00643-x. [DOI] [Google Scholar]
  • 7.Javaid A., Oloketuyi S.F., Khan M.M., Khan F. Diversity of bacterial synthesis of silver nanoparticles. Bionanoscience. 2018;8:43–59. doi: 10.1007/s12668-017-0496-x. [DOI] [Google Scholar]
  • 8.Mahendran D., Geetha N., Venkatachalam P. Springer Singapore; 2019. Role of silver nitrate and silver nanoparticles on tissue culture medium and enhanced the plant growth and development; pp. 59–74. (Vitr. Plant Breed. Towar. Nov. Agron. Trait. Biot. Abiotic Stress Toler.). [DOI] [Google Scholar]
  • 9.Salama D.M., Abd El-Aziz M.E., Osman S.A., Abd Elwahed M.S.A., Shaaban E.A. Foliar spraying of MnO2-NPs and its effect on vegetative growth, production, genomic stability, and chemical quality of the common dry bean. Arab J. Basic Appl. Sci. 2022;29:26–39. doi: 10.1080/25765299.2022.2032921. [DOI] [Google Scholar]
  • 10.Sadak M.S. Impact of silver nanoparticles on plant growth, some biochemical aspects, and yield of fenugreek plant (Trigonella foenum-graecum) Bull. Natl. Res. Cent. 2019;43:1–6. doi: 10.1186/S42269-019-0077-Y. [DOI] [Google Scholar]
  • 11.Salama D.M., Abd El-Aziz M.E., Shaaban E.A., Osman S.A., Abd El-Wahed M.S. The impact of nanofertilizer on agro-morphological criteria, yield, and genomic stability of common bean (Phaseolus vulgaris L.) Sci. Rep. 2022;12:1–15. doi: 10.1038/s41598-022-21834-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Arnott A., Galagedara L., Thomas R., Cheema M., Sobze J.M. The potential of rock dust nanoparticles to improve seed germination and seedling vigor of native species: a review. Sci. Total Environ. 2021;775 doi: 10.1016/j.scitotenv.2021.145139. [DOI] [Google Scholar]
  • 13.Salama D.M., Abd El-Aziz M.E., Rizk F.A., Abd Elwahed M.S.A. Applications of nanotechnology on vegetable crops. Chemosphere. 2021;266 doi: 10.1016/j.chemosphere.2020.129026. [DOI] [PubMed] [Google Scholar]
  • 14.Geisler-Lee J., Wang Q., Yao Y., Zhang W., Geisler M., Li K., Huang Y., Chen Y., Kolmakov A., Ma X. Phytotoxicity, accumulation and transport of silver nanoparticles by Arabidopsis thaliana. Nanotoxicology. 2013;7:323–337. doi: 10.3109/17435390.2012.658094. [DOI] [PubMed] [Google Scholar]
  • 15.Abd El-Aziz M.E., Salama D.M., Morsi S.M.M., Youssef A.M., El-Sakhawy M. Development of polymer composites and encapsulation technology for slow-release fertilizers. Rev. Chem. Eng. 2022;38:603–616. doi: 10.1515/revce-2020-0044. [DOI] [Google Scholar]
  • 16.Research of the effect of nanometer materials on germination and growth enhancement of Glycine max and its mechanism - Abstract - Europe PMC. https://europepmc.org/article/cba/371541 (n.d.) (accessed April 14, 2022)
  • 17.Zuverza-Mena N., Armendariz R., Peralta-Videa J.R., Gardea-Torresdey J.L. Effects of silver nanoparticles on radish sprouts: root growth reduction and modifications in the nutritional value. Front. Plant Sci. 2016;7:90. doi: 10.3389/fpls.2016.00090. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Sharif Mughal S., Mona Hassan S. Comparative study of AgO nanoparticles synthesize via biological, chemical and physical methods: a review. Am. J. Mater. Synth. Process. 2022;7:15–28. http://article.ajmsp.net/pdf/10.11648.j.ajmsp.20220702.11.pdf (accessed February 7, 2023) [Google Scholar]
  • 19.Iravani S., Korbekandi H., Mirmohammadi S.V., Zolfaghari B. Synthesis of silver nanoparticles: chemical, physical and biological methods. Res. Pharm. Sci. 2014;9:385–406. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326978/ (accessed February 7, 2023) [PMC free article] [PubMed] [Google Scholar]
  • 20.Iacono S.T., Jennings A.R. Recent studies on fluorinated silica nanometer-sized particles. Nanomaterials. 2019;9 doi: 10.3390/nano9050684. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Hwang J.S., Park J.E., Kim G.W., Nam H., Yu S., Jeon J.S., Kim S., Lee H., Yang M. Recycling silver nanoparticle debris from laser ablation of silver nanowire in liquid media toward minimum material waste. Sci. Rep. 2021;11:1–11. doi: 10.1038/s41598-021-81692-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Chugh H., Sood D., Chandra I., Tomar V., Dhawan G., Chandra R. Role of gold and silver nanoparticles in cancer nano-medicine, Artif. Cells. Nanomedicine Biotechnol. 2018;46:1210–1220. doi: 10.1080/21691401.2018.1449118. [DOI] [PubMed] [Google Scholar]
  • 23.Scaiano J.C., Billone P., Gonzalez C.M., Maretti L., Marin M.L., McGilvray K.L., Yuan N. Photochemical routes to silver and gold nanoparticles. Pure Appl. Chem. 2009:635–647. doi: 10.1351/PAC-CON-08-09-11. [DOI] [Google Scholar]
  • 24.dos Santos M.A., Paterno L.G., Moreira S.G.C., Sales M.J.A. Original photochemical synthesis of Ag nanoparticles mediated by potato starch. SN Appl. Sci. 2019;1 doi: 10.1007/s42452-019-0586-1. [DOI] [Google Scholar]
  • 25.El-Sheikh M.A. A novel photosynthesis of carboxymethyl starch-stabilized silver nanoparticles. Sci. World J. 2014;2014 doi: 10.1155/2014/514563. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Mathew S., Prakash A., Radhakrishnan E.K. Sunlight mediated rapid synthesis of small size range silver nanoparticles using Zingiber officinale rhizome extract and its antibacterial activity analysis. Inorg. Nano-Metal Chem. 2018;48:139–145. doi: 10.1080/24701556.2017.1373295. [DOI] [Google Scholar]
  • 27.Zare-Bidaki M., Mohammadparast-Tabas P., Peyghambari Y., Chamani E., Siami-Aliabad M., Mortazavi-Derazkola S. Photochemical synthesis of metallic silver nanoparticles using Pistacia khinjuk leaves extract (PKL@AgNPs) and their applications as an alternative catalytic, antioxidant, antibacterial, and anticancer agents. Appl. Organomet. Chem. 2022;36:e6478. doi: 10.1002/aoc.6478. [DOI] [Google Scholar]
  • 28.Yaqoob A.A., Umar K., Ibrahim M.N.M. Silver nanoparticles: various methods of synthesis, size affecting factors and their potential applications–a review. Appl. Nanosci. 2020;10:1369–1378. doi: 10.1007/s13204-020-01318-w. [DOI] [Google Scholar]
  • 29.Arokiyaraj S., Vincent S., Saravanan M., Lee Y., Oh Y.K., Kim K.H. Green synthesis of silver nanoparticles using Rheum palmatum root extract and their antibacterial activity against Staphylococcus aureus and Pseudomonas aeruginosa, Artif. Cells. Nanomedicine Biotechnol. 2017;45:372–379. doi: 10.3109/21691401.2016.1160403. [DOI] [PubMed] [Google Scholar]
  • 30.Patra S., Mukherjee S., Barui A.K., Ganguly A., Sreedhar B., Patra C.R. Green synthesis, characterization of gold and silver nanoparticles and their potential application for cancer therapeutics. Mater. Sci. Eng., C. 2015;53:298–309. doi: 10.1016/j.msec.2015.04.048. [DOI] [PubMed] [Google Scholar]
  • 31.Abou El-Nour K.M.M., Eftaiha A., Al-Warthan A., Ammar R.A.A. Synthesis and applications of silver nanoparticles. Arab. J. Chem. 2010;3:135–140. doi: 10.1016/j.arabjc.2010.04.008. [DOI] [Google Scholar]
  • 32.Mukherjee P., Ahmad A., Mandal D., Senapati S., Sainkar S.R., Khan M.I., Parishcha R., Ajaykumar P.V., Alam M., Kumar R., Sastry M. Fungus-mediated synthesis of silver nanoparticles and their immobilization in the mycelial matrix: a novel biological approach to nanoparticle synthesis. Nano Lett. 2001;1:515–519. doi: 10.1021/nl0155274. [DOI] [Google Scholar]
  • 33.Khatami M., Sharifi I., Nobre M.A.L., Zafarnia N., Aflatoonian M.R. Waste-grass-mediated green synthesis of silver nanoparticles and evaluation of their anticancer, antifungal and antibacterial activity. Green Chem. Lett. Rev. 2018;11:125–134. doi: 10.1080/17518253.2018.1444797. [DOI] [Google Scholar]
  • 34.Mandal D., Bolander M.E., Mukhopadhyay D., Sarkar G., Mukherjee P. The use of microorganisms for the formation of metal nanoparticles and their application. Appl. Microbiol. Biotechnol. 2006;69:485–492. doi: 10.1007/s00253-005-0179-3. [DOI] [PubMed] [Google Scholar]
  • 35.Slepička P., Kasálková N.S., Siegel J., Kolská Z., Švorčík V. Methods of gold and silver nanoparticles preparation. Materials. 2020;13:1. doi: 10.3390/ma13010001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Jiang Z., Li L., Huang H., He W., Ming W. Progress in laser ablation and biological synthesis processes: “Top-Down” and “Bottom-Up” approaches for the green synthesis of Au/Ag nanoparticles. Int. J. Mol. Sci. 2022;23 doi: 10.3390/ijms232314658. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Küünal S., Visnapuu M., Volubujeva O., Soares Rosario M., Rauwel P., Rauwel E. Optimisation of plant mediated synthesis of silver nanoparticles by common weed Plantago major and their antimicrobial properties. IOP Conf. Ser. Mater. Sci. Eng. 2019 doi: 10.1088/1757-899X/613/1/012003. [DOI] [Google Scholar]
  • 38.Mohamed S., Hashim S.N., Rahman H.A. Seaweeds: a sustainable functional food for complementary and alternative therapy. Trends Food Sci. Technol. 2012;23:83–96. doi: 10.1016/j.tifs.2011.09.001. [DOI] [Google Scholar]
  • 39.Mahdavi M., Namvar F., Bin Ahmad M., Mohamad R. Green biosynthesis and characterization of magnetic iron oxide (Fe 3O4) nanoparticles using seaweed (Sargassum muticum) aqueous extract. Molecules. 2013;18:5954–5964. doi: 10.3390/molecules18055954. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Acharya P., Jayaprakasha G.K., Crosby K.M., Jifon J.L., Patil B.S. Nanoparticle-mediated seed priming improves germination, growth, yield, and quality of watermelons (Citrullus lanatus) at multi-locations in Texas. Sci. Rep. 2020;10 doi: 10.1038/s41598-020-61696-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Mahakham W., Sarmah A.K., Maensiri S., Theerakulpisut P. Nanopriming technology for enhancing germination and starch metabolism of aged rice seeds using phytosynthesized silver nanoparticles. Sci. Rep. 2017;7:1–21. doi: 10.1038/s41598-017-08669-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Sable S.V., Ranade S., Joshi S. Role of AgNPs in the enhancement of seed germination and its effect on plumule and radicle length of Pennisetum glaucum. IET Nanobiotechnol. 2018;12:922–926. doi: 10.1049/iet-nbt.2017.0304. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Hojjat S.S. The Effect of silver nanoparticle on lentil Seed Germination under drought stress. Int. J. Farming Allied Sci. 2016:208–212. www.ijfas.com (accessed April 13, 2022) [Google Scholar]
  • 44.Yin L., Colman B.P., McGill B.M., Wright J.P., Bernhardt E.S. Effects of silver nanoparticle exposure on germination and early growth of eleven Wetland plants. PLoS One. 2012;7 doi: 10.1371/journal.pone.0047674. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Sabir S., Arshad M., Satti S.H. Effect of green synthesized silver nanoparticles on seed germination and seedling growth in wheat. Int. J. Agric. Biosyst. Eng. 2018;12:14–16. https://innspub.net/ijaar/effect-green-synthesized-silver-nanoparticles-seed-germination-seedling-growth-wheat/ (accessed April 15, 2022) [Google Scholar]
  • 46.Khalaki M.A., Ghorbani A., Moameri M. Effects of silica and silver nanoparticles on seed germination traits of Thymus kotschyanus in laboratory conditions. J. Rangel. Sci. 2016;6:221–231. http://www.rangeland.ir/index.php/2-volume-1/article_523964.html (accessed April 15, 2022) [Google Scholar]
  • 47.Hojjat S.S., Kamyab M. The effect of silver nanoparticle on Fenugreek seed germination under salinity levels. Russ. Agric. Sci. 2017;43:61–65. doi: 10.3103/s1068367417010189. [DOI] [Google Scholar]
  • 48.Almutairi Z., Alharbi A. Effect of silver nanoparticles on seed germination of crop plants. J. Adv. Agric. 2015;4:280–285. doi: 10.24297/jaa.v4i1.4295. [DOI] [Google Scholar]
  • 49.Asanova A.A., Yashin S.E., V Trofimova T., Polonskiy V.I. Application of silver nanoparticles to improve wheat seedlings growth. IOP Conf. Ser. Earth Environ. Sci. 2019 doi: 10.1088/1755-1315/315/5/052041. [DOI] [Google Scholar]
  • 50.Pandey C., Khan E., Mishra A., Sardar M., Gupta M. Silver nanoparticles and its effect on seed germination and physiology in Brassica juncea L. (Indian mustard) plant. Adv. Sci. Lett. 2014;20:1673–1676. doi: 10.1166/asl.2014.5518. [DOI] [Google Scholar]
  • 51.Nejatzadeh F. Effect of silver nanoparticles on salt tolerance of Satureja hortensis l. during in vitro and in vivo germination tests. Heliyon. 2021;7 doi: 10.1016/j.heliyon.2021.e05981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Khan I., Raza M.A., Awan S.A., Khalid M.H.B., Raja N.I., Min S., Zhang A., Naeem M., Meraj T.A., Iqbal N., Zhang X., Huang L. In vitro effect of metallic silver nanoparticles (AgNPs): a novel approach toward the feasible production of biomass and natural antioxidants in pearl millet (Pennisetum glaucum L.) Appl. Ecol. Environ. Res. 2019;17:12877–12892. doi: 10.15666/aeer/1706_1287712892. [DOI] [Google Scholar]
  • 53.Khan S., Khan R.S., Zahoor M., khan Sikandar, Islam N.U., Khan T., Muhammad Z., Ullah R., Bari A. Alnus nitida and urea-doped Alnus nitida-based silver nanoparticles synthesis, characterization, their effects on the biomass and elicitation of secondary metabolites in wheat seeds under in vitro conditions. Heliyon. 2023;9 doi: 10.1016/j.heliyon.2023.e14579. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Mazumdar H., Ahmed G.U. Synthesis of silver nanoparticles and its adverse effect on seed germinations in oryza sativa, vigna radiata and BRASSICA campestris. Int. J. Adv. Biotechnol. Res. 2011;2:404–413. http://www.bipublication.com (accessed April 24, 2022) [Google Scholar]
  • 55.El-Temsah Y.S., Joner E.J. Impact of Fe and Ag nanoparticles on seed germination and differences in bioavailability during exposure in aqueous suspension and soil. Environ. Toxicol. 2012;27:42–49. doi: 10.1002/tox.20610. [DOI] [PubMed] [Google Scholar]
  • 56.Abdullah E.R.E.N. Biyolojik Olarak Sentezlenen Gümüş Nanopartiküllerin Buğday (Triticum aestivum L.) Tohumlarının Çimlenmesine Etkisi. ISPEC J. Agric. Sci. 2020;4:358–365. doi: 10.46291/ispecjasvol4iss2pp223-230. [DOI] [Google Scholar]
  • 57.Geisler-Lee J., Brooks M., Gerfen J.R., Wang Q., Fotis C., Sparer A., Ma X., Berg R.H., Geisler M. Reproductive toxicity and life history study of silver nanoparticle effect, uptake and transport in arabidopsis thaliana. Nanomaterials. 2014;4:301–318. doi: 10.3390/nano4020301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Guzmán-Báez G.A., Trejo-Téllez L.I., Ramírez-Olvera S.M., Salinas-Ruíz J., Bello-Bello J.J., Alcántar-González G., Hidalgo-Contreras J.V., Gómez-Merino F.C. Silver nanoparticles increase nitrogen, phosphorus, and potassium concentrations in leaves and stimulate root length and number of roots in tomato seedlings in a hormetic manner. Dose Response. 2021;19:1–15. doi: 10.1177/15593258211044576. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Mirzajani F., Askari H., Hamzelou S., Farzaneh M., Ghassempour A. Effect of silver nanoparticles on Oryza sativa L. And its rhizosphere bacteria. Ecotoxicol. Environ. Saf. 2013;88:48–54. doi: 10.1016/j.ecoenv.2012.10.018. [DOI] [PubMed] [Google Scholar]
  • 60.Tymoszuk A. Silver nanoparticles effects on in vitro germination, growth, and biochemical activity of tomato, radish, and kale seedlings. Materials. 2021;14:5340. doi: 10.3390/ma14185340. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Pallavi, Mehta C.M., Srivastava R., Arora S., Sharma A.K. Impact assessment of silver nanoparticles on plant growth and soil bacterial diversity. 3 Biotech. 2016;6 doi: 10.1007/s13205-016-0567-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Tomacheski D., Pittol M., Simões D.N., Ribeiro V.F., Santana R.M.C. Impact of silver ions and silver nanoparticles on the plant growth and soil microorganisms. Glob. J. Environ. Sci. Manag. 2017;3:341–350. doi: 10.22034/gjesm.2017.03.04.001. [DOI] [Google Scholar]
  • 63.Sharma P., Bhatt D., Zaidi M.G.H., Saradhi P.P., Khanna P.K., Arora S. Silver nanoparticle-mediated enhancement in growth and Antioxidant Status of Brassica juncea. Appl. Biochem. Biotechnol. 2012;167:2225–2233. doi: 10.1007/s12010-012-9759-8. [DOI] [PubMed] [Google Scholar]
  • 64.Rani P.U., Yasur J., Loke K.S., Dutta D. Effect of synthetic and biosynthesized silver nanoparticles on growth, physiology and oxidative stress of water hyacinth: Eichhornia crassipes (Mart) Solms. Acta Physiol. Plant. 2016;38:1–9. doi: 10.1007/s11738-016-2074-1. [DOI] [Google Scholar]
  • 65.Zea L., Salama H.M.H. Effects of silver nanoparticles in some crop plants , Common bean (Phaseolus vulgaris L.) and corn. Int. Res. J. Bacteriol. 2012;3:190–197. http://www.interesjournals.org/IRJOB (accessed April 25, 2022) [Google Scholar]
  • 66.Q. Yang, K.-C. Yung, K. Eisawi, M. Tash, W. Khalifa, N. Quang, H. Vu, T. Hoang, H. Kim, H.T. Quang, Effects of different treatments of silver nanoparticles (AgNPs) on the growth & physiological characteristics of lotus (Nelumbo nucifera), Iopscience.Iop.Org. (n.d.). 10.1088/1755-1315/947/1/012038. [DOI]
  • 67.Al-Huqail A.A., Hatata M.M., AL-Huqail A.A., Ibrahim M.M. Preparation, characterization of silver phyto nanoparticles and their impact on growth potential of Lupinus termis L. seedlings. Saudi J. Biol. Sci. 2018;25:313–319. doi: 10.1016/j.sjbs.2017.08.013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Khan I., Awan S.A., Raza M.A., Rizwan M., Tariq R., Ali S., Huang L. Silver nanoparticles improved the plant growth and reduced the sodium and chlorine accumulation in pearl millet: a life cycle study. Environ. Sci. Pollut. Res. 2021;28:13712–13724. doi: 10.1007/s11356-020-11612-3. [DOI] [PubMed] [Google Scholar]
  • 69.Iqbal M., Raja N.I., Mashwani Z.U.R., Hussain M., Ejaz M., Yasmeen F. Effect of silver nanoparticles on growth of wheat under heat stress, Iran. J. Sci. Technol. Trans. A Sci. 2019;43:387–395. doi: 10.1007/s40995-017-0417-4. [DOI] [Google Scholar]
  • 70.Khan M., Khan A.U., Moon I.S., Felimban R., Alserihi R., Alsanie W.F., Alam M. Synthesis of biogenic silver nanoparticles from the seed coat waste of pistachio (Pistacia vera) and their effect on the growth of eggplant. Nanotechnol. Rev. 2021;10:1789–1800. doi: 10.1515/ntrev-2021-0107. [DOI] [Google Scholar]
  • 71.Budhani S., Egboluche N.P., Arslan Z., Yu H., Deng H. Phytotoxic effect of silver nanoparticles on seed germination and growth of terrestrial plants. J. Environ. Sci. Health Part C Environ. Carcinog. Ecotoxicol. Rev. 2019;37:330–355. doi: 10.1080/10590501.2019.1676600. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Vishwakarma K., Shweta, Upadhyay N., Singh J., Liu S., Singh V.P., Prasad S.M., Chauhan D.K., Tripathi D.K., Sharma S. Differential phytotoxic impact of plant mediated silver nanoparticles (AgNPs) and silver nitrate (AgNO3) on Brassica sp. Front. Plant Sci. 2017;8:1501. doi: 10.3389/fpls.2017.01501. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Yang J., Jiang F., Ma C., Rui Y., Rui M., Adeel M., Cao W., Xing B. Alteration of crop yield and quality of wheat upon exposure to silver nanoparticles in a life cycle study. J. Agric. Food Chem. 2018;66:2589–2597. doi: 10.1021/acs.jafc.7b04904. [DOI] [PubMed] [Google Scholar]
  • 74.De Paiva Pinheiro S.K., De Medeiros Chaves M., Rangel Miguel T.B.A., De Freitas Barros F.C., Farias C.P., Ferreira O.P., De Castro Miguel E. Toxic effects of silver nanoparticles on the germination and root development of lettuce (Lactuca sativa) Aust. J. Bot. 2020;68:127–136. doi: 10.1071/BT19170. [DOI] [Google Scholar]
  • 75.Vinković T., Štolfa-čamagajevac I., Tkalec M., Goessler W., Domazet-Jurašin D., Vinković-Vrček I. Does plant growing condition affects biodistribution and biological effects of silver nanoparticles? Spanish J. Agric. Res. 2018;16 doi: 10.5424/sjar/2018164-13580. [DOI] [Google Scholar]
  • 76.García-Sánchez S., Bernales I., Cristobal S. Early response to nanoparticles in the Arabidopsis transcriptome compromises plant defence and root-hair development through salicylic acid signalling. BMC Genom. 2015;16 doi: 10.1186/s12864-015-1530-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Abd-Alla M.H., Nafady N.A., Khalaf D.M. Assessment of silver nanoparticles contamination on faba bean-Rhizobium leguminosarum bv. viciae-Glomus aggregatum symbiosis: implications for induction of autophagy process in root nodule. Agric. Ecosyst. Environ. 2016;218:163–177. doi: 10.1016/j.agee.2015.11.022. [DOI] [Google Scholar]
  • 78.Dimkpa C.O., McLean J.E., Martineau N., Britt D.W., Haverkamp R., Anderson A.J. Silver nanoparticles disrupt wheat (Triticum aestivum L.) growth in a sand matrix. Environ. Sci. Technol. 2013;47:1082–1090. doi: 10.1021/ES302973Y/SUPPL_FILE/ES302973Y_SI_001.PDF. [DOI] [PubMed] [Google Scholar]
  • 79.Babu M., Devi V., Ramakritinan C.M., Umarani R., Taredahalli N., Kumaraguru A.K. Application of biosynthesized silver nanoparticles in agricultural and marine pest control. Curr. Nanosci. 2013;10:374–381. doi: 10.2174/15734137113096660103. [DOI] [Google Scholar]
  • 80.Amin H.H. Biosynthesized silver nanoparticles using Ulva lactuca as a safe synthetic pesticide (in vitro) Open Agric. 2020;5:291–299. doi: 10.1515/opag-2020-0032. [DOI] [Google Scholar]
  • 81.Bhattacharyya A., Prasad R., Buhroo A.A., Duraisamy P., Yousuf I., Umadevi M., Bindhu M.R., Govindarajan M., Khanday A.L. One-pot fabrication and characterization of silver nanoparticles using Solanum lycopersicum : an eco-friendly and potent control tool against rose aphid. Macrosiphum rosae, J. Nanosci. 2016;2016:1–7. doi: 10.1155/2016/4679410. [DOI] [Google Scholar]
  • 82.Rankic I., Zelinka R., Ridoskova A., Gagic M., Pelcova P., Huska D. Nano/microparticles in conjunction with microalgae extract as novel insecticides against Mealworm beetles, Tenebrio molitor. Sci. Rep. 2021;11 doi: 10.1038/s41598-021-96426-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Yasur J., Usha Rani P. Lepidopteran insect susceptibility to silver nanoparticles and measurement of changes in their growth, development and physiology. Chemosphere. 2015;124:92–102. doi: 10.1016/j.chemosphere.2014.11.029. [DOI] [PubMed] [Google Scholar]
  • 84.Yuvaraj M., Sevathapandian Subramanian K. Novel slow release nanocomposite fertilizers. Nanotechnol. Environ. 2020 doi: 10.5772/intechopen.93267. [DOI] [Google Scholar]
  • 85.Gosavi V., Daspute A., Patil A., Gangurde A. Researchgate.Net.; 2020. Synthesis of Green Nanobiofertilizer Using Silver Nanoparticles of Allium cepa Extract Short Title: Green Nanofertilizer from Allium cepa. S.W.- IJCS, undefined 2020. [DOI] [Google Scholar]
  • 86.Sayed A.M.M., Kim S. 2018. Myco-silver Nanoparticles Synthesized Using Beauveria bassiana and Metarhizium brunneum as a Smart Pest Control Article History.http://www.ejppri.eg.net/pdf/v1n1/1.pdf (accessed April 16, 2022) [Google Scholar]
  • 87.Feizi H., Pour S.J., Rad K.H. 2013. Biological Response of Muskmelon (Cucumis Melo L.) to Magnetic Field and Silver Nanoparticles.http://journalarrb.com/index.php/ARRB/article/view/24894 (accessed April 13, 2023) [Google Scholar]
  • 88.Jhanzab H.M., Razzaq A., Hafeez A., Jilani G., Rehman A., Yasmeen F. Silver nano-particles enhance the growth, yield and nutrient use efficiency of wheat. Int. J. Agron. Agric. Res. 2015;7:15–22. https://citeseerx.ist.psu.edu/viewdoc/download?doi=10.1.1.735.7696&rep=rep1&type=pdf (accessed April 25, 2022) [Google Scholar]
  • 89.Mehmood A., Murtaza G. Impact of biosynthesized silver nanoparticles on protein and carbohydrate contents in seeds of pisum sativum L, Crop Breed. Appl. Biotechnol. 2017;17:334–340. doi: 10.1590/1984-70332017v17n4a51. [DOI] [Google Scholar]
  • 90.Crystals P. Nanotechnology for insect pest. Researchgate.Net. 2016;3:528–545. https://www.researchgate.net/profile/Vladimir-Kulchitsky/post/How_nanotechnology_could_be_used_as_potential_tool_against_insect_pests/attachment/5b77e357cfe4a7f7ca5b21e9/AS%3A660905838792704%401534583639531/download/IJSET+17.pdf (accessed April 16, 2022) [Google Scholar]
  • 91.Singh R.P., Handa R., Manchanda G. Nanoparticles in sustainable agriculture: an emerging opportunity. J. Contr. Release. 2021;329:1234–1248. doi: 10.1016/j.jconrel.2020.10.051. [DOI] [PubMed] [Google Scholar]
  • 92.Chen X., Chen Y., Zou L., Zhang X., Dong Y., Tang J., McClements D.J., Liu W. Plant-based nanoparticles prepared from proteins and phospholipids consisting of a core-multilayer-Shell structure: fabrication, stability, and foamability. J. Agric. Food Chem. 2019;67:6574–6584. doi: 10.1021/acs.jafc.9b02028. [DOI] [PubMed] [Google Scholar]
  • 93.Gour N., Upadhyaya P., Patel J. Elsevier B.V.; 2019. Nanomaterials as Therapeutic and Diagnostic Tool for Controlling Plant Diseases; pp. 225–261. (Compr. Anal. Chem.). [DOI] [Google Scholar]
  • 94.Alif Alisha A.S., Thangapandiyan S. Comparative bioassay of silver nanoparticles and malathion on infestation of red flour beetle, Tribolium castaneum. J. Basic Appl. Zool. 2019;80 doi: 10.1186/s41936-019-0124-0. [DOI] [Google Scholar]
  • 95.Babu M., Devi V., Ramakritinan C.M., Umarani R., Taredahalli N., Kumaraguru A.K. Application of biosynthesized silver nanoparticles in agricultural and marine pest control. Curr. Nanosci. 2013;10:374–381. doi: 10.2174/15734137113096660103. [DOI] [Google Scholar]
  • 96.Sayed A.M.M., Kim S., Behle R.W. Characterisation of silver nanoparticles synthesised by Bacillus thuringiensis as a nanobiopesticide for insect pest control. Biocontrol Sci. Technol. 2017;27:1308–1326. doi: 10.1080/09583157.2017.1397597. [DOI] [Google Scholar]
  • 97.Kamil D., Prameeladevi T., Ganesh S., Prabhakaran N., Nareshkumar R., Thomas S.P. Green synthesis of silver nanoparticles by entomopathogenic fungus Beauveria bassiana and their bioefficacy against mustard aphid (Lipaphis erysimi Kalt.) Indian J. Exp. Biol. 2017;55:555–561. http://nopr.niscair.res.in/handle/123456789/42555 (accessed April 16, 2022) [Google Scholar]
  • 98.Manimegalai T., Raguvaran K., Kalpana M., Maheswaran R. Green synthesis of silver nanoparticle using Leonotis nepetifolia and their toxicity against vector mosquitoes of Aedes aegypti and Culex quinquefasciatus and agricultural pests of Spodoptera litura and Helicoverpa armigera. Environ. Sci. Pollut. Res. 2020;27:43103–43116. doi: 10.1007/s11356-020-10127-1. [DOI] [PubMed] [Google Scholar]
  • 99.Biswas P.K., Dey S. Effects and applications of silver nanoparticles in different fields. Int. J. Recent Sci. Res. 2015;6:5880–5883. http://www.rikilt.wur.nl/NR/rdonlyres/BDEEDD31- (accessed April 17, 2022) [Google Scholar]
  • 100.Ibrahimović A., Stambolić A., Omanović-Mikličanin E. 2021. Application of Nanotechnology in Food Packaging; pp. 979–984. (Lect. Notes Networks Syst.). [DOI] [Google Scholar]
  • 101.Carbone M., Donia D.T., Sabbatella G., Antiochia R. Silver nanoparticles in polymeric matrices for fresh food packaging. J. King Saud Univ. Sci. 2016;28:273–279. doi: 10.1016/j.jksus.2016.05.004. [DOI] [Google Scholar]
  • 102.De Moura M.R., Mattoso L.H.C., Zucolotto V. Development of cellulose-based bactericidal nanocomposites containing silver nanoparticles and their use as active food packaging. J. Food Eng. 2012;109:520–524. doi: 10.1016/j.jfoodeng.2011.10.030. [DOI] [Google Scholar]
  • 103.Kumar S., Shukla A., Baul P.P., Mitra A., Halder D. Biodegradable hybrid nanocomposites of chitosan/gelatin and silver nanoparticles for active food packaging applications. Food Packag. Shelf Life. 2018;16:178–184. doi: 10.1016/j.fpsl.2018.03.008. [DOI] [Google Scholar]
  • 104.Yu Z., Wang W., Kong F., Lin M., Mustapha A. Cellulose nanofibril/silver nanoparticle composite as an active food packaging system and its toxicity to human colon cells. Int. J. Biol. Macromol. 2019;129:887–894. doi: 10.1016/j.ijbiomac.2019.02.084. [DOI] [PubMed] [Google Scholar]
  • 105.Becaro A.A., Puti F.C., Correa D.S., Paris E.C., Marconcini J.M., Ferreira M.D. Polyethylene films containing silver nanoparticles for applications in food packaging: characterization of physico-chemical and anti-microbial properties. J. Nanosci. Nanotechnol. 2015;15:2148–2156. doi: 10.1166/jnn.2015.9721. [DOI] [PubMed] [Google Scholar]
  • 106.He Y., Li H., Fei X., Peng L. Carboxymethyl cellulose/cellulose nanocrystals immobilized silver nanoparticles as an effective coating to improve barrier and antibacterial properties of paper for food packaging applications. Carbohydr. Polym. 2021;252 doi: 10.1016/j.carbpol.2020.117156. [DOI] [PubMed] [Google Scholar]
  • 107.Ernest Ravindran R.S., Subha V., Ilangovan R. Silver nanoparticles blended PEG/PVA nanocomposites synthesis and characterization for food packaging. Arab. J. Chem. 2020;13:6056–6060. doi: 10.1016/j.arabjc.2020.05.005. [DOI] [Google Scholar]
  • 108.Brito S. da C., Bresolin J.D., Sivieri K., Ferreira M.D. Low-density polyethylene films incorporated with silver nanoparticles to promote antimicrobial efficiency in food packaging. Food Sci. Technol. Int. 2020;26:353–366. doi: 10.1177/1082013219894202. [DOI] [PubMed] [Google Scholar]
  • 109.Rizzo D.M., Lichtveld M., Mazet J.A.K., Togami E., Miller S.A. Plant health and its effects on food safety and security in a One Health framework: four case studies, One Heal. Outlook. 2021;3 doi: 10.1186/s42522-021-00038-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.Gruère G.P. Implications of nanotechnology growth in food and agriculture in OECD countries. Food Pol. 2012;37:191–198. doi: 10.1016/j.foodpol.2012.01.001. [DOI] [Google Scholar]
  • 111.Chavan R.R., Bhinge S.D., Bhutkar M.A., Randive D.S., Wadkar G.H., Todkar S.S., Urade M.N. Characterization, antioxidant, antimicrobial and cytotoxic activities of green synthesized silver and iron nanoparticles using alcoholic Blumea eriantha DC plant extract. Mater. Today Commun. 2020;24 doi: 10.1016/j.mtcomm.2020.101320. [DOI] [Google Scholar]
  • 112.Giljohann D.A., Seferos D.S., Daniel W.L., Massich M.D., Patel P.C., Mirkin C.A. Gold nanoparticles for biology and medicine. Angew. Chem., Int. Ed. 2010;49:3280–3294. doi: 10.1002/anie.200904359. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 113.Panyala N.R., Peña-Méndez E.M., Havel J. Silver or silver nanoparticles: a hazardous threat to the environment and human health? J. Appl. Biomed. 2012;10:117–129. https://www.researchgate.net/file.PostFileLoader.html?id=5952abbd615e277b0269930e&assetKey=AS%3A509941484093441%401498590932135 (accessed April 17, 2022) [Google Scholar]
  • 114.Swathy J.R., Udhaya Sankar M., Chaudhary A., Aigal S., Anshup, Pradeep T. Antimicrobial silver: an unprecedented anion effect. Sci. Rep. 2014;11 doi: 10.1038/srep07161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 115.Shao W., Liu X., Min H., Dong G., Feng Q., Zuo S. Preparation, characterization, and antibacterial activity of silver nanoparticle-decorated graphene oxide nanocomposite. ACS Appl. Mater. Interfaces. 2015;7:6966–6973. doi: 10.1021/acsami.5b00937. [DOI] [PubMed] [Google Scholar]
  • 116.Guimarães M.L., da Silva F.A.G., da Costa M.M., de Oliveira H.P. Green synthesis of silver nanoparticles using Ziziphus joazeiro leaf extract for production of antibacterial agents. Appl. Nanosci. 2020;10:1073–1081. doi: 10.1007/s13204-019-01181-4. [DOI] [Google Scholar]
  • 117.Vanti G.L., Kurjogi M., Basavesha K.N., Teradal N.L., Masaphy S., Nargund V.B. Synthesis and antibacterial activity of solanum torvum mediated silver nanoparticle against Xanthomonas axonopodis pv.punicae and Ralstonia solanacearum. J. Biotechnol. 2020;309:20–28. doi: 10.1016/j.jbiotec.2019.12.009. [DOI] [PubMed] [Google Scholar]
  • 118.Chen J., Li S., Luo J., Wang R., Ding W. Enhancement of the antibacterial activity of silver nanoparticles against phytopathogenic bacterium Ralstonia solanacearum by stabilization. J. Nanomater. 2016;2016 doi: 10.1155/2016/7135852. [DOI] [Google Scholar]
  • 119.Jacob J.A., Mahal H.S., Biswas N., Mukherjee T., Kapoor S. Role of phenol derivatives in the formation of silver nanoparticles. Langmuir. 2008;24:528–533. doi: 10.1021/la702073r. [DOI] [PubMed] [Google Scholar]
  • 120.Jo Y.K., Kim B.H., Jung G. Antifungal activity of silver ions and nanoparticles on phytopathogenic fungi. Plant Dis. 2009;93:1037–1043. doi: 10.1094/PDIS-93-10-1037. [DOI] [PubMed] [Google Scholar]
  • 121.Mahdizadeh V., Safaie N., Khelghatibana F. Evaluation of antifungal activity of silver nanoparticles against some phytopathogenic fungi and Trichoderma harzianum. J. Crop Prot. 2015;4:291–300. https://jcp.modares.ac.ir/browse.php?a_id=12407&sid=3&slc_lang=fa (accessed April 17, 2022) [Google Scholar]
  • 122.Balashanmugam P., Balakumaran M.D., Murugan R., Dhanapal K., Kalaichelvan P.T. Phytogenic synthesis of silver nanoparticles, optimization and evaluation of in vitro antifungal activity against human and plant pathogens. Microbiol. Res. 2016;192:52–64. doi: 10.1016/j.micres.2016.06.004. [DOI] [PubMed] [Google Scholar]
  • 123.Xiang S., Ma X., Shi H., Ma T., Tian C., Chen Y., Chen H., Chen X., Luo K., Cai L., Wang D., Xue Y., Huang J., Sun X. Green synthesis of an alginate-coated silver nanoparticle shows high antifungal activity by enhancing its cell membrane penetrating ability. ACS Appl. Bio Mater. 2019;2:4087–4096. doi: 10.1021/acsabm.9b00590. [DOI] [PubMed] [Google Scholar]
  • 124.Chowdappa P., Shivakumar G. Antifungal activity of chitosan-silver nanoparticle composite against Colletotrichum gloeosporioides associated with mango anthracnose. Afr. J. Microbiol. Res. 2014;8:1803–1812. doi: 10.5897/ajmr2013.6584. [DOI] [Google Scholar]
  • 125.Bahrami-Teimoori B., Nikparast Y., Hojatianfar M., Akhlaghi M., Ghorbani R., Pourianfar H.R. Characterisation and antifungal activity of silver nanoparticles biologically synthesised by Amaranthus retroflexus leaf extract. J. Exp. Nanosci. 2017;12:129–139. doi: 10.1080/17458080.2017.1279355. [DOI] [Google Scholar]
  • 126.Kim S.W., Jung J.H., Lamsal K., Kim Y.S., Min J.S., Lee Y.S. Antifungal effects of silver nanoparticles (AgNPs) against various plant pathogenic fungi. MYCOBIOLOGY. 2012;40:53–58. doi: 10.5941/MYCO.2012.40.1.053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 127.Tyagi P.K., Mishra R., Khan F., Gupta D., Gola D. Antifungal effects of silver nanoparticles against various plant pathogenic fungi and its safety evaluation on Drosophila melanogaster. Biointerface Res. Appl. Chem. 2020;10:6587–6596. doi: 10.33263/BRIAC106.65876596. [DOI] [Google Scholar]
  • 128.Li R., Cui L., Chen M., Huang Y. Nanomaterials for Airborne virus inactivation: a Short review. Aerosol Sci. Eng. 2021;5:1–11. doi: 10.1007/s41810-020-00080-4. [DOI] [Google Scholar]
  • 129.xi Xiang D., Chen Q., Pang L., long Zheng C. Inhibitory effects of silver nanoparticles on H1N1 influenza A virus in vitro. J. Virol. Methods. 2011;178:137–142. doi: 10.1016/j.jviromet.2011.09.003. [DOI] [PubMed] [Google Scholar]
  • 130.Galdiero S., Falanga A., Vitiello M., Cantisani M., Marra V., Galdiero M. Silver nanoparticles as potential antiviral agents. Molecules. 2011;16:8894–8918. doi: 10.3390/molecules16108894. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 131.Belanger J.M., Raviv Y., Viard M., de la Cruz M.J., Nagashima K., Blumenthal R. Effects of UVA irradiation, aryl azides, and reactive oxygen species on the orthogonal inactivation of the human immunodeficiency virus (HIV-1) Virology. 2011;417:221–228. doi: 10.1016/j.virol.2011.06.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 132.Elbeshehy E.K.F., Elazzazy A.M., Aggelis G. Silver nanoparticles synthesis mediated by new isolates of Bacillus spp., nanoparticle characterization and their activity against Bean Yellow Mosaic Virus and human pathogens. Front. Microbiol. 2015;6:453. doi: 10.3389/fmicb.2015.00453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 133.El Gamal A.Y., Tohamy M.R., Abou-Zaid M.I., Atia M.M., El Sayed T., Farroh K.Y. Silver nanoparticles as a viricidal agent to inhibit plant-infecting viruses and disrupt their acquisition and transmission by their aphid vector. Arch. Virol. 2022;167:85–97. doi: 10.1007/s00705-021-05280-y. [DOI] [PubMed] [Google Scholar]
  • 134.Mahfouze H.A., El-Dougdoug N.K., Mahfouze S.A. Virucidal activity of silver nanoparticles against Banana bunchy top virus (BBTV) in banana plants. Bull. Natl. Res. Cent. 2020;44 doi: 10.1186/s42269-020-00433-6. [DOI] [Google Scholar]
  • 135.Shafie R.M., Salama A.M., Farroh K.Y. Silver nanoparticles activity against Tomato spotted wilt virus. Middle East J. Agric. Res. 2018:1251–1267. https://www.curresweb.com/mejar/mejar/2018/1251-1267.pdf (accessed April 27, 2022) [Google Scholar]
  • 136.Ahsan T. Biofabrication of silver nanoparticles from Pseudomonas fluorescens to control tobacco mosaic virus, Egypt. J. Biol. Pest Control. 2020;30 doi: 10.1186/s41938-020-00268-3. [DOI] [Google Scholar]
  • 137.El-Dougdoug N.K., Bondok A.M., El-Dougdoug K.A. Evaluation of silver nanoparticles as antiviral agent against ToMV and PVY in tomato plants, Middle East. J. Appl. Sci. 2018:100–111. https://www.curresweb.com/mejas/mejas/2018/100-111.pdf (accessed April 27, 2022) [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

No data was used for the research described in the article.


Articles from Heliyon are provided here courtesy of Elsevier

RESOURCES