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. 2014 Sep;30(3):169–178. doi: 10.5487/TR.2014.30.3.169

New Paradigm Shift for the Green Synthesis of Antibacterial Silver Nanoparticles Utilizing Plant Extracts

Youmie Park 1,
PMCID: PMC4206743  PMID: 25343010

Abstract

This review covers general information regarding the green synthesis of antibacterial silver nanoparticles. Owing to their antibacterial properties, silver nanoparticles are widely used in many areas, especially biomedical applications. In green synthesis practices, the chemical reducing agents are eliminated, and biological entities are utilized to convert silver ions to silver nanoparticles. Among the various biological entities, natural plant extracts have emerged as green reducing agents, providing eco-friendly routes for the preparation of silver nanomaterials. The most obvious merits of green synthesis are the increased biocompatibility of the resulting silver nanoparticles and the ease with which the reaction can be carried out. This review summarizes some of the plant extracts that are used to produce antibacterial silver nanoparticles. Additionally, background information regarding the green synthesis and antibacterial activity of silver nanoparticles is provided. Finally, the toxicological aspects of silver nanoparticles are briefly mentioned.

Keywords: Plant extracts, Green synthesis, Silver nanoparticles, Antibacterial activity

INTRODUCTION

As an important aspect of nanotechnology, nanoparticles (NPs, less than 100 nm in one dimension) have been developed for a variety of applications, especially in the area of nanomedicine (1). NPs possess characteristic properties that differ from those of their bulk counterparts. In the area of nanomedicine, NPs are commonly employed as drug delivery vehicles. Recently, NPs have been employed in therapeutic applications to target specific sites, such as lung tissue, as well as in cancer therapy and vaccinations (1). Additionally, the use of NPs continues to increase in microbial applications due to the potential of NPs to circumvent microbial resistance while satisfying the current need for novel antibiotics (2-4). The number of infections and outbreaks associated with multi-drug-resistant (MDR) bacteria has increased, threatening public health. The NPs used to overcome microbial resistance include nitric oxide-releasing NPs, chitosan NPs and metallic NPs (3). Among the metallic NPs, the medicinal potentials of gold NPs (AuNPs) and silver NPs (AgNPs) have been extensively discussed elsewhere (5). AgNPs possess excellent antibacterial, antiviral and antifungal activities (6). Metallic NPs are commonly synthesized by traditional chemical and physical methods (7). However, current sustainability issues have led to explorations of eco-friendly synthesis and green synthesis for the production of metallic NPs based on diverse biological entities (7). This review is not meant to be inclusive of all plant extracts utilized for the green synthesis of AgNPs. There are extensive reviews that address this area (8-12). Instead, this review focuses on the preparation of antibacterial AgNPs by using plant extracts as reducing agents.

GREEN SYNTHESIS OF AgNPs

Advantages and applications. The chemical synthesis of AgNPs employs chemical reducing agents to convert Ag ions to AgNPs. One of the most widely used chemical reducing agents is sodium borohydride. This process involves the undesired use of hazardous chemicals, and the biocompatibility of the resulting AgNPs is too low for application in biological systems. Relative to this traditional chemical method, methods of green synthesis that use environmentally friendly or eco-friendly compounds as reducing agents are emerging (13-19). The biological entities used for green synthesis include bacteria, fungi, plants, pure compounds from plants, algae, carbohydrates, microorganisms, etc. The process of green synthesis requires the use of water as an environmentally friendly solvent; of note is the fact that water is more biocompatible than organic solvents.

Green synthesis possesses the following advantages over traditional chemical methods. (1) green synthesis is simple and usually involves a one-pot reaction; (2) it is amenable to scale up; (3) the toxicity-associated hazardous chemicals are eliminated, increasing the biocompatibility of the resulting product with normal tissues for in vivo applications; and (4) green biological entities can be used as reducing agents and capping agents, providing AgNPs with enhanced colloidal stability. Colloidal stability is an important factor when making claims regarding the biological activity of AgNPs. (5) Finally, the process is cost-effective. These advantages are not limited to AgNPs. Other metallic NPs can be greensynthesized and have many uses in biomedical and industrial applications. There are extensive reviews elsewhere regarding the applications of green-synthesized metallic NPs (20,21). The applications of metallic NPs include (1) biomedical applications, such as antimicrobial applications, drug delivery vehicles, medical imaging and diagnostics; (2) environmental remediation applications, such as the catalytic degradation of pollutants; and (3) industrial applications, such as energy-related applications and catalysis in organic synthesis (20). Borase et al. have extensively reviewed AgNPs in a variety of applications, including anticancer, catalysis, biosensor, drug delivery, textiles and cosmetics, antituberculosis, antiviral, insect management and water purification (12).

Procedures and characterization. We utilized various biological entities, including plant extracts (Leonurus japonicus, Artemisia capillaris, Polygala tenuifolia, and Caesalpinia sappan), a pure compound from plants (chlorogenic acid), polysaccharides (chondroitin sulfate and acharan sulfate), an oligosaccharide (sialyllactose) and invertebrate extracts (an African giant snail Achatina fulica and an earthworm Eisenia andrei), for the green synthesis of AgNPs (22-29). The green synthesis of AgNPs is a simple and facile approach that is carried out by mixing silver nitrate (the Ag ion source) with a biological entity (the reducing agent). A schematic representation of the synthesis process is depicted in Fig. 1. In our experiment, an external source of energy, for example, oven incubation, is used to facilitate the reaction. The applications that we evaluated were mainly antibacterial (minimum inhibitory concentration, MIC) and in vivo wound-healing activities. Remarkably, AgNPs synthesized with the extract of Leonurus japonicus exhibited enhanced antibacterial activities (approximately 127-fold increase) against Pseudomonas aeruginosa, Escherichia coli and Enterobacter cloacae (22). The aerial portion of Leonurus japonicus was utilized. In the case of AgNPs synthesized with the root extract of Polygala tenuifolia, the strain of Escherichia coli DC2 was shown to be the most effective when treated with AgNPs (approximately 16-fold increase) (24). The aerial portion of Artemisia capillaris was also used as a reducing agent for the synthesis of AgNPs and AgNPs enhance the antibacterial activity against Pseudomonas aeruginosa, Escherichia coli, Enterobacter cloacae, Klebsiella oxytoca and Klebsiella areogenes (23). In each case, MIC values are compared with values recorded for the original plant extract alone. Generally, AgNPs synthesized with the three plant extracts mentioned above show more effective antibacterial activities against Gram-negative than Gram-positive bacteria.

Fig. 1. A schematic of the procedure followed to synthesize AgNPs by using plant extracts as reducing agents.

Fig. 1.

The formation of AgNPs is generally characterized with spectroscopic and microscopic methods, including UV-visible spectrophotometry, Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), X-ray diffraction (XRD) and zeta potential measurements. The formation of AgNPs is initially judged based on the color change of the solution, using the naked eye. The characteristic absorbance is observed in the range of 380~450 nm (yellow color), in which predominantly spherical AgNPs are synthesized. When the synthesis is completed, the size, shape and dispersion state of AgNPs are commonly visualized and measured by microscopic methods, such as TEM, AFM and SEM. Next, the crystalline nature of AgNPs is confirmed by XRD analysis. FT-IR spectra provide information regarding the functional groups of the reducing agents that are involved in the reduction of Ag+ to AgNPs. Further, zeta potential measurements give information regarding the surface charges of AgNPs, which affect their colloidal stability. The reaction yield is measured by using both ultracentrifugation and inductively coupled plasma mass spectrometry (ICP-MS). After performing ultracentrifugation, AgNPs settle to the bottom of the tube. The colorless supernatant solution containing the unreacted Ag+ is pooled and analyzed by ICP-MS. Then, the yield can be calculated by measuring the concentrations of both the total Ag in the solution of AgNPs and the unreacted Ag in the supernatant.

PLANT EXTRACTS AS REDUCING AGENTS FOR THE GREEN SYNTHESIS OF AgNPs

Following various sustainability initiatives, plant extracts are emerging as potential reducing agents for the green synthesis of AgNPs. Various categories of plant extracts further act as stabilizing agents. Approximately 321,212 species of plants are known on earth, according to the Botanic Gardens Conservation International, indicating that researchers have access to a significant variety of natural plant material (12). The author extensively reviewed the green synthesis of AuNPs and AgNPs using polysaccharides and phytochemicals as reducing agents (13). Phytochemicals and plant-derived polysaccharides, such as cellulose, starch, dextran, and alginic acid, play dual roles as reducing and stabilizing agents. The oxidation of the hydroxyl groups of polysaccharides to carbonyl groups is most likely involved in the reduction of metal ions to produce metallic NPs (13).

Researchers have reported that four factors—pH, temperature, reaction time and the ratio of plant extracts to silver nitrate—affect the synthesis of AgNPs based on plant extracts (8,12). (1) By changing the pH, the charges of the biomolecules in extracts are altered. Because the Ag ion is a cation, the charge of the biomolecules also affects the synthesis of AgNPs. (2) Generally, increasing the reaction temperature leads to a higher reaction rate. In high-temperature reactions, thermo-stable compounds can play a major role in obtaining higher yields. (3) Additionally, by increasing the reaction time, the reaction rate generally increases. (4) Finally, the ratio of plant extract to silver nitrate is a very important factor for obtaining AgNPs with various sizes and shapes.

Table 1. Plant extracts used for the green synthesis of antibacterial AgNPs.

Antibacterial AgNPs

Scientific name Intrinsic biological activities of plants Plant part used for the green synthesis of AgNPs Refs.

Azadirachta indica 1) antiinflammatory and antinociceptive activities leaves (40)
2) antioxidant and antiproliferative activities
3) cytotoxic and melanogenesis-inhibitory activity
Boswellia ovalifoliolata 1) antioxidant activity stem barks (41)
Caesalpinia sappan 1) antiinflammatory activity heartwoods (25)
2) vasorelaxant activity
Camellia sinensis 1) antioxidant activity leaves (42)
2) blood anticoagulation and antiplatelet activities
3) neuroprotective effect
4) antimicrobial activity
5) hypoglycaemic and hypolipidemic activities
6) wound healing activity
Carica papaya 1) antiplasmodial activity fruits (43)
2) antioxidant activity
3) anxiolytic and sedative effects
Catharanthus roseus 1) larvicidal efficacy leaves (44)
2) antidiabetic and antioxidant activities
3) hypoglycemic activity
4) hypolipidemic activity
5) AchE inhibitory activity
Chrysanthemum morifolium 1) antiinflammatory activity flower (45)
2) anti HIV activity
3) antitumor activity
Cinnamon zeylanicum 1) improves insulin sensitivity in the brain bark (46)
2) antihypertension effect
3) effects neurodegenerative diseases and its potent antineuroinflammatory capacity
Citrullus colocynthis 1) antimicrobial potentials leaves (47)
2) analgesic and antiinflammatory activities
3) antibacterial activity
4) antioxidant activity
5) antitumor activity
Citrus sinensis 1) antioxidant and antifungal activities peel (48)
Cochlospermum gossypium none gum (49)
Coleus aromaticus 1) wound healing activity leaves (50)
2) diuretic activity
Coleus forskohlii 1) wound healing activity root (51)
2) anti HIV activity
3) diuretic activity
4) antifungal activity
Curcuma longa 1) antioxidant, antiinflammatory and chemosensitizer activities tuber (52)
2) hepatoprotective effect
Desmodium triflorum 1) antioxidant and antiproliferative activities whole plant (53)
2) analgesic and antiinflammatory activities
Dioscorea batatas 1) antiinflammatory activity rhizome (54)
2) antioxidant activity
Dioscorea bulbifera 1) antibacterial activity tuber (55)
2) antitumor activity
3) antidiabetic activity
4) analgesic and antiinflammatory
Eucalyptus citriodora 1) antiinflammatory activity leaves (56)
2) analgesic activity
3) antiproliferative effect
4) antituberculosis
5) antibacterial activity
Euphorbia hirta 1) antimicrobial activity leaves (57,58)
2) mosquito larvicidal and pupicidal activities
3) antidiabetic and antioxidant potentials
4) immunomodulatory activity
5) antianaphylactic effect
6) burn-wound healing activity
7) antidiarrhoeic activity
8) analgesic, antipyretic and antiinflammatory properties
Euphorbia nivulia 1) wound healing activity latex (59)
2) haemostatic activity
3) antibacterial activity
Ficus benghalensis 1) antimicrobial activity leaves (60)
2) antiinflammatory activity
3) antidiabetic activity
4) antiatherogenic activity
5) antioxidant activity
6) antiinflammatory and analgesic activities
Fissidens minutus none mosses (61)
Garcinia mangostana 1) neuroprotective effect leaves (62)
2) antiinflammatory effect
3) antioxidant and antitumor activities
4) antimicrobial and antiprotozoal activities
5) antiangiogenic effect
6) antihyperglycemic activity
7) analgesic activity
8) antiviral activity
Gliricidia sepium 1) larvicidal, ovicidal and pupicidal activities leaves (63)
Hibiscus sabdariffa 1) nephroprotective effect leaves, stems (64)
2) antimicrobial effect
3) hypolipidemic activity
4) wound healing activity
5) antidiabetic activity
6) diuretic effect
7) antioxidant activity
Leonurus japonicus 1) antioxidant activity aerial parts (22)
2) anticancer activity
3) cardioprotective effect
4) antibacterial activity
5) antiinflammatory activity
Mangifera indica 1) ameliorates diabetes and decrease in high density lipoprotein peel (65)
2) inhibitory effects of mango leaves against S. typhi
3) chemopreventive activity
4) antiphotoaging activity in UVB-irradiated hairless mice
Mentha piperita 1) prevents chemotherapy-induced nausea and vomiting leaves (66)
2) antifungal activity
3) antioxidant and free radical scavenging activities
4) a potential source of natural antimicrobial products
5) analgesic effect
6) antispasmodic activity on rat trachea
Mimusops elengi 1) antioxidant activity fruits (67)
Moringa oleifera 1) antimicrobial, anticancer, antiinflammatory, antidiabetic, and antioxidant effects leaves (68)
2) antidiabetic and antioxidant activities
3) antiinflammatory activity
4) hypoglycemia and hypolipidemia activities
5) antioxidant capacity and antimicrobial activities
6) antifungal activity
7) recovery from hepatic damage
8) antispasmodic, antiinflammatory and diuretic activities
9) induces apoptosis
Musa paradisiaca 1) antioxidant, antimutagenic, anticarcinogenic, and cytoprotective activities peel (69)
Nerium indicum 1) antifungal activity leaves (58)
2) antioxidant activity
3) anticancer effects
4) antidiabetic activity
Nicotiana tobaccum none leaves (70)
Ocimum tenuiflorum 1) antihyperglycemic activity leaves (71)
Opuntia ficus-indica 1) activity of the coagulants leaves (72)
2) antibacterial activity
3) inhibits the ulcerogenic activity
4) wound healing activity
5) reduces hangover symptoms and inhibites the production of inflammatory mediators
6) hepatoprotective effect
Polygala tenuifolia 1) antiinflammatory activity roots (24)
2) antitumor activity
3) anxiolytic activity
Sesuvium portulacastrum 1) potential antimicrobial agent leaves, callus (73)
2) cholinesterase inhibitory activity
Shorea tumbuggaia 1) decreases cholesterol and triglycerides stem barks (41)
Svensonia hyderabadensis none leaves (74)
Tribulus terrestris 1) antitumor and antiangiogenic activities fruits (75)
2) large gains in strength and lean muscle mass
3) inhibits oxidative stress
4) reduces Cd load
5) conventional analgesic drugs
6) antihypertensive effect both systolic and diastolic
7) antidepressive effect
Vitex negundo 1) treats various inflammatory disorders leaves (76)
2) analgesic and antiinflammatory activities

ANTIBACTERIAL ACTIVITIES OF AgNPs

MDR bacteria. One of the most remarkable properties of AgNPs is their antibacterial activity. For 7,000 years, mankind has used Ag metal in coins, cutlery, textiles, cosmetics and medical implants. Ag has also been used as an antibacterial agent in the form of ions, NPs and bulk metal (30). Currently, the increased use of AgNPs in medicine is closely associated with the antibacterial potential of AgNPs. The emergence of MDR bacteria requires novel antibiotics with improved antibacterial activities. In most respects, AgNPs have appeared as prospective alternatives for overcoming antibiotic resistance problems because AgNPs utilize multivalent or polyvalent mechanisms to exert their antibacterial activities. Additionally, the high surface-areato-volume ratio and the specific physical and chemical characteristics of AgNPs make them effective antibacterial agents against MDR bacteria, which includes methicillinresistant Staphylococcus aureus (MRSA), methicillin-sensitive Staphylococcus aureus (MSSA), methicillin-resistant Staphylococcus epidermis (MRSE), ampicillin-resistant Escherichia coli, vancomycin-resistant Staphylococcus aureus (VRSA), erythromycin-resistant Streptococcus pyogenes and multidrug-resistant Pseudomonas aeruginosa (31).

Mechanisms. The antibacterial mechanisms of AgNPs are not yet fully understood; however, the research community has put forward several hypotheses, which follow (31). (1) AgNPs penetrate the cell wall of Gram-negative bacteria, leading to increased cell permeability followed by cell death; (2) the formation of free radicals by AgNPs is attributed to membrane damage; and (3) the strong binding capacity of Ag+ with thiol groups and phosphorous-containing bases, such as vital enzymes and DNA bases, causes the inhibition of bacterial growth and death. Key factors, such as size and shape, affect the antibacterial activity of AgNPs (31). With decreasing size, the surface-area-to-volume ratio increases. The large surface area provides many opportunities for interactions with bacteria; thus, the small particle size is effective as an antibacterial agent. Pal et al. reported that triangular AgNPs are more active than spherical and rod-shaped AgNPs against Escherichia coli, suggesting that the shape of AgNPs should be considered to develop highly efficient antibacterial agents (32).

Stabilizers. For antibacterial applications of AgNPs, the colloidal stability is a major consideration. Thus, stabilizers are commonly employed to increase the stability of AgNPs. The most widely used stabilizers are anionic, cationic, and nonionic surfactants and polymers. Carmona-Ribeiro and de Melo Carrasco have reported that cationic compounds, especially compounds with quaternary ammonium groups, are promising candidates for the development of antimicrobial agents (33). One cationic surfactant, cetyltrimethylammonium bromide (CTAB), has been employed as a stabilizing agent during the synthesis of AgNPs. The mechanism of CTAB adsorption onto the AgNPs is not clearly understood; however, the formation of a CTAB bilayer is a possibility (34). As shown in Fig. 2A, the cationic head group of CTAB binds to the surface of AgNPs, with the hydrophilic group of the surfactant attaching to the AgNPs. Then, the outward hydrophobic tail binds to the hydrophobic tail of another CTAB molecule to form a bilayer structure. Consequently, due to the bilayer formation, the hydrophilic head group of CTAB is directed outward, contributing to the overall positive charge of CTAB-stabilized AgNPs (Fig. 2B). We performed a green synthesis reaction for AgNPs by using extract of Caesalpinia sappan in both the absence and presence of stabilizers. The stabilizers used were a nonionic polymer (PVP) and cationic (CTAB), anionic (SDS, NaDDSS) and nonionic (Tween 20 and 80) surfactants (25). Among the tested stabilizers, CTAB-stabilized AgNPs were found to be the most potent antibacterial agents against 19 strains of MRSA (25). The bilayer shell of CTAB provides improved colloidal stability to the AgNPs, which is closely connected to their enhanced antibacterial activity against MRSA. The overall positive charge of the CTAB-stabilized AgNPs offers many opportunities for the NPs to interact with the negatively charged bacterial cell wall.

Fig. 2. The binding of CTAB on the AgNP surface. (A) The bilayer formation of CTAB, and (B) CTAB-stabilized AgNPs with overall positive charges (34).

Fig. 2.

PERSPECTIVES

Currently, AgNPs-based consumer products are widespread in medical devices, clothing, industry, household goods, healthcare products and cosmetics (35). The potent antimicrobial activity of AgNPs is a key feature being utilized in the development of nanosilver products. Additionally, as a result of the increasing interest in the use of AgNPs in medical applications, the number of scientific publications on this subject has risen 41-fold since the last decade (2000~2011) (35). Whereas there were only four related publications in 2000, the number of publication increased to 164 in 2011 when a PubMed database search was performed using the keyword ‘nanosilver’ (35). In spite of the broad range of AgNP therapeutic applications, the limited information has been reported regarding the toxicity of AgNPs. One mechanism of AgNPs-induced toxicity is cellular apoptosis, which decreases cell viability (6). Safety issues concerning the environment should also be considered because AgNPs from consumer products enter ecosystems. However, understanding the toxicity and fate of AgNPs in ecosytems requires further investigation (6). The green synthetic strategy of AgNPs based on plant extracts, as reported in the current review, contributes to the protection of the ecosystem and our health by decreasing the use of toxicity-associated hazardous chemicals. Again, due to the increasing number of applications of AgNPs, the associated toxicity and safety issues should be investigated in depth to further the safe use of AgNPs.

Acknowledgments

This work was supported by a National Research Foundation of Korea (NRF) grant funded by the Korean government through the Ministry of Education (NRF-2012R1A1A2042224). The author thanks Ms. Sang Hui Jun and Ms. Hye Sung Lee for their assistance with manuscript preparation.

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