Abstract
Establishing biological synthesis of nanoparticles is increasing nowadays in the field of nanotechnology. The search for an optimal source with durability, stability, capacity to withstand higher environmental conditions with excellent characteristics is yet to meet. Consequently, there is need to create an eco‐friendly strategy for metal nanoparticle synthesis. One approach investigated in this review is the use of biosurfactants to enhance the synthesis biologically. In comparison with the other technologies, biosurfactants are less toxic and exhibit higher properties. This method is different from the conventional practice like physical and chemical methods. Several research studies represented that the biosurfactant influences the production of nanoparticles about 2–50 nm. In this manner, the research towards the biosurfactant has raised. This review also addressed the feasibility of biosurfactant and their benefits in the synthesis of metallic nanoparticles. The findings from this review can recommend a conceivable use of biosurfactant as a source for metal nanoparticle synthesis.
Inspec keywords: nanoparticles, microorganisms, nanotechnology, biotechnology, nanofabrication, durability, surfactants, reviews
Other keywords: biological synthesis, bacterial biosurfactants, environmental conditions, metallic nanoparticles synthesis, nanotechnology, durability, review, stability, size 2.0 nm to 50.0 nm
1 Introduction
The present progression in nanomaterials welcomes new items for wide applications in different fields of studies and in particular, nanomaterials for science, hardware, transport, data innovation, physics, chemistry, medicine and instrument engineering. The advancement in the field of life sciences and healthcare can be developed by nanotechnology, which makes the researchers work on the cellular and molecular levels. Nanotechnology research was increasing all over the world in the twenty‐first century. The nanomaterials are usually in the range of 1–100 nm [1]. In the case of large‐scale usage of nanoparticles in the field like biosensors, catalysis, drug delivery and biotechnology, the most inventive method is required. The metal nanoparticles act as biomedical agents and therapeutic agents for the various disorders. The metal nanoparticles were raise from silver, gold, platinum, palladium, titanium, copper, zinc etc. Metal nanoparticle was utilised in catalysis, sensing, electronics because they are based on properties like magnetic, catalytic, medicinal and electrical properties. Creation of nanoparticles with high monodispersity is very difficult in case of material science. Synthesis of nanoparticles has been a dynamic research region in the ongoing years because of extensive properties of the nanomaterials. In addition, these properties could provide a promising result in the biological field. The development of material science research is based on the size and composition of nanomaterials. Nanomaterials can be integrated by utilising an assortment of strategies like sol–gel, co‐precipitation, laser ablation, microemulsion, electrospinning and pyrolysis [2]. The above‐mentioned techniques are expensive, generates toxic substances and produce less stable nanoparticles. In addition, these techniques involve atomic, molecular and particulate processing in the medium [3]. Physical and chemical methods use high temperature and pressure and biologically toxic compounds, which creates the toxicity to the environment and human health. The most famous method is the chemical reduction method that transfers the metal salts into metal atoms by using certain reducing agents such as citrate, hydrides, ethylene glycol and hydrazine. However, all these agents have the capacity to create environmental issues [4, 5].
The major topic in various investigations is a synthesis of metallic nanoparticles using the biological material as a reducing agent. To synthesise the nanoparticles in a controlled shape and size, development of synthesis procedures is required. Thus, the environmental friendly inventive process is required to enhance the nanoparticles synthesis for industrial and medical applications. Microorganisms have a higher potential towards the synthesis of nanoparticles. Generally, two sorts of biological synthesis of metal nanoparticles have been so far been recognised. The first choice is the utilisation of every single microbial framework (all living beings) and the second alternative is to utilise the metabolites combined by various living beings (microorganisms or plants). Due to microorganisms, the nanoparticles are delivered either intracellular or extracellular [6]. The progressing research is looking for more refined conventions to determine the polydispersity and to control over size and shape of nanoparticles and a few investigations have obtained great outcomes utilising biomolecules [7, 8]. Various reports suggested that biosurfactant mediated process is developing on the biosynthesis [9, 10]. This method is particularly utilised for the metal nanoparticles. The sources needed for the nanoparticles require surfactants either chemically or biologically. However, the chemical surfactants are highly useful it brings out toxic substances to the living beings. For the fast synthesis of nanoparticles, bacterial biosurfactants (organisms delivering surfactants) are rising as a substitute hotspot due to the necessities of eco‐friendly bioprocess and novel enhancer. Like above mentioned, microemulsion technique is a most promising approach in the nanoparticle synthesis which utilises oil–water–surfactant mixture. Some of the disadvantages of chemical and physical methods of nanoparticle synthesis are represented (Table 1). Biosurfactants are biological surfactants got from microbial source made generally out of sugar and unsaturated fat moieties, they have higher biodegradability and bring down harmfulness.
Table 1.
Method | Demerits | References |
---|---|---|
deposition of gas phase | dangerous in controlling the size of the particle | [11] |
electron beam lithography | requires costly and complex machines | [12] |
sol–gel method | high permeability, weak bonding, | [13] |
oxidation | small size of colloids | [14, 15] |
chemical coprecipitation | usage of toxic chemicals | [16] |
flow injection | continuous mixing | [17] |
electrochemical | recreation is not possible | [13] |
aerosol/vapour phase | works under high temperature | [18] |
sonochemical decomposition | not easy to understand the mechanism | [19] |
supercritical fluid method | need high pressure and temperature | [20] |
using nanoreactors | complicated | [21] |
2 Biosurfactants
The biological method synthesis of nanoparticles plays a vital role among the research scientists. The major advantages of a biological method like cost‐effectiveness, eco‐friendly and so on, influences the biosynthesis of nanoparticles. Some of the organisms possess biosurfactants, which acts as a substitute for the chemical synthesis of nanoparticles [22]. Biosurfactants are the emulsifiers, which help to decrease the surface tension of the compound. It is accessible in the intracellular and extracellular part of the bacterial cell. It is comprised of hydrophobic and hydrophilic moieties, which helps in the reduction of surface tension of compounds and leads to easy degradation by the bacteria [23].
2.1 Biosurfactants classification
It consists of the non‐polar group comprised of fatty acid and a polar group comprised of sugars (glycolipids like rhamnolipids, trehalolipids, mannosylerythritol lipids and sophorolipids), peptides (lipopeptides) or polysaccharides (polymeric surfactants). Based on the molecular mass of biosurfactants, they were divided into two types. They are low molecular mass biosurfactants consists of glycolipids such as rhamnolipids and sophorolipids, or high molecular mass biosurfactants consists of lipopeptides such as surfactin and polymyxin. Glycolipids contain rhamnose sugar, which is linked to the myrmicacin, which is a derivative of β‐hydroxycarboxylic acid hydroxyl group [24]. Glycolipids are commercially produced from the microorganisms like Bacillus subtilis and Pseudomonas aeruginosa [25]. The disaccharide sugar in the trehalose linked to the carbon backbone to long chain fatty acids of mycolic acid. The morphology of the mycolic acid varies based on the atoms of carbons. Trehalose is produced from the organisms like Arthrobacter sp. and Rhodococcus erythropolis. Macrolactones and a free acidic group are present in the sophorolipids. From the sophorolipids, lactones are extracted which is the ester groups of hydroxyl carboxylic acids and these lactones are widely used for the various biomedical applications [26]. The microorganisms involved in the production of glycolipids are Pseudomonas, Burkholderia, Acinetobacter, Mycobacterium, Rhodococcus, Nocardia, Candida, Arthrobacter and Corynebacterium etc. Aspergillus, Acinetobacter, Arthrobacter, Corynebacterium and Nocardia have been utilised for the synthesis of phospholipids and fatty acids. Lipopeptides have reported to produce mostly by the organisms like Bacillus, Actinoplanes, Aspergillus, Serratia and Streptomyces [27, 28].
2.2 Characteristics of biosurfactants
Based on critical micelle concentration (CMC), hydrophilic–lipophilic balance (HLB), charge and chemical structure, the biosurfactants are characterised [29]. The efficiency of biosurfactants is determined using critical micelle concentration. For example, low critical micelle concentration indicates high efficiency, which means that low concentration of biosurfactant is required to decrease the surface tension. Usually, the CMC is lower than chemical surfactants, because of this reason biosurfactants requirement is low in case of reducing the surface tension [30]. In a study, the surface tension of water gets decreased by using rhamnolipid biosurfactant produced by Pseudomonas aeruginosa [31]. Hence, surface tension and interfacial tension are the major properties of biosurfactants. The list of studies, which depicts the surface tension, and critical micelle concentration of various biosurfactants are explained (Table 2). Conductivity, viscosity, density, osmotic pressure, turbidity can be characterised with the help of HLB property. The water‐in‐oil emulsion and oil‐in‐water emulsion are identified in biosurfactant by using HLB property. The environmental conditions do not affect the parameters of biosurfactants like temperature and pH. For example, a recent study suggested that lipopeptides produced by Bacillus subtilis was found to be more stable for about 180 days at an autoclavable temperature (121°C) and at low temperatures below −15°C. At the same NaCl concentration, more than 15% the activity of biosurfactant are more stable [49].
Table 2.
Group | Surface tension, mN m−1 | Critical micelle concentration, mg L−1 | References |
---|---|---|---|
glycolipids | 72–33.9 | 50 | [32] |
74–38 | 120 | [33] | |
72–31.4 | 30 | [34] | |
31.1 | 600 | [35] | |
72–39.5 | 2.5 | [36] | |
72–28 | 35 | [37] | |
29.73 | 100 | [38] | |
31 | 50 | [39] | |
72–31 | 0.130 | [40] | |
33.8 | 37.9 | [41] | |
phospholipids and fatty acids | 31.2 | 400 | [42] |
lipopeptides and lipoproteins | 36 | 225 | [43] |
72–32 | 185 | [44] | |
71.6–30.2 | 56 | [45] | |
36 | 300 | [46] | |
30 | 0.12 | [47] | |
29 | 110 | [48] |
2.3 Upsides of biosurfactants
In a natural form, the biosurfactants can be obtained that exhibits some good characteristics like restorative properties, expanded degradability, great diminishing property and these properties are lagging in the chemical surfactants. It is highly used because of its benefits like low toxicity and high degradability. Biosurfactants can also be generated from the microbes with the help of enzymes and they play a vital role in the synthesis of biosurfactants [50]. Surfactants help to decrease the surface tension, hence its application has been raised in the industrial process containing emulsification, foaming, detergency, wetting etc. In the recovery of oil and hydrocarbons from the wastewater, it acts as an emulsifier [51]. The activity of biosurfactants varies based on the chemical composition. Several reports depicted that the bacteria have the capability to produce the surface‐active agents called biosurfactants. The various properties of biosurfactants influence its application in different fields like cosmetics, pharmaceuticals, emulsifying agents in food etc. Some other applications in case of increasing the surface area and bioavailability of pollutants are heavy metal binding, bacterial pathogenesis, quorum sensing, and biofilm formation. The consequences of biosurfactants produced by bacterial strain listed (Table 3). In comparison with the chemical surfactants, the biosurfactants exhibit higher properties and they are less toxic compared to the chemical surfactants. In this manner, the research towards the biosurfactant has increased in the last decades. A few analysts investigated the bioprocess in lab scale reactors for a more noteworthy creation from known biosurfactant‐creating microbes [70, 71] and others concentrated on the detachment of new species and studying the qualities of surface active products [72, 73]. In any case, while the industrial interest for surfactants has expanded almost 300% in the US industry during the most recent decade [73]. However, the surfactants used in the industries are usually synthesised by chemical method. An expanding interest of biosurfactants and the need of cost‐focused bioprocess of biosurfactants for business usage, influence the scientists to create cost‐effective methodologies for biosurfactant creation.
Table 3.
Type of biosurfactant | Bacterial strain | Importance of biosurfactant | References |
---|---|---|---|
rhamnolipid | Pseudomonas aeruginosa | bioremediation of oil | [52] |
biocontrol agent | [53] | ||
solubilisation and mobilisation of hydrocarbons | [54] | ||
anti‐tumour activity | [55] | ||
emulsifying activity and washing of hydrocarbons | [56] | ||
Pseudomonas. alcaligenes | mobilisation of hydrocarbons | [57] | |
Pseudomonas desmolyticum | dyes solubilisation | [58] | |
glycolipid | Nocardioides sp. | induce hemolysis | [59] |
P. aeruginosa | enhanced oil recovery | [60] | |
Aeromonas sp. | thermostable emulsifier of various hydrocarbons | [61] | |
lipopeptide | Brevibacillus laterosporus | antimicrobial agent | [62] |
Bacillus circulans | polyaromatic hydrocarbon solubilisation | [63] | |
trehalose lipid | Rhodococcus sp. | hemolytic activity | [64] |
Rhodococcus sp. | membrane permeabilising activity | [65] | |
R. erythropolis | dissolution of hydrocarbons | [66] | |
sophorolipids | Candida bombicola | antimicrobial activity | [67] |
Wickerhamiella domercqiae | anticancer activity | [68] | |
Wickerhamiella domercqiae | surface active property | [69] |
The advancement of an environmental friendly process for the synthesis of nanoparticles is developing as a vital part of nanotechnology. The most important source for the nanoparticle synthesis from biological systems are bacteria, fungi, algae and plant extracts [74, 75]. Several studies reported the production of metal nanoparticles using above‐mentioned biological sources [76, 77]. Though the biological synthesis influences the system complex, it restricts the understanding about the reduction and capping process. This disadvantage can overcome easily using a microbial surfactant. They can be considered as a good appropriate method for the nanoparticle synthesis. The biosurfactants‐mediated nanoparticle synthesis examined as an environmentally acceptable procedure due to its less toxicity. It is more advantageous than other methods because of its reduction in aggregate formation and provides uniform morphology among the nanoparticles. The other benefits like biodegradability, biocompatibility, availability, specificity, the effectiveness of biosurfactants at temperature, pH, and salinity influences the many authors for the generation of materials for future utilisation. In this review, we have provided a summary of available works representing the use of biosurfactants for the synthesis of metallic nanoparticles. Due to the huge applications of biosurfactants [78, 79, 80], it is a need to expand the research.
3 Types of nanoparticles synthesised through bacterial biosurfactants
In connection with biotechnology and nanotechnology, a new area like bionanotechnology has raised. The aim of this new area is to understand the communication between the nanoparticle and biological systems. The current trend is to develop a technique for the production of nanoparticles in which various biological substances have used because of its benefits like renewable, less expensive and so on. The major downside in the synthesis of nanoparticles from the bacterial mass is that complex downstream process. Therefore, there is a need to introduce an ever‐growing environmentally benign procedure for the synthesis of metal nanoparticles. Based on the concern, i.e. minimise the generation of waste, Anastas and Warner [81] introduced certain principles, some of them are less hazardous synthesis route, use of safe chemicals and renewable feedstocks, degradable substrates [82]. The significance of creating eco‐friendly strategies for the synthesis of metal nanoparticles, researchers have started investigating based on it. This can overcome by the biosurfactant‐mediated nanoparticle synthesis. It is the simplest method of synthesising the metal nanoparticles. It was noted that biosurfactants created by microorganisms can be a critical part in the synthesis of nanoparticles through aggregation and stabilisation process. The mode of action of biosurfactant is adsorbing onto metallic nanoparticles (MeNPs), surface settling the nanoparticles and avoiding consequent aggregation. The surfactant adsorption relies upon the kind of surfactant (ionic, non‐ionic, polymeric, and so on.) and the thickness of the adsorbed layer [83, 84]. The research has inspected that several biosurfactants can be used as stabiliser and modifier in the synthesis of metallic nanoparticles.
3.1 Silver nanoparticles
It is generally utilised in the health care products, medical devices, optical receptors, as catalysts in chemical reactions, for biolabelling, water purification systems, antimicrobial agents in industries and so on [85, 86, 87, 88]. The silver nanoparticles display some of the properties like catalytic property, electrical conductivity, catalytic property, magnetic property, antimicrobial activity etc. The available methodologies for the synthesis of nanoparticles are chemical reduction, photochemical reduction, aerosol approach, and electrostatic spraying approach. These are widely used techniques for the synthesis of nanoparticles. Based on the size, the application of silver nanoparticle synthesis is large. Boutonnet et al. [89] were the first who used reverse micelle technique to form metal nanoparticles but they used chemical surfactants, which will pollute the environment easily. This is the major drawback found in this study. Reddy et al. [90] investigated the utilisation of a biosurfactant, a lipopeptide biosurfactant created by Bacillus subtilis has exhibited for the stabilisation of silver nanoparticles. In this study, the size and morphology of nanoparticles depend on the pH and temperature of biosurfactants. This procedure gives a less complex for nanoparticle synthesis contrasted with existing frameworks. An attempt made by Das et al. [91] to isolate the rhamnolipid biosurfactant from Pseudomonas aeruginosa with an enhanced method. Synthesis of spherical shape silver nanoparticles carried out with the help of biosurfactants and then applied in microemulsion technique. Additionally, they have done antimicrobial and cytotoxic activities for both biosurfactants and synthesised nanoparticles in which the result suggested that biosurfactants show best antimicrobial activity than the silver nanoparticle. Zeta potential results from this study suggested that nanoparticle is more stable in the suspension [91]. Hence, several reports represented that rhamnolipid biosurfactants are highly useful in the synthesis of silver nanoparticles [92, 93, 94]. Moreover, some of the other researchers used the rhamnolipid biosurfactant, which was isolated from Pseudomonas fluorescens for the synthesis of silver nanoparticles [95]. They obtained a stable silver nanoparticle that was found to be uniform and has the capability to be stable for about 3 months. They concluded that this study is an appropriate method for green synthesis of silver nanoparticles. Kiran et al. [96] reported the rhamnolipid production using marine bacteria called Brevibacterium casei. They depicted that this biosurfactant acts as a reasonable stabiliser in Ag nanoparticles biosynthesis under solid‐state fermentation. Like different perceptions detailed for rhamnolipids created nanoparticles were steady for two months and the biosurfactant acted as the best stabilisation agent. Saikia et al. [97] portrayed a new part of rhamnolipid in the conservation of silver nanoparticles against salt. Rhamnolipids delivered by a Pseudomonas aeruginosa strain utilised as a part of testing the stability of colloidal silver nanoparticles (AgNPs) regarding salt fixations (2–60 mg NaCl/mL). It was proposed that rhamnolipid might be an intense stabiliser of the AgNPs in the colloidal frame. Additionally, reports by Kasture et al. [98] described on utilising sophorolipids as a reducing and stabilising agent for the silver nanoparticle synthesis, which carried out at room temperature, 40, 60, 80 and 100°C. Two sorts of sophorolipids were generated on either oleic acid or linoleic acid, which may influence the fatty acid chain length of the sophorolipid molecule. At the lower temperatures, bigger particles with wide size obtained. At increasing temperatures, the silver nanoparticles with narrow size are obtained.
3.2 Gold nanoparticles
Based on the size and morphology, the physical properties of nanoparticles are determined. The gold nanoparticles exhibit the shape‐dependent properties. In the synthesis of gold nanoparticles, chemical methods are not only followed but it results in environmental pollution due to the usage of toxic chemicals like borohydrate, citrate and acetylene [99]. Since gold nanoparticles are a shape dependent, stabilising agents like surfactants, thiols, amines, phosphines, phosphine oxides and carboxylates are used in the synthesis process for the control of shape and size. Nowadays, researchers focused on the synthesis of stabilised gold nanoparticles by the biological method. Recently, the demand is increasing towards the clean, non‐toxic, eco‐friendly synthesis of gold nanoparticles. Also hence many studies are now turned their interest into the biological microorganism. The benefits of the biological method include avoidance of toxic reagents, compatible, and so on. By seeing these benefits, biosurfactants could prove to be an appropriate method for enhancing the nanoparticle synthesis biologically. Only a few reports elucidated the synthesis of gold nanoparticles using biosurfactants. An ongoing methodology in this field is the utilisation of biosurfactant delivering microbial strain. Reddy et al. [100] examined the surfactant‐mediated gold nanoparticle synthesis. Using the bacteria Bacillus subtilis lipopeptide biosurfactant generated and the changes in the structure of lipopeptide alter the shape of the gold nanoparticles in this study. They conducted the study at acid, basic and neutral conditions in which aggregation does not occur at basic and neutral conditions. The results showed that the biosurfactant‐mediated gold nanoparticles are spherical in shape and very stable at basic and neutral [100]. Tomar et al. [101] synthesised the gold nanoparticles with the help of biosurfactant produced from Pseudomonas aeruginosa in which the biosurfactant acted as a capping agent. To make the gold nanoparticles synthesis more economical, more research needs to done in the biosurfactants.
3.3 Nickel nanoparticles
Nickel is an essential progress metal and nickel nanoparticles have boundless applications. Many authors are focused on the nickel nanoparticles because of its properties like catalytic activity and insulating property [102]. These enhanced properties make them a perfect for the application in battery cathode, electrochromic devices and gas sensors [103]. Due to these reasons, the nickel nanoparticles’ synthesis has attracted in incredible focal point of numerous researchers. Nickel nanoparticles are widely utilised as a part of different fields and are manufactured by different physico‐synthetic techniques including, i.e. sol–gel, micro‐emulsion, sonochemical, vapour phase and co‐precipitation methods [104, 105, 106, 107]. Palanisamy [108] depicted that they used rhamnolipid biosurfactants for the synthesis of nanoparticles. The results show that the pH of the biosurfactant plays a vital role in the morphology of nickel nanoparticles. This study was carried out in the microemulsion technique by using biosurfactant in the dispersed in n ‐heptane hydrocarbon phase. They identified that the morphology of the nanoparticles is changing with varying pH without affecting the environment. When the pH was increased, the morphology changed to the spherical shape and when pH was decreased, the morphology changes over to flaky shape.
3.4 Zinc nanoparticles
Zinc nanoparticles contain unique properties such as UV‐absorbing properties, sunscreen agents, anticancer and antibacterial activities, electronic, thermal and structural properties [109, 110, 111, 112]. It is considered as a most important nanoparticle because of its applications in various areas like a catalyst, sensors, optoelectronic, and photoelectron devices [113]. Zinc nanoparticles have high surface area and catalytic activity and hence they are helpful in the medical and pharmaceutical fields. Some of the applications as antimicrobial agents in baby powder, calamine cream, anti‐dandruff shampoos and antiseptic ointments [114]. When the size of the zinc oxide nanoparticles >100 nm, they are assumed to be biocompatible and then used for drug delivery. Several methods such as precipitation method, wet chemical synthesis, solid‐state pyrolytic method, sol–gel method are refined to synthesise zinc metal nanoparticles yet many disadvantages are explained in reports like aggregation, broadening the size of the particles, poor reproducibility, need high temperature and high pressure and so on [115, 116]. Zinc nanoparticles are less toxic and more compatible when compared with the other metal nanoparticles. The interaction of zinc with the pharmaceutical compounds is less, which was reported by Sahdev et al. [117]. The ‘biosynthesis’ is an ecologically well‐disposed process in science and chemical method is ending up progressively because of overall issues related with environmental contaminants [118]. To avoid the toxic waste, there is a need to develop an approach by using bacteria, algae, and fungi plant extracts [119]. During the synthesis of nanoparticles, the outcomes form microbes such as biosurfactants gets involved in the capping process [120]. Zinc oxide nanoparticles exhibit antioxidant property, which aroused the interest in synthesis [121].
In the last decades, chemical strategies have been utilised for the synthesis of zinc nanoparticles. The greater part of these strategies exhibits extreme ecological issues and natural dangers. Therefore, certain researchers reported a biological way using biosurfactants, i.e. rhamnolipids from Pseudomonas aeruginosa [122]. They analysed for the antioxidant property of biosurfactant mediated zinc nanoparticle and found that zinc nanoparticle is a promising antioxidant. This approach exploits the low‐cost eco‐friendly approach for the synthesis of nanoparticles [122]. In an attempt to synthesise zinc sulphide nanoparticles, they used biosurfactant (rhamnolipid) produced by Pseudomonas aeruginosa [123]. In this study, zinc sulphide nanoparticles synthesised using biosurfactants showed less degradation rate of direct brown MR textile dye. Yet the researchers concluded that ZnS nanoparticles demonstrated the best nanophotocatalyst. Narayanan et al. [124] utilised water‐dissolvable rhamnolipids delivered by Pseudomonas aeruginosa for capping ZnS nanoparticles and they also represented the metal affinity, size and optical properties of the rhamnolipid ZnS nanoparticles. FT‐IR spectra acquired for rhamnolipid‐topped ZnS nanoparticles demonstrated an affinity between COOH of rhamnolipid and metal ions.
3.5 Cadmium nanoparticles
A cadmium nanoparticle has a wide range of applications in the field like solar energy conversion, photoelectrochemical cells and photocatalysis etc., because of its unique properties. Chemical precipitation, thermal decomposition and γ‐irradiation were used for the synthesis of cadmium nanoparticles. These methods have certain downsides like the instability of nanoparticles, precipitation, broad particle size and so on [125]. Recently, the microbial synthesis of nanoparticles has been emerging alternative to the chemical and physical method [126, 127]. Still, this method also has restrictions like capping process is required for the increment of stability of the nanoparticles [128] and for this purpose bacterial biosurfactants can overcome this drawback, which could be a substitute for the conventional techniques. Singh et al. [115] investigated the synthesis of stable cadmium sulphide nanoparticles using surfactin produced by Bacillus amyloliquifaciens strain. In this study, a renewable bioresource obtained for surfactin production and applied in the nanotechnology in which it acts as a stabiliser for nanoparticle synthesis. The average yield of about 160 mg/L of surfactin was obtained, mixed with 1 Mm Cd(NO3)2 in ratio 1:1. The synthesised cadmium nanoparticle was stable up to 120 days and characterised using XRD, TEM and spectroscopic studies. The results suggested that biosurfactant is a significant biocompatible and effective stabilising agent for the development of stable cadmium nanoparticles [115]. This study elucidated that biosurfactant could be utilised as a renewable source for the development of nanoparticles.
3.6 Iron nanoparticles
Nanoparticle synthesis using different organic and inorganic materials provides novel properties [129]. The essential class of nanoparticles is iron nanoparticles because it possesses technological importance. The parameters, which influence the synthesis of iron nanoparticles, are temperature, pH, the concentration of precursor etc. The behaviour of magnetic nanoparticles depends on the size of the nanoparticles. Using the external magnetic field, the iron nanoparticles can modified for its usage in target tissue [130]. The iron nanoparticles have gained the interest as they are applied in biomedical applications like cell labelling, cell targeting, and separation of cells, tissue repair, radioactive therapies, magnetic resonance imaging, magnetofection and tumour hyperthermia due to its chemical, thermal, mechanical properties [131, 132, 133]. The other important application of iron nanoparticles is magnetic storage media, solar energy transformation, electronics and catalysis. A microemulsion, thermal decomposition, co‐precipitation methods, γ‐ray radiation and microwave plasma synthesis are widely used for preparing magnetic nanoparticles [134, 135, 136]. The formation of aggregation and wide particle size production occurs in the above‐mentioned methods. Hence, researchers are focused on the generation of magnetic nanoparticles using the biological method.
The iron nanoparticles can be synthesised using sophorolipids [137]. The acidic structures of sophorolipids were appropriate for use as surface complexing agents in the synthesis of iron oxide nanoparticles. Dynamic light scattering tests showed that sophorolipids‐determined nanoparticles had amazing colloidal stability both in water and in salt‐containing water. Baccile et al. [137] proposed that the availability of the sophorose aggregate at the surface of the nanoparticles is an imperative issue for biocompatibility properties of iron oxide nanoparticles. This study demonstrated that sophorose layer covered the iron oxide nanoparticles. A type of lipopeptide called surfactin was utilised by Liao et al. [138] for the stabilisation of super magnetic iron oxide nanoparticles. They found that the obtained nanoparticle is spherical in shape and dispersed easily in the aqueous phase.
4 Conclusion and future outlook
A wide assortment of microorganisms are known to create surface active compounds called biosurfactants with large ecological applications that give benefits over the chemical surfactants with high specificity, biodegradability, and biocompatibility. The investigation on the synthesis of nanoparticles will give a quick and novel indicative option for the biological method. This review represents the development of a green protocol for nanoparticle synthesis. The renewable biosurfactant‐based nanoparticles have appeared to be helpful in the creation of advanced materials. Biosurfactants delivered by microorganisms is an alternative to the petroleum‐based surfactants in the synthesis of advanced materials, not just for pharmaceutical and ecological applications, yet in addition to every aspect of the industry. In any case, their utilisation requires additional research to accomplish expansive scale creation and repeatability, tending to danger and security issues also. The biochemical and atomic components of biosynthesis of metallic nanoparticles should better comprehend to enhance the rate of synthesis of particles. The effect of biosurfactants on the shape, size and properties of metallic nanoparticles are required to explain the components that stimulate microbial growth to permit control of size, shape and crystallinity of the created nanoparticles. Future research on the part of biosurfactants in the biosynthesis of nanoparticles with remarkable properties is of extraordinary significance for particular applications in science, chemistry, agriculture and medicine.
5 References
- 1. Hudlikar M. Joglekar S. Dhaygude M. et al.: ‘Latex‐mediated synthesis of ZnS nanoparticles: green synthesis approach’, J. Nanoparticle Res., 2012, 14, (5), pp. 865 –871 [Google Scholar]
- 2. Tartaj P. Morales M.d.P.M. Veintemillas‐Verdaguer S. et al.: ‘Progress in the preparation of magnetic nanoparticles for applications in biomedicine’, J. Phys. D., Appl. Phys., 2003, 42, (22), pp. 182 –197 [Google Scholar]
- 3. Anandan S. Grieser F. Ashokkumar M.: ‘Sonochemical synthesis of Au–Ag core–shell bimetallic nanoparticles’, J. Phys. Chem. C, 2008, 112, pp. 15102 –15105 [Google Scholar]
- 4. Patel K. Kapoor S. Dave D.P. et al.: ‘Synthesis of Pt, Pd, Pt/Ag and Pd/Ag nanoparticles by microwave – polyol method’, J. Chem. Sci., 2005, 117, (4), pp. 311 –316 [Google Scholar]
- 5. Chen Z. Gao L.: ‘A facile and novel way for the synthesis of nearly monodisperse silver nanoparticles’, Mater. Res. Bull., 2007, 42, (9), pp. 1657 –1661 [Google Scholar]
- 6. Rangarajan V. Majumder S. Sen R.: ‘Biosurfactant‐mediated nanoparticle synthesis a green and sustainable approach’ (CRC Press Taylor & Francis Group, Boca Raton, 2014), pp. 221 –234 [Google Scholar]
- 7. Xie J. Lee J.Y. Wang D.I.C. et al.: ‘Silver nanoplates: from biological to biomimetic synthesis’, ACS Nano, 2007, 1, (5), pp. 429 –439 [DOI] [PubMed] [Google Scholar]
- 8. Xie J. Lee J.Y. Wang D.I.C. et al.: ‘Identification of active biomolecules in the high‐yield synthesis of single‐crystalline gold nanoplates in algal solutions’, Small, 2007, 3, (4), pp. 672 –682 [DOI] [PubMed] [Google Scholar]
- 9. Sharma V.K. Yngard R.A. Lin Y.: ‘Silver nanoparticles: green synthesis and their antimicrobial activities’, Adv. Colloid Interface Sci., 2009, 145, (1–2), pp. 83 –96 [DOI] [PubMed] [Google Scholar]
- 10. Bhattacharya D. Gupta R.K.: ‘Nanotechnology and potential of microorganisms’, Crit. Rev. Biotechnol., 2005, 25, (4), pp. 199 –204 [DOI] [PubMed] [Google Scholar]
- 11. Cuenya B.R.: ‘Synthesis and catalytic properties of metal nanoparticles: size, shape, support, composition, and oxidation state effects’, Thin Solid Films, 2010, 518, (12), pp. 3127 –3150 [Google Scholar]
- 12. Lin X.M. Samia A.C.S.: ‘Synthesis, assembly and physical properties of magnetic nanoparticles’, J. Magn. Magn. Mater., 2006, 305, (1), pp. 100 –109 [Google Scholar]
- 13. Laurent S. Forge D. Port M. et al.: ‘Magnetic iron oxide nanoparticles: synthesis, stabilization, vectorization, physicochemical characterizations and biological applications’, Chem. Rev., 2008, 108, (6), pp. 2064 –2110 [DOI] [PubMed] [Google Scholar]
- 14. Soenen S.J.H. Brisson A.R. De Cuyper M.: ‘Addressing the problem of cationic lipid‐mediated toxicity: the magneto liposome model’, Biomaterials, 2009, 30, (22), pp. 3691 –3701 [DOI] [PubMed] [Google Scholar]
- 15. Woo K. Hong J. Choi S. et al.: ‘Easy synthesis and magnetic properties of iron oxide nanoparticles’, Chem. Mater., 2004, 16, (14), pp. 2814 –2818 [Google Scholar]
- 16. Wu S. Sun A. Zhai F. et al.: ‘Fe3 O4 magnetic nanoparticles synthesis from tailings by ultrasonic chemical co‐precipitation’, Mater. Lett., 2011, 65, (12), pp. 1882 –1884 [Google Scholar]
- 17. Salazar‐Alvarez G. Muhammed M. Zagorodni A.A.: ‘Novel flow injection synthesis of iron oxide nanoparticles with narrow size distribution’, Chem. Eng. Sci., 2006, 61, (14), pp. 4625 –4633 [Google Scholar]
- 18. Ling D. Hyeon T.: ‘Chemical design of biocompatible iron oxide nanoparticles for medical applications’, Small, 2013, 9, (9–10), pp. 1450 –1466 [DOI] [PubMed] [Google Scholar]
- 19. Unsoy G. Yalcin S. Khodadust R. et al.: ‘Synthesis optimization and characterization of chitosan coated iron oxide nanoparticles produced for biomedical applications’, J. Nanoparticle Res., 2012, 14, (11), pp. 1 –13 [Google Scholar]
- 20. Teja A.S. Koh P.Y.: ‘Synthesis, properties, and applications of magnetic iron oxide nanoparticles’, Prog. Cryst. Growth Charact. Mater., 2009, 55, (1–2), pp. 22 –45 [Google Scholar]
- 21. Thorek D.L.J. Chen A.K. Czupryna J. et al.: ‘Superparamagnetic iron oxide nanoparticle probes for molecular imaging’, Ann. Biomed. Eng., 2006, 34, (1), pp. 23 –38 [DOI] [PubMed] [Google Scholar]
- 22. Kumar Sur U. Ankamwar B. Karmakar S. et al.: ‘Green synthesis of silver nanoparticles using the plant extract of Shikakai and Reetha ’, Mater. Today Proc., 2018, 5, (1), pp. 2321 –2329 [Google Scholar]
- 23. Xia W. Du Z. Cui Q. et al.: ‘Biosurfactant produced by novel Pseudomonas sp. WJ6 with biodegradation of n‐alkanes and polycyclic aromatic hydrocarbons’, J. Hazard. Mater., 2014, 276, pp. 489 –498 [DOI] [PubMed] [Google Scholar]
- 24. Nickzad A. Deziel E.: ‘Adaptive significance of quorum sensing‐dependent regulation of rhamnolipids by integration of growth rate in Burkholderia glumae: a trade‐off between survival and efficiency’, Front. Microbiol., 2016, 7, pp. 1 –15 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25. Banat I.M. Franzetti A. Gandolfi I. et al.: ‘Microbial biosurfactants production, applications and future potential’, Appl. Microbiol. Biotechnol., 2010, 87, (2), pp. 427 –444 [DOI] [PubMed] [Google Scholar]
- 26. Jimenez‐Penalver P. Gea T. Sánchez A. et al.: ‘Production of sophorolipids from winterization oil cake by solid‐state fermentation: optimization, monitoring and effect of mixing’, Biochem. Eng. J., 2016, 115, pp. 93 –100 [Google Scholar]
- 27. Silva R.d.C.F.S. Almeida D.G. Rufino R.D. et al.: ‘Applications of biosurfactants in the petroleum industry and the remediation of oil spills’, Int. J. Mol. Sci., 2014, 15, (7), pp. 12523 –12542 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28. Santos D.K.F. Rufino R.D. Luna J.M. et al.: ‘Biosurfactants: multifunctional biomolecules of the 21st century’, Int. J. Mol. Sci., 2016, 17, (3), pp. 1 –13 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29. Marchant R. Banat I.M.: ‘Microbial biosurfactants: challenges and opportunities for future exploitation’, Trends Biotechnol., 2012, 30, (11), pp. 558 –565 [DOI] [PubMed] [Google Scholar]
- 30. Anjum F. Gautam G. Edgard G. et al.: ‘Biosurfactant production through Bacillus sp. MTCC 5877 and its multifarious applications in food industry’, Bioresour. Technol., 2016, 213, pp. 262 –269 [DOI] [PubMed] [Google Scholar]
- 31. Kim L.H. Jung Y. Yu H.W. et al.: ‘Physicochemical interactions between rhamnolipids and Pseudomonas aeruginosa biofilm layers’, Environ. Sci. Technol., 2015, 49, (6), pp. 3718 –3726 [DOI] [PubMed] [Google Scholar]
- 32. Yin H. Qiang J. Jia Y. et al.: ‘Characteristics of biosurfactant produced by Pseudomonas aeruginosa S6 isolated from oil‐containing wastewater’, Process Biochem., 2009, 44, (3), pp. 302 –308 [Google Scholar]
- 33. Wang W. Cai B. Shao Z.: ‘Oil degradation and biosurfactant production by the deep sea bacterium Dietzia maris As‐13‐3’, Front. Microbiol., 2014, 5, pp. 1 –11 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34. Van Dyke M.I. Couture P. Brauer M. et al.: ‘ Pseudomonas aeruginosa UG2 rhamnolipid biosurfactants: structural characterization and their use in removing hydrophobic compounds from soil’, Can. J. Microbiol., 1993, 39, (11), pp. 1071 –1078 [DOI] [PubMed] [Google Scholar]
- 35. Soares da Silva R.d.C.F. Almeida D.G. Meira H.M. et al.: ‘Production and characterization of a new biosurfactant from Pseudomonas cepacia grown in low‐cost fermentative medium and its application in the oil industry’, Biocatal. Agric. Biotechnol., 2017, 12, pp. 206 –215 [Google Scholar]
- 36. Sharma D. Saharan B.S.: ‘Functional characterization of biomedical potential of biosurfactant produced by Lactobacillus helveticus ’, Biotechnol. Rep., 2016, 11, pp. 27 –35 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37. Chandankere R. Yao J. Cai M. et al.: ‘Properties and characterization of biosurfactant in crude oil biodegradation by bacterium Bacillus methylotrophicus USTBa’, Fuel, 2014, 122, pp. 140 –148 [Google Scholar]
- 38. Aparna A. Srinikethan G. Smitha H.: ‘Production and characterization of biosurfactant produced by a novel Pseudomonas sp. 2B’, Colloids Surf. B Biointerfaces, 2012, 95, pp. 23 –29 [DOI] [PubMed] [Google Scholar]
- 39. Wei Y.H. Chou C.L. Chang J.S.: ‘Rhamnolipid production by indigenous Pseudomonas aeruginosa J4 originating from petrochemical wastewater’, Biochem. Eng. J., 2005, 27, (2), pp. 146 –154 [Google Scholar]
- 40. Janek T. Łukaszewicz M. Krasowska A.: ‘Identification and characterization of biosurfactants produced by the Arctic bacterium Pseudomonas putida BD2’, Colloids Surf. B, Biointerfaces, 2013, 110, pp. 379 –386 [DOI] [PubMed] [Google Scholar]
- 41. Jimenez‐Penalver P. Castillejos M. Koh A. et al.: ‘Production and characterization of sophorolipids from stearic acid by solid‐state fermentation, a cleaner alternative to chemical surfactants’, J. Clean. Prod., 2018, 172, pp. 2735 –2747 [Google Scholar]
- 42. Marti M.E. Colonna W.J. Patra P. et al.: ‘Production and characterization of microbial biosurfactants for potential use in oil‐spill remediation’, Enzyme Microb. Technol., 2014, 55, pp. 31 –39 [DOI] [PubMed] [Google Scholar]
- 43. Bezza F.A. Beukes M. Chirwa E.M.N.: ‘Application of biosurfactant produced by Ochrobactrum intermedium CN3 for enhancing petroleum sludge bioremediation’, Process Biochem., 2015, 50, (11), pp. 1911 –1922 [Google Scholar]
- 44. Bezza F.A. Chirwa E.M.N.: ‘Production and applications of lipopeptide biosurfactant for bioremediation and oil recovery by Bacillus subtilis CN2’, Biochem. Eng. J., 2015, 101, pp. 168 –178 [Google Scholar]
- 45. Li J. Deng M. Wang Y. et al.: ‘Production and characteristics of biosurfactant produced by Bacillus pseudomycoides BS6 utilizing soybean oil waste’, Int. Biodeterior. Biodegrad., 2016, 112, pp. 72 –79 [Google Scholar]
- 46. Ohadi M. Dehghannoudeh G. Forootanfar H. et al.: ‘Investigation of the structural, physicochemical properties, and aggregation behavior of lipopeptide biosurfactant produced by Acinetobacter junii B6’, Int. J. Biol. Macromol., 2018, 112, pp. 712 –719 [DOI] [PubMed] [Google Scholar]
- 47. Fooladi T. Moazami N. Abdeshahian P. et al.: ‘Characterization, production and optimization of lipopeptide biosurfactant by new strain Bacillus pumilus 2IR isolated from an Iranian oil field’, J. Pet. Sci. Eng., 2016, 145, pp. 510 –519 [Google Scholar]
- 48. Khopade A. Ren B. Liu X.Y. et al.: ‘Production and characterization of biosurfactant from marine Streptomyces species B3’, J. Colloid Interface Sci., 2012, 367, (1), pp. 311 –318 [DOI] [PubMed] [Google Scholar]
- 49. Shivlata L. Satyanarayana T.: ‘Thermophilic and alkaliphilic actinobacteria: biology and potential applications’, Front. Microbiol., 2015, 6, p. 1014 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50. Capek I.: ‘Preparation of metal nanoparticles in water‐in‐oil (w/o) microemulsions’, Adv. Colloid Interface Sci., 2004, 110, (1–2), pp. 49 –74 [DOI] [PubMed] [Google Scholar]
- 51. Rahman K.S.M. Banat I.M. Thahira J. et al.: ‘Bioremediation of gasoline contaminated soil by a bacterial consortium amended with poultry litter, coir pith and rhamnolipid biosurfactant’, Bioresour. Technol., 2002, 81, (1), pp. 25 –32 [DOI] [PubMed] [Google Scholar]
- 52. Amani H. Müller M.M. Syldatk C. et al.: ‘Production of microbial rhamnolipid by Pseudomonas aeruginosa MM1011 for Ex situ enhanced oil recovery’, Appl. Biochem. Biotechnol., 2013, 170, (5), pp. 1080 –1093 [DOI] [PubMed] [Google Scholar]
- 53. Kulkarni M. Chaudhari R. Chaudhari A.: ‘Novel tensio‐active microbial compounds for biocontrol applications’, Appl. Microbiol., 2007, pp. 295 –304 [Google Scholar]
- 54. Whang L.M. Liu P.W.G. Ma C.C. et al.: ‘Application of rhamnolipid and surfactin for enhanced diesel biodegradation‐effects of pH and ammonium addition’, J. Hazard. Mater., 2009, 164, (2–3), pp. 1045 –1050 [DOI] [PubMed] [Google Scholar]
- 55. Christova N. Tuleva B. Kril A. et al.: ‘Chemical structure and in vitro antitumor activity of rhamnolipids from Pseudomonas aeruginosa BN10’, Appl. Biochem. Biotechnol., 2013, 170, (3), pp. 676 –689 [DOI] [PubMed] [Google Scholar]
- 56. Gudina E.J. Rodrigues A.I. Alves E. et al.: ‘Bioconversion of agro‐industrial by‐products in rhamnolipids toward applications in enhanced oil recovery and bioremediation’, Bioresour. Technol., 2015, 177, pp. 87 –93 [DOI] [PubMed] [Google Scholar]
- 57. Oliveira F.J.S. Vazquez L. de Campos N.P. et al.: ‘Production of rhamnolipids by a Pseudomonas alcaligenes strain’, Process Biochem., 2009, 44, (4), pp. 383 –389 [Google Scholar]
- 58. Jadhav M. Kalme S. Tamboli D. et al.: ‘Rhamnolipid from Pseudomonas desmolyticum NCIM‐2112 and its role in the degradation of Brown 3REL’, J. Basic Microbiol., 2011, 51, (4), pp. 385 –396 [DOI] [PubMed] [Google Scholar]
- 59. Vasileva‐Tonkova E. Gesheva V.: ‘Glycolipids produced by Antarctic Nocardioides sp. during growth on n‐paraffin’, Process Biochem., 2005, 40, (7), pp. 2387 –2391 [Google Scholar]
- 60. Thaniyavarn J. Chongchin A. Wanitsuksombut N. et al.: ‘Biosurfactant production by Pseudomonas aeruginosa A41 using palm oil as carbon source’, J. Gen. Appl. Microbiol., 2006, 52, pp. 215 –222 [DOI] [PubMed] [Google Scholar]
- 61. Ilori M.O. Amobi C.J. Odocha A.C.: ‘Factors affecting biosurfactant production by oil degrading Aeromonas sp. Isolated from a tropical environment’, Chemosphere, 2005, 61, (7), pp. 985 –992 [DOI] [PubMed] [Google Scholar]
- 62. Desjardine K. Pereira A. Wright H. et al.: ‘Tauramamide, a lipopeptide antibiotic produced in culture by Brevibacillus laterosporus isolated from a marine habitat: structure elucidation and synthesis’, J. Nat. Prod., 2007, 70, (12), pp. 1850 –1853 [DOI] [PubMed] [Google Scholar]
- 63. Das P. Mukherjee S. Sen R.: ‘Improved bioavailability and biodegradation of a model polyaromatic hydrocarbon by a biosurfactant producing bacterium of marine origin’, Chemosphere, 2008, 72, (9), pp. 1229 –1234 [DOI] [PubMed] [Google Scholar]
- 64. Zaragoza A. Aranda F.J. Espuny M.J. et al.: ‘Mechanism of membrane permeabilization by a bacterial trehalose lipid biosurfactant produced by Rhodococcus sp’, Langmuir, 2009, 25, (14), pp. 7892 –7898 [DOI] [PubMed] [Google Scholar]
- 65. Ortiz A. Teruel J.A. Manresa A. et al.: ‘Effects of a bacterial trehalose lipid on phosphatidylglycerol membranes’, Biochim. Biophys. Acta – Biomembr., 2011, 1808, (8), pp. 2067 –2072 [DOI] [PubMed] [Google Scholar]
- 66. Urum K. Pekdemir T.: ‘Evaluation of biosurfactants for crude oil contaminated soil washing’, Chemosphere, 2004, 57, (9), pp. 1139 –1150 [DOI] [PubMed] [Google Scholar]
- 67. Solaiman D.K.Y. Ashby R.D. Zerkowski J.A. et al.: ‘Simplified soy molasses‐based medium for reduced‐cost production of sophorolipids by Candida bombicola ’, Biotechnol. Lett., 2007, 29, (9), pp. 1341 –1347 [DOI] [PubMed] [Google Scholar]
- 68. Chen J. Song X. Zhang H. et al.: ‘Production, structure elucidation and anticancer properties of sophorolipid from Wickerhamiella domercqiae ’, Enzyme Microb. Technol., 2006, 39, (3), pp. 501 –506 [Google Scholar]
- 69. Li H. Ma X.J. Wang S. et al.: ‘Production of sophorolipids with eicosapentaenoic acid and docosahexaenoic acid from Wickerhamiella domercqiae var. sophorolipid using fish oil as a hydrophobic carbon source’, Biotechnol. Lett., 2013, 35, (6), pp. 901 –908 [DOI] [PubMed] [Google Scholar]
- 70. Pornsunthorntawee O. Maksung S. Huayyai O. et al.: ‘Biosurfactant production by Pseudomonas aeruginosa SP4 using sequencing batch reactors: effects of oil loading rate and cycle time’, Bioresour. Technol., 2009, 100, (2), pp. 812 –818 [DOI] [PubMed] [Google Scholar]
- 71. Pansiripat S. Pornsunthorntawee O. Rujiravanit R. et al.: ‘Biosurfactant production by Pseudomonas aeruginosa SP4 using sequencing batch reactors: effect of oil‐to‐glucose ratio’, Biochem. Eng. J., 2010, 49, (2), pp. 185 –191 [DOI] [PubMed] [Google Scholar]
- 72. Gudina E.J. Teixeira J.A. Rodrigues L.R.: ‘Isolation and functional characterization of a biosurfactant produced by Lactobacillus paracasei ’, Colloids Surf. B, Biointerfaces, 2010, 76, (1), pp. 298 –304 [DOI] [PubMed] [Google Scholar]
- 73. Seghal Kiran G. Anto Thomas T. Selvin J. et al.: ‘Optimization and characterization of a new lipopeptide biosurfactant produced by marine Brevibacterium aureum MSA13 in solid state culture’, Bioresour. Technol., 2010, 101, (7), pp. 2389 –2396 [DOI] [PubMed] [Google Scholar]
- 74. Duran N. Marcato P.D. Alves O.L. et al.: ‘Mechanistic aspects of biosynthesis of silver nanoparticles by several Fusarium oxysporum strains’, J. Nanobiotechnology, 2005, 3, pp. 1 –7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 75. Tabassum Khan N. Jamil Khan M.: ‘Mycofabricated silver nanoparticles: an overview of biological organisms responsible for its synthesis’, Process. Biochem., 2007, 42, pp. 919 –923 [Google Scholar]
- 76. Narayanan K.B. Sakthivel N.: ‘Biological synthesis of metal nanoparticles by microbes’, Adv. Colloid Interface Sci., 2010, 156, (1–2), pp. 1 –13 [DOI] [PubMed] [Google Scholar]
- 77. Quester K. Avalos‐Borja M. Castro‐Longoria E.: ‘Biosynthesis and microscopic study of metallic nanoparticles’, Micron, 2013, 54–55, pp. 1 –27 [DOI] [PubMed] [Google Scholar]
- 78. Cameotra S.S. Makkar R.S.: ‘Recent applications of biosurfactants as biological and immunological molecules’, Curr. Opin. Microbiol., 2004, 7, (3), pp. 262 –266 [DOI] [PubMed] [Google Scholar]
- 79. Sen R.: ‘Biotechnology in petroleum recovery: the microbial EOR’, Prog. Energy Combust. Sci., 2008, 34, (6), pp. 714 –724 [Google Scholar]
- 80. Kanlayavattanakul M. Lourith N.: ‘Lipopeptides in cosmetics’, Int. J. Cosmet. Sci., 2010, 32, (1), pp. 1 –8 [DOI] [PubMed] [Google Scholar]
- 81. Anastas P.T. Warner J.C.: Green Chemistry: Theory and Practice, Oxford University Press, Oxford, UK, 1998, p. 30 [Google Scholar]
- 82. Raveendran P. Fu J. Wallen S.L.: ‘Completely ‘Green’ synthesis and stabilization of metal nanoparticles’, J. Am. Chem. Soc., 2003, 125, (46), pp. 13940 –13941 [DOI] [PubMed] [Google Scholar]
- 83. Chou K.S. Lai Y.S.: ‘Effect of polyvinyl pyrrolidone molecular weights on the formation of nanosized silver colloids’, Mater. Chem. Phys., 2004, 83, (1), pp. 82 –88 [Google Scholar]
- 84. Kvitek L. Panácek A. Soukupova J. et al.: ‘Effect of surfactants and polymers on stability and antibacterial activity of silver nanoparticles (NPs)’, J. Phys. Chem. C, 2008, 112, (15), pp. 5825 –5834 [Google Scholar]
- 85. Falletta E. Bonini M. Fratini E. et al.: ‘Clusters of poly(acrylates) and silver nanoparticles: structure and applications for antimicrobial fabrics’, J. Phys. Chem., 2008, 112, pp. 11758 –11766 [Google Scholar]
- 86. Jain P. Pradeep T.: ‘Potential of silver nanoparticle‐coated polyurethane foam as an antibacterial water filter’, Biotechnol. Bioeng., 2005, 90, (1), pp. 59 –63 [DOI] [PubMed] [Google Scholar]
- 87. Kim K.J. Sung W.S. Suh B.K. et al.: ‘Antifungal activity and mode of action of silver nano‐particles on Candida albicans ’, BioMetals, 2009, 22, (2), pp. 235 –242 [DOI] [PubMed] [Google Scholar]
- 88. Rai M. Yadav A. Gade A.: ‘Silver nanoparticles as a new generation of antimicrobials’, Biotechnol. Adv., 2009, 27, (1), pp. 76 –83 [DOI] [PubMed] [Google Scholar]
- 89. Boutonnet M. Kizling J. Mintsa‐Eya V. et al.: ‘Monodisperse colloidal metal particles from nonaqueous solutions: catalytic behavior in hydrogenation of but‐1‐ene of platinum, palladium, and rhodium particles supported on pumice’, J. Catal., 1987, 103, (1), pp. 95 –104 [Google Scholar]
- 90. Reddy A.S. Chen C.Y. Baker S.C. et al.: ‘Synthesis of silver nanoparticles using surfactin: a biosurfactant as stabilizing agent’, Mater. Lett., 2009, 63, (15), pp. 1227 –1230 [Google Scholar]
- 91. Das M. Patowary K. Vidya R. et al.: ‘Microemulsion synthesis of silver nanoparticles using biosurfactant extracted from Pseudomonas aerugin osa MKVIT3 strain and comparison of their antimicrobial and cytotoxic activities’, IET Nanobiotechnol., 2016, 10, (6), pp. 1 –8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 92. Kumar C.G. Mamidyala S.K. Das B. et al.: ‘Synthesis of biosurfactant‐based silver nanoparticles with purified rhamnolipids isolated from Pseudomonas aeruginosa BS‐161R’, J. Microbiol. Biotechnol., 2010, 20, (7), pp. 1061 –1068 [DOI] [PubMed] [Google Scholar]
- 93. Farias C.B.B. Silva A.F. Rufino R.D. et al.: ‘Synthesis of silver nanoparticles using a biosurfactant produced in low‐costmediumas stabilizing agent’, Electron. J. Biotechnol., 2014, 17, pp. 122 –125 [Google Scholar]
- 94. Xie Y. Ye R. Liu H.: ‘Synthesis of silver nanoparticles in reverse micelles stabilized by natural biosurfactant’, Colloids Surf. A, Physicochem. Eng. Asp., 2006, 279, (1–3), pp. 175 –178 [Google Scholar]
- 95. Maragatham I. Govindammal M. Maragatham A.I. et al.: ‘Biosynthesis of silver nanoparticles by rhamnolipid produced by Pseudomonas fluorescens MFS‐1 from mangrove soil’, Int. J. Pharm. Biol. Arch., 2014, 5, (5), pp. 135 –140 [Google Scholar]
- 96. Kiran G.S. Sabu A. Selvin J.: ‘Synthesis of silver nanoparticles by glycolipid biosurfactant produced from marine Brevibacterium casei MSA19’, J. Biotechnol., 2010, 148, (4), pp. 221 –225 [DOI] [PubMed] [Google Scholar]
- 97. Saikia J.P. Bharali P. Konwar B.K.: ‘Possible protection of silver nanoparticles against salt by using rhamnolipid’, Colloids Surf. B, Biointerfaces, 2013, 104, pp. 330 –332 [DOI] [PubMed] [Google Scholar]
- 98. Kasture M.B. Patel P. Prabhune A.A. et al.: ‘Synthesis of silver nanoparticles by sophorolipids: effect of temperature and sophorolipid structure on the size of particles’, J. Chem. Sci., 2008, 120, (6), pp. 515 –520 [Google Scholar]
- 99. Wang Z. Chen J. Yang P. et al.: ‘Biomimetic synthesis of gold nanoparticles and their aggregates using a polypeptide sequence’, Appl. Organometal. Chem., 2007, 21, pp. 645 –651 [Google Scholar]
- 100. Reddy A.S. Chen C.‐Y. Chen C.‐C. et al.: ‘Synthesis of gold nanoparticles via an environmentally benign route using a biosurfactant’, J. Nanosci. Nanotechnol., 2009, 9, (11), pp. 6693 –6699 [DOI] [PubMed] [Google Scholar]
- 101. Tomar R.S. Banerjee S. Kaushik S. et al.: ‘Microbial synthesis of gold nanoparticles by biosurfactant producing Pseudomonas aeruginosa ’, Int. J. Adv. Life Sci., 2015, 8, (4), pp. 520 –527 [Google Scholar]
- 102. Kunes J. Anisimov V.I. Skornyakov S.L. et al.: ‘NiO: correlated band structure of a charge‐transfer insulator’, Phys. Rev. Lett., 2007, 99, (15), pp. 1 –4 [DOI] [PubMed] [Google Scholar]
- 103. Palanisamy P. Raichur A.M.: ‘Synthesis of spherical NiO nanoparticles through a novel biosurfactant mediated emulsion technique’, Mater. Sci. Eng. C, 2009, 29, (1), pp. 199 –204 [Google Scholar]
- 104. Bibi I. Kamal S. Ahmed A. et al.: ‘Nickel nanoparticle synthesis using Camellia sinensis as reducing and capping agent: growth mechanism and photo‐catalytic activity evaluation’, Int. J. Biol. Macromol., 2017, 103, pp. 783 –790 [DOI] [PubMed] [Google Scholar]
- 105. Babu R.S. Prabhu P. Narayanan S.S.: ‘Green synthesized nickel nanoparticles modified electrode in ionic liquid medium and its application towards determination of biomolecules’, Talanta, 2013, 110, pp. 135 –143 [DOI] [PubMed] [Google Scholar]
- 106. Eluri R. Paul B.: ‘Microwave assisted greener synthesis of nickel nanoparticles using sodium hypophosphite’, Mater. Lett., 2012, 76, pp. 36 –39 [Google Scholar]
- 107. Xu W. Liew K.Y. Liu H. et al.: ‘Microwave‐assisted synthesis of nickel nanoparticles’, Mater. Lett., 2008, 62, (17–18), pp. 2571 –2573 [Google Scholar]
- 108. Palanisamy P.: ‘Biosurfactant mediated synthesis of NiO nanorods’, Mater. Lett., 2008, 62, (4–5), pp. 743 –746 [Google Scholar]
- 109. Shoeb M. Singh B.R. Khan J.A. et al.: ‘ROS‐dependent anticandidal activity of zinc oxide nanoparticles synthesized by using egg albumen as a biotemplate’, Adv. Nat. Sci. Nanosci. Nanotechnol., 2013, 4, (3), p. 035015 [Google Scholar]
- 110. Vijayakumar S. Vaseeharan B. Malaikozhundan B. et al.: ‘ Laurus nobilis leaf extract mediated green synthesis of ZnO nanoparticles: characterization and biomedical applications’, Biomed. Pharmacother., 2016, 84, pp. 1213 –1222 [DOI] [PubMed] [Google Scholar]
- 111. Sruthi S. Millot N. Mohanan P.V.: ‘Zinc oxide nanoparticles mediated cytotoxicity, mitochondrial membrane potential and level of antioxidants in presence of melatonin’, Int. J. Biol. Macromol., 2017, 103, pp. 808 –818 [DOI] [PubMed] [Google Scholar]
- 112. Condello M. De Berardis B. Ammendolia M.G. et al.: ‘ZnO nanoparticle tracking from uptake to genotoxic damage in human colon carcinoma cells’, Toxicol. Vitr., 2016, 35, pp. 169 –179 [DOI] [PubMed] [Google Scholar]
- 113. Nel A. Xia T. Mädler L. et al.: ‘Toxic potential of materials at the nanolevel’, Science, 2006, 311, (5761), pp. 622 –627 [DOI] [PubMed] [Google Scholar]
- 114. Ansari S.A. Husain Q. Qayyum S. et al.: ‘Designing and surface modification of zinc oxide nanoparticles for biomedical applications’, Food Chem. Toxicol., 2011, 49, (9), pp. 2107 –2115 [DOI] [PubMed] [Google Scholar]
- 115. Singh B.R. Dwivedi S. Al‐Khedhairy A.A. et al.: ‘Synthesis of stable cadmium sulfide nanoparticles using surfactin produced by Bacillus amyloliquifaciens strain KSU‐109’, Colloids Surf. B, Biointerfaces, 2011, 85, (2), pp. 207 –213 [DOI] [PubMed] [Google Scholar]
- 116. Bai H.J. Zhang Z.M. Gong J.: ‘Biological synthesis of semiconductor zinc sulfide nanoparticles by immobilized Rhodobacter sphaeroides ’, Biotechnol. Lett., 2006, 28, (14), pp. 1135 –1139 [DOI] [PubMed] [Google Scholar]
- 117. Sahdev P. Podaralla S. Kaushik R.S. et al.: ‘Calcium phosphate nanoparticles for transcutaneous vaccine delivery’, J. Biomed. Nanotechnol., 2013, 9, (1), pp. 132 –141 [DOI] [PubMed] [Google Scholar]
- 118. Kharissova O.V. Dias H.V.R. Kharisov B.I. et al.: ‘The greener synthesis of nanoparticles’, Trends Biotechnol., 2013, 31, (4), pp. 240 –248 [DOI] [PubMed] [Google Scholar]
- 119. Wei X. Luo M. Li W. et al.: ‘Synthesis of silver nanoparticles by solar irradiation of cell‐free Bacillus amyloliquefaciens extracts and AgNO3 ’, Bioresour. Technol., 2012, 103, (1), pp. 273 –278 [DOI] [PubMed] [Google Scholar]
- 120. Singh B.R. Singh B.N. Khan W. et al.: ‘ROS‐mediated apoptotic cell death in prostate cancer LNCaP cells induced by biosurfactant stabilized CdS quantum dots’, Biomaterials, 2012, 33, (23), pp. 5753 –5767 [DOI] [PubMed] [Google Scholar]
- 121. Das D. Nath B.C. Phukon P. et al.: ‘Synthesis of ZnO nanoparticles and evaluation of antioxidant and cytotoxic activity’, Colloids Surf. B, Biointerfaces, 2013, 111, pp. 556 –560 [DOI] [PubMed] [Google Scholar]
- 122. Singh B.N. Rawat A.K.S. Khan W. et al.: ‘Biosynthesis of stable antioxidant ZnO nanoparticles by Pseudomonas aeruginosa rhamnolipids’, PLoS One, 2014, 9, (9), p. 106937 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 123. Hazra C. Kundu D. Chaudhari A. et al.: ‘Biogenic synthesis, characterization, toxicity and photocatalysis of zinc sulfide nanoparticles using rhamnolipids from Pseudomonas aeruginosa BS01 as capping and stabilizing agent’, J. Chem. Technol. Biotechnol., 2013, 88, (6), pp. 1039 –1048 [Google Scholar]
- 124. Narayanan J. Ramji R. Sahu H. et al.: ‘Synthesis, stabilisation and characterisation of rhamnolipid‐capped ZnS nanoparticles in aqueous medium’, IET Nanobiotechnol., 2010, 4, (2), p. 29 [DOI] [PubMed] [Google Scholar]
- 125. Mandal S. Phadtare S. Sastry M.: ‘Interfacing biology with nanoparticles’, Curr. Appl. Phys., 2005, 5, (2), pp. 118 –127 [Google Scholar]
- 126. Verma V.C. Kharwar R.N. Gange A.C.: ‘Biosynthesis of antimicrobial silver nanoparticles by the endophytic fungus Aspergillus clavatus ’, Nanomedicine, 2010, 5, (1), pp. 33 –40 [DOI] [PubMed] [Google Scholar]
- 127. Musarrat J. Dwivedi S. Singh B.R. et al.: ‘Production of antimicrobial silver nanoparticles in water extracts of the fungus Amylomyces rouxii strain KSU‐09’, Bioresour. Technol., 2010, 101, (22), pp. 8772 –8776 [DOI] [PubMed] [Google Scholar]
- 128. Reddy A.S. Chen C.‐Y. Chen C.‐C. et al.: ‘Biological synthesis of gold and silver nanoparticles mediated by the bacteria Bacillus subtilis ’, J. Nanosci. Nanotechnol., 2010, 10, (10), pp. 6567 –6574 [DOI] [PubMed] [Google Scholar]
- 129. Wu W. He Q. Jiang C.: ‘Magnetic iron oxide nanoparticles: synthesis and surface functionalization strategies’, Nanoscale Res. Lett., 2008, 3, (11), pp. 397 –415 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 130. Prijic S. Sersa G.: ‘Magnetic nanoparticles as targeted delivery systems in oncology’, Radiol. Oncol., 2011, 45, (1), pp. 1 –16 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 131. Hong R.Y. Pan T.T. Han Y.P. et al.: ‘Magnetic field synthesis of Fe3 O4 nanoparticles used as a precursor of ferrofluids’, J. Magn. Magn. Mater., 2007, 310, (1), pp. 37 –47 [Google Scholar]
- 132. Arbab A.S. Bashaw L.A. Miller B.R. et al.: ‘Characterization of biophysical and metabolic properties of cells labeled with superparamagnetic iron oxide nanoparticles and transfection agent for cellular MR imaging’, Radiology, 2003, 229, (3), pp. 838 –846 [DOI] [PubMed] [Google Scholar]
- 133. Bárcena C. Sra A.K. Gao J.: ‘Applications of magnetic nanoparticles in biomedicine’, in Liu J.P. Fullerton E. Gutfleisch O. Sellmyer D.J. (Ed.): ‘Nanoscale magnetic materials and applications’, (Springer, USA, Boston, MA, 2009), pp. 591 –626 [Google Scholar]
- 134. Shokuhfar A. Alibeigi S. Vaezi M.R. et al.: ‘Synthesis of Fe3 O4 nanoparticles prepared by various surfactants and studying their characterizations’, Defect Diffus. Forum, 2008, 273–276, pp. 22 –27 [Google Scholar]
- 135. Wang X. Zhuang J. Peng Q. et al.: ‘A general strategy for nanocrystal synthesis’, Nature, 2005, 437, (7055), pp. 121 –124 [DOI] [PubMed] [Google Scholar]
- 136. Park J. An K. Hwang Y. et al.: ‘Ultra‐large‐scale syntheses of monodisperse nanocrystals’, Nat. Mater., 2004, 3, (12), pp. 891 –895 [DOI] [PubMed] [Google Scholar]
- 137. Baccile N. Noiville R. Stievano L. et al.: ‘Sophorolipids‐functionalized iron oxide nanoparticles’, Phys. Chem. Chem. Phys., 2013, 15, (5), pp. 1606 –1620 [DOI] [PubMed] [Google Scholar]
- 138. Liao Z. Wang H. Wang X. et al.: ‘Biocompatible surfactin‐stabilized superparamagnetic iron oxide nanoparticles as contrast agents for magnetic resonance imaging’, Colloids Surf. A, Physicochem. Eng. Aspects, 2010, 370, (1–3), pp. 1 –5 [Google Scholar]