|SYMPOSIUM - REVIEW ARTICLE
|Year : 2012 | Volume
| Issue : 1 | Page : 74-81
Bio-inspired nanomaterials and their applications as antimicrobial agents
Smita Sachin Zinjarde
Institute of Bioinformatics and Biotechnology, University of Pune, Pune, Maharashtra, India
|Date of Web Publication||27-Mar-2012|
Smita Sachin Zinjarde
Associate Professor, Institute of Bioinformatics and Biotechnology, University of Pune, Pune - 411 007, Maharashtra
Source of Support: None, Conflict of Interest: None
| Abstract|| |
In the recent decades, the interdisciplinary field of nanotechnology has expanded extensively. A variety of nanoparticles (NPs) have been used for a number of specialized applications. In this era facing a major problem of microorganisms developing antibiotic resistance, NPs are a lucrative option. Most physical and chemical processes of NP synthesis are associated with drawbacks and bio-inspired NPs have now become popular. This review summarizes the recent developments on the biosynthesis, characterization, and applications of NPs with particular reference to their use as antimicrobial agents. Reviewed here is the synthesis of gold and silver NPs (AgNPs) by a variety of biological forms and biomolecules as well as their effectiveness toward different fungal and bacterial pathogens. The use of gold NPs (bio-inspired by plants, fungi, and bacteria) and AgNPs, synthesized by carbohydrates (of plant, animal, and microbial origin), plant parts (bark, callus, leaves, peels, and tubers), fungi, and bacteria have been highlighted. In addition, the use of zinc oxide NPs (although not bio-inspired) as novel antimicrobial agents have also been discussed.
Keywords: Antimicrobial agents, bio-inspired, nanoparticles
|How to cite this article:|
Zinjarde SS. Bio-inspired nanomaterials and their applications as antimicrobial agents. Chron Young Sci 2012;3:74-81
| Introduction|| |
In the past few decades, the field of nanotechnology has developed extensively. Nanotechnology, in general, refers to the synthesis, characterization, and applications of materials that are in the nanometer range (1 m = 10 9 nm). Nanometric material properties differ from the bulk properties. This difference is due to the very small size and high surface area of the former. Such nanoscale structures are known to bridge the gap between bulk materials and the atomic and molecular structures. Nanotechnology is thus an interdisciplinary field that involves physical, chemical, biological, and engineering sciences. Nanomaterials can be broadly grouped into two main categories: (i) organic which include carbon nanoparticles (NPs) such as fullerenes and (ii) inorganic particles such as those of noble metals (gold, silver, and platinum), magnetic NPs (iron, cobalt, and nickel), and those of semiconductors (oxides of titanium, zinc, cadmium) to mention a few. NPs from each of these categories have been used for a variety of specialized applications as detailed in relevant reviews. ,,,,,,,
Two major approaches have been used for the synthesis of metallic NPs. The "Top-down" approach begins with a suitable starting structure. This structure is decreased in size by employing a variety of physical or chemical methods. The "Bottom-up" methods involve the formation of nanostructures through the self-assembly in an atom-by-atom, molecule-by-molecule, or cluster-by-cluster manner. Biological synthesis of NPs, in general, involves this approach wherein, biomolecules mediate reductive processes and stabilize nanostructures. Most of the earlier studies on NP synthesis have involved the use of chemical or physical methods. These processes use high temperatures, apply radiations, include toxic chemicals, involve the generation of hazardous by-products, need specialized apparatus, and consume energy. On account of these issues, biological systems have emerged as effective alternatives for the rapid, cost-effective, and "green" synthesis of NPs. In general, biological systems (plant and microorganisms) display a vast variety of biomolecules with reductive properties. These mediate a reduction of metal salts to nanostructural elemental forms. The nanostructures thus formed are capped by additional biomolecules present in the biological material. Microorganisms are constantly exposed to metals and often have inherent defense reductive mechanisms that mediate the synthesis of a variety of NPs. This property makes them some of the most lucrative bio-machines for the synthesis of novel materials. There are several reviews on bio-inspired nanomaterials with respect to their synthesis, the mechanisms involved, and applications in different fields. ,,,[,13],,,,,, However, a review on the applications of these bio-inspired NPs as antimicrobial agents is missing. The present review hopes to fill this void in the literature.
| Nanoparticles as antimicrobial agents|| |
Infectious diseases are major cause of mortality worldwide. The appearance of antibiotic-resistant pathogenic strains has been threatening public health globally. In some cases, microorganisms display multiple drug resistance. This has triggered a need for the development of novel therapeutic agents. With nanotechnology emerging as a forefront area in integrated science, the use of NP-based therapeutics for controlling pathogenic bacteria has emerged as an important alternative.
A variety of NPs have been explored for their antimicrobial properties. These include NPs of silica, silica/iron oxide, bi-functional Fe 3 O 4 -Ag NPs, titanium, copper and aluminum, and those of silver, gold, and zinc, as discussed in this review. ,,,, The NPs when studied as antimicrobial agents have not necessarily been synthesized through biological systems. Although there are a few dedicated reviews on the use of bio-inspired silver NPs (AgNPs) as antimicrobial agents, , the present review describes recent update on the antimicrobial properties of bio-inspired NPs. In the following sections, the synthesis and application of a variety of NPs of the two major noble metals (gold and silver) has been presented in a classified manner. In addition, the applications of ZnONPs (although not bio-inspired) have also been discussed as they are becoming popular as antimicrobial agents with regard to medical applications.
| Gold nanoparticles as antimicrobial agents|| |
Gold NPs (AuNPs) have been studied extensively as they display several unique features. They can be synthesized by relatively simple methods, exhibit good water solubility, and display excellent stability. In recent years, green approaches for the generation of AuNPs are on the rise and their antimicrobial properties have also been evaluated. There are a few reports on AuNPs mediated by plant material, fungi, and bacteria, as shown in [Figure 1]. The following section summarizes the reports on bio-inspired AuNPs and their antimicrobial activities.
|Figure 1: Summary of bio-inspired gold nanoparticles as antimicrobial agents|
Click here to view
A few plant products have been applied for synthesizing antimicrobial AuNPs. For example, bioreduction of chloroauric acid (HAuCl 4 ) to Auº by the plant extract of Mentha piperita (Lamiaceae) has been reported recently.  Amide groups in the extract were thought to be involved in the synthetic process. The NPs were 150 nm and exhibited strong antibacterial activity against Escherichia More Details coli. AuNPs have also been synthesized by using banana peel (Musa paradisiaca) extract (BPE).  This simple, non-toxic, eco-friendly "green material" reduced HAuCl 4 to AuNPs. Dynamic light scattering studies revealed the average size of the NPs to be 300 nm. Fourier transform infra red (FTIR) spectroscopy indicated the involvement of carboxyl, amine, and hydroxyl groups in the synthetic process. The BPE-mediated NPs displayed efficient antimicrobial activity toward Candida albicans, Shigella sp., Citrobacter koseri, E. coli, Proteus vulgaris, and Enterobacter aerogenes. However, antibacterial activity was not observed with Klebsiella sp. and Pseudomonas aeruginosa.
A few microbial systems including fungi, yeasts, and bacteria have been used in the synthesis of antimicrobial AuNPs. A green method to synthesize nanogold-bioconjugate (NGBC) has been described.  The AuNPs (10 nm average diameter) were produced on the surface of Rhizopus oryzae by in situ reduction of HAuCl 4 . The NGBC showed high antimicrobial activity against Gram-negative and Gram-positive pathogenic bacteria as well as against yeasts (Saccharomyces cerevisiae and C. albicans). The NGBC has been proposed as a promising candidate for obtaining potable water free from pathogens. Extracellular synthesis of AuNPs by a yeast (Candida guilliermondii) has also been described.  The biosynthesized NPs were 50 to 70 nm and displayed antimicrobial activity against five pathogenic bacterial strains. The highest efficiency was observed against Staphylococcus aureus. In another report, the metal-reducing bacterium Shwanella oneidensis brought about the reduction of tetrachloroaurate (III) ions to extracellular homogenous spherical gold nanocrystallites with an average size of 12±5 nm.  The particles were possibly fabricated by reducing agents present in the cell membrane and were capped by a detachable protein/peptide. The antibacterial activity of these AuNPs was assessed against E. coli, S. oneidensis, and Bacillus subtilis. However, these AuNPs were neither toxic nor inhibitory toward any of the test bacteria.
Cefaclor is a well-known second-generation antibiotic belonging to the β-lactam class of antibiotics derived from the fungus Acremonium (previously Cephalosporium). There is a report on a one-pot synthetic method for the development of AuNPs (52-22 nm) using this antibiotic.  The primary amine group of cefaclor acted as the reducing as well as the capping agent leaving the β-lactam ring available for antibacterial activity. The cefaclor-reduced AuNPs displayed potent antimicrobial activity against S. aureus and E. coli as compared with cefaclor or AuNPs individually. The minimum inhibitory concentration (MIC) values of cefaclor-reduced AuNPs were found to be 10 μg/ml and 100 μg/ml for S. aureus and E. coli, respectively. The AuNPs thus obtained were also coated onto polyethyleneimine-modified glass surfaces to obtain antimicrobial coatings (inhibiting growth of E. coli) suitable for biomedical applications. The antibacterial activity of these particles was through the combined action of cefaclor inhibiting the synthesis of the peptidoglycan layer and AuNPs generating "holes" in bacterial cell walls.
| Silver nanoparticles as antimicrobial agents|| |
An extensive literature survey has shown that AgNPs are the most popular inorganic NPs to be used as antimicrobial agents. There are a few reviews that summarize the green methods for AgNP synthesis. ,,, This review will focus on the recent literature on bio-inspired NPs that have been tested for their antimicrobial activities. This literature has been classified in subsequent sections as (i) carbohydrate-mediated, (ii) plant-mediated, (iii) fungal biomass-mediated, and (iv) bacteria-mediated synthesis of AgNPs [Figure 2].
|Figure 2: Summary of bio-inspired silver nanoparticles as antimicrobial agents|
Click here to view
Carbohydrate polymer-mediated synthesis of silver nanoparticles and their antimicrobial activities
Plant- and animal-derived carbohydrates have been employed in the synthesis of AgNPs. [Table 1] summarizes carbohydrate polymer-mediated synthesis and properties of antimicrobial AgNPs.
|Table 1: Carbohydrate-mediated synthesis of antimicrobial silver nanoparticles|
Click here to view
Plant-inspired synthesis of silver nanoparticles and their applications as antimicrobial agents
A variety of plant parts including barks, callus, leaves, tubers, and fruit peels have been used for the synthesis of AgNPs that display antimicrobial properties. Cinnamon zeylanicum bark powder (CBP) and powder extracts (CBPE) have been applied for this purpose. CBPE was more effective in the reduction of Ag + to AgΊ. The antimicrobial activity of the AgNPs was tested against E. coli (BL 12). The effective concentrations required to induce a 50% effect (EC 50 ) were found to be 11 ± 1.72 mg/l and MIC values were 50 mg/l. 
The callus and leaf extracts of the coastal sea marsh plant Sesuvium portulacastrum L have also been investigated for their ability to synthesize AgNPs.  The former was more effective in NP synthesis. The size of the NPs was between 5 to 20 nm. Proteins, flavones, and terpenoids were responsible for stabilizing the AgNPs. Among P. aeruginosa, S. aureus, Listeria monocytogenes, Micrococcus luteus, Klebsiella pneumonia, Alternaria alternata, Penicillium italicum, Fusarium equiseti, and C. albicans that were tested, highest zone of inhibition (ZOI) of 23 mm was formed against S. aureus. On the other hand, M. luteus was approximately three-fold less affected (8 mm ZOI). The ZOI obtained with Penicillium sp. was 18 mm and with C. albicans, it was 12 mm.
The aqueous leaf extract of Acalypha indica, an Indian traditional medicinal plant, was also able to rapidly (within 30 minutes) reduce ionic silver and stabilize AgNPs that were 20 to 30 nm in size.  These AgNPs showed effective antibacterial activity against E. coli and Vibrio cholera. The MIC values (lowest concentration at which no visible growth of the test pathogens was observed) for both the cultures were 10 μg/ml. The leaf extracts of Eucalyptus citriodora and Ficus bengalensis have also been successfully employed for the "green" synthesis of cotton fibers loaded with AgNPs.  These extracts that were rich in polysaccharides composed of p-menthane-3,8-diol, β-sitosterol, α-d-glucose, and mesoinositol reduced silver salts and stabilized AgNPs (average size of 21 nm). Cotton fibers loaded with NPs were also fabricated by the in situ reduction of silver nitrate into AgNPs. The biological synthesis of AgNPs using Solanum torvum leaf extracts has been reported recently.  The reduction of the AgNO 3 to AgNPs was completed in 60 minutes. Carboxylate groups in the biological material were important in the reductive process. The average size of the NPs was 14 mm. The growth of P. aeruginosa, S. aureus, Aspergillus flavus, and Aspergillus niger was inhibited by these bio-inspired NPs.
A rapid, convenient, and extracellular method for synthesis of AgNPs has been developed with the help of onion (Allium cepa) leaf extract.  The average size of AgNPs was 33.6 nm. The effect of AgNPs on the bacterial growth was monitored on the basis of optical density measurements. As the concentration of AgNPs was increased, there was a decrease in bacterial growth of E. coli and Salmonella More Details typhimurium. Another simple eco-friendly mechanism for the biosynthesis of AgNPs has been reported by using leaf extracts of Garcinia mangostana (mangosteen).  Silver ions when exposed to leaf extract were reduced to AgNPs with an average size of 35 nm. Furthermore, these NPs were highly effective against a variety of multidrug-resistant human pathogens. For E. coli, the ZOI with AgNPs (20 μg/ ml) was 15 mm and for S. aureus, it was 20 mm. In a recent report, the bioreduction of silver nitrate to AgNPs by the plant extract of Mentha pipertita has also been described.  The amide groups were involved in NP synthesis that were 90 nm in size. The synthesized AgNPs exhibited strong antibacterial activity against E. coli and S. aureus, the test cultures that were used.
Synthesis of AgNPs by Curcuma longa tuber powder and extract has also been described.  The tuber extracts were more efficient in AgNP synthesis. In the extract, the content of the reducing agents was large and these were easily available for the reductive process. C. longa tubers are known to be rich in terpenoids such as cineol, borneol, and in zingiberene, sabinene, a-phellandrene, sesquiterpines, and curcumin. These along with protein components were believed to play a role in silver nanoparticle biosynthesis. The minimum bactericidal concentration of these AgNPs for E. coli BL-21 strain was found to be 50 mg/l. Immobilization of AgNPs on cotton cloth showed better bactericidal activity when compared with polyvinylidene fluoride-immobilized cloth.
The use of fruit peels for the synthesis of AgNPs with antimicrobial activity has also been reported. Bio-inspired AgNPs were synthesized with the aid of BPE (Musa paradisiaca), a non-toxic, eco-friendly biological material.  Boiled, crushed, acetone precipitated, air-dried peel powder brought about a reduction of silver nitrate. Silver nanosized crystallites were obtained after short incubation periods. FTIR analysis indicated the role of different functional groups (carboxyl, amine, and hydroxyl) in the synthetic process. These AgNPs displayed antimicrobial activity against fungi such as C. albicans and Candida lipolytica. They were also antibacterial against E. coli, E. aerogenes, Klebsiella sp., and Shigella sp. Other bacteria such as C. koseri, P. vulgaris, and P. aeruginosa, however, did not display the characteristic zones of inhibition, indicating that these cultures were not inhibited by the AgNPs.
The aqueous extracts of Citrus sinensis (orange) peels for the synthesis of starch-supported AgNPs is also reported.  The antimicrobial activity of these NPs was tested against B. subtilis in the presence and absence of rifampicin. In the absence of rifampicin, a larger ZOI (20 mm) was obtained. However, in the presence of rifampicin, this was 17 mm. The starch associated with the NPs allowed lesser diffusion of the NPs, thereby explaining the observed results.
Antimicrobial activities of silver nanoparticles synthesized by fungi
Fungi have been used extensively for the synthesis of AgNPs. [Table 2] summarizes the synthesis of AgNPs by a variety of fungi. The most frequent reports are on Aspergillus and Fusarium sp.
Bacterial synthesis of silver nanoparticles
A few Gram-negative bacteria have been used to synthesize antimicrobial AgNPs. AgNPs were synthesized by using Klebsiella pneumoniae and their antimicrobial activity against S. aureus and E. coli was evaluated.  The experimentation showed that the antibacterial activities of antibiotics such as penicillin G, amoxicillin, erythromycin, clindamycin, and vancomycin were enhanced in the presence of AgNPs against both the test cultures. With erythromycin, the highest synergistic activity was observed against the test S. aureus culture. In another study, the culture supernatant of P. aeruginosa strain BS-161R was effective in the simple and cost-effective green synthesis of AgNPs.  The reduction of silver ions resulted in mono-dispersed and spherical particles with an average size of 13 nm. The enzyme nitrate reductase and rhamnolipids present in the culture supernatant were thought to be responsible for the reduction and capping, respectively. The prepared AgNPs exhibited strong antimicrobial activity against S. aureus, Micrococcus luteus, C. albicans, and C. krusei at 8 μg/ml concentrations, suggesting a broad-spectrum nature of their antimicrobial activity. Another recent report describes the facile biosynthesis of small, spherical, nearly mono-dispersed silver nanocrystallites with average size of 4±1.5 nm by using the metal-reducing bacterium, Shwanella oneidensis MR-1.  Carbonyl, hydroxyl, amide, and carboxyl groups were involved in the synthetic process. Additionally, the antibacterial properties of these biogenic AgNPs were compared with those of chemically synthesized NPs (colloidal-Ag) and (oleate-Ag) on E. coli, S. oneidensis, and B. subtilis. The different chemical/biological coatings on the NPs significantly influenced their toxicity. The authors have suggested that such a strategy could in turn provide a means for adapting NPs for different applications or for altering their fate in biological and environmental systems.
There are a few reports on Gram-positive bacteria producing AgNPs. For example, the extracellular components of Streptomyces hygroscopicus resulted in the development of spherical AgNPs that were 20 to 30 nm.  Furthermore, the biosynthesized AgNPs significantly inhibited the growth of medically important pathogenic Gram-positive bacteria (B. subtilis and Enterococcus faecalis), Gram-negative bacteria (E. coli and S. typhimurium), and the yeast C. albicans. In another study, a strain of B. licheniformis was used to synthesize AgNPs.  These bio-inspired AgNPs were able to disrupt biofilms of two common bacterial pathogens, P. aeruginosa and S. epidermidis, a major cause of microbial keratitis. Observations in microtiter plate assays disclosed the potential of AgNPs in the effective inhibition of biofilm formation by these two cultures. The results strongly suggested the futuristic applications of AgNP-based contact lens care solutions, for biofilm-based human ocular problems.
| Other (non-bioinspired) inorganic nanoparticles as antimicrobial agents|| |
Oxides of titanium, copper, aluminum, and zinc are some of the other inorganic nanoscale materials that have antimicrobial activity. An extensive literature survey has shown that most of these NPs have not generally been synthesized by using biological systems. Although the aforementioned variety of metal oxides have been investigated for their antimicrobial activities, ZnONPs have received particular attention in medical settings.  Similar to other metal oxides, these ZnONPs have also been synthesized chemically. ZnONPs have several advantageous features. They display photo-catalytic and -oxidizing capacities against biological and chemical species. They are stable under harsh conditions and can be fabricated at ambient temperature. The most important character is that they are generally regarded as safe. [Table 3] summarizes the use of such chemically synthesized ZnONPs individually or in combinations with other agents in being effective as antimicrobial agents.
| Conclusion|| |
In conclusion, a variety of biological systems have been employed for the synthesis of NPs displaying antimicrobial properties. An important point that arises from the literature survey involved is that bio-inspired NPs of noble metals (silver, in particular) are very popular as antimicrobial agents. Most of the studies have involved the testing of antimicrobial properties against potential pathogens. However, these may also possess antimicrobial properties toward the normal flora. In the future, a possible line of investigation would be the development of nanomachines specifically destroying pathogenic microorganisms. However, it must be noted that there are a few constraints on the use of these NPs as antimicrobial agents. First, a dramatic increase in the prices of these noble metals worldwide would restrict their widespread use. Second, microorganisms are capable of developing resistance to metals through natural selection or horizontal gene transfer. Third, not all type of gold and AgNPs are antimicrobial in nature. There is thus a need to determine additional factors involved in the biosynthetic processes that make such nanoparticle preparations antimicrobial or non-antimicrobial. Another aspect is related to the use of crude extracts in the synthetic procedures. Components of these extracts should be tested for their detrimental effects on human health. It may thus be necessary to isolate and purify the components in the extract that mediate the synthetic process. It is also evident that apart from gold and AgNPs, oxides of other metals are less expensive, lucrative alternatives. There is scope for studies on the synthesis of such metal oxide NPs through biological routes and examination of their potential as antimicrobial agents.
| References|| |
|1.||Lee KS, El-Sayed MA. Gold and silver nanoparticles in sensing and imaging: Sensitivity of plasmon response to size, shape, and metal composition. J Phys Chem B 2006;110:19220-5. |
|2.||Li X, Elliott DW, Zhang W. Zero-valent iron nanoparticles for abatement of environmental pollutants: materials and engineering aspects. Crit Rev Solid State Mater Sci 2006;31:111-22. |
|3.||Liu WT. Nanoparticles and their biological and environmental applications. J Biosci Bioeng 2006;102:1-7. |
|4.||Jain PK, Huang X, El-Sayed IH, EL-Sayed MA. Noble metals on the nanoscale: Optical and photothermal properties and some applications in imaging, sensing, biology, and medicine. Acc Chem Res 2008;41:1578-86. |
|5.||Bhattacharya R, Mukherjee P. Biological properties of "naked" metal nanoparticles. Adv Drug Deliv Rev 2008;60:1289-306. |
|6.||Rasmussen JW, Martinez E, Louka P, Wingett DG. Zinc oxide nanoparticles for selective destruction of tumor cells and potential for drug delivery applications. Expert Opin Drug Deliv 2010;7:1063-77. |
|7.||Mahmoudi M, Simchi A, Imani M. Recent advances in surface engineering of superparamagnetic iron oxide nanoparticles for biomedical applications. J Iranian Chem Soc 2010;7:1-27. |
|8.||Mahmoudi M, Sahraian MA, Laurent S. Superparamagnetic iron oxide nanoparticles: Promises for diagnosis and treatment of multiple sclerosis. ACS Chem Neurosci 2011;2:118-40. |
|9.||Dujaradin E, Mann S. Bioinspired materials chemistry. Adv Mater 2002;14:1-13. |
|10.||Salata OV. Applications of nanoparticles in biology and medicine. J Nanobiotechnol 2004;2 Available from: http://www.jnanobiotechnology.com/content/2/1/3. [Last cited 2011 May 01]. |
|11.||Bhattacharya D, Gupta RK. Nanotechnology and potential of microorganisms. Crit Rev Biotechnol 2005;25:199-204. |
|12.||Mandal D, Bolander ME, Mukhopadhyay D, Sarkar G, Mukherjee P. The use of microorganisms for the formation of metal nanoparticles and their application. Appl Microbiol Biotechnol 2006;69:485-92. |
|13.||Thakkar KN, Mhatre SS, Parikh RY. Biological synthesis of metallic nanoparticles. Nanomed: Nanotechnol Biol Med 2010;6:257-62. |
|14.||Gade A, Ingle A, Whiteley C, Rai M. Mycogenic metal nanoparticles: progress and applications. Biotechnol Lett 2010;32:593-600. |
|15.||Sharma VK, Yngard RA, Lin Y. Silver nanoparticles: Green synthesis and their antimicrobial activities. Adv Coll Interf Sci 2009;145:83-96. |
|16.||Vijayaraghavan K, Nalini SP. Biotemplates in the green synthesis of silver nanoparticles. Biotechnol J 2010;5:1098-110. |
|17.||Tolaymat TM, El Badawy AM, Genaidy A, Scheckel KG, Luxton TP, Suidan M. An evidence-based environmental perspective of manufactured silver nanoparticle in syntheses and applications: A systematic review and critical appraisal of peer-reviewed scientific papers. Sci Total Environ 2010;408:999-1006. |
|18.||Rai M, Yadav A, Gade A. Silver nanoparticles as a new generation of antimicrobials. Biotechnol Adv 2009;27:76-83. |
|19.||Zhang X, Yan S, Tyagi RD, Surampalli RY. Synthesis of nanoparticles by microorganisms and their application in enhancing microbiological reaction rates. Chemosphere 2011;82:489-94. |
|20.||Williams DN, Ehrman SH, Holoman TR. Evaluation of the microbial growth response to inorganic Nanoparticles. J Nanobiotechnology 2006;4:3. |
|21.||Gong P, Li H, He X, Wang K, Hu J, Tan W, et al. Preparation and antibacterial activity of Fe 3 O 4 @Ag nanoparticles. Nanotechnol 2007;18:285604. |
|22.||Chung CJ, Lin HI, Chou CM, Hsieh PY, Hsiao CH, Shi ZY, et al. Inactivation of Staphylococcus aureus and Escherichia coli under various light sources on photocatalytic titanium dioxide thin film. Surf Coatings Technol 2009;203:1081-5. |
|23.||Ren G, Hu D, Cheng EW, Vargas-Reus MA, Reip P, Allaker RP. Characterisation of copper oxide nanoparticles for antimicrobial applications. Int J Antimicrob Agents 2009;33:587-90. |
|24.||Sadiq IM, Chowdhury B, Chandrasekaran N, Mukherjee A. Antimicrobial sensitivity of Escherichia coli to alumina nanoparticles. Nanomedicine 2009;5:282-6. |
|25.||MubarakAli D, Thajuddin N, Jeganathan K, Gunasekaran M. Plant extract mediated synthesis of silver and gold nanoparticles and its antibacterial activity against clinically isolated pathogens. Colloids Surf B Biointerfaces 2011;85:360-5. |
|26.||Bankar AV, Joshi BS, Kumar AR, Zinjarde SS. Banana peel extract mediated synthesis of gold nanoparticles. Colloids Surf B Biointerfaces 2010;80:45-50. |
|27.||Das SK, Das AR, Guha AK. Gold nanoparticles: Microbial synthesis and application in water hygiene management. Langmuir 2009;25:8192-9. |
|28.||Mishra A, Tripathy SK, Yun SI. Bio-synthesis of gold and silver nanoparticles from Candida guilliermondii and their antimicrobial effect against pathogenic bacteria. J Nanosci Nanotechnol 2011;11:243-8. |
|29.||Suresh AK, Pelletier DA, Wang W, Broich ML, Moon JW, Gu B, et al. Biofabrication of discrete spherical gold nanoparticles using the metal-reducing bacterium Shewanella oneidensis. Acta Biomaterialia 2011;7:2148-52. |
|30.||Rai A, Prabhune A, Perry CC. Antibiotic mediated synthesis of gold nanoparticles with potent antimicrobial activity and their application in antimicrobial coatings. J Mater Chem 2010;20:6789-98. |
|31.||Wei D, Sun W, Qian W, Ye Y, Ma X. The synthesis of chitosan-based silver nanoparticles and their antibacterial activity. Carbohydr Res 2009;344:2375-82. |
|32.||Kora AJ, Shashdhar RB, Arunachalam J. Gum kondagogu (Cochlospermum gossypium): A template for the green synthesis and stabilization of silver nanoparticles with antibacterial application. Carbohydr Polymers 2010;82:670-9. |
|33.||Bo¡zani´c DK, Dimitrijevi´c-Brankovi´c S, Bibi´c N, Luyt AS, Djokovi´c V. Silver nanoparticles encapsulated in glycogen biopolymer: Morphology, optical and antimicrobial properties. Carbohydr Polymers 2011;83:883-90. |
|34.||Venkatpurwar V, Pokharkar V. Green synthesis of silver nanoparticles using marine polysaccharide: Study of in-vitro antibacterial activity. Mater Lett 2011;65:999-1002. |
|35.||Sathishkumar M, Sneha K, Won SW, Cho CW, Kim S, Yun YS. Cinnamon zeylanicum bark extract and powder mediated green synthesis of nano-crystalline silver particles and its bactericidal activity. Colloids Surf B Biointerfaces 2009;73:332-8. |
|36.||Nabikhan A, Kandasamy K, Raj A, Alikunhi NM. Synthesis of antimicrobial silver nanoparticles by callus and leaf extracts from saltmarsh plant, Sesuvium portulacastrum L. Colloids Surf B Biointerfaces 2010;79:488-93. |
|37.||Krishnaraj C, Jagan EG, Rajasekar S, Selvakumar P, Kalaichelvan PT, Mohan N. Synthesis of silver nanoparticles using Acalypha indica leaf extracts and its antibacterial activity against water borne pathogens. Colloids Surf B Biointerfaces 2010;76:50-6. |
|38.||Ravindra S, Mohan YM, Reddy NN, Raju KM. Fabrication of antibacterial cotton fibres loaded with silver nanoparticles via "Green Approach" Coll Surf A. Physicochem Eng Asp 2010;367:31-40. |
|39.||Govindaraju K, Tamilselvan S, Kiruthiga V, Singaravelu G. Biogenic silver nanoparticles by Solanum torvum and their promising antimicrobial activity. J Biopesticides 2010;3:394-9. |
|40.||Saxena A, Tripathi RM, Singh RP. Biological synthesis of silver nanoparticles by using onion (Allium cepa) extract and their antibacterial activity. Digest J Nanomater Biostr 2010;5:427-32. |
|41.||Veerasamy R, Xin TZ, Gunasagaran S, Xiang TF, Yang EF, Jeyakumar N, et al. Biosynthesis of silver nanoparticles using mangosteen leaf extract and evaluation of their antimicrobial activities. J Saudi Chem Soc 2011;15:113-20. |
|42.||Sathishkumar M, Sneha K, Yun YS. Immobilization of silver nanoparticles synthesized using Curcuma longa tuber powder and extract on cotton cloth for bactericidal activity. Bioresour Technol 2010;101:7958-65. |
|43.||Bankar A, Joshi B, Kumar AR, Zinjarde S. Banana peel extract mediated novel route for the synthesis. Coll Surf A: Physicochem Eng Asp 2010;368:58-63. |
|44.||Konwarh R, Gogoi B, Philip R, Laskar MA, Karak N. Biomimetic preparation of polymer-supported free radical scavenging, cytocompatible and antimicrobial "green" silver nanoparticles using aqueous extract of Citrus sinensis peel. Colloids Surf B Biointerfaces 2011;84:338-45. |
|45.||Gade AK, Bonde P, Ingle AP, Marcato PD, Duran N, Rai MK. Exploitation of Aspergillus niger for synthesis of silver nanoparticles. J Biobased Mater Bioener 2008;2:243-7. |
|46.||Jaidev LR, Narasimha G. Fungal mediated biosynthesis of silver nanoparticles, characterization and antimicrobial activity. Colloids Surf B Biointerfaces 2010;81:430-3. |
|47.||Kathiresan K, Alikunhi NM, Pathmanaban S, Nabikhan A, Kandasamy S. Analysis of antimicrobial silver nanoparticles synthesized by coastal strains of Escherichia coli and Aspergillus niger. Can J Microbiol 2010;56:1050-9. |
|48.||Verma VC, Kharwar RN, Gange AC. Biosynthesis of antimicrobial silver nanoparticles by the endophytic fungus Aspergillus clavatus. Nanomed (Lond) 2010;5:33-40. |
|49.||Saravanan M, Nanda A. Extracellular synthesis of silver bionanoparticles from Aspergillus clavatus and its antimicrobial activity against MRSA and MRSE. Colloids Surf B Biointerfaces 2010;77:214-8. |
|50.||Binupriya AR, Sathishkumar M, Yun SI. Myco-crystallization of silver ions to nano-sized particles by live and dead cell filtrates of Aspergillus oryzae var viridis and its bactericidal activity towards Staphylococcus aureus KCCM 12256. Ind Eng Chem Res 2010;49:852-8. |
|51.||Ingle A, Gade A, Pierrat S, Sonnichsen C, Rai M. Mycosynthesis of silver nanoparticles using the fungus Fusarium acuminatum and its activity against some human pathogenic bacteria. Curr Nano. 2008;4:141-4. |
|52.||El-Rafie MH, Mohamed AA, Shaheen TI, Hebeish A. Antimicrobial effect of silver nanoparticles produced by fungal process on cotton fabrics. Carbohydr Polymers 2010;80:779-82. |
|53.||Birla SS, Tiwari VV, Gade AK, Ingle AP, Yadav AP, Rai MK. Fabrication of silver nanoparticles by Phoma glomerata and its combined effect against Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus. Letts Appl Microbiol 2009;48:173-9. |
|54.||Musarrat J, Dwivedi S, Singh BR, Al-Khedhairy AA, Azam A, Naqvi A. Production of antimicrobial silver nanoparticles in water extracts of the fungus Amylomyces rouxii strain KSU-09. Bioresour Technol 2010;101:8772-6. |
|55.||Fayaz AM, Balaji K, Girilal M, Yadav R, Kalaichelvan PT, Venketesan R. Biogenic synthesis of silver nanoparticles and their synergistic effect with antibiotics: A study against gram-positive and gram-negative bacteria. Nanomedicine 2010;6:103-9. |
|56.||Gajbhiye MB, Kesharwani JG, Ingle AP, Gade AK, Rai MK. Fungus mediated synthesis of silver nanoparticles and its activity against pathogenic fungi in combination of Fluconazole. Nanomedicine 2009;5:382-6. |
|57.||Maliszewska I, Sadowski Z. Synthesis and antibacterial activity of of silver nanoparticles. J Phys Conf Ser 2009;146:012024. |
|58.||Shahverdi AR, Fakhimi A, Shahverdi HR, Minaian S. Synthesis and effect of silver nanoparticles on the antibacterial activity of different antibiotics against Staphylococcus aureus and Escherichia coli. Nanomedicine 2007;3:168-71. |
|59.||Kumar GC, Mamidyala SK. Extracellular synthesis of silver nanoparticles using culture supernatant of Pseudomonas aeruginosa. Colloids Surf B Biointerfaces 2011;84:462-6. |
|60.||Suresh AK, Pelletier DA, Wang W, Moon JW, Gu B, NP Mortensen, et al. Silver nanocrystallites: Biofabrication using Shewanella oneidensis, and an evaluation of their comparative toxicity on Gram-negative and Gram-positive bacteria. Environ Sci Technol 2010;44:5210-5. |
|61.||Sadhasivam S, Shanmugam P, Yun K. Biosynthesis of silver nanoparticles by Streptomyces hygroscopicus and antimicrobial activity against medically important pathogenic microorganisms. Colloids Surf B Biointerfaces 2010;81:358-62. |
|62.||Kalishwaralal K, Manikanth SB, Pandian SR, Deepak V, Gurunathan S. Silver nanoparticles impede the biofilm formation by Pseudomonas aeruginosa and Staphylococcus epidermidis. Colloids Surf B Biointerfaces 2010;79:340-4. |
|63.||Jones N, Ray B, Ranjit KT, Manna AC. Antibacterial activity of ZnO nanoparticle suspensions on a broad spectrum of microorganisms. FEMS Microbiol Lett 2008;279:271-6. |
|64.||Gordon T, Perlstein B, Houbara O, Felner I, Banin E, Margel S. Synthesis and characterization of zinc/iron oxide composite nanoparticles and their antibacterial properties. Colloids Surf A: Physicochem Eng Asp 2011;374:1-8. |
|65.||Sharma D, Rajput J, Kaith BS, Kaur M, Sharma S. Synthesis of ZnO nanoparticles and study of their antibacterial and antifungal properties. Thin Solid Films 2010;519:1224-9. |
|66.||Wahab R, Mishra A, Yun SI, Kim YS, Shin HS. Antibacterial activity of ZnO nanoparticles prepared via non-hydrolytic solution route. Appl Microbiol Biotechnol 2010;87:1917-25. |
|67.||Nair S, Sasidharan A, Divya Rani VV, Menon D, Nair S, Manzoor K, et al. Role of size scale of ZnO nanoparticles and microparticles on toxicity toward bacteria and osteoblast cancer cells. J Mater Sci Mater Med 2009;20: S235-41. |
|68.||Rekha K, Nirmala M, Nair MG, Anukaliani A. Structural, optical, photocatalytic and antibacterial activity of zinc oxide and manganese doped zinc oxide nanoparticles. Physica B 2010;405:3180-5. |
|69.||Jin T, Sun D, Su JY, Zhang H, Sue HJ. Antimicrobial efficacy of zinc oxide quantum dots against Listeria monocytogenes, Salmonella enteritidis, and Escherichia coli O157: H7. J Food Sci 2009;74: M46-52. |
|70.||Reddy KM, Feris K, Bell J, Wingett DG, Hanley C, Punnoose A. Selective toxicity of zinc oxide nanoparticles to prokaryotic and eukaryotic systems. Appl Phys Lett 2007;90:2139021-3. |
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3]
|This article has been cited by|
||Autoclave mediated one-pot-one-minute synthesis of AgNPs and Au–Ag nanocomposite from Melia azedarach bark extract with antimicrobial activity against food pathogens
| ||Alok Pani,Joong Hee Lee,Soon-II Yun |
| ||Chemistry Central Journal. 2016; 10(1) |
|[Pubmed] | [DOI]|
||Nanoparticles: Alternatives Against Drug-Resistant Pathogenic Microbes
| ||Gudepalya Rudramurthy,Mallappa Swamy,Uma Sinniah,Ali Ghasemzadeh |
| ||Molecules. 2016; 21(7): 836 |
|[Pubmed] | [DOI]|
||“Green” seed-mediated synthesis and morphology of Au nanoparticles using ß-cyclodextrin
| ||F. R. Castiello,J. M. Romo-Herrera,M. H. Farías,E. D. Guerra,O. E. Contreras,G. Berhault,H. Kochkar,S. Fuentes,G. Alonso-Nuñez |
| ||Gold Bulletin. 2016; |
|[Pubmed] | [DOI]|
||3, 4-dihydroxy-L-phenylalanine-derived melanin from Yarrowia lipolytica mediates the synthesis of silver and gold nanostructures
| ||Mugdha Apte,Gauri Girme,Ashok Bankar,Ameeta RaviKumar,Smita Zinjarde |
| ||Journal of Nanobiotechnology. 2013; 11(1): 2 |
|[Pubmed] | [DOI]|
||Psychrotrophic yeast Yarrowia lipolytica NCYC 789 mediates the synthesis of antimicrobial silver nanoparticles via cell-associated melanin
| ||Mugdha Apte,Devashree Sambre,Shital Gaikawad,Swanand Joshi,Ashok Bankar,Ameeta Kumar,Smita Zinjarde |
| ||AMB Express. 2013; 3(1): 32 |
|[Pubmed] | [DOI]|