A green chemistry approach for synthesizing biocompatible gold nanoparticles
© Gurunathan et al.; licensee Springer. 2014
Received: 22 January 2014
Accepted: 8 May 2014
Published: 21 May 2014
Gold nanoparticles (AuNPs) are a fascinating class of nanomaterial that can be used for a wide range of biomedical applications, including bio-imaging, lateral flow assays, environmental detection and purification, data storage, drug delivery, biomarkers, catalysis, chemical sensors, and DNA detection. Biological synthesis of nanoparticles appears to be simple, cost-effective, non-toxic, and easy to use for controlling size, shape, and stability, which is unlike the chemically synthesized nanoparticles. The aim of this study was to synthesize homogeneous AuNPs using pharmaceutically important Ganoderma spp. We developed a simple, non-toxic, and green method for water-soluble AuNP synthesis by treating gold (III) chloride trihydrate (HAuCl4) with a hot aqueous extract of the Ganoderma spp. mycelia. The formation of biologically synthesized AuNPs (bio-AuNPs) was characterized by ultraviolet (UV)-visible absorption spectroscopy, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray (EDX), dynamic light scattering (DLS), and transmission electron microscopy (TEM). Furthermore, the biocompatibility of as-prepared AuNPs was evaluated using a series of assays, such as cell viability, lactate dehydrogenase leakage, and reactive oxygen species generation (ROS) in human breast cancer cells (MDA-MB-231). The color change of the solution from yellow to reddish pink and strong surface plasmon resonance were observed at 520 nm using UV-visible spectroscopy, and that indicated the formation of AuNPs. DLS analysis revealed the size distribution of AuNPs in liquid solution, and the average size of AuNPs was 20 nm. The size and morphology of AuNPs were investigated using TEM. The biocompatibility effect of as-prepared AuNPs was investigated in MDA-MB-231 breast cancer cells by using various concentrations of AuNPs (10 to 100 μM) for 24 h. Our findings suggest that AuNPs are non-cytotoxic and biocompatible. To the best of our knowledge, this is the first report to describe the synthesis of monodispersed, biocompatible, and soluble AuNPs with an average size of 20 nm using Ganoderma spp. This study opens up new possibilities of using an inexpensive and non-toxic mushroom extract as a reducing and stabilizing agent for the synthesis of size-controlled, large-scale, biocompatible, and monodispersed AuNPs, which may have future diagnostic and therapeutic applications.
KeywordsAuNPs Biocompatibility Ganoderma spp Human breast cancer cells Transmission electron microscopy UV-visible spectroscopy
In recent years, gold nanoparticles (AuNPs) have been of great research interest because of their unique properties, such as size- and shape-dependent optoelectronic, physiochemical, and biological properties as well as various potential therapeutic applications. AuNPs possess distinct physical and chemical properties that make them excellent tools for creating novel chemical and biological sensors[1–3]. First, AuNPs can be synthesized using a simple method and made highly stable. Second, they possess unique optoelectronic properties. Third, they provide high surface-to-volume ratios with excellent biocompatibility when using appropriate ligands. Fourth, these AuNP properties can be readily tuned by varying their size and shape as well as the surrounding chemical environment.
Because of their stability, oxidation resistance, and biocompatibility, AuNPs have a wide range of potential applications, such as in electronics and photonics, catalysis, information storage, chemical sensing and imaging, drug delivery, and biological labeling[4, 5]. The tuning of AuNPs is an important process to enhance versatility in defining and controlling the shape. Thus, new methodologies are essential for designing shape-controlled synthesis of AuNPs[6–8].
Several synthetic chemical methods have been adopted for AuNP synthesis, including physical methods, such as attrition and pyrolysis, which were previously utilized for the synthesis of metallic nanoparticles. Alternatively, chemical methods are the most widely and traditionally used methods and incorporate various reducing agents, such as hydrazine and sodium borohydride. However, many of these methods can be cumbersome and involve the use of toxic chemicals, high temperatures, and pressures and, most importantly, can cause the particles to become unstable or aggregate upon interaction with biological media or biomolecules. At the same time, these approaches produce multi-shaped nanoparticles that require purification by differential centrifugation, and consequently have a low yield[12, 13]. Therefore, there is a constant need for new methodologies to produce shape-controlled synthesis of AuNPs.
Recently, several labs have been interested in developing methodologies for synthesis of nanomaterials using a green chemistry approach, which is an alternate approach to biosynthesizing nanomaterials that relies on natural organisms for the reduction of metal ions into stable nanocrystals[14–21]. Biological methods are supposed to yield novel and complex structural entities, unlike those obtained using conventional techniques[14, 15, 22]. A number of microbial species have been used for synthesis of metal nanoparticles but without much success in achieving shape control. The shape-controlled microbial synthesis of nanostructures is an exciting new area with considerable potential for development. Recently, Das et al. reported the synthesis of single-crystalline AuNPs and different nanostructures from HAuCl4 using Rhizopus oryzae.
Biological methods exhibit size and shape control over a diverse array of materials, and they also facilitate mass production, high yield, and reproducibility[23, 24]. Biosynthesis of AuNPs and silver nanoparticles (AgNPs) have been reported in different prokaryotic organisms, including Bacillus licheniformis, Brevibacterium casei, Bacillus subtilis, Escherichia coli, Lactobacillus, Pseudomonas aeruginosa, and Rhodopseudomonas capsulate. Several researchers exploited fungi as reducing agents for AgNP synthesis, including fungi such as Verticillium, Fusarium oxysporum, Aspergillus fumigatus, Penicillium fellutanum, Volvariella volvacea, Pleurotus florida, Candida, Ganoderma lucidum, and Neurospora crassa.
Among nanoparticles, AuNPs have immense potential for cancer diagnosis and therapy. Conjugation of AuNPs to ligands on cancer cells allows molecular imaging and detection of cancer. Further, AuNPs have potential applications in electronics, catalysis, biological sensors, cancer diagnostics, therapeutics, nanomedicine, and environmental work, because they have several merits, such as the fact that they are easy to synthesize, cost effective, and non-toxic, and they have easy functionalization, optical properties, facile surface chemistry, and biocompatibility[37, 38]. Moreover, biological processes could provide significant yield and are free from downstream processing; therefore, many researchers are interested in synthesizing nanoparticles with green manufacturing technology that uses bacteria, fungi, plants, and plant products.
In most studies, either AuNPs or AgNPs were synthesized using bacteria. Many fungi have not been explored, including those mentioned above, and only a few fungi have been investigated for AuNP and AgNP synthesis. Among fungi that have not been tested, Ganoderma spp. have long been used as medicinal mushrooms in Asia, and they have an array of pharmacological properties, including immunomodulatory activity and pharmacological properties. Ganoderma spp. have several advantages: They have large quantities of viable mycelia, they are cost-effective, there is easy downstream processing, and they are non-pathogenic. Moreover, the synthesized AuNPs are highly soluble in water. Therefore, the aim of this study was to investigate the possible use of Ganoderma spp. as green producers for AuNP synthesis and to further evaluate the biocompatibility effect of as-prepared AuNPs in human breast cancer cells (MDA-MB-231).
Gold (III) chloride trihydrate was purchased from Sigma (St. Louis, MO, USA). Penicillin-streptomycin solution, trypsin-EDTA solution, Dulbecco's modified Eagle's medium (DMEM/F-12), and 1% antibiotic-antimycotic solution were obtained from Life Technologies GIBCO (Grand Island, NY, USA). All the other chemicals and reagents were purchased from Sigma (St. Louis, MO, USA), unless otherwise specified.
Culturing and maintenance of Ganoderma spp
The culture of Ganoderma spp. was collected from a tropical forest near Pollachi, Tamilnadu, India. Culturing and maintenance were conducted as described in previous studies, with suitable modifications[40, 41]. Briefly, the mycelia were cultured on potato dextrose agar (PDA) and incubated at 28°C ± 2°C for 7 days. The mycelia were then transferred to glucose yeast malt peptone broth (GYMP). The inoculated medium was incubated at 28°C ± 2°C and agitated at 150 rpm for 10 days. After incubation, the mycelia were harvested, washed with distilled water, freeze-dried, and stored at 4°C in air-tight containers, prior to use.
Preparation of mycelia hot aqueous extract
The preparation of mushroom extract was carried out according to a method described in previous studies[40, 41], with suitable modifications. In brief, the freeze-dried mycelia were soaked in distilled water at a ratio of 1:20 and double boiled for 45 min, left to cool, and filtered through Whatman filter paper No. 4. The hot aqueous extract was then freeze-dried at -70°C ± 2°C for 48 h and stored at 4°C in airtight containers. The freeze-dried hot aqueous extract of the mycelia was used as the reducing and stabilizing agent for AuNP synthesis.
Synthesis of AuNPs
Synthesis of AuNPs was carried out according to the method described earlier. In a typical reaction, 1 mg/mL of freeze-dried hot aqueous mushroom mycelia extract was mixed with an aqueous solution of 1 mM HAuCl4 solution and kept at room temperature for 24 h. Synthesis was observed using ultraviolet (UV)-visible spectroscopy. The color change observed was from pale yellow to purple. To compare the efficiency of biologically prepared AuNPs, we used citrate-mediated synthesis of AuNPs (chem-AuNPs) from Sigma.
Characterization of AuNPs
Characterization of synthesized AuNPs was carried out according to previously described methods. The nanoparticles were primarily characterized by UV-visible spectroscopy, which has proven to be a very useful technique for nanoparticle analysis. UV-visible (UV-vis) spectra were obtained using a WPA (Biowave II, Biochrom, Cambridge, UK). Dispersion particle size was measured by Zetasizer Nano ZS90 (Malvern Instruments Limited, Malvern, UK).
The synthesized AuNPs were freeze dried, powdered, and used for X-ray diffraction (XRD) analysis. The spectra were evaluated using an X-ray diffractometer (PHILIPS X'Pert-MPD diffractometer, Amsterdam, the Netherlands) and Cu-Kα radiation (1.5405 Å) over an angular range of 10° to 80° at 40 kV and 30 mA. The dried powder was diluted with potassium bromide at a the ratio of 1:100, and the results were recorded using the Fourier transform infrared spectroscopy (FTIR; PerkinElmer Inc., Walham, MA, USA) and spectrum GX spectrometry within the range of 500 to 4,000 cm-1.
Transmission electron microscopy (TEM, JEM-1200EX, JEOL Ltd., Tokyo, Japan) was used to determine the size and morphology of AuNPs. AuNPs were prepared by dropping a small amount of aqueous dispersion on copper grids, which were dried and then examined in the TEM. Further, the presence of Au metals in the sample was analyzed by energy dispersive X-ray analysis (EDX) combined with a field emission SEM.
MDA-MB-231 human breast cancer cells were kindly provided by Kyung Jin Lee, Institute for Life Sciences, ASAN Medical Center, University of Ulsan College of Medicine. MDA-MB-231 breast cancer cell lines were grown adherently and maintained in DMEM containing 10% fetal calf serum (FCS) and 1% antibiotic solution containing penicillin and streptomycin at 37°C under 5% CO2. All the experiments were performed in six-well plates, unless stated otherwise. Cells were seeded onto plates at a density of 1 × 106 cells per well and incubated for 24 h prior to the experiments. The cells were washed with phosphate buffered saline (PBS, pH 7.4) and incubated in fresh medium containing different concentrations of AuNPs dissolved in water.
Cell viability assay
In order to evaluate the biocompatibility of the as-prepared AuNPs, we carried out cell viability assay in breast cancer cells (MDA-MB-231) by using MTT reagents. In addition, to compare the biocompatibility effect of bio-AuNPs, we used chemical-mediated synthesis of chem-AuNPs as a positive control. Cell viability was measured using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide dye reduction assay performed to determine the cytotoxic effect of the AuNPs at various concentrations. Briefly, the cells were plated onto 96-well flat-bottom culture plates with various concentrations of AuNPs (0 to100 μM). All the cultures were incubated for 24 h at 37°C in a humidified incubator. After 24 h of incubation (37°C, 5% CO2 in a humid atmosphere), 10 μL of MTT (5 mg/mL in PBS) was added to each well, and the plate was incubated for another 4 h at 37°C. The resulting formazan was dissolved in 100 μL of DMSO with gentle shaking at 37°C, and the absorbance was measured at 595 nm by using an ELISA reader (Spectra MAX; Molecular Devices, Sunnyvale, CA, USA). The results are shown as the mean of three independent experiments.
Cell membrane integrity of MDA-MB-231 cells was evaluated by determining the activity of lactate dehydrogenase (LDH) leaking out of the cell, according to the manufacturer's instructions (in vitro toxicology assay kit, TOX7, Sigma, USA). The LDH assay is based on the release of the cytosolic enzyme LDH from cells with damaged cellular membranes. Thus, in cell culture, AuNPs induced cytotoxicity and were quantitatively analyzed by measuring the activity of LDH in the supernatant. Briefly, cells were exposed to various concentrations of AuNPs for 24 h, and then 100 μL per well of each cell-free supernatant was transferred in triplicates into wells in a 96-well plate, and 100 μL of LDH-assay reaction mixture was added to each well. After 3-h incubation under standard conditions, the optical density of the generated color was determined at a wavelength of 490 nm using a Microplate Reader.
Determination of ROS
Intracellular reactive oxygen species (ROS) were measured based on the intracellular peroxide-dependent oxidation of 2′,7′-dichlorodihydrofluorescein diacetate (DCFH-DA, Molecular Probes, Eugene, OR, USA) to form the fluorescent compound 2′,7′-dichlorofluorescein (DCF), as previously described. Cells were seeded onto 24-well plates at a density of 5 × 104 cells per well and cultured for 24 h. After washing twice with PBS, fresh medium containing 100 μM of AuNPs, 1 mM H2O2, or AgNPs (5 μg/mL) was added, and the cells were incubated for 24 h. For the control, cells were added to 20 μM of DCFH-DA and incubation continued for 30 min at 37°C. The cells were rinsed with PBS, 2 mL of PBS was added to each well, and fluorescence intensity was determined with a spectrofluorometer (Gemini EM) with excitation at 485 nm and emission at 530 nm. For the control, had antioxidant N-acetyl-l-cystein (NAC, 5 mM) was added to the cells grown in 24-well plates (for 24 h) for 1 h prior to exposure to AuNPs, 1 mM H2O2, or AgNPs (5 μg/mL) for 24 h. We then added 20 μM of DCFH-DA, and the cells were incubated for 30 min at 37°C before measuring DCF fluorescence changes as described.
Results and discussion
Extracellular synthesis of AuNPs
Further, to determine if there was AuNP synthesis, the biosynthesis of nanoparticle reactions was monitored by UV-vis spectroscopy. UV-vis absorption spectroscopy is the most widely used technique for characterizing the optical properties and electronic structure of nanoparticles, because the absorption bands are related to the diameter and different aspect ratios of metal nanoparticles, including size and shape. As shown in Figure 1, the spectra of AuNP synthesis showed a gradual increase in the surface plasmon resonance (SPR) excitation peak centered at 520 nm, which is characteristic of AuNPs[11, 43]. This further indicates that the mushroom extract could be useful as a reducing agent for AuNP synthesis. Control reactions in the absence of mushroom extract exhibited no change in color or absorbance at 520 nm, clearly indicating that the protein and polysaccharides found in the extract are responsible for biosynthesis of AuNPs.
Previous studies demonstrated that metal biotransformation might involve a complex of either capping proteins/peptides and reductases, quinines, cytochromes, phytochelatins, or electron shuttles that are known to reduce various metals and metal oxides[11, 43–46]. Das et al. proposed possible mechanisms of AuNP synthesis in Rhizopus oryzae. The first mechanism is binding of Au (III) on the cell wall through electrostatic interaction followed by reduction to AuNPs by proteins/enzymes present on the cell wall, and the second is diffusion or transportation of Au (III) into the cytoplasm and protein/enzymatic reduction to form AuNPs. Taken together, these results indicate that AuNP synthesis could be facilitated by the presence of proteins in the extract.
XRD analysis of AuNPs
Gupta and Bector observed four different intense peaks at 2θ angle: 38.22, 44.42, 64.71, and 77.62 with Bragg reflections corresponding to (111), (200), (220), and (311) in biomass-associated AuNPs. Alternatively, only a single prominent peak was observed at 2θ angle: 38.22 with a Bragg reflection corresponding to (111) in extracellular AuNPs. Our present findings are consistent with earlier studies that used biological methods to synthesize AuNPs using plant extracts[49–51], yeast, and bacteria.
It is well known that proteins can bind to AuNPs either through free amine groups or cysteine residues in the proteins; therefore, stabilization of the AuNPs by surface-bound proteins is a possibility in the case of AuNPs synthesized by Ganoderma spp. Additionally, the bands at 1,636 cm-1 can be assigned to the vibrational modes of C=C double bonds of these molecules. The large peak between 1,500 and 1,700 cm-1 falls in the region of C=O stretching frequency, and the bands at 3,492 cm-1 correspond to carbonyl and hydroxyl functional groups in alcohols and phenol derivatives[11, 16, 55]. The FTIR results show that the surface capping of AuNPs synthesized by the mushroom extract is predominantly by proteins. Moreover, our results are consistent with those reported earlier for biosynthesized nanoparticles[11, 16, 50, 51, 55].
Particle size analysis
In our results, we found that the absorption peak is at 520 nm, which corresponds to a particle size of 20 nm. Moreover, our results are consistent with the absorption spectra and particle size analysis data obtained for chemically prepared AuNPs that have a characteristic band at 524 nm, corresponding to a 20-nm particle size. To confirm the particular size and shape, synthesized AuNPs were further analyzed using TEM.
Homogeneous nanoparticles with specific shapes are important for applications in biological and chemical sensing as well as for optical, medical, and electronic devices because the optical properties of AuNPs are dependent on the size and shape. Several studies have reported synthesis of various size AuNPs using different fungi. Fusarium oxysporum produced spherical and triangular morphologies of particles with a size range of 20 to 40 nm. Honary et al. reported that Penicillium aurantiogriseum, Penicillium citrinum, and Penicillium waksmanii synthesized AuNPs that were fairly uniform with spherical shapes and had average diameters of 153.3, 172, and 160.1 nm, respectively. Alternatively, the fungi Aspergillus fumigates and Neurospora crassa produced average AuNP sizes of 25 and 32 nm, respectively.
Effect of AuNPs on cell viability
The use of nontoxic and biocompatible nanoparticles with capping materials is an important aspect of biomedical applications. Consequently, the cytotoxic effects and future health problems caused by nanoparticles must be considered in the engineering of such materials. It is essential to validate whether as-prepared AuNPs are toxic or biocompatible, because biomedical applications of any nanomaterial involves intentional exposure to nanoparticles. Therefore, understanding the properties of nanoparticles and their effects on the human body are crucial before they are clinically applied.
Shukla et al. suggested that AuNPs are not cytotoxic, reduce the production of reactive oxygen and nitrite species, and do not stimulate secretion of proinflammatory cytokines, such as TNF-alpha and IL1-beta, making them suitable candidates for nanomedicine. Using a human leukaemia cell line, gold nanospheres of different sizes (4, 12, and 18 nm in diameter) and capping agents were found to be nontoxic based on the MTT assay. Similarly, Arnida et al. found that plain spherical AuNPs and PEGylated spheres and rods did not interfere with the proliferation of PC-3 cells when cells were exposed to as high as 1.5 nM of AuNPs for a period of over two population doubling times (88 h). Plain spherical particles that were 50 and 90 nm in diameter slightly stimulated the proliferation of PC-3 cells. Parab et al. investigated the biocompatibility effect of sodium hexametaphosphate (HMP)-stabilized AuNPs (Au-HMPs) in tumor and fibroblast cells. Synthesized Au-HMP nanoparticles and their surface-modified counterparts revealed non-cytotoxic properties in tested cells and showed biocompatibility.
Mukherjee et al. designed and developed an AuNP-based drug delivery system (DDS) (Au-DOX) containing doxorubicin (DOX). Administration of this DDS to breast cancer cells (MCF-7 and MDA-MB-231) showed significant inhibition of breast cancer cell proliferation compared with pristine doxorubicin. The viability of the bovine retinal pigment epithelial cells was not affected with an AuNP concentration of up to 300 nM, and increasing the concentrations above 300 nM resulted in significant cell death. AuNPs have anti-oxidative and anti-hyperglycemic activities in streptozotocin-induced diabetic mice by balancing or inhibiting ROS generation in hyperglycemic conditions by scavenging free radicals and leading to increased anti-oxidant defense enzymes in mice.
Effect of AuNPs on LDH leakage
Pan et al. found that 1.4-nm gold nanospheres triggered necrosis and mitochondrial damage and induced oxidative stress in endothelial and epithelial cells. In contrast, they found no evidence of cellular damage for 15-nm gold nanospheres bearing the same surface group, and these results also suggest that the toxicity of AuNPs depends on size. Interestingly, citrate-capped AuNPs (13 nm in diameter) were found to be toxic to a human carcinoma lung cell line but not to a human liver carcinoma cell line at the same dosage.
Uboldi et al. reported that, after 24 to 48 h of exposure, AuNPs induced a mild LDH release in the human ATII-like cell line A549, independent of the presence or absence of surface contaminants. Additionally, after 72 h of exposure to AuNPs, there was a dose-dependent release of LDH in the supernatant, and the amount of LDH released was significantly higher compared with shorter exposure times. Zhang et al. reported that chloroplast-mediated synthesis of AuNPs retained up to 85% better viability in both GES-1 and MGC-803 cells, even up to 150 μg/mL after 36 h of treatment. Freese et al. studied the effect of AuNPs on the amount of LDH released into the supernatant, and they suggest that up to 100 μM of AuNPs did not induce cytotoxicity in human dermal microvascular endothelial cells (HDMECs) and human cardiac microvascular endothelial cells (hCMECs). Altogether, our findings suggest that the biologically derived AuNPs with an average size of 20 nm are biocompatible.
ROS, which are a specific type of oxygen-containing reactive molecule, play important roles in various cellular processes and are known to be essential for basal cell proliferation. Higher concentrations of ROS lead to cell death[69, 70]. Several studies suggested that nanoparticle-mediated cytotoxicity is associated with ROS production.
Chuang et al. extensively studied the exposure of three different-sized AuNPs in human gastric carcinoma (AGS) and human lung adenocarcinoma epithelial (A549) cells. Their results suggest that significant increases of ROS generation occur with certain concentrations of AuNPs in AGS cells. Conversely, no obvious increases were observed for A549 cells in any of the three sizes of AuNPs. The authors eventually concluded that ROS signaling may play a role in AuNP-induced apoptotic cell death in AGS cells.
Furthermore, western blot analyses revealed that the expression of proteins involved in the anti-oxidative defense system was not significantly modulated any of the three sizes of AuNPs in both lines, except for a modest increase in TrxR-1 and SOD-1 in AGS cells. Altogether, our results suggest that biologically synthesized AuNPs have significant biocompatibility and could possibly be used for ultrasensitive detection, gene transfer, biomolecular imaging, drug delivery, and cancer therapy.
Synthesis of nanoparticles using biological systems is an important area of nanobiotechnology. Here we show a simple, rapid, clean, efficient, cost-effective, and green method for the synthesis of biocompatible AuNPs using Ganoderma spp. extract as a reducing and stabilizing agent. The as-prepared AuNPs were characterized via UV-vis, XRD, FTIR, EDX, DLS, and TEM. The biologically derived AuNPs were spherical, discrete, and the average size was 20 nm. The biocompatibility effect of AuNPs was investigated using cell viability, LDH, and ROS assays. The results indicate that biologically derived AuNPs are biocompatible. Finally, this eco-friendly method provides an alternative route for large-scale production of biocompatible AuNPs that can be used in catalysis, sensors, electronics, and biomedical applications, especially for cancer therapy.
This work was supported by the KU-Research Professor Program of Konkuk University. Dr Sangiliyandi Gurunathan was supported by a Konkuk University KU-Full-time Professorship.
This work was supported by the Woo Jang-Choon project (PJ007849) and the next generation of Biogreen 21 (PJ009107) from the Rural Development Administration (RDA), Republic of Korea.
- Daniel MC, Astruc D: Gold nanoparticles: assembly, supramolecular chemistry, quantum-size-related properties, and applications toward biology, catalysis, and nanotechnology. Chem Rev 2004, 104(1):293–346. 10.1021/cr030698+View ArticleGoogle Scholar
- Boisselier E, Astruc D: Gold nanoparticles in nanomedicine: preparations, imaging, diagnostics, therapies and toxicity. Chem Soc Rev 2009, 38(5):1759–1782.View ArticleGoogle Scholar
- Saha K, Agasti SS, Kim C, Li XN, Rotello VM: Gold nanoparticles in Chemical and Biological Sensing. Chem Rev 2012, 112(5):2739–2779. 10.1021/cr2001178View ArticleGoogle Scholar
- Corti CW, Holiday RJ: Commercial aspects of gold applications: from materials science to chemical science. Gold Bull 2004, 37(1–2):20–26.View ArticleGoogle Scholar
- Das SK, Das AR, Guha AK: Microbial synthesis of multishaped gold nanostructures. Small 2010, 6(9):1012–1021. 10.1002/smll.200902011View ArticleGoogle Scholar
- Wong SS, Joselevich E, Woolley AT, Cheung CL, Lieber CM: Covalently functionalized nanotubes as nanometre-sized probes in chemistry and biology. Nature 1998, 394(2):52–55.Google Scholar
- Tang Z, Kotov NA, Giersig M: Spontaneous organization of single CdTe nanoparticles into luminescent nanowires. Science 2002, 297(12):237–240.View ArticleGoogle Scholar
- Grubbs RB: Nanoparticle assembly: solvent-tuned structures. Nat Mater 2007, 6(8):553–555.View ArticleGoogle Scholar
- Li C, Price JE, Milas L, Hunter NR, Ke S, Yu DF, Charnsangavej C, Wallace S: Antitumor activity of poly( L -glutamic acid)-paclitaxel on syngeneic and xenografted tumors. Clin Cancer Res 1999, 5: 891–897.Google Scholar
- Kim JS, Kuk E, Yu KN, Kim JH, Park SJ, Lee HJ, Kim SH, Park YK, Park YH, Hwang CY, Kim YK, Lee YS, Jeong DH, Cho MH: Antimicrobial effects of silver nanoparticles. Nanomedicine 2007, 3(1):95–101. 10.1016/j.nano.2006.12.001View ArticleGoogle Scholar
- Suresh AK, Pelletier DA, Wang W, Broich ML, Moon JW, Gu B, Allison DP, Joy DC, Phelps TJ, Doktycz MJ: Biofabrication of discrete spherical gold nanoparticles using the metal-reducing bacterium Shewanella oneidensis . Acta Biomater 2011, 7(5):2148–2152. 10.1016/j.actbio.2011.01.023View ArticleGoogle Scholar
- Puntes VF, Krishnan KM, Alivisatos AP: Colloidal nanocrystal shape and size control: the case of cobalt. Science 2001, 291(16):2115–2117.View ArticleGoogle Scholar
- Murphy CJ: Nanocubes and nanoboxes. Science 2002, 298(5601):2139–2141. 10.1126/science.1080007View ArticleGoogle Scholar
- Mukherjee P, Ahmad A, Mandal D, Senapati S, Sainkar SR, Khan MI, Ramani R, Parischa R, Ajayakumar PV, Alam M, Sastry M, Kumar R: Bioreduction of AuCl4- ions by the fungus, Verticillium sp. and surface trapping of the gold nanoparticles formed. Angew Chem Int Ed Engl 2001, 40(19):3585–3588. 10.1002/1521-3773(20011001)40:19<3585::AID-ANIE3585>3.0.CO;2-KView ArticleGoogle Scholar
- Mukherjee P, Senapati S, Mandal D, Ahmad A, Khan MI, Kumar R, Sastry M: Extracellular synthesis of gold nanoparticles by the fungus Fusarium oxysporum . ChemBioChem 2002, 3(5):461–463. 10.1002/1439-7633(20020503)3:5<461::AID-CBIC461>3.0.CO;2-XView ArticleGoogle Scholar
- Ahmad A, Mukherjee P, Senapati S, Mandal D, Khan MI, Kumar R, Sastry M: Extracellular biosynthesis of silver nanoparticles using the fungus Fusarium oxysporum . Colloids Surf B: Biointer 2003, 28(4):313–318. 10.1016/S0927-7765(02)00174-1View ArticleGoogle Scholar
- Kumar V, Yadav SK: Plant-mediated synthesis of silver and gold nanoparticles and their applications. J Chem Technol Biot 2009, 84(2):151–157. 10.1002/jctb.2023View ArticleGoogle Scholar
- Bhambure R, Bule M, Shaligram N, Kamat M, Singhal R: Extracellular biosynthesis of gold nanoparticles using Aspergillus niger – its characterization and stability. Chem Eng Technol 2009, 32(7):1036–1041. 10.1002/ceat.200800647View ArticleGoogle Scholar
- Das SK, Das AR, Guha AK: Gold nanoparticles: microbial synthesis and application in water hygiene management. Langmuir 2009, 25(14):8192–8199. 10.1021/la900585pView ArticleGoogle Scholar
- Kalishwaralal K, Deepak V, Pandian Ram Kumar S, Gurunathan S: Biological synthesis of gold nanocubes from Bacillus licheniformis . Bioresour Technol 2009, 100(21):5356–5358. 10.1016/j.biortech.2009.05.051View ArticleGoogle Scholar
- Kalishwaralal K, Deepak V, Pandian SRK, Kottaisamy M, BarathManiKanth S, Kartikeyan B, Gurunathan S: Biosynthesis of silver and gold nanoparticles using Brevibacterium casei . Colloids Surf B: Biointerf 2010, 77(2):257–262. 10.1016/j.colsurfb.2010.02.007View ArticleGoogle Scholar
- Klaus T, Joerger R, Olsson E, Granqvist CG: Silver-based crystalline nanoparticles, microbially fabricated. Proc Natl Acad Sci USA 1999, 96(24):13611–13614. 10.1073/pnas.96.24.13611View ArticleGoogle Scholar
- Jin Y, Li H, Bai J: Homogeneous selecting of a quadruplex-binding ligand-based gold nanoparticle fluorescence resonance energy transfer assay. Anal Chem 2009, 81(14):5709–5715. 10.1021/ac900482pView ArticleGoogle Scholar
- Narayanan KB, Sakthivel N: Biological synthesis of metal nanoparticles by microbes. Adv Colloid Interface Sci 2010, 156(1–2):1–13.View ArticleGoogle Scholar
- Beveridge TJ, Murray RG: Sites of metal deposition in the cell wall of Bacillus subtilis . J Bacteriol 1980, 141(2):876–887.Google Scholar
- Gurunathan S, Kalishwaralal K, Vaidyanathan R, Venkataraman D, Pandian SR, Muniyandi J, Hariharan N, Eom SH: Biosynthesis, purification and characterization of silver nanoparticles using Escherichia coli . Colloids Surf B: Biointerf 2009, 74(1):328–335. 10.1016/j.colsurfb.2009.07.048View ArticleGoogle Scholar
- Nair B, Pradeep T: Coalescence of nanoclusters and formation of submicron crystallites assisted by Lactobacillus strains. Cryst Growth Des 2002, 2(4):293–298. 10.1021/cg0255164View ArticleGoogle Scholar
- Husseiny MI, El-Aziz MA, Badr Y, Mahmoud MA: Biosynthesis of gold nanoparticles using Pseudomonas aeruginosa . Spectrochim Acta A 2007, 67(3–4):1003–1006.View ArticleGoogle Scholar
- He S, Guo Z, Zhang Y, Zhang S, Wang J, Gu N: Biosynthesis of gold nanoparticles using the bacteria Rhodopseudomonas capsulata . Mater Lett 2007, 61(18):3984–3987. 10.1016/j.matlet.2007.01.018View ArticleGoogle Scholar
- Bhainsa KC, D’Souza SF: Extracellular biosynthesis of silver nanoparticles using the fungus Aspergillus fumigatus . Colloids Surf B: Biointerf 2006, 47(2):160–164. 10.1016/j.colsurfb.2005.11.026View ArticleGoogle Scholar
- Kathiresan K, Manivannan S, Nabeel MA, Dhivya B: Studies on silver nanoparticles synthesized by a marine fungus, Penicillium fellutanum isolated from coastal mangrove sediment. Colloids Surf B: Biointerf 2009, 71(1):133–137. 10.1016/j.colsurfb.2009.01.016View ArticleGoogle Scholar
- Philip D: Biosynthesis of Au, Ag and Au–Ag nanoparticles using edible mushroom extract. Spectrochim Acta A Mol Biomol Spectrosc 2009, 73(2):374–381. 10.1016/j.saa.2009.02.037View ArticleGoogle Scholar
- Bhat R, Deshpande R, Ganachari SV, Huh DS, Venkataraman A: Photo-irradiated biosynthesis of silver nanoparticles using edible mushroom Pleurotus florida and their antibacterial activity studies. Bioinorg Chem Appl 2011, 2011(2011):7.Google Scholar
- Ahmad T, Wani IA, Manzoor N, Ahmed J, Asiri AM: Biosynthesis, structural characterization and antimicrobial activity of gold and silver nanoparticles. Colloids Surf B: Biointerf 2013, 107: 227–234.View ArticleGoogle Scholar
- Karwa A, Gaikwad S, Rai MK: Mycosynthesis of silver nanoparticles using Lingzhi or Reishi medicinal mushroom, Ganoderma lucidum (W. Curt.:Fr.) P. Karst . and their role as antimicrobials and antibiotic activity enhancers. Int J Medicinal Mushrooms 2011, 13(5):483–491. 10.1615/IntJMedMushr.v13.i5.80View ArticleGoogle Scholar
- Castro-Longoria E, Vilchis-Nestor AR, Avalos-Borja M: Biosynthesis of silver, gold and bimetallic nanoparticles using the filamentous fungus Neurospora crassa . Colloids Surf B: Biointerf 2011, 83(1):42–48. 10.1016/j.colsurfb.2010.10.035View ArticleGoogle Scholar
- Jain PK, El-Sayed IH, El-Sayed MA: Au nanoparticles target cancer. Nanotoday 2007, 2(1):18–29. 10.1016/S1748-0132(07)70016-6View ArticleGoogle Scholar
- Mukherjee S, Sushma V, Patra S, Barui AK, Bhadra MP, Sreedhar B, Ranjan Patra C: Green chemistry approach for the synthesis and stabilization of biocompatible gold nanoparticles and their potential applications in cancer therapy. Nanotechnology 2012, 23(45):455103. 10.1088/0957-4484/23/45/455103View ArticleGoogle Scholar
- Seow SLS, Naidu M, David P, Wong KH, Sabaratnam V: Potentiation of neuritogenic activity of medicinal mushrooms in rat pheochromocytoma cells. BMC Complement Altern Med 2013, 13: 157. 10.1186/1472-6882-13-157View ArticleGoogle Scholar
- Lin ES, Chen YH: Factors affecting mycelial biomass and exopolysaccharide production in submerged cultivation of Antrodia cinnamomea using complex media. Bioresour Technol 2007, 98(13):2511–2517. 10.1016/j.biortech.2006.09.008View ArticleGoogle Scholar
- Wong KH, Sabaratnam V, Abdullah N, Naidu M, Keynes R: Activity of aqueous extracts of lion’s mane mushroom Hericium erinaceus (Bull.: Fr.) Pers. (Aphyllophoromycetideae) on the neural cell line NG108–15. Int J Medicinal Mushrooms 2007, 9(1):57–65. 10.1615/IntJMedMushr.v9.i1.70View ArticleGoogle Scholar
- Phillips RL, Miranda OR, You CC, Rotello VM, Bunz UHF: Rapid and efficient identification of bacteria using gold-nanoparticle–poly(para-phenyleneethynylene) constructs. Angew Chem Int Ed Engl 2008, 47(14):2590–2594. 10.1002/anie.200703369View ArticleGoogle Scholar
- Anil Kumar S, Abyaneh MK, Gosavi SW, Kulkarni SK, Pasricha R, Ahmad A, Khan MI: Nitrate reductase-mediated synthesis of silver nanoparticles from AgNO3. Biotechnol Lett 2007, 29(3):439–445. 10.1007/s10529-006-9256-7View ArticleGoogle Scholar
- Marsili E, Baron DB, Shikhare ID, Coursolle D, Gralnick JA, Bond DR: Shewanella secretes flavins that mediate extracellular electron transfer. Proc Natl Acad Sci USA 2008, 105(10):3968–3973. 10.1073/pnas.0710525105View ArticleGoogle Scholar
- Fredrickson JK, Romine MF, Beliaev AS, Auchtung JM, Driscoll ME, Gardner TS, Nealson KH, Osterman AL, Pinchuk G, Reed JL, Rodionov DA, Rodrigues JL, Saffarini DA, Serres MH, Spormann AM, Zhulin IB, Tiedje JM: Towards environmental systems biology of Shewanella . Nat Rev Microbiol 2008, 6(8):592–603. 10.1038/nrmicro1947View ArticleGoogle Scholar
- Kumar SA, Peter YA, Nadeau JL: Facile biosynthesis, separation and conjugation of AuNPs to doxorubicin. Nanotechnology 2008, 19(49):495101. 10.1088/0957-4484/19/49/495101View ArticleGoogle Scholar
- Das SK, Dickinson C, Lafir F, Brougham DF, Marsili E: Synthesis, characterization and catalytic activity of AuNPs biosynthesized with Rhizopus oryzae protein extract. Green Chem 2012, 14(5):1322–1334. 10.1039/c2gc16676cView ArticleGoogle Scholar
- Gupta S, Bector S: Biosynthesis of extracellular and intracellular AuNPs by Aspergillus fumigatus and A. flavus . Antonie Van Leeuwenhoek 2013, 103(5):1113–1123. 10.1007/s10482-013-9892-6View ArticleGoogle Scholar
- Gardea-Torresdey JL, Parsons JG, Gomez E, Peralta-Videa J, Troiani HE, Santiago P, Jose Yacaman M: Formation and growth of Au nanoparticles inside live Alfalfa plants. Nano Lett 2002, 2(4):397–401. 10.1021/nl015673+View ArticleGoogle Scholar
- Shankar SS, Rai A, Ankamwar B, Singh A, Ahmad A, Sastry M: Biological synthesis of triangular gold nanoprisms. Nat Mater 2004, 3(7):482–488. 10.1038/nmat1152View ArticleGoogle Scholar
- Shankar SS, Ahmad A, Pasrichaa R, Sastry M: Bioreduction of chloroaurate ions by geranium leaves and its endophytic fungus yields gold nanoparticles of different shapes. J Mater Chem 2003, 13(7):1822–1826. 10.1039/b303808bView ArticleGoogle Scholar
- Caruso F, Furlong DN, Ariga K, Ichinose I, Kunitake T: Characterization of polyelectrolyte-protein multilayer films by atomic force microscopy, scanning electron microscopy, and Fourier transform infrared reflection-absorption spectroscopy. Langmuir 1998, 14(16):4559–4565. 10.1021/la971288hView ArticleGoogle Scholar
- Mehra RK, Winge DR: Metal ion resistance in fungi: molecular mechanisms and their regulated expression. J Cell Biochem 1991, 45(1):30–40. 10.1002/jcb.240450109View ArticleGoogle Scholar
- Gole A, Dash C, Ramachandran V, Mandale AB, Sainkar SR, Rao M, Sastry M: Pepsin-gold colloid conjugates: preparation, characterization, and enzymatic activity. Langmuir 2001, 17(5):1674–1679. 10.1021/la001164wView ArticleGoogle Scholar
- Suresh AK, Pelletier DA, Wang W, Moon JW, Gu B, Mortensen NP, Allison DP, Phelps TJ, Doktycz MJ: 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(13):5210–5215. 10.1021/es903684rView ArticleGoogle Scholar
- Rao CNR, Cheetham AK: Science and technology of nanomaterials: current status and future prospects. J Mate Chem 2001, 11(12):2887–2894. 10.1039/b105058nView ArticleGoogle Scholar
- Honary S, Gharaei-Fathabad E, Barabadi H, Naghibi F: Fungus-mediated synthesis of gold nanoparticles: a novel biological approach to nanoparticle synthesis. J Nanosci Nanotechnol 2013, 13(2):1427–1430. 10.1166/jnn.2013.5989View ArticleGoogle Scholar
- Parab HJ, Huang JH, Lai TC, Jan YH, Liu RS, Wang JL, Hsiao M, Chen CH, Hwu YK, Tsai DP, Chuang SY, Pang JH: Biocompatible transferrin-conjugated sodium hexametaphosphate-stabilized AuNPs: synthesis, characterization, cytotoxicity and cellular uptake. Nanotechnology 2011, 22(39):395706. 10.1088/0957-4484/22/39/395706View ArticleGoogle Scholar
- Shukla R, Bansal V, Chaudhary M, Basu A, Bhonde RR, Sastry M: Biocompatibility of AuNPs and their endocytotic fate inside the cellular compartment: a microscopic overview. Langmuir 2005, 21(23):10644–10654. 10.1021/la0513712View ArticleGoogle Scholar
- Connor EE, Mwamuka J, Gole A, Murphy CJ, Wyatt MD: Gold nanoparticles are taken up by human cells but do not cause acute cytotoxicity. Small 2005, 1(3):325–327. 10.1002/smll.200400093View ArticleGoogle Scholar
- Arnida , Malugin A, Ghandehari H: Cellular uptake and toxicity of gold nanoparticles in prostate cancer cells: a comparative study of rods and spheres. J Appl Toxicol 2010, 30(3):212–217.Google Scholar
- Karthikeyan B, Kalishwaralal K, Sheikpranbabu S, Deepak V, Haribalaganesh R, Gurunathan S: Gold nanoparticles downregulate VEGF-and IL-1β-induced cell proliferation through Src kinase in retinal pigment epithelial cells. Exp Eye Res 2010, 91(5):769–778. 10.1016/j.exer.2010.09.003View ArticleGoogle Scholar
- Pan Y, Leifert A, Ruau D, Neuss S, Bornemann J, Schmid G, Brandau W, Simon U, Jahnen-Dechent W: AuNPs of diameter 1.4 nm trigger necrosis by oxidative stress and mitochondrial damage. Small 2009, 5(18):2067–2076. 10.1002/smll.200900466View ArticleGoogle Scholar
- Patra HK, Banerjee S, Chaudhuri U, Lahiri P, Dasgupta AK: Cell selective response to gold nanoparticles. Nanomed 2007, 3(2):111–119.View ArticleGoogle Scholar
- Uboldi C, Bonacchi D, Lorenzi G, Hermanns MI, Pohl C, Baldi G, Unger RE, Kirkpatrick CJ: AuNPs induce cytotoxicity in the alveolar type-II cell lines A549 and NCIH441. Part Fibre Toxicol 2009, 6: 18. 10.1186/1743-8977-6-18View ArticleGoogle Scholar
- Zhang YX, Zheng J, Gao G, Kong YF, Zhi X, Wang K, Zhang XQ, Cuida X: Biosynthesis of gold nanoparticles using chloroplasts. Int J Nanomedicine 2011, 6: 2899–2906.View ArticleGoogle Scholar
- Freese C, Uboldi C, Gibson MI, Unger RE, Weksler BB, Romero IA, Couraud PO, Kirkpatrick CJ: Uptake and cytotoxicity of citrate-coated gold nanospheres: comparative studies on human endothelial and epithelial cells. Part Fibre Toxicol 2012, 9: 23. 10.1186/1743-8977-9-23View ArticleGoogle Scholar
- Burdon RH: Superoxide and hydrogen peroxide in relation to mammalian cell proliferation. Free Radic Biol Med 1995, 18(4):775–794. 10.1016/0891-5849(94)00198-SView ArticleGoogle Scholar
- Fiers W, Beyaert R, Declercq W, Vandenabeele P: More than one way to die: apoptosis, necrosis and reactive oxygen damage. Oncogene 1999, 18(54):7719–7730.View ArticleGoogle Scholar
- Matés JM, Segura JA, Alonso FJ, Márquez J: Intracellular redox status and oxidative stress: implications for cell proliferation, apoptosis, and carcinogenesis. Arch Toxicol 2008, 82(5):273–299. 10.1007/s00204-008-0304-zView ArticleGoogle Scholar
- Chuang SM, Lee YH, Liang RY, Roam GD, Zeng ZM, Tu HF, Wang SK, Chueh PJ: Extensive evaluations of the cytotoxic effects of gold nanoparticles. Biochim Biophys Acta 2013, 1830(10):4960–4973. 10.1016/j.bbagen.2013.06.025View ArticleGoogle Scholar
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