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Microwave-Mediated Rapid Synthesis of Gold Nanoparticles Using Calotropis procera Latex and Study of Optical Properties

DOI: 10.5402/2012/650759

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Abstract:

We report a microwave-mediated simple and rapid method of gold nanoparticles (GNPs) synthesis using latex of Calotropis procera. UV-Vis spectroscopic studies indicated the formation of GNPs. The GNPs were stable at room temperature (25°C) for six months. Transmission electron microscope (TEM) micrographs of the synthesized GNPs showed the formation of spherical nanoparticles with an average size of 13 ± 5?nm. SAED and XRD confirmed the crystalline nature of GNPs. Fourier transform infrared (FTIR) analysis indicated the presence of organic coating on the nanoparticles. Cytotoxicity of the GNPs was tested on HeLa and A549 and found to be nontoxic which was indicating that latex of Calotropis procera provided the nontoxic coating on GNPs, thus can be used as biomedical and pharmacological applications. 1. Introduction Gold nanoparticles (GNPs) have been of immense interest for their unique chemical and physical properties and potential technological applications in various fields ranging from catalysis to disease diagnosis [1–15]. Conventional methods of GNPs synthesis mostly rely on the use of synthetic chemicals and prolonged heating [16–19]. Owing to the increased awareness for potential toxicity of GNPs associated with biological applications, alternative methodologies for biocompatible GNPs synthesis are gaining importance. Replacement of toxic chemicals as a reducing and stabilizing agent is the prime concern of this new approach. Reports about the successful synthesis and subsequent stability of GNPs by using different biomaterials sourced from plant and microbes are now increasing day by day [20–27]. On the other hand, microwave (MW) dielectric heating is a fast emerging and widely accepted new processing technology for a variety of inorganic synthesis and biomedical applications [28–33]. Compared to the conventional heating, MW irradiation shortens reaction times and improve yield without causing any appreciable alteration in the composition of products of a chemical reaction. In contrast to general heating treatment, MW synthesis favors homogeneous heating through the entire bulk of the reaction mixture in a container, leading to a more homogeneous and easy nucleation of noble metal nanoparticles [34–37]. We found that latex of the plant C. procera, a multifarious plant having many remedial properties, can act as both reducing and capping agent in the GNPs synthesis through conventional heating [38]. This motivated us to further explore the synthesis of GNPs through MW irradiation. We found remarkable shortening in the reaction time and GNPs of

References

[1]  J. M. Thomas, “Colloidal metals: past, present and future,” Pure and Applied Chemistry, vol. 60, no. 10, pp. 1517–1528, 1998.
[2]  G. Schmid, “Large clusters and colloids. Metals in the embryonic state,” Chemical Reviews, vol. 92, no. 8, pp. 1709–1727, 1992.
[3]  L. N. Lewis, “Chemical catalysis by colloids and clusters,” Chemical Reviews, vol. 93, no. 8, pp. 2693–2730, 1993.
[4]  B. C. Gates, “Supported metal clusters: synthesis, structure, and catalysis,” Chemical Reviews, vol. 95, no. 3, pp. 511–522, 1995.
[5]  H. Hirai and N. Toshima, “ploymer-attached catalyst,” in Tailored Metal Catalysts, Y. Iwasawa, Ed., pp. 121–140, Reidel, Dordrecht, The Netherlands, 1986.
[6]  H. Bonnemann, W. Brijoux, R. Brinkmann et al., “Preparation, characterization, and application of fine metal particles and metal colloids using hydrotriorganoborates,” Journal of Molecular Catalysis, vol. 86, no. 1-3, pp. 129–177, 1994.
[7]  H. Liu, G. Mao, and S. Meng, “Preparation and characterization of the polymer-protected palladium-gold colloidal bimetallic catalysts,” Journal of Molecular Catalysis, vol. 74, no. 1-3, pp. 275–284, 1992.
[8]  W. Yu, Y. Wang, H. Liu, and W. Zheng, “Preparation and characterization of polymer-protected Pt/Co bimetallic colloids and their catalytic properties in the selective hydrogenation of cinnamaldehyde,” Journal of Molecular Catalysis A, vol. 112, no. 1, pp. 105–113, 1996.
[9]  Y. Wang, H. Liu, and Y. Jiang, “A new method for immobilization of polymer-protective colloidal platinum metals via co-ordination capture with anchored ligands. Synthesis of the first example of a mercapto-containing supported metallic catalyst for hydrogenation of alkenes with high activity,” Journal of the Chemical Society, Chemical Communications, no. 24, pp. 1878–1879, 1989.
[10]  W. Y. Yu, H. F. Liu, and Q. Tao, “Modification of metal cations to metal clusters in liquid medium,” Chemical Communications, no. 15, pp. 1773–1774, 1996.
[11]  G. Schmid, S. Emde, V. Maihack, W. Meyer-Zaika, and S. Peschel, “Synthesis and catalytic properties of large ligand stabilized palladium clusters,” Journal of Molecular Catalysis A, vol. 107, no. 1–3, pp. 95–104, 1996.
[12]  R. F. Ziolo, E. P. Giannelis, B. A. Weinstein et al., “Matrix-mediated synthesis of nanocrystalline γ-Fe2O3: a new optically transparent magnetic material,” Science, vol. 257, no. 5067, pp. 219–223, 1992.
[13]  U. Simon, G. Sch?n, and G. Schmid, “Die Verwendung von Au55-Clustern als Quantenpunkte,” Angewandte Chemie, vol. 32, no. 2, pp. 250–254, 1993.
[14]  J. F. Hainfeld, D. N. Slatkin, T. M. Focella, and H. M. Smilowitz, “Gold nanoparticles: a new X-ray contrast agent,” British Journal of Radiology, vol. 79, no. 939, pp. 248–253, 2006.
[15]  C. Alric, J. Taleb, G. Le Duc et al., “Gadolinium chelate coated gold nanoparticles as contrast agents for both X-ray computed tomography and magnetic resonance imaging,” Journal of the American Chemical Society, vol. 130, no. 18, pp. 5908–5915, 2008.
[16]  Z. Zhang, R. C. Patel, R. Kothari, C. P. Johnson, S. E. Friberg, and P. A. Aikens, “Stable silver clusters and nanoparticles prepared in polyacrylate and inverse micellar solutions,” Journal of Physical Chemistry B, vol. 104, no. 6, pp. 1176–1182, 2000.
[17]  S. Chen, K. Huang, and J. A. Stearns, “Alkanethiolate-protected palladium nanoparticles,” Chemistry of Materials, vol. 12, no. 2, pp. 540–547, 2000.
[18]  A. Manna, T. Imae, M. Iida, and N. Hisamatsu, “Formation of silver nanoparticles from a N-hexadecylethylenediamine silver nitrate complex,” Langmuir, vol. 17, no. 19, pp. 6000–6004, 2001.
[19]  S. He, J. Yao, P. Jiang et al., “Formation of silver nanoparticles and self-assembled two-dimensional ordered superlattice,” Langmuir, vol. 17, no. 5, pp. 1571–1575, 2001.
[20]  R. K. Das, B. B. Borthakur, and U. Bora, “Green synthesis of gold nanoparticles using ethanolic leaf extract of Centella asiatica,” Materials Letters, vol. 64, no. 13, pp. 1445–1447, 2010.
[21]  P. Mohanpuria, N. K. Rana, and S. K. Yadav, “Biosynthesis of nanoparticles: technological concepts and future applications,” Journal of Nanoparticle Research, vol. 10, no. 3, pp. 507–517, 2008.
[22]  P. Raveendran, J. Fu, and S. L. Wallen, “Completely "green" synthesis and stabilization of metal nanoparticles,” Journal of the American Chemical Society, vol. 125, no. 46, pp. 13940–13941, 2003.
[23]  H. Huang and X. Yang, “Synthesis of polysaccharide-stabilized gold and silver nanoparticles: a green method,” Carbohydrate Research, vol. 339, no. 15, pp. 2627–2631, 2004.
[24]  P. Mukherjee, A. Ahmad, D. Mandal et al., “Fungus-mediated synthesis of silver nanoparticles and their immobilization in the mycelial matrix: a novel biological approach to nanoparticle synthesis,” Nano Letters, vol. 1, no. 10, pp. 515–519, 2001.
[25]  P. Mukherjee, A. Ahmad, D. Mandal et al., “Bioreduction of AuCl4? ions by the fungus, Verticillium sp. and surface trapping of the gold nanoparticles formed,” Angewandte Chemie, vol. 40, pp. 3585–3588, 2001.
[26]  Y. Xiao, V. Pavlov, S. Levine, T. Niazov, G. Markovitch, and I. Willner, “Catalytic growth of Au nanoparticles by NAD(P)H cofactors: optical sensors for NAD(P)+-dependent biocatalyzed transformations,” Angewandte Chemie, vol. 43, no. 34, pp. 4519–4522, 2004.
[27]  P. J. Babu, P. Sharma, B. B. Borthakur, R. K. Das, P. Nahar, and U. Bora, “Synthesis of gold nanoparticles using Mentha arvensis leaf extract,” International Journal of Green Nanotechnology, vol. 2, no. 2, pp. P62–P68, 2010.
[28]  Y. Wada, H. Kuramoto, T. Sakata et al., “Preparation of nano-sized nickel metal particles by microwave irradiation,” Chemistry Letters, no. 7, pp. 607–608, 1999.
[29]  Y. Wada, H. Kuramoto, J. Anand et al., “Microwave-assisted size control of CdS nanocrystallites,” Journal of Materials Chemistry, vol. 11, no. 7, pp. 1936–1940, 2001.
[30]  H. Yin, T. Yamamoto, Y. Wada, and S. Yanagida, “Large-scale and size-controlled synthesis of silver nanoparticles under microwave irradiation,” Materials Chemistry and Physics, vol. 83, no. 1, pp. 66–70, 2004.
[31]  K. Patel, S. Kapoor, D. P. Dave, and T. Mukherjee, “Synthesis of nanosized silver colloids by microwave dielectric heating,” Journal of Chemical Sciences, vol. 117, no. 1, pp. 53–60, 2005.
[32]  P. Nahar and U. Bora, “Microwave-mediated rapid immobilization of enzymes onto an activated surface through covalent bonding,” Analytical Biochemistry, vol. 328, no. 1, pp. 81–83, 2004.
[33]  A. Sahu, P. Goswami, and U. Bora, “Microwave mediated rapid synthesis of chitosan,” Journal of Materials Science, vol. 20, no. 1, pp. 171–175, 2009.
[34]  J. M. Thiebaut, G. Roussy, M. S. Medjram, F. Garin, L. Seyfried, and G. Maire, “Durable changes of the catalytic properties of alumina-supported platinum induced by microwave irradiation,” Catalysis Letters, vol. 21, no. 1-2, pp. 133–138, 1993.
[35]  R. Correa, G. Gonzalez, and V. Dougar, “Emulsion polymerization in a microwave reactor,” Polymer, vol. 39, no. 6-7, pp. 1471–1474, 1998.
[36]  H. Yin, T. Yamamoto, Y. Wada, and S. Yanagida, “Large-scale and size-controlled synthesis of silver nanoparticles under microwave irradiation,” Materials Chemistry and Physics, vol. 83, no. 1, pp. 66–70, 2004.
[37]  K. Patel, S. Kapoor, D. P. Dave, and T. Mukherjee, “Synthesis of nanosized silver colloids by microwave dielectric heating,” Journal of Chemical Sciences, vol. 117, no. 1, pp. 53–60, 2005.
[38]  R. K. Das, P. Sharma, P. Nahar, and U. Bora, “Synthesis of gold nanoparticles using aqueous extract of Calotropis procera latex,” Materials Letters, vol. 65, no. 4, pp. 610–613, 2011.
[39]  O. H. Lowry, N. J. Rosebrough, A. L. Farr, and R. J. Randall, “Protein measurement with the Folin phenol reagent,” The Journal of Biological Chemistry, vol. 193, no. 1, pp. 265–275, 1951.
[40]  M. Horisberger and M. Vauthe, “Labelling of colloidal gold with protein,” Histochemistry, vol. 80, no. 1, pp. 13–18, 1984.
[41]  T. Mosmann, “Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays,” Journal of Immunological Methods, vol. 65, no. 1-2, pp. 55–63, 1983.
[42]  C. Basset, J. Vadrot, J. Denis, J. Poupon, and E. S. Zafrani, “Prolonged cholestasis and ductopenia following gold salt therapy,” Liver International, vol. 23, no. 2, pp. 89–93, 2003.
[43]  C. Frank Shaw III, “Gold-based therapeutic agents,” Chemical Reviews, vol. 99, no. 9, pp. 2589–2600, 1999.

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