Single-step green synthesis and characterization of gold-conjugated polyphenol nanoparticles with antioxidant and biological activities

International Journal of Nanomedicine

Volumn 9, Issue 1, 2014, Pages 4935-4951

  Sanna, Vanna ^a   Pala, Nicolino ^a   DessÌ, Giuseppina ^a   Manconi, Paola ^a   Mariani, Alberto ^a   Dedola, Sonia ^a   Rassu, Mauro ^a   Crosio, Claudia ^a   Iaccarino, Ciro ^a   Sechi, Mario ^a  

^a UNIVERSITY OF SASSARI   (Italy)

Author keywords

Antioxidant activity; Epigallocatechin 3 gallate; Fsetin; Gold nanoparticles; Resveratrol; SH SY5Y CFP DEVD YFP cells

Indexed keywords

CYAN FLUORESCENT PROTEIN; EPIGALLOCATECHIN CONJUGATED GALLATE GOLD NANOPARTICLE; EPIGALLOCATECHIN GALLATE; FISETIN; FISETIN CONJUGATED GOLD NANOPARTICLE; GOLD NANOPARTICLE; GOLD SALT; POLYPHENOL; RESVERATROL; RESVERATROL CONJUGATED GOLD NANOPARTICLE; UNCLASSIFIED DRUG; YELLOW FLUORESCENT PROTEIN; ANTIOXIDANT; CATECHIN; FLAVONOID; GOLD; METAL NANOPARTICLE; STILBENE DERIVATIVE;

ABTS RADICAL SCAVENGING ASSAY; ANTIOXIDANT ACTIVITY; ANTIPROLIFERATIVE ACTIVITY; APOPTOSIS; ARTICLE; BIOLOGICAL ACTIVITY; CARDIOVASCULAR DISEASE; CELL CLONE; CELL VIABILITY; CONJUGATION; CONTROLLED STUDY; CORRELATION COEFFICIENT; CULTURE MEDIUM; DEGENERATIVE DISEASE; DPPH RADICAL SCAVENGING ASSAY; DRUG STRUCTURE; HUMAN; HUMAN CELL; IN VITRO STUDY; MOLECULAR STABILITY; MTS ASSAY; NANODEVICE; NEOPLASM; NEUROBLASTOMA CELL LINE; OXIDATIVE STRESS; PARTICLE SIZE; REDUCTION; REPORTER GENE; SINGLE STEP GREEN NANOSYNTHESIS; SYNTHESIS; ANALOGS AND DERIVATIVES; CELL PROLIFERATION; CHEMISTRY; DRUG EFFECTS; DRUG STABILITY; GREEN CHEMISTRY; TUMOR CELL LINE;

RICE STRIPE VIRUS;

ANTIOXIDANTS; APOPTOSIS; CATECHIN; CELL LINE, TUMOR; CELL PROLIFERATION; DRUG STABILITY; FLAVONOIDS; GOLD; GREEN CHEMISTRY TECHNOLOGY; HUMANS; METAL NANOPARTICLES; POLYPHENOLS; STILBENES;

EID: 84924872629     PISSN: 11769114     EISSN: 11782013     Source Type: Journal    
DOI: 10.2147/IJN.S70648     Document Type: Article

References (57)

1. Sperling RA, Rivera-Gil P, Zhang F, Zanella M, Parak WJ. Biological applications of gold nanoparticles. Chem Soc Rev. 2008;37(9): 1896-1908.
2. Dykman L, Khlebtsov N. Gold nanoparticles in biomedical applications: recent advances and perspectives. Chem Soc Rev. 2012;41(6): 2256-2282.
3. Dreaden EC, Alkilany AM, Huang X, Murphy CJ, El-Sayed MA. The golden age: gold nanoparticles for biomedicine. Chem Soc Rev. 2012; 41(7):2740-2779.
4. Vigderman L, Zubarev ER. Therapeutic platforms based on gold nanoparticles and their covalent conjugates with drug molecules. Adv Drug Deliv Rev. 2013;65(5):663-676.
5. Thomas M, Klibanov AM. Conjugation to gold nanoparticles enhances polyethylenimine’s transfer of plasmid DNA into mammalian cells. Proc Natl Acad Sci USA. 2003;100(16):9138–9143.
6. Du J, Jin J, Yan M, Lu Y. Synthetic nanocarriers for intracellular protein delivery. Curr Drug Metab. 2012;13(1):82-92.
7. Giljohann DA, Seferos DS, Daniel WL, Massich MD, Patel PC, Mrkin CA. Gold nanoparticles for biology and medicine. Angew Chem Int Ed Engl. 2010;49(19):3280-3294.
8. Llevot A, Astruc D. Applications of vectorized gold nanoparticles to the diagnosis and therapy of cancer. Chem Soc Rev. 2012;41(1): 242-257.
9. Cai W, Gao T, Hong H, Sun J. Applications of gold nanoparticles in cancer nanotechnology. Nanotechnol Sci Appl. 2008;1:17-32.
10. Turkevich J, Stevenson PC, Hillier J. A study of the nucleation and growth processes in the synthesis of colloidal gold. Discuss Faraday Soc. 1951;11:55-75.
11. Daniel MC, Astruc D. Gold nanoparticles: assembly, supramolecular chemistry, quantum-size-related properties, and applications toward biology, catalysis, and nanotechnology. Chem Rev. 2004;104: 293-346.
12. Corbierre MK, Cameron NS, Lennox RB. Polymer-stabilized gold nanoparticles with high grafting densities. Langmuir 2004; 20(7):2867-2873.
13. DeLong RK, Reynolds CM, Malcolm Y, Schaeffer A, Severs T, Wanekaya A. Functionalized gold nanoparticles for the binding, stabilization, and delivery of therapeutic DNA, RNA, and other biological macromolecules. Nanotechnol Sci App. 2010;3(1):53-63.
14. Chompoosor A, Han G, Rotello VM. Charge dependence of ligand release and monolayer stability of gold nanoparticles by biogenic thiols. Bioconjug Chem. 2008;19(7):1342-1345.
15. Katti K, Chanda N, Shukla R, et al. Green nanotechnology from cumin phytochemicals: generation of biocompatible gold nanoparticles. Int J Green Nanotechnol Biomed. 2009;1(1):B39-B52.
16. Menon D, Basanth A, Retnakumari A, Manzoor K, Nair SV. Green synthesis of biocompatible gold nanocrystals with tunable surface plasmon resonance using garlic phytochemicals. J Biomed Nanotechnol. 2012;8(6):901-911.
17. Mukherjee S, Sushma V, Patra S, et al. Green chemistry approach for the synthesis and stabilization of biocompatible gold nanoparticles and their potential applications in cancer therapy. Nanotechnology. 2012;23(45):455103.
18. Das S, Roy P, Mondal S, Bera T, Mukherjee A. One pot synthesis of gold nanoparticles and application in chemotherapy of wild and resistant type visceral leishmaniasis. Colloids Surf B Biointerfaces. 2013;107:27-34.
19. Arunachalam KD, Annamalai SK, Hari S. One-step green synthesis and characterization of leaf extract-mediated biocompatible silver and gold nanoparticles from Memecylon umbellatum. Int J Nanomedicine. 2013;8:1307-1315.
20. Arunachalam KD, Annamalai SK. Chrysopogon zizanioides aqueous extract mediated synthesis, characterization of crystalline silver and gold nanoparticles for biomedical applications. Int J Nanomedicine. 2013;8:2375-2384.
21. Han X, Shen T, Lou H. Dietary polyphenols and their biological signifcance. Int J Mol Sci. 2007;8(9):950-988.
22. Scalbert A, Johnson IT, Saltmarsh M. Polyphenols: antioxidants and beyond. Am J Clin Nutr. 2005;81(1 Suppl):215S-217S.
23. Higdon JV, Frei B. Tea catechins and polyphenols: health effects, metabolism, and antioxidant functions. Crit Rev Food Sci Nutr. 2003; 43(1):89–143.
24. Khan N, Mukhtar H. Tea polyphenols for health promotion. Life Sci. 2007;81(7):519-533.
25. Pervaiz S, Holme AL. Resveratrol: its biologic targets and functional activity. Antioxid Redox Signal. 2009;11(11):2851-2897.
26. Khan N, Asim M, Afaq F, Abu Zaid M, Mukhtar H. A novel dietary favonoid fsetin inhibits androgen receptor signaling and tumor growth in athymic nude mice. Cancer Res. 2008;68(20):8555-8563.
27. Siddiqui IA, Adhami VM, Bharali DJ, et al. Introducing nanochemo-prevention as a novel approach for cancer control: proof of principle with green tea polyphenol epigallocatechin-3-gallate. Cancer Res. 2009;69(5):1712-1716.
28. Sanna V, Pintus G, Roggio AM, et al. Targeted biocompatible nanoparticles for the delivery of (-)-epigallocatechin 3-gallate to prostate cancer cells. J Med Chem. 2011;54(5):1321-1332.
29. Sanna V, Sechi M. Nanoparticle therapeutics for prostate cancer treatment. Nanomedicine. 2012;8:S31-S36.
30. Sanna V, Roggio AM, Siliani S, et al. Development of novel cationic chitosan- and anionic alginate-coated poly(D,L-lactide-co-glycolide) nanoparticles for controlled release and light protection of resveratrol. Int J Nanomedicine. 2012;7:5501-5516.
31. Sanna V, Siddiqui IA, Sechi M, Mukhtar H. Nanoformulation of natural products for prevention and therapy of prostate cancer. Cancer Lett. 2013;334:142-151.
32. Nune SK, Chanda N, Shukla R, et al. Green nanotechnology from tea: phytochemicals in tea as building blocks for production of biocompatible gold nanoparticles. J Mater Chem. 2009;19(19): 2912-2920.
33. Shukla R, Chanda N, Zambre A, et al. Laminin receptor specifc therapeutic gold nanoparticles (198AuNP-EGCg) show effcacy in treating prostate cancer. Proc Natl Acad Sci USA. 2012;109(31): 12426-12431.
34. Hsieh DS, Lu HC, Chen CC, Wu CJ, Yeh MK. The preparation and characterization of gold-conjugated polyphenol nanoparticles as a novel delivery system. Int J Nanomedicine. 2012;7:1623-1633.
35. Huang X, Wu H, Liao X, Shi B. One-step, size-controlled synthesis of gold nanoparticles at room temperature using plant tannin. Green Chem. 2010;12:395-399.
36. Wu H, Huang X, Gao M, Liao X, Shi B. Polyphenol-grafted collagen fber as reductant and stabilizer for one-step synthesis of size-controlled gold nanoparticles and their catalytic application to 4-nitrophenol reduction. Green Chem. 2011;13:651-658.
37. Zhu H, Du ML, Zou ML, Xu CS, Li N, Fu YQ. Facile and green synthesis of well-dispersed Au nanoparticles in PAN nanofbers by tea polyphenols. J Mater Chem. 2012;22:9301-9307.
38. Singh DK, Jagannathan R, Khandelwal P, Abraham PM, Poddar P. In situ synthesis and surface functionalization of gold nanoparticles with curcumin and their antioxidant properties: an experimental and density functional theory investigation. Nanoscale. 2013;5:1882-1893.
39. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the folin phenol reagent. J Biol Chem. 1951;193:265-275.
40. George S, Brat P, Alter P, Amiot MJ. Rapid determination of polyphenols and vitamin C in plant-derived products. J Agric Food Chem. 2005;53(5):1370-1373.
41. Blois MS. Antioxidant determinations by the use of a stable free radical. Nature. 1958;181:1199-1200.
42. Gülçin I. Antioxidant properties of resveratrol: a structure-activity insight. Innov Food Sci Emerg Technol. 2010;11(1):210-218.
43. Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice-Evans C. Antioxidant activity applying an improved ABTS radical cation decol-orization assay. Free Radic Biol Med. 1999;26(9-10):1231-1237.
44. Gülçin I, Elias R, Gepdiremen A, Boyer L. Antioxidant activity of lignans from fringe tree (chionanthus virginicus L.). Eur Food Res Technol. 2006;223(6):759-767.
45. Baschong W, Suetterlin R, Laeng RH. Control of autofuorescence of archival formaldehyde-fxed, paraffn-embedded tissue in confo-cal laser scanning microscopy (CLSM). J Histochem Cytochem. 2001;49:1565-1572.
46. Iaccarino C, Mura ME, Esposito S, et al. Bcl2-A1 interacts with pro-caspase-3: implications for amyotrophic lateral sclerosis. Neurobiol Dis. 2011;43:642-650.
47. Philip D. Synthesis and spectroscopic characterization of gold nanopar-ticles. Spectrochim Acta A Mol Biomol Spectrosc. 2008;71(1):80-85.
48. Philip D. Green synthesis of gold and silver nanoparticles using hibiscus rosa sinensis. Phys E. 2010;42(5):1417-1424.
49. Singleton VL, Orthofer R, Lamuela-Raventós RM. Analysis of total phenols and other oxidation substrates and antioxidants by means of folin-ciocalteu reagent. Methods Enzymol. 1998;299:152-178.
50. Dauthal P, Mukhopadhyay M. In-vitro free radical scavenging activity of biosynthesized gold and silver nanoparticles using prunus armeniaca (apricot) fruit extract nanomaterials in energy, health and environment. J Nanopart Res. 2013;1:15.
51. Gao D, Tian Y, Bi S, Chen Y, Yu A, Zhang H. Studies on the interaction of colloidal gold and serum albumins by spectral methods. Spectrochim Acta A Mol Biomol Spectrosc. 2005;62(4-5):1203-1208.
52. Rice-Evans CA, Miller NJ, Paganga G. Structure-antioxidant activity relationships of favonoids and phenolic acids. Free Radic Biol Med. 1996;20(7):933-956.
53. Osman AM, Wong KKY, Fernyhough A. ABTS radical-driven oxidation of polyphenols: isolation and structural elucidation of covalent adducts. Biochem Biophys Res Comm. 2006;346:321-329.
54. Qanungo S, Das M, Haldar S, Basu A. Epigallocatechin-3-gallate induces mitochondrial membrane depolarization and caspase-dependent apoptosis in pancreatic cancer cells. Carcinogenesis. 2005;26: 958-967.
55. Islam S, Islam N, Kermode T, et al. Involvement of caspase-3 in epigallocatechin-3-gallate-mediated apoptosis of human chondrosarcoma cells. Biochem Biophys Res Commun. 2000;270;793-797.
56. Tyas L, Brophy VA, Pope A, Rivett AJ, Tavaré JM. Rapid caspase-3 activation during apoptosis revealed using fuorescence-resonance energy transfer. EMBO Rep. 2000;3:267–270.
57. Srivastava AK, Bhatnagar P, Singh M, et al. Synthesis of PLGA nanoparticles of tea polyphenols and their strong in vivo protective effect against chemically induced DNA damage. Int J Nanomedicine. 2013;8:1451-1462.