Comparative in vitro cytotoxicity study of silver nanoparticle on two mammalian cell lines

Toxicology in Vitro

Volumn 26, Issue 2, 2012, Pages 238-251

  Mukherjee, Sanchali Gupta ^a   O'Claonadh, Niall ^a   Casey, Alan ^a   Chambers, Gordon ^a  

^a DUBLIN INSTITUTE OF TECHNOLOGY   (Ireland)

Author keywords

Adenylate kinase; Alamar Blue assay; Apoptosis; Cellular proliferative capacity; Comparative cytotoxicity; Coomassie Blue assay; Cytotoxicity assessment; Glutathione; LD50; Lysosomal activity; Mitochondrial metabolism; Physical characterization; ROS

Indexed keywords

ADENYLATE KINASE; CELL PROTEIN; GLUTATHIONE; SILVER NANOPARTICLE; WATER;

APOPTOSIS; ARTICLE; CANCER CELL CULTURE; CELL CULTURE; CELL MEMBRANE; CELL METABOLISM; CELL PROLIFERATION; CONCENTRATION RESPONSE; CONTROLLED STUDY; CULTURE MEDIUM; CYTOTOXICITY; ENZYME ASSAY; HUMAN; HUMAN CELL; IN VITRO STUDY; LIGHT SCATTERING; LYSOSOME; MAMMAL CELL; MEMBRANE DAMAGE; MITOCHONDRIAL RESPIRATION; OXIDATIVE STRESS; PARTICLE SIZE; PROTEIN CONTENT; SCANNING ELECTRON MICROSCOPY; SKIN CANCER; TIME; TRANSMISSION ELECTRON MICROSCOPY; UTERINE CERVIX CANCER;

ADENYLATE KINASE; APOPTOSIS; CELL LINE; CELL SURVIVAL; GLUTATHIONE; HELA CELLS; HUMANS; LETHAL DOSE 50; METAL NANOPARTICLES; REACTIVE OXYGEN SPECIES; SILVER;

MAMMALIA;

EID: 84856433451     PISSN: 08872333     EISSN: 18793177     Source Type: Journal    
DOI: 10.1016/j.tiv.2011.12.004     Document Type: Article

References (52)

1. Ahn M.H., Kang C.M., Park C.S., Park S.J., Rhim T., Yoon P.O., Chang H.S., Kim S.H., Kyono H., Kim K.C. Titanium dioxide particle-induced goblet cell hyperplasia: association with mast cells and IL-13. Respir. Res. 2005, 13:34.
2. AshaRani P.V., Mun G.L.K., Hande M.P., Valiyaveettil S. Cytotoxicity and genotoxicity of silver nanoparticles in human cells. ACS Nano 2009, 3:279-290.
3. Boukamp P., Petrussevska R.T., Breitkreutz D., Hornung J., Markham A., Fusenig N.E. Normal human keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line. J. Cell Biol. 1988, 106:761-771.
4. Bradbury D., Simmons T., Slater K., Crouch S. Measurement of ADP:ATP ratio in human leukaemic cell lines can be used as an indicator of cell viability, necrosis and apoptosis. J. Immunol. Methods 2000, 243:167-190.
5. Brown D.M., Donaldson K., Borm P.J., Schins R.P., Dehnhardt M., Gilmour P., Jimenez L.A., Stone V. Calcium and ROS-mediated activation of transcription factors and TNF- a cytokine gene expression in macrophages exposed to ultrafine particles. Am. J. Physiol. Lung Cell. Mol. Physiol. 2004, 286:L344-L353.
6. Casey A., Davoren M., Herzog E., Lyng F.M., Byrne H.J., Chambers G. Probing the interaction of single walled carbon nanotubes within cell culture medium as a precursor to toxicity testing. Carbon 2007, 45:34-40.
7. Casey A., Herzog E., Lyng F.M., Byrne H.J., Chambers G., Davoren M. Single walled carbon nanotubes induce indirect cytotoxicity by medium depletion in A549 lung cells. Toxicol. Lett. 2008, 179:78-84.
8. Cathcart R., Schwiers E., Ames B.N. Detection of picomole levels of hydrogenperoxide using a fluorescent dichlorofluorescein assay. Anal. Biochem. 1983, 134:111-116.
9. Chen H.W., Su S.F., Chien C.T., Lin W.H., Yu S.L., Chou C.C., Chen J.J., Yang P.C. Titanium dioxide nanoparticles induce emphysema-like lung injury in mice. FASEB J. 2006, 20:2393-2395.
10. Cheng D., Yang J., Zhao Y. Antibacterial materials of silver nanoparticles application in medical appliances and appliances for daily use. Chin. Med. Equip. J. 2004, 4:26-32.
11. Cho K.-H., Park J.-E., et al. The study of antimicrobial activity and preservative effects of nanoAg ingredient. Electrochim. Acta 2005, 51(5):956-960.
12. Choi O., Clevenger T.E., Deng B., Surampalli R.Y., Ross L., Hu Z. Role of sulfide and ligand strength in controlling nanosilver toxicity. Water Res. 2009, 43(7):1879-1886.
13. Clare M.G., Cormack H.L. Can in-vitro assays predict chemically-induced skin damage?. Inflammopharmacology 1996, 4(2):195-204.
14. Cohen M.S., Stern J.M., Vanni A.J., Kelley R.S., Baumgart E., Field D., Libertino J.A., Summerhayes I.C. In vitro analysis of a nanocrystalline silver-coated surgical mesh. Surg. Infect. 2007, 8:397-403.
15. Cooke M.C., Evans M.D., Dizdaroglu M., Lunec J. Oxidative DNA damage: mechanisms, mutation, and disease. FASEB J. 2003, 17:1195-1214.
16. Crouch S., Kozlowski R., Slater K., Fletcher J. The use of ATP bioluminescence as a measure of cell proliferation and cytotoxicity. J. Immunol. Methods 1993, 160:81-88.
17. De Fries R., Mitsuhashi M. Quantification of mitogen induced human lymphocyte proliferation: Comparison of alamarbluetm assay to 3h-thymidine incorporation assay. J. Clin. Lab. Anal. 1995, 9:89-95.
18. Donaldson K., Stone V., Tran C.L., Kreyling W., Borm P.J.A. Nanotoxicology. Occup. Environ. Med. 2004, 61:727-728.
19. Eturska M., Obreshkova E. Argyria in the prolonged use of adsorgan. Vutr. Boles. 1979, 18:121-123.
20. Franken N.A.P., Rodermond H.M., Stap J., Haveman J., Bree C.V. Clonogenic assay of cells in vitro. Nat. Protoc. 2006, 1:2315-2319.
21. Hussain S.M., Hess K.L., et al. In vitro toxicity of nanoparticles in BRL 3A rat liver cells. Toxicol. In Vitro 2005, 19(7):975-983.
22. Kim S., Choi J.E., Choi J., Chung K.-H., Park K., Yi J., Ryu D.-Y. Oxidative stress-dependent toxicity of silver nanoparticles in human hepatoma cells. Toxicol. In Vitro 2009, 23:1076-1084.
23. Lansdown A.B. Silver in health care: antimicrobial effects and safety in use. Curr. Probl. Dermatol. 2006, 33:17-34.
24. Lee H.Y., Park H.K., Lee Y.M., Kim K., Park S.B. A practical procedure for producing silver nanocoated fabric and its antibacterial evaluation for biomedical applications. Chem. Commun. (Camb.) 2007, 28:2959-2961.
25. Liau S.Y., Read D.C., et al. Interaction of Ag nitrate with readily identifiable groups: relationship to the antibacterial action of Ag ions. Lett. Appl. Microbiol. 1997, 25(4):279-283.
26. Lundqvist M., Stigler J., Elia G., Lynch I., Cedervall T., Dawson K. Nanoparticle size and surface properties determine the protein corona with possible implications for biological impacts. PNAS 2008, 105:14265-14270.
27. Lynch I., Dawson K. Protein-nanoparticle interactions. Nanotoday 2008, 3:40-47.
28. Magrez A., Kasas S., Sallicio V., Pasquier N., Seo J.W., Celio M., Catsicas S., Schwaller B., Forro L. Cellular toxicity of carbon-based nanomaterials. Nano Lett. 2006, 6(6):1121-1125.
29. Moaddab S., Ahari H., Shahbazzadeh D., Motallebi A.A., Anvar A.A., Rahman-Nya J., Shokrgozar M.R. Toxicity study of nanosilver (nanocid®) on osteoblast cancer cell line. Int. Nano Lett. 2011, 1:11-16.
30. Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 1983, 65(1-2):55-63.
31. Muangman P., Chuntrasakul C., Silthram S., Suvanchote S., Benjathanung R., Kittidacha S., Rueksomtawin S. Comparison of efficacy of 1% silver sulfadiazine and Acticoat for treatment of partial-thickness burn wounds. J. Med. Assoc. Thai. 2006, 89:953-958.
32. Mukherjee S.P., Davoren M., Byrne H.J. In vitro mammalian cytotoxicological study of PAMAM dendrimers - towards quantitative structure activity relationships. Toxicol. In Vitro 2010, 24(1):1169-1177.
33. Mukherjee S.P., Lyng F.M., Garcia A., Davoren M., Byrne H.J. Mechanistic studies of in vitro cytotoxicity of poly(amidoamine) dendrimers in mammalian cells. Toxicol. Appl. Pharmacol. 2010, 248(3):259-268.
34. Naha P.C., Casey A., Tenuta T., Lynch I., Dawson K.A., Byrne H.J., Davoren M. Preparation, characterization of NIPAM and NIPAM/BAM copolymer nanoparticles and their acute toxicity testing using an aquatic test battery. Aquat. Toxicol. 2009, 92:146-154.
35. Oberdörster, G., Finkelstein, J.N., Johnston, C., Gelein, R., Cox, C., Baggs, R., Elder, A.C.P., 2000. Acute pulmonary effects of ultrafine particles in rats and mice. HEI Research Report 96. Health Effects Institute, http://www.healtheffects.org/.
36. O'Brien J., Wilson I., Orton T., Pognan F. Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity. Eur. J. Biochem. 2000, 267:5421-5426.
37. Percival S.L., Bowler P.G., Russell D. Bacterial resistance to Ag in wound care. J. Hosp. Infect. 2005, 60:1-7.
38. Puck T.T., Marcus P.L. Action of X-rays on mammalian cells. J. Exp. Med. 1956, 103:653-666.
39. Renwick L.C., Brown D., Clouter A., Donaldson K. Increased inflammation and altered macrophage chemotactic responses caused by two ultrafine particle types. Occup. Environ. Med. 2004, 61:442-446.
40. Shuval H., Fattal B., Nassar A., Lev O., Pedahzur R. The study of the synergism between oligodynamic Ag and hydrogen peroxide as a long-acting water disinfectant. Water Supply 1995, 13:241-251.
41. Shvedova A.A., Kisin E.R., Mercer R., Murray A.R., Johnson V.J., Potapovich A.I., Tyurina Y.Y., Gorelik O., Arepalli S., Schwegler-Berry D., Hubbs A.F., Antonini J., Evans D.E., Ku B.K., Ramsey D., Maynard A., Kagan V.E., Castranova V., Baron P. Unusual inflammatory and fibrogenic pulmonary responses to single-walled carbon nanotubes in mice. Am. J. Physiol. Lung Cell. Mol. Physiol. 2005, 289:L698-L708.
42. Snow E.T., Sykora P., Durham T.R., Klein C.B. Arsenic, mode of action at biologically plausible low doses: What are the implications for low dose cancer risk? Toxicol. Appl. Pharm. 2005, 207:S557-S564.
43. Spencer W.H., Garron L.K., Contreras F., Hayes T.L., Lai C. Endogenous and exogenous ocular and systemic silver deposition. Trans. Ophthalmol. Soc. UK 1980, 100:171-178.
44. Stennicke H.R., Jürgensmeier J.M., Shin H., Deveraux Q., Wolf B.B., Yang X., Zhou Q., Ellerby H.M., Ellerby L.M., Bredesen D., Green D.R., Reed J.C., Froelich C.J., Salvesen G.S. Pro-caspase-3 Is a Major Physiologic Target of Caspase-8. J. Biol. Chem. 1998, 273:27084-27090.
45. Tipnis S.R., Blake D.G., Shepherd A.G., McLellan L.I. Overexpression of the regulatory subunit of c-glutamylcysteine synthetase in HeLa cells increases c-glutamylcysteine synthetase activity and confers drug resistance. Biochem. J. 1999, 337:559-566.
46. Valko M., Izakovic M., Mazur M., Rhodes C.J., Telser J. Role of oxygen radicals in DNA damage and cancer incidence. Mol. Cell. Biochem. 2004, 266:37-56.
47. Van deVoorde K., Nijsten T., Schelfhout K., Moorkens G., Lambert J. Long-term use of silver containing nose-drops resulting in systemic argyria. Acta Clin. Belg. 2005, 60:33-35.
48. Vigneshwaran N., Kathe A.A., Varadarajan P.V., Nachane R.P., Balasubramanya R.H.J. Functional finishing of cotton fabrics using silver nanoparticles. Nanosci. Nanotechnol. 2007, 7:1893-1897.
49. Vila A., Sanchez A., Tobío M., Calvo P., Alonso M.J. Design of biodegradable particles for protein delivery. J. Control. Release 2002, 78:15-24.
50. Xia T., Kovochich M., Brant J., Hotze M., Sempf J., Oberley T., Sioutas C., Yeh J.I., Wiesner M.R., Nel A.E. Comparison of the abilities of ambient and manufactured nanoparticles to induce cellular toxicity according to an oxidative stress paradigm. Nano Lett. 2006, 6:1794-1807.
51. York J.D., Majerus P.W. Nuclear phosphatidylinositols decrease during S-phase of the cell cycle in HeLa cells. J. Biol. Chem. 1994, 269:7847-7850.
52. Zhang Y., Sun J. A study on the bio-safety for nano-silver as anti-bacterial materials. Chin. J. Med. Instrum. 2007, 31:35-38.