Generation of reactive oxygen species from porous silicon microparticles in cell culture medium

被引:33
作者
Low, Suet Peng [1 ]
Williams, Keryn A. [2 ]
Canham, Leigh T. [3 ]
Voelcker, Nicolas H. [1 ]
机构
[1] Flinders Univ S Australia, Fac Sci & Engn, Sch Chem Phys & Earth Sci, Adelaide, SA, Australia
[2] Flinders Univ S Australia, Dept Ophthalmol, Adelaide, SA, Australia
[3] PSiMedica, Malvern, Worcs, England
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
porous silicon; microparticles; biodegradable materials; reactive oxygen species; MESOPOROUS SILICON; OXIDATIVE STRESS; SURFACE; DAMAGE; SILANIZATION; DEGRADATION; DISSOLUTION; PEROXIDES; DELIVERY;
D O I
10.1002/jbm.a.32610
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Nanostructured (porous) silicon is a promising biodegradable biomaterial, which is being intensively researched as a tissue engineering scaffold and drug-delivery vehicle. Here, we tested the biocompatibility of non-treated and thermally-oxidized porous silicon particles using an indirect cell viability assay. Initial direct cell culture on porous silicon determined that human lens epithelial cells only poorly adhered to non-treated porous silicon. Using an indirect cell culture assay, we found that non-treated microparticles caused complete cell death, indicating that these particles generated a toxic product in cell culture medium. In contrast, thermally-oxidized microparticles did not reduce cell viability significantly. We found evidence for the generation of reactive oxygen species (ROS) by means of the fluorescent probe 2',7'-dichlorofluorescin. Our results suggest that non-treated porous silicon microparticles produced ROS, which interacted with the components of the cell culture medium, leading to the formation of cytotoxic species. Oxidation of porous silicon microparticles not only mitigated, but also abolished the toxic effects. (C) 2009 Wiley Periodicals, Inc. J Biomed Mater Res 93A: 1124-1131, 2010
引用
收藏
页码:1124 / 1131
页数:8
相关论文
共 61 条
[1]   ETCHING OF SILICON IN NAOH SOLUTIONS .2. ELECTROCHEMICAL STUDIES OF N-SI(111) AND N-SI(100) AND MECHANISM OF THE DISSOLUTION [J].
ALLONGUE, P ;
COSTAKIELING, V ;
GERISCHER, H .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1993, 140 (04) :1018-1026
[2]   Dissolution of different forms of partially porous silicon wafers under simulated physiological conditions [J].
Anderson, SHC ;
Elliott, H ;
Wallis, DJ ;
Canham, LT ;
Powell, JJ .
PHYSICA STATUS SOLIDI A-APPLICATIONS AND MATERIALS SCIENCE, 2003, 197 (02) :331-335
[3]   Porous silicon in drug delivery devices and materials [J].
Anglin, Emily J. ;
Cheng, Lingyun ;
Freeman, William R. ;
Sailor, Michael J. .
ADVANCED DRUG DELIVERY REVIEWS, 2008, 60 (11) :1266-1277
[4]   Phosphate and cell growth on nanostructured semiconductors [J].
Bayliss, SC ;
Harris, PJ ;
Buckberry, LD ;
Rousseau, C .
JOURNAL OF MATERIALS SCIENCE LETTERS, 1997, 16 (09) :737-740
[5]  
Bayliss SC, 1999, ADV MATER, V11, P318, DOI 10.1002/(SICI)1521-4095(199903)11:4<318::AID-ADMA318>3.0.CO
[6]  
2-Z
[7]   Molecular events associated with reactive oxygen species and cell cycle progression in mammalian cells [J].
Boonstra, J ;
Post, JA .
GENE, 2004, 337 :1-13
[8]   SILICON QUANTUM WIRE ARRAY FABRICATION BY ELECTROCHEMICAL AND CHEMICAL DISSOLUTION OF WAFERS [J].
CANHAM, LT .
APPLIED PHYSICS LETTERS, 1990, 57 (10) :1046-1048
[9]  
Canham LT, 1999, ADV MATER, V11, P1505, DOI 10.1002/(SICI)1521-4095(199912)11:18<1505::AID-ADMA1505>3.0.CO
[10]  
2-C