In vitro cytotoxicity of porous silicon microparticles: Effect of the particle concentration, surface chemistry and size

被引:141
|
作者
Santos, Helder A. [1 ]
Riikonen, Joakim [2 ]
Salonen, Jarno [3 ]
Makila, Ermei [3 ]
Heikkila, Teemu [3 ]
Laaksonen, Timo [1 ]
Peltonen, Leena [1 ]
Lehto, Vesa-Pekka [2 ]
Hirvonen, Jouni [1 ]
机构
[1] Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, FI-00014 Helsinki, Finland
[2] Univ Kuopio, Dept Phys, FI-70211 Kuopio, Finland
[3] Univ Turku, Dept Phys, Lab Ind Phys, FI-20014 Turku, Finland
基金
芬兰科学院;
关键词
Porous silicon; Microparticles; Cytotoxicity; Oral drug delivery; Caco-2; cells; MESOPOROUS SILICON; DRUG-DELIVERY; MODEL; NANOPARTICLES; MOLECULES; APOPTOSIS; TOXICITY; RELEASE; CELLS; TCPSI;
D O I
10.1016/j.actbio.2009.12.043
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
We report here the in vitro cytotoxicity of mesoporous silicon (PSI) microparticles on the Caco-2 cells as a function of particle size fractions (1.2-75 mu m), particle concentration (0.2-4 mg ml(-1)) and incubation times (3, 11 and 24 h). The particle size (smaller PSI particles showed higher cytotoxicity) and the surface chemistry treatment of the PSi microparticles were considered to be the key factors regarding the toxicity aspects. These effects were significant after the 11 and 24 h exposure times, and were explained by cell-particle interactions involving mitochondrial disruption resulting from ATP depletion and reactive oxygen species production induced by the PSi surface. These events further induced an increase in cell apoptosis and consequent cell damage and cell death in a dose-dependent manner and as a function of the PSi particle size. These effects were, however, less pronounced with thermally oxidized PSi particles. Under the experimental conditions tested and at particle sizes >25 mu m, the non-toxic threshold concentration for thermally hydrocarbonized and carbonized PSi particles was <2 mg ml(-1), and for thermally oxidized PSI microparticles was <4 mg ml(-1). (C) 2009 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2721 / 2731
页数:11
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