Cytotoxicity of mesoporous silica nanomaterials

被引:189
作者
Di Pasqua, Anthony J. [1 ]
Sharma, Krishna K. [1 ]
Shi, Yan-Li [1 ]
Toms, Bonnie B. [2 ]
Ouellette, Wayne [1 ]
Dabrowiak, James C. [1 ]
Asefa, Tewodros [1 ]
机构
[1] Syracuse Univ, Dept Chem, Syracuse, NY 13244 USA
[2] SUNY Syracuse, Upstate Med Univ, Dept Paediat, Syracuse, NY 13210 USA
基金
美国国家科学基金会;
关键词
cells; cytotoxicity; nanomaterials; mesoporous silica;
D O I
10.1016/j.jinorgbio.2007.12.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We here measure the toxicity of MCM-41, a mesoporous silica nanomaterial, two of its functionalized analogs, AP-T, which has grafted aminopropyl groups and MP-T, which has grafted mercaptopropyl groups, and spherical silica nanoparticles (SiO2), toward human neuroblastorna (SK-N-SH) cells. Since the particles studied are not soluble in aqueous media, the metric used to report the cytotoxicity of these materials is a new quantity, Q(50), which is the number of particles required to inhibit normal cell growth by 50%. Determining the number of particles per gram of material applied to the cells required both the calculated and experimentally determined surface areas of these nanomaterials. This study shows that Q50 increases in the order, MCM-41 < MP-T < AP-T approximate to SiO2, showing that on a per particle basis, MCM-41 is the-most cytotoxic material studied. For the three mesoporous silica materials in this study, cytotoxicity appears related to the adsorptive surface area of the particle, although the nature of the functional group cannot be ruled out. Silica nanospheres have the lowest surface area of the particles studied but since they exhibit a Q(50) value similar to that of AP-T, shape may also be important in the cytotoxicity of these materials. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1416 / 1423
页数:8
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