Processing nanoparticles with A4F-SAXS for toxicological studies: Iron oxide in cell-based assays

被引:13
作者
Knappe, Patrick [1 ]
Boehmert, Linda [2 ]
Bienert, Ralf [1 ]
Karmutzki, Silvana [2 ]
Niemann, Birgit [2 ]
Lampen, Alfonso [2 ]
Thuenemann, Andreas F. [1 ]
机构
[1] BAM Fed Inst Mat Res & Testing, D-12489 Berlin, Germany
[2] BfR Fed Inst Risk Assessment, D-14195 Berlin, Germany
关键词
Field-flow-fractionation; Small-angle X-ray scattering; Nanoparticle; FIELD-FLOW FRACTIONATION; PARTICLE-SIZE; METAL-OXIDE; CYTOTOXICITY; STABILITY; TOXICITY; PROTEIN;
D O I
10.1016/j.chroma.2010.11.012
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nanoparticles are not typically ready-to-use for in vitro cell culture assays. Prior to their use in assays, powder samples containing nanoparticles must be dispersed, de-agglomerated, fractionated by size, and characterized with respect to size and size distribution. For this purpose we report exemplarily on polyphosphate-stabilized iron oxide nanoparticles in aqueous suspension. Fractionation and online particle size analysis was performed in a time-saving procedure lasting 50 min by combining asymmetrical flow field-now fractionation (A4F) and small-angle X-ray scattering (SAXS). Narrowly distributed nanoparticle fractions with radii of gyration (R-g) from 7 to 21 nm were obtained from polydisperse samples. The A4F-SAXS combination is introduced for the preparation of well-characterized sample fractions originating from a highly polydisperse system as typically found in engineered nanoparticles. A4F-SAXS processed particles are ready-to-use for toxicological studies. The results of preliminary tests of the effects of fractionated iron oxide nanoparticles with a R-g of 15 nm on a human colon model cell line are reported. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:4160 / 4166
页数:7
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