Superparamagnetic nanoparticle-polystyrene bead conjugates as pathogen capture mimics: A parametric study of factors affecting capture efficiency and specificity

被引:21
作者
Kell, Arnold J. [1 ]
Somaskandan, Kanchana [1 ]
Stewart, Gale [2 ]
Bergeron, Michel G. [2 ]
Simard, Benoit [1 ]
机构
[1] Natl Res Council Canada, Steacie Inst Mol Sci, Ottawa, ON K1A 0R6, Canada
[2] Univ Laval, Ctr Hosp Univ Quebec, Ctr Rech & Infectiol, Pavillon CHUL, Quebec City, PQ G1V 4G2, Canada
关键词
D O I
10.1021/la7037476
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
There is Currently significant interest in the miniaturization of disease detection platforms. As detection platforms decrease in size there is a need for the development of sample preparation protocols by which cells or biomarkers of interest can be concentrated from large volumes down to volumes more amenable to analysis within microfluidic devices. To address this issue, we present a series of magnetic confinement assays for polystyrene (PS) beads mediated through their covalent modification with a series of superparamagnetic nanoparticles, where the PS beads have many properties similar to bacteria, but are not pathogenic. The magnetic confinement of the PS beads is investigated as a function of (1) the overall nanoparticle size, (2) the loading of superparamagnetic content within the nanoparticle matrix, and (3) the viscosity and volume of the dispersion medium. We demonstrate that the time required for the magnetic capture of the PS beads by the superparamagnetic nanoparticles (I) decreases as the loading of superparamagnetic material into the nanoparticles increases and (2) increases as the viscosity and volume of the dispersion medium are increased. However, limitations in the magnetic confinement efficiency for the PS beads labeled with nanoparticles comprised of low loadings of superparamagnetic material can be overcome through the use of magnetic columns. These magnetic Columns Provide a practical and fast mode of sample preparation that should facilitate the magnetic concentration of cells and biomarkers from large volumes to volumes more amenable to incorporation into a microfluidic-based analysis system, where they can be analyzed/detected.
引用
收藏
页码:3493 / 3502
页数:10
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