Burnham Daniel R, Schneider Thomas, Chiu Daniel T
Department of Chemistry, University of Washington, Box 351700, Seattle, WA 98195-1700.
Proc SPIE Int Soc Opt Eng. 2010 Aug 27;7762:77621T. doi: 10.1117/12.862519.
We have developed a method that employs nanocapsules, optical trapping, and single-pulse laser photolysis for delivering bioactive molecules to cells with both high spatial and temporal resolutions. This method is particularly suitable for a cell-culture setting, in which a single nanocapsule can be optically trapped and positioned at a pre-defined location next to the cell, followed by single-pulse laser photolysis to release the contents of the nanocapsule onto the cell. To parallelize this method such that a large array of nanocapsules can be manipulated, positioned, and photolyzed simultaneously, we have turned to the use of spatial light modulators and holographic beam shaping techniques. This paper outlines the progress we have made so far and details the issues we had to address in order to achieve efficient parallel optical manipulations of nanocapsules and particles.
我们开发了一种方法,该方法利用纳米胶囊、光镊和单脉冲激光光解技术,以高空间和时间分辨率将生物活性分子递送至细胞。此方法特别适用于细胞培养环境,在这种环境中,单个纳米胶囊可通过光镊捕获并定位在细胞旁边的预定义位置,随后通过单脉冲激光光解将纳米胶囊的内容物释放到细胞上。为了使该方法并行化,以便能够同时操纵、定位和光解大量纳米胶囊阵列,我们开始使用空间光调制器和全息光束整形技术。本文概述了我们迄今为止取得的进展,并详细阐述了为实现纳米胶囊和粒子的高效并行光学操纵而必须解决的问题。