Anal Chem. 2011 Apr 15;83(8):2858-61. doi: 10.1021/ac200410v. Epub 2011 Mar 28.
In recent years, there has been a growing interest in using porous microbeads such as agarose beads as solid supports to bind target molecules from complex fluid samples. Porous beads have large surface area to volume ratios and high receptor concentrations, and they facilitate relatively high sensitivity detection and multiplexing. Unfortunately, to take full advantage of the porous beads' attributes, long incubation times are needed due to the relatively slow mass transfer of target molecules from the exterior solution into the beads' interior. To accelerate the mass transfer process, we propose a novel assay in which functionalized porous beads are periodically compressed and expanded. Preliminary experiments were carried out to compare the performance of the pulsating beads with that of conventional, nonpulsating beads. These experiments indicate that the pulsating beads significantly accelerate binding rates with minimal increase in nonspecific binding. Thus, pulsing has the potential of significantly reducing assay time.
近年来,人们越来越感兴趣地使用多孔微珠(如琼脂糖珠)作为固体载体,从复杂的流体样品中结合目标分子。多孔珠具有较大的表面积与体积比和较高的受体浓度,并且它们有利于相对较高的灵敏度检测和多重检测。不幸的是,为了充分利用多孔珠的属性,由于目标分子从外部溶液进入珠内的相对较慢的质量转移,需要较长的孵育时间。为了加速质量转移过程,我们提出了一种新的分析方法,其中功能化的多孔珠周期性地被压缩和扩张。初步实验比较了脉动珠与传统非脉动珠的性能。这些实验表明,脉动珠在最小化非特异性结合的情况下显著提高了结合速率。因此,脉动有可能显著缩短分析时间。