Chabinyc M L, Chiu D T, McDonald J C, Stroock A D, Christian J F, Karger A M, Whitesides G M
Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Anal Chem. 2001 Sep 15;73(18):4491-8. doi: 10.1021/ac010423z.
This paper describes a prototype of an integrated fluorescence detection system that uses a microavalanche photodiode (microAPD) as the photodetector for microfluidic devices fabricated in poly(dimethylsiloxane) (PDMS). The prototype device consisted of a reusable detection system and a disposable microfluidic system that was fabricated using rapid prototyping. The first step of the procedure was the fabrication of microfluidic channels in PDMS and the encapsulation of a multimode optical fiber (100-microm core diameter) in the PDMS; the tip of the fiber was placed next to the side wall of one of the channels. The optical fiber was used to couple light into the microchannel for the excitation of fluorescent analytes. The photodetector, a prototype solid-state microAPD array, was embedded in a thick slab (1 cm) of PDMS. A thin (80 microm) colored polycarbonate filter was placed on the top of the embedded microAPD to absorb scattered excitation light before it reached the detector. The microAPD was placed below the microchannel and orthogonal to the axis of the optical fiber. The close proximity (approximately 200 microm) of the microAPD to the microchannel made it unnecessary to incorporate transfer optics; the pixel size of the microAPD (30 microm) matched the dimensions of the channels (50 microm). A blue light-emitting diode was used for fluorescence excitation. The microAPD was operated in Geiger mode to detect the fluorescence. The detection limit of the prototype (approximately 25 nM) was determined by finding the minimum detectable concentration of a solution of fluorescein. The device was used to detect the separation of a mixture of proteins and small molecules by capillary electrophoresis; the separation illustrated the suitability of this integrated fluorescence detection system for bioanalytical applications.
本文描述了一种集成荧光检测系统的原型,该系统使用微雪崩光电二极管(microAPD)作为聚二甲基硅氧烷(PDMS)中制造的微流控装置的光电探测器。该原型装置由一个可重复使用的检测系统和一个使用快速成型制造的一次性微流控系统组成。该过程的第一步是在PDMS中制造微流控通道,并将多模光纤(芯径100微米)封装在PDMS中;光纤尖端放置在其中一个通道的侧壁旁边。光纤用于将光耦合到微通道中以激发荧光分析物。光电探测器是一个原型固态微APD阵列,嵌入在一块厚1厘米的PDMS平板中。在嵌入式微APD顶部放置一个薄(80微米)的彩色聚碳酸酯滤光片,以在散射的激发光到达探测器之前将其吸收。微APD放置在微通道下方并与光纤轴正交。微APD与微通道的近距离(约200微米)使得无需并入传输光学器件;微APD的像素尺寸(30微米)与通道尺寸(50微米)匹配。使用蓝色发光二极管进行荧光激发。微APD以盖革模式运行以检测荧光。通过找到荧光素溶液的最低可检测浓度来确定原型的检测限(约25 nM)。该装置用于通过毛细管电泳检测蛋白质和小分子混合物的分离;该分离说明了这种集成荧光检测系统在生物分析应用中的适用性。