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一种无需标记即可通过磁梯度进行连续血细胞分选的玻璃微流控芯片。

A glass microfluidic chip for continuous blood cell sorting by a magnetic gradient without labeling.

作者信息

Qu Bai-Yan, Wu Zhi-Yong, Fang Fang, Bai Zhi-Ming, Yang Dong-Zhi, Xu Shu-Kun

机构信息

Research Center for Analytical Sciences, Northeastern University, 110004, Shenyang, China.

出版信息

Anal Bioanal Chem. 2008 Dec;392(7-8):1317-24. doi: 10.1007/s00216-008-2382-4. Epub 2008 Sep 20.

DOI:10.1007/s00216-008-2382-4
PMID:18807015
Abstract

This paper presents a microfluidic chip for highly efficient separation of red blood cells (RBCs) from whole blood on the basis of their native magnetic properties. The glass chip was fabricated by photolithography and thermal bonding. It consisted of one inlet and three outlets, and a nickel wire of 69-microm diameter was positioned in the center of a separation channel with 149-microm top width and 73-microm depth by two parallel ridges (about 10 microm high). The two ridges were formed simultaneously during the wet etching of the channels. The nickel wire for generating the magnetic gradient inside the separation channel was introduced from the side of the chip through a guide channel. The external magnetic field was applied by a permanent magnet of 0.3 T placed by the side of the chip and parallel to the main separation channel. The RBCs were separated continuously from the 1:40 (v/v) diluted blood sample at a flow rate in the range 0.12-0.92 microL/min (9-74 mm/min) with the chip, and up to 93.7% of the RBCs were collected in the middle outlet under a flow rate of 0.23 microL/min. The cell sedimentation was alleviated by adjusting the specific density of the supporting media with bovine serum albumin. Quantum dot labeling was introduced for visual fluorescence tracking of the separation process. The uneven distribution phenomenon of the blood cells around the nickel wire was reported and discussed.

摘要

本文介绍了一种基于红细胞固有磁性从全血中高效分离红细胞的微流控芯片。该玻璃芯片通过光刻和热键合工艺制造。它由一个入口和三个出口组成,一根直径为69微米的镍丝通过两条平行的脊(约10微米高)位于顶部宽度为149微米、深度为73微米的分离通道中央。这两条脊在通道的湿法蚀刻过程中同时形成。用于在分离通道内产生磁梯度的镍丝通过一个引导通道从芯片侧面引入。外部磁场由置于芯片侧面且与主分离通道平行的0.3T永久磁铁施加。使用该芯片以0.12 - 0.92微升/分钟(9 - 74毫米/分钟)的流速从1:40(v/v)稀释血样中连续分离红细胞,在0.23微升/分钟的流速下,高达93.7%的红细胞收集在中间出口。通过用牛血清白蛋白调节支撑介质的比重来减轻细胞沉降。引入量子点标记用于分离过程的可视化荧光追踪。报道并讨论了镍丝周围血细胞的不均匀分布现象。

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