Separation media for microchips.
Separation media for microchips.
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微芯片的分离介质。
DOI:
10.1021/ac0718703
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发表时间:
2007
影响因子:
7.4
通讯作者:
Wirth,MaryJ
中科院分区:
文献类型:
--
作者:
Wirth,MaryJ
Chemical separations are essential for analyses of complex samples. Biological samples, in particular, are extremely complex and require multiple preparatory steps before the separation, yet the sample size is often limited. In view of these challenges, Manz et al. pointed out the need for miniaturized total chemical analysis systems, or µTAS (1). The idea is that tiny samples can best be injected, prepared, separated, and analyzed in one integrated system to minimize sample loss or contamination. Microchip, or lab-on-a-chip, technology has emerged from this vision, in which all of the steps are performed on a miniaturized platform. Each of these steps has been done individually on a microchip, and multiple steps have been combined on microchips. Specimens such as saliva, urine, and plasma obviously do not require cell lysis. Often, the chemical separation can be avoided by use of a microarray, as in hybridization assays or immunoassays. Today, the interest in microchips is growing because of the need for ever-increasing speed and throughput in biological analyses. Target applications for µTAS devices include point-of-care clinical diagnostics (2), forensic DNA fingerprinting (3), and real-time monitoring for biodefense (4).Here, two case studies illustrate the research activity in microchip analyses with chemical separations—one involves DNA analysis and the other proteomics. The goal is to see why a particular type of analysis might work better when integrated on a chip. We can then assess which separation media exist and what needs to be developed to make µTAS on microchips possible.