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使用SU-8作为介电层将数字微流控与常压质谱联用

Interfacing Digital Microfluidics with Ambient Mass Spectrometry Using SU-8 as Dielectric Layer.

作者信息

Sathyanarayanan Gowtham, Haapala Markus, Sikanen Tiina

机构信息

Drug Research Program, Faculty of Pharmacy, Division of Pharmaceutical Chemistry and Technology, University of Helsinki, Viikinkaari 5E, 00790 Helsinki, Finland.

出版信息

Micromachines (Basel). 2018 Dec 8;9(12):649. doi: 10.3390/mi9120649.

Abstract

This work describes the interfacing of electrowetting-on-dielectric based digital microfluidic (DMF) sample preparation devices with ambient mass spectrometry (MS) via desorption atmospheric pressure photoionization (DAPPI). The DMF droplet manipulation technique was adopted to facilitate drug distribution and metabolism assays in droplet scale, while ambient mass spectrometry (MS) was exploited for the analysis of dried samples directly on the surface of the DMF device. Although ambient MS is well-established for bio- and forensic analyses directly on surfaces, its interfacing with DMF is scarce and requires careful optimization of the surface-sensitive processes, such as sample precipitation and the subsequent desorption/ionization. These technical challenges were addressed and resolved in this study by making use of the high mechanical, thermal, and chemical stability of SU-8. In our assay design, SU-8 served as the dielectric layer for DMF as well as the substrate material for DAPPI-MS. The feasibility of SU-8 based DMF devices for DAPPI-MS was demonstrated in the analysis of selected pharmaceuticals following on-chip liquid-liquid extraction or an enzymatic dealkylation reaction. The lower limits of detection were in the range of 1⁻10 pmol per droplet (0.25⁻1.0 µg/mL) for all pharmaceuticals tested.

摘要

这项工作描述了基于介电层上电润湿的数字微流控(DMF)样品制备装置通过解吸大气压光电离(DAPPI)与常压质谱(MS)的联用。采用DMF液滴操控技术以促进液滴尺度下的药物分布和代谢分析,同时利用常压质谱(MS)直接对DMF装置表面上的干燥样品进行分析。尽管常压质谱在直接对表面进行生物和法医分析方面已得到广泛应用,但其与DMF的联用却很少见,并且需要对诸如样品沉淀以及随后的解吸/电离等表面敏感过程进行仔细优化。在本研究中,通过利用SU-8的高机械稳定性、热稳定性和化学稳定性,解决了这些技术难题。在我们的分析设计中,SU-8既用作DMF的介电层,又用作DAPPI-MS的基底材料。基于SU-8的DMF装置用于DAPPI-MS的可行性在对选定药物进行芯片上液-液萃取或酶促脱烷基反应后的分析中得到了证明。所有测试药物的检测下限在每滴1⁻10皮摩尔(0.25⁻1.0微克/毫升)范围内。

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