Silicon micropillar array electrospray chip for drug and biomolecule analysis

被引:34
作者
Nissila, Teemu
Sainiemi, Lauri
Sikanen, Tiina
Kotiaho, Tapio
Franssila, Sami
Kostiainen, Risto
Ketola, Raimo A.
机构
[1] Univ Helsinki, Div Pharmaceut Chem, FI-00014 Helsinki, Finland
[2] Drug Discovery & Dev Technol Ctr, FI-00014 Helsinki, Finland
[3] Aalto Univ, Micro & Nanosci Lab, FI-02015 Helsinki, Finland
[4] Analyt Chem Lab, FI-00014 Helsinki, Finland
关键词
D O I
10.1002/rcm.3266
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have developed a lidless micropillar array electrospray ionization chip (mu PESI) combined with mass spectrometry (MS) for analysis of drugs and biomolecules. The mu PESI chip, made of silicon, contains a sample introduction spot for a liquid sample, an array of micropillars (diameter, height, and distance between pillars in the range of 15-200, 20-40, and 2-80 mu m, respectively), and a sharpened tip for direct electrospray formation. The microchips were fabricated using deep reactive ion etching (DRIE) which results in accurate dimensional control. The chip, providing a reliable open-channel filling structure based on capillary forces and a electrospray emitter tip for ionization, allows an easy operation and reliable, non-clogging liquid transfer. The mu PESI chip can be used for a fast analysis using single sampling or for continuous infusion measurements using a syringe pump for sample introduction. The mu PESI-MS shows high sensitivity, with limit of detection 30 pmol/L (60 amol or 28 fg) for verapamil measured with tandem mass spectrometry (MS/MS) and using a sample volume of 2.5 mu L. The system shows also good quantitative linearity (r(2) > 0.99) with linear dynamic range of at least six orders of magnitude and good ion current stability (standard deviation <5%) in 1-h continuous flow measurement. The mu PESI-MS is shown to be a very potential method for direct analysis of drugs and biomolecules. Copyright (C) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:3677 / 3682
页数:6
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