A fully automated nanoelectrospray tandem mass spectrometric method for analysis of Caco-2 samples

被引:48
作者
Van Pelt, CK
Zhang, S
Fung, E
Chu, IH
Liu, TT
Li, C
Korfmacher, WA
Henion, J
机构
[1] Adv Biosci Inc, Ithaca, NY 14850 USA
[2] Schering Plough Res Inst, Kenilworth, NJ 07033 USA
关键词
D O I
10.1002/rcm.1087
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Caco-2 cells offer a means to rapidly screen permeability of drug candidates, allowing pharmaceutical companies to eliminate candidates unable to cross the intestinal barrier early in the discovery process. This screening process is typically performed by conventional liquid chromatography/tandem mass spectrometry (LC/MS/MS), which can require time-consuming method development. An alternative to LC/MS/MS, automated nanoelectrospray tandem mass spectrometry (nanoESI-MS/MS), is introduced. This novel approach requires an off-line ZipTip(TM) desalting step followed by automated nanoESI-MS/MS, using the NanoMate(TM) 100 and ESI Chip(TM). In addition to reduced method development time, automated nanoESI-MS/MS also offers no carry-over between samples, low sample consumption, and ease-of-use as compared with conventional pulled-capillary nanoelectrospray. Furthermore, the infusion system described has the potential to be high-throughput. A comparison of Caco-2 samples analyzed both by LC/MS/MS and by automated nanoESI-MS/MS is presented. The permeability and recovery data of the two compounds analyzed in this study obtained from conventional LC/MS/MS and by automated nanoESI-MS/MS were in excellent agreement. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:1573 / 1578
页数:6
相关论文
共 12 条
[1]   CORRELATION BETWEEN ORAL-DRUG ABSORPTION IN HUMANS AND APPARENT DRUG PERMEABILITY COEFFICIENTS IN HUMAN INTESTINAL EPITHELIAL (CACO-2) CELLS [J].
ARTURSSON, P ;
KARLSSON, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 175 (03) :880-885
[2]  
ARTURSSON P, 1991, CRIT REV THER DRUG, V8, P305
[3]   Demonstration of direct bioanalysis of drugs in plasma using nanoelectrospray infusion from a silicon chip coupled with tandem mass spectrometry [J].
Dethy, JM ;
Ackermann, BL ;
Delatour, C ;
Henion, JD ;
Schultz, GA .
ANALYTICAL CHEMISTRY, 2003, 75 (04) :805-811
[4]   127 CULTURED HUMAN TUMOR-CELL LINES PRODUCING TUMORS IN NUDE MICE [J].
FOGH, J ;
FOGH, JM ;
ORFEO, T .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1977, 59 (01) :221-226
[5]  
HIDALGO IJ, 1989, GASTROENTEROLOGY, V96, P736
[6]  
JACKSON MJ, 1987, PHYSL GASTROINTESTIN, P1597
[7]   Human drug absorption kinetics and comparison to Caco-2 monolayer permeabilities [J].
Polli, JE ;
Ginski, MJ .
PHARMACEUTICAL RESEARCH, 1998, 15 (01) :47-52
[8]   A fully integrated monolithic microchip electrospray device for mass spectrometry [J].
Schultz, GA ;
Corso, TN ;
Prosser, SJ ;
Zhang, S .
ANALYTICAL CHEMISTRY, 2000, 72 (17) :4058-4063
[9]  
Van Pelt Colleen K, 2002, J Biomol Tech, V13, P72
[10]  
Wang Z, 2000, J MASS SPECTROM, V35, P71, DOI 10.1002/(SICI)1096-9888(200001)35:1<71::AID-JMS915>3.0.CO