Automated protein precipitation by filtration in the 96-well format

被引:60
作者
Biddlecombe, RA [1 ]
Pleasance, S [1 ]
机构
[1] GlaxoWellcome R&D, Div Bioanal & Drug Metab, Dept Int Bioanal, Ware SG12 0DP, Herts, England
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 1999年 / 734卷 / 02期
关键词
automated protein precipitation; filtration; salbutamol;
D O I
10.1016/S0378-4347(99)00355-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The use of automated protein precipitation by filtration in the 96-well format as a rapid sample preparation technique for high throughput bioanalysis using Liquid chromatography tandem mass spectrometry is reported. A robotic sample processor is used to aspirate sequentially a plasma sample and acetonitrile separated by air gaps. These are then mixed by being dispensed into individual channels of a 96-well filter block. The resulting supernatant is separated from the precipitated plasma proteins by the application of gentle vacuum using a custom manifold. The filtered supernatants are collected into a deep well microtitre plate, evaporated to dryness using a heated 96-well dry down station and reconstituted in water prior to analysis. The efficiency-df the extraction procedure is measured by the Lowry method for determining protein concentration. This method was used to optimise both the volume and the order of reagent addition, and to compare several prototype 96-well filter blocks. Using the optimised procedure a specific, precise and accurate method was developed for the P-agonist salbutamol in rabbit plasma with a calibration range of 1 to 100 ng/ml from 100 mu l of sample. (C) 1999 Elsevier Science B.V, All rights reserved.
引用
收藏
页码:257 / 265
页数:9
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