Automated method for the determination of a new matrix metalloproteinase inhibitor in ovine plasma and serum by coupling of restricted access material for on-line sample clean-up to liquid chromatography

被引:10
作者
Chiap, P
Piette, M
Evrard, B
Frankenne, F
Christiaens, B
Piel, G
Cataldo, D
Foidart, JM
Delattre, L
Crommen, J
Hubert, P
机构
[1] Univ Liege, Inst Pharm, Dept Pharmaceut Analyt Chem, CHU, B-4000 Liege, Belgium
[2] Univ Liege, Inst Pharm, Dept Pharmaceut Technol, CHU, B-4000 Liege, Belgium
[3] Univ Liege, Lab Biol Tumors & Dev, CHU, B-4000 Liege, Belgium
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2005年 / 817卷 / 01期
关键词
matrix metalloproteinase inhibitor; Ro; 28-2653; plasma; serum; sample preparation; column-switching; restricted access material; liquid chromatography;
D O I
10.1016/j.jchromb.2004.08.042
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A fully automated liquid chromatographic method was developed for the determination of Ro 28-2653, a new synthetic inhibitor of matrix metalloproteinases (MMPs), in ovine serum and plasma. The method was based on the coupling of a pre-column packed with restricted access material, namely LiChrospher RP-8 ADS (alkyl diol silica), for sample clean-up to an analytical column containing octyl silica stationary phase. One hundred mul of biological sample, to which 2-propanol was automatically added, were injected onto the ADS pre-column, which was then washed with a washing liquid consisting of a mixture of 25 mM phosphate buffer (pH 7.0) and acetonitrile (90: 10; v/v) for 10 min. By rotation of the switching valve, the analyte was then eluted in the back-flush mode with the LC mobile phase composed of a mixture of acetonitrile and 25 mM phosphate buffer (pH 7.0) (57:43; v/v). The UV detection was performed at 395 nm. The main parameters likely to influence the sample preparation technique were investigated. The method was then validated over a concentration range from 17.5 to 1950 ng/mI, the first concentration level corresponding to the lower limit of quantitation. At this concentration level, the mean bias and the R.S.D. value for intermediate precision were -2.4% and 4.2%, respectively. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:109 / 117
页数:9
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