Quantitative determination of peptide drug in human plasma samples at low pg/ml levels using coupled column liquid chromatography-tandem mass spectrometry

被引:19
作者
Lovgren, Ulf [1 ]
Johansson, Sara [1 ]
Jensen, Lasse Skov [1 ]
Ekstrom, Carina [1 ]
Carlshaf, Alf [1 ]
机构
[1] Ferring Pharmaceut AS, Dept Bioanal Expt Med & Bioanal, Clin & Nonclin R&D, DK-2300 Copenhagen S, Denmark
关键词
Peptide; Drug; Plasma; Coupled column liquid chromatography; Mass spectrometry; LC-MS-MS; SEPARATION; PHOSPHOLIPIDS; BIOANALYSIS; HPLC;
D O I
10.1016/j.jpba.2010.03.024
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Plasma concentrations after administration of peptide drugs are often low clue to the high potency often seen with this class of compounds In this work a bioanalytical method based on coupled column liquid chromatography-tandem mass spectrometry (LC-MS/MS) is presented for quantification of a peptide drug, FE 202158. under clinical development A volume of 0 5 ml human plasma is solid phase extracted on a weak cationic exchanger After evaporation of the solvent to dryness, the reconstituted sample is injected into a coupled column liquid chromatography system A heart-cut from the initial column, a cyano column, is trapped on a C(4) column and thereafter injected into a microbore C(18) column For the detection a triple quadrupole mass spectrometer, equipped with a TurbolonSpray interface working in positive ion mode, is used. The design of the system is described and the gain in sensitivity and selectivity, compared to a conventional system, is discussed Data from validation of the bioanalytical method are presented For human plasma samples a lower limit of quantification (LLOQ) of 5.00 pg/ml (=4.77 pmol/l) was achieved The inter-assay precision was less than 11% and bias was within +/- 4% over the whole validated range of 5.00-860 pg/ml. (c) 2010 Elsevier B V All rights reserved
引用
收藏
页码:537 / 545
页数:9
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