A flexible and high throughput liquid chromatography-tandem mass spectrometric assay for the quantitation of telcagepant in human plasma

被引:1
|
作者
Du, Lihong [1 ]
Miller-Stein, Cynthia M. [1 ]
Valesky, Robert J. [1 ]
Martucci, Ashley N. [1 ]
Woolf, Eric J. [1 ]
机构
[1] Merck & Co Inc, Dept Clin PK PD, Merck Res Labs, West Point, PA 19486 USA
关键词
Telcagepant (MK-0974); Protein precipitation; Human plasma; LC-MS/MS; RECEPTOR ANTAGONIST; MIGRAINE; CGRP; MK-0974; ELECTROSPRAY; STRATEGIES; SAMPLES;
D O I
10.1016/j.jchromb.2009.03.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Telcagepant (MK-0974) is a novel oral calcitonin gene-related peptide (CGRP) receptor antagonist and is currently under clinical development. Results from phases II and III clinical trials have Suggested that telcagepant is effective for migraine treatment. A reliable and high throughput protein precipitation (PPT) method for determination of telcagepant in human plasma using liquid chromatography coupled with atmospheric pressure chemical ionization (APCI) tandem mass spectrometry has been developed. Clinical samples, internal standard (IS) and acetonitrile are transferred into 96-well plates using a robotic liquid handling system. An aliquot of 10 mu L supernatant is directly injected into the LC-MS/MS system where separation is performed on a FluoPhase RP (150 x 2.1 mm, 5 mu m) column with an isocratic mobile phase (60% acetonitrile with 0.1% formic acid and 40% water with 0.1% formic acid)at 0.2 mL/min. The interfering 3S-diastereomer of telcagepant, which is observed in clinical samples, is chromatographically resolved from telcagepant. The PPT procedure significantly reduces the time required for sample processing and the assay is sufficiently sensitive for detection using both API 4000 and API 3000 mass spectrometers. The linear calibration range is 5-5000 nM using 200 mu L of plasma. Assay intraday validation was conducted using Six calibration Curves derived from six lots of human control plasma. Calibration standard accuracy did not deviate by more than 3% and 6% of nominal values, and precision did not exceed 4% coefficient of variation (CV) and 10% CV, respectively on the Apt 4000 and API 3000. Several clinical phases IIb and III Studies have been successfully supported with this assay. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1465 / 1471
页数:7
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