Sensitive and cost-effective LC-MS/MS method for quantitation of CVT-6883 in human urine using sodium dodecylbenzenesulfonate additive to eliminate adsorptive losses

被引:19
作者
Chen, Chungwen [1 ]
Bajpai, Lakshmikant [1 ]
Mollova, Nevena [1 ]
Leung, Kwan [1 ]
机构
[1] CV Therapeut Inc, Dept Preclin & Dev, Palo Alto, CA 94304 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2009年 / 877卷 / 10期
关键词
CVT-6883; A(2B) adenosin receptor antagonist; Human urine; Sodium dodecylbenzenesulfonate; SDBS; Adsorptive losses; Non-specific binding; LC-MS/MS; Method validation; PERFORMANCE LIQUID-CHROMATOGRAPHY; ASSAY;
D O I
10.1016/j.jchromb.2009.02.045
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
CVT-6883, a novel selective A(2B) adenosine receptor antagonist currently under clinical development, is highly lipophilic and exhibits high affinity for non-specific binding to container surfaces, resulting in very low recovery in urine assays. Our study showed the use of sodium dodecylbenzenesulfonate (SDBS). a low-cost additive, eliminated non-specific binding problems in the analysis of CVT-6883 in human urine without compromising sensitivity. A new sensitive and selective LC-MS/MS method for quantitation of CVT-6883 in the range of 0.200-80.0 ng/mL using SDBS additive was therefore developed and validated for the analysis of human urine samples. The recoveries during sample collection, handling and extraction for the analyte and internal standard (d(5)-CVT-6883) were higher than 87%. CVT-6883 was found stable under the following conditions: in extract - at ambient temperature for 3 days, under refrigeration (5 degrees C) for 6 days: in human urine (containing 4 mM SDBS) - after three freeze/thaw cycles, at ambient temperature for 26 h, under refrigeration (5 degrees C) for 94 h, and in a freezer set to -20 degrees C for at least 2 months. The results demonstrated that the validated method is sufficiently sensitive, specific, and cost-effective for the analysis of CVT-6883 in human urine and will provide a powerful tool to support the clinical programs for CVT-6883. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:943 / 947
页数:5
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