Evaluation of glucuronide metabolite stability in dried blood spots

被引:0
|
作者
Bowen, Chester L. [1 ]
Volpatti, Jonathan [2 ]
Cades, Jessica [3 ]
Licea-Perez, Hermes [1 ]
Evans, Christopher A. [1 ]
机构
[1] GlaxoSmithKline, Platform Technol & Sci, Drug Metab & Pharmacokinet, Bioanalyt Sci & Toxicokinet, King Of Prussia, PA 19406 USA
[2] Drexel Univ, Dept Chem, Philadelphia, PA 19104 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Biol, Baltimore, MD 21205 USA
关键词
ACYL GLUCURONIDES; N-GLUCURONIDE; COTININE; PHARMACOKINETICS; QUANTIFICATION; ACETAMINOPHEN; MINOXIDIL; PLASMA; MS/MS;
D O I
10.4155/BIO.12.269
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Stabilization of phase II metabolites is an important consideration during bioanalytical method development, method validation and sample analysis. Generic approaches to stabilize these metabolites during storage in liquid-based matrices include pH adjustment of samples prior to storage and/or temperature control; although a variety of other compound-specific stabilization techniques exist. Dried blood spot (DBS) technology is becoming a popular alternative to liquid matrix sampling in many preclinical and clinical applications. However, concerns remain regarding the stability of metabolites stored under ambient conditions using DBS. Results: Experimental data have shown that, under ambient storage conditions, the stability of the glucuronides investigated herein stored as DBS is equivalent to that of liquid samples stored at -80 degrees C. Conclusion: The decision to employ DBS technology for a given study needs to be considered on a case-by-case basis with an understanding of compound-specific metabolism characteristics and clinical study design.
引用
收藏
页码:2823 / 2832
页数:10
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