Assessing mass balance in pharmaceutical drug products: New insights into an old topic

被引:13
作者
Baertschi, Steven W. [1 ]
Pack, Brian W. [1 ]
Hyzer, Cherokee S. Hoaglund [1 ]
Nussbaum, Mark A. [2 ]
机构
[1] Eli Lilly & Co, Small Mol Design & Dev, Indianapolis, IN 46285 USA
[2] Hillsdale Coll, Dept Chem, Hillsdale, MI 49242 USA
关键词
Analytical methodology; Assay variability; Degradation; Detection; Drug product; Mass balance; Pharmaceutical; Reactant; Reaction stoichiometry; Response factor (Rf); PERFORMANCE LIQUID-CHROMATOGRAPHY; INDICATING LC METHOD; ASSAY-METHOD; PEAK PURITY; HPLC METHOD; DEGRADATION-PRODUCTS; RESPONSE FACTORS; VALIDATION; IDENTIFICATION; IMPURITIES;
D O I
10.1016/j.trac.2013.06.006
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Mass balance is an important concept in pharmaceutical development, but it often proves challenging to assess accurately. This article explores the various methods by which mass balance can and should be measured, expressed, and evaluated in conjunction with degradation chemistry. Causes of mass-balance issues and potential solutions are summarized, as are the advantages and the disadvantages of various detection strategies. The importance of reactants other than the parent drug, reaction stoichiometry, response factors, and assay variability are discussed, and recommendations for obtaining reliable and informative mass-balance information are provided. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:126 / 136
页数:11
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