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Assessing mass balance in pharmaceutical drug products: New insights into an old topic
Journal article   Peer reviewed

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

Steven W Baertschi, Brian W Pack, Cherokee S Hoaglund Hyzer and Mark A Nussbaum
TrAC, Trends in analytical chemistry (Regular ed.), Vol.49, pp.126-136
09/2013

Abstract

Analytical methodology Assay variability Degradation Detection Drug product Mass balance Pharmaceutical Reactant Reaction stoichiometry Response factor (Rf)
•Approaches for measuring and conveying mass balance.•Primary causes of mass imbalance with general approaches to mitigation.•The contribution of analytical variability to assessments of mass balance.•Importance of other reactants and stoichiometry in determinations of mass balance.•Examples of problems of mass balance associated with analytical methodology. 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.

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