Literature DB >> 18940251

Predicting drug hydrolysis based on moisture uptake in various packaging designs.

Klemen Naversnik1, Simona Bohanec.   

Abstract

An attempt was made to predict the stability of a moisture sensitive drug product based on the knowledge of the dependence of the degradation rate on tablet moisture. The moisture increase inside a HDPE bottle with the drug formulation was simulated with the sorption-desorption moisture transfer model, which, in turn, allowed an accurate prediction of the drug degradation kinetics. The stability prediction, obtained by computer simulation, was made in a considerably shorter time frame and required little resources compared to a conventional stability study. The prediction was finally upgraded to a stochastic Monte Carlo simulation, which allowed quantitative incorporation of uncertainty, stemming from various sources. The resulting distribution of the outcome of interest (amount of degradation product at expiry) is a comprehensive way of communicating the result along with its uncertainty, superior to single-value results or confidence intervals.

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Year:  2008        PMID: 18940251     DOI: 10.1016/j.ejps.2008.09.007

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  2 in total

Review 1.  Impact of excipient interactions on solid dosage form stability.

Authors:  Ajit S Narang; Divyakant Desai; Sherif Badawy
Journal:  Pharm Res       Date:  2012-06-16       Impact factor: 4.200

2.  The application of the Accelerated Stability Assessment Program (ASAP) to quality by design (QbD) for drug product stability.

Authors:  Kenneth Craig Waterman
Journal:  AAPS PharmSciTech       Date:  2011-07-12       Impact factor: 3.246

  2 in total

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