Literature DB >> 30550816

Degradation Rate Observations as a Function of Drug Load in Solid-State Drug Products.

Steven W Baertschi1, Allison L Dill2, Timothy T Kramer3, Garry Scrivens4, Miroslav Suruzhon5.   

Abstract

Degradation rates of solid-state drug products generally increase as the drug load decreases. A model for quantifying this effect based on surface area ratios is proposed here. This model relates the degradation rate to an estimate of the proportion of drug substance in contact with the excipient, and that the drug substance in contact with excipients degrades more quickly. Degradation data from previously published case studies and from 5 new case studies were found to be consistent with our proposed model; our model performed better than similar previously published models. It was also found that the relationship between degradation rate and drug load is largely independent of the temperature and humidity conditions, suggesting that drug load solely affects the pre-exponential factor of the Arrhenius equation and does not significantly affect the activation energy of the degradation process. A second method for calculating the proportion of the drug substance surface in contact with the excipient surface is presented in the Supplementary Material. Fundamentally, the 2 methods are very similar and provide almost identical fits to the experimental data.
Copyright © 2019 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

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Keywords:  chemical stability; drug-excipient interactions; formulation; hydrolysis; in silico modeling; kinetics; mathematical models; oxidation; solid-state stability; surface chemistry

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Year:  2018        PMID: 30550816     DOI: 10.1016/j.xphs.2018.12.003

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  1 in total

1.  Understanding and Kinetic Modeling of Complex Degradation Pathways in the Solid Dosage Form: The Case of Saxagliptin.

Authors:  Blaž Robnik; Blaž Likozar; Baifan Wang; Tijana Stanić Ljubin; Zdenko Časar
Journal:  Pharmaceutics       Date:  2019-09-02       Impact factor: 6.321

  1 in total

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