AI Article Synopsis

  • The ICH Q1B guidance outlines the necessary protocols for conducting photostability testing of pharmaceutical drugs, focusing on aspects like manufacturing, packaging, and storage.
  • Previous papers addressed photostability testing for injectable and topical drug products, highlighting a gap in guidance for oral drug formulations.
  • This third paper expands on the topic by detailing experimental approaches that simulate extreme photoexposure conditions using ICH-defined light sources to ensure the safety and effectiveness of photosensitive oral medications.

Article Abstract

The ICH Q1B guidance and additional clarifying manuscripts provide the essential information needed to conduct photostability testing for pharmaceutical drug products in the context of manufacturing, packaging, and storage. As the previous 2 papers in this series highlight for drug products administered by injection (part 1) and drug products administered via topical application (part 2), there remains a paucity of guidance and methodological approaches to conducting photostability testing to ensure effective product administration. Part 3 in the series is presented here to provide a similar approach and commentary for photostability testing for oral drug products. The approach taken, as was done previously, is to examine "worst case" photoexposure scenarios in combination with ICH-defined light sources to derive a set of practical experimental approaches to support the safe and effective administration of photosensitive oral drug products.

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Source
http://dx.doi.org/10.1016/j.xphs.2016.02.035DOI Listing

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