Reichard J F, Phelps S E, Lehnhardt K R, Young M, Easter B D
NASA Johnson Space Center, Houston, TX, US.
Department of Environmental and Public Health Sciences, University of Cincinnati, Cincinnati, OH, USA.
NPJ Microgravity. 2023 May 5;9(1):35. doi: 10.1038/s41526-023-00271-6.
Pharmaceuticals selected for exploration space missions must remain stable and effective throughout mission timeframes. Although there have been six spaceflight drug stability studies, there has not been a comprehensive analytical analysis of these data. We sought to use these studies to quantify the rate of spaceflight drug degradation and the time-dependent probability of drug failure resulting from the loss of active pharmaceutical ingredient (API). Additionally, existing spaceflight drug stability studies were reviewed to identify research gaps to be addressed prior to exploration missions. Data were extracted from the six spaceflight studies to quantify API loss for 36 drug products with long-duration exposure to spaceflight. Medications stored for up to 2.4 years in low Earth orbit (LEO) exhibit a small increase in the rate of API loss with a corresponding increase in risk of product failure. Overall, the potency for all spaceflight-exposed medications remains within 10% of terrestrial lot-matched control with a ~1.5 increase in degradation rate. All existing studies of spaceflight drug stability have focused primarily on repackaged solid oral medications, which is important because non-protective repackaging is a well-established factor contributing to loss of drug potency. The factor most detrimental to drug stability appears to be nonprotective drug repackaging, based on premature failure of drug products in the terrestrial control group. The result of this study supports a critical need to evaluate the effects of current repackaging processes on drug shelf life, and to develop and validate suitable protective repackaging strategies that help assure the stability of medications throughout the full duration of exploration space missions.
为探索太空任务所选的药品必须在整个任务期间保持稳定且有效。尽管已经进行了六项太空飞行药物稳定性研究,但尚未对这些数据进行全面的分析。我们试图利用这些研究来量化太空飞行药物的降解速率以及因活性药物成分(API)损失导致药物失效的时间依赖性概率。此外,对现有的太空飞行药物稳定性研究进行了审查,以确定在探索任务之前需要解决的研究空白。从六项太空飞行研究中提取数据,以量化36种长期暴露于太空飞行的药品的API损失情况。在低地球轨道(LEO)中储存长达2.4年的药物,其API损失速率略有增加,产品失效风险相应增加。总体而言,所有暴露于太空飞行的药物的效力仍在地面批次匹配对照的10%以内,降解速率增加了约1.5倍。现有的所有太空飞行药物稳定性研究主要集中在重新包装的固体口服药物上,这很重要,因为非保护性重新包装是导致药物效力丧失的一个公认因素。基于地面对照组药物产品的过早失效,对药物稳定性最不利的因素似乎是非保护性药物重新包装。这项研究的结果支持迫切需要评估当前重新包装过程对药物保质期的影响,并开发和验证合适的保护性重新包装策略,以确保药物在整个探索太空任务期间的稳定性。