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Exploring the Complexities of Drug Formulation Selection, Storage, and Shelf-Life for Exploration SpaceflightMedications have been a part of space travel dating back as far as the Apollo missions. Currently, medical kits aboard the ISS contain medications and supplies to help crew members cope with a variety of possible medical events. NASA reported that 1,867 medical events occurred from 1981 to 1998 on space shuttle flights, STS-1 to STS-89; 498 out of the 508 crewmembers on those flights reported experiencing a medical event other than space motion sickness. In 2000, the Institute of Medicine (IOM) convened a committee of experts, Committee on Creating a Vision for Space Medicine during Travel beyond Earth Orbit, to examine the issues surrounding astronaut health and safety for long duration space missions. The primary theme of the committee’s final report is that there is not enough known about the risks to human health during long-duration missions beyond Earth’s orbit and ways to effectively mitigate those risks in an environment of deep space. In 2014, the IOM convened the Committee on Ethics Principles and Guidelines for Health Standards for Long Duration and Exploration Spaceflights and released a report emphasizing the importance of prevention, mitigation, and treatment of major risks to human health during exploration spaceflight. NASA’s Human Research Program has organized five distinct categories of spaceflight hazards summarized by the acronym “RIDGE” (Space Radiation, Isolation and Confinement, Distance from Earth, Gravity fields, and Hostile/Closed Environments) that astronauts may encounter during exploration spaceflight. From those hazards, NASA further derived 30 of the most critical human health and performance risks, including limits to medical care resulting from pharmaceutical degradation. As we prepare for more distant exploration missions to Mars and beyond, risk management planning for astronaut healthcare should include the assembly of a medication formulary that is comprehensive enough to prevent or treat anticipated medical events, remains safe and chemically stable, and retains sufficient potency to last for the duration of the mission. The present editorial will summarize the current state of knowledge regarding innovative formulary optimization strategies, pharmaceutical stability assessment techniques, and storage and packaging solutions that could enhance drug safety and efficacy for future exploration spaceflight missions.
Document ID
20230009066
Acquisition Source
Johnson Space Center
Document Type
Accepted Manuscript (Version with final changes)
Authors
Vernie R Daniels ORCID
(KBR (United States) Houston, Texas, United States)
Edward S Williams
(Johnson Space Center Houston, Texas, United States)
Date Acquired
June 14, 2023
Publication Date
November 8, 2023
Publication Information
Publication: British Journal of Clinical Pharmacology
Publisher: British Pharmacological Society
Issue Publication Date: November 8, 2023
ISSN: 0306-5251
e-ISSN: 1365-2125
Subject Category
Aerospace Medicine
Funding Number(s)
CONTRACT_GRANT: NNJ15HK11B
Distribution Limits
Public
Copyright
Public Use Permitted.
Technical Review
Single Expert
Keywords
drug degradation risk assessment
drug repurposing
drug storage and packaging
innovative drug delivery systems
spaceflight drug formulary optimization
spaceflight pharmaceutical stability
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