4.5 Article

Dried Urine Spot Analysis for assessing cardiovascular drugs exposure applicable in spaceflight conditions

出版社

ELSEVIER
DOI: 10.1016/j.jchromb.2022.123539

关键词

Antihypertensive drugs; Dried urine spot; Microsampling; Liquid chromatography; Mass spectrometry; Space pharmacology

向作者/读者索取更多资源

Cardiovascular pharmacological countermeasures are needed for long-term space travelers to prevent cardiovascular deconditioning and early vascular aging. Due to the limitations and constraints of the extreme space environment, implementing drug studies is challenging. To address this, a simple sampling method using dried urine spots (DUS) was developed to quantify five antihypertensive drugs in human urine. The method was validated and showed stability of the targeted drugs under various storage conditions. It has been successfully implemented in space test programs conducted in 2022.
Cardiovascular pharmacological countermeasures will be required as a preventive measure of cardiovascular deconditioning and early vascular ageing for long term space travelers. Physiological changes during spaceflight could have severe implications on drug pharmacokinetics and pharmacodynamics (PK/PD). However, limitations exist for the implementation of drug studies due to the requirements and constraints of this extreme environ-ment. Therefore, we developed an easy sampling method on dried urine spot (DUS), for the simultaneous quantification of 5 antihypertensive drugs in human urine: irbesartan, valsartan, olmesartan, metoprolol and furosemide analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS), considering spaceflight parameters. This assay was validated in terms of linearity, accuracy, and precision with satisfactory results. There were no relevant carry-over, matrix interferences. The targeted drugs were stable in urine collected by DUS until 6 months at +21 degrees C, +4 degrees C,-20 degrees C (with or without desiccants) and at 30 degrees C during 48 h. Irbesartan, valsartan and olmesartan were not stable at 50 degrees C during 48 h. This method was found to be eligible for space pharma-cology studies in terms of practicality, safety, robustness and energy costs. It has been successfully implemented in space tests programs led in 2022.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据