Volumetric Absorptive Microsampling During Spaceflight for Analysis of Acetaminophen Pharmacokinetics in Whole Blood

Abstract Spaceflight induces altered physiology that has the potential to alter medication pharmacokinetics due to factors including gastrointestinal motility, fluid balance, circulatory dynamics, hormonal changes, and metabolic alterations. Here, we report the first pharmacokinetic analysis using blood samples during spaceflight. The four SpaceX Polaris Dawn crewmembers ingested 500 mg of oral acetaminophen pre‐flight, in‐flight, and post‐flight. Post‐ingestion capillary blood samples were collected using volumetric absorptive microsampling (VAMS). Samples were analyzed using liquid chromatography‐tandem mass spectrometry. All samples collected in microgravity were adequate for post‐flight analysis. Compared to pre‐flight baseline, in‐flight increases were observed in the C max (mean [SD] ng/mL: pre‐flight = 9110 [3290], in‐flight = 43,300 [5700], P < .001 ), AUC 0–last (mean [SD] h ng/mL: pre‐flight = 26,100 [4520], in‐flight = 109,000 [29,400]), and λ z (mean [SD] 1/h: pre‐flight = 0.227 [0.0688], in‐flight = 0.336 [0.0209]). Compared to pre‐flight baseline, in‐flight decreases were observed in t max (mean [SD] h: pre‐flight = 1.06 [0.657], in‐flight = 0.688 [0.239]), t 1/2 (mean [SD] h: pre‐flight = 3.27 [0.950], in‐flight = 2.07 [0.130]), CL/F (mean [SD] mL/h: pre‐flight = 16,200 [2990], in‐flight = 3890 [559]), and V z /F (mean [SD] mL: pre‐flight = 74,700 [18,800], in‐flight = 11,500 [1100]). Compared to pre‐flight baseline, C max , AUC, and λ z increased in‐flight, while t max , t 1/2 , V z /F, and CL/F decreased in‐flight. C max , AUC, V z /F, and CL/F showed residual changes 3 days post‐flight (R + 3). Supratherapeutic blood levels with standard terrestrial dosing raises concern for inadvertent toxicity in the spaceflight environment, and highlights the value of further pharmacokinetic study of medications commonly included within spaceflight medical systems. Overall, VAMS enabled pharmacokinetic study during spaceflight and could serve as a platform for future pharmacokinetic studies.

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Publication Details

Journal
The Journal of Clinical Pharmacology
Published
2026-07-30
DOI
https://doi.org/10.1002/jcph.70240
Primary Topic
Spaceflight effects on biology
Type
article
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article

Volumetric Absorptive Microsampling During Spaceflight for Analysis of Acetaminophen Pharmacokinetics in Whole Blood

John Donehoo, Nicolas Heft, Jaime Mateus, James Rudge et al.
The Journal of Clinical Pharmacology
Spaceflight effects on biology
article

Volumetric Absorptive Microsampling During Spaceflight for Analysis of Acetaminophen Pharmacokinetics in Whole Blood

John Donehoo, Nicolas Heft, Jaime Mateus, James Rudge, Jennifer Zimmer, Marissa Rosenberg, Amran Asadi, David Mampre, Erik Burns, Robert Guttendorf, James Huggins, Chad Christianson, Brooke Whitson, Takako Mizuno
article en

Abstract

Abstract Spaceflight induces altered physiology that has the potential to alter medication pharmacokinetics due to factors including gastrointestinal motility, fluid balance, circulatory dynamics, hormonal changes, and metabolic alterations. Here, we report the first pharmacokinetic analysis using blood samples during spaceflight. The four SpaceX Polaris Dawn crewmembers ingested 500 mg of oral acetaminophen pre‐flight, in‐flight, and post‐flight. Post‐ingestion capillary blood samples were collected using volumetric absorptive microsampling (VAMS). Samples were analyzed using liquid chromatography‐tandem mass spectrometry. All samples collected in microgravity were adequate for post‐flight analysis. Compared to pre‐flight baseline, in‐flight increases were observed in the C max (mean [SD] ng/mL: pre‐flight = 9110 [3290], in‐flight = 43,300 [5700], P < .001 ), AUC 0–last (mean [SD] h ng/mL: pre‐flight = 26,100 [4520], in‐flight = 109,000 [29,400]), and λ z (mean [SD] 1/h: pre‐flight = 0.227 [0.0688], in‐flight = 0.336 [0.0209]). Compared to pre‐flight baseline, in‐flight decreases were observed in t max (mean [SD] h: pre‐flight = 1.06 [0.657], in‐flight = 0.688 [0.239]), t 1/2 (mean [SD] h: pre‐flight = 3.27 [0.950], in‐flight = 2.07 [0.130]), CL/F (mean [SD] mL/h: pre‐flight = 16,200 [2990], in‐flight = 3890 [559]), and V z /F (mean [SD] mL: pre‐flight = 74,700 [18,800], in‐flight = 11,500 [1100]). Compared to pre‐flight baseline, C max , AUC, and λ z increased in‐flight, while t max , t 1/2 , V z /F, and CL/F decreased in‐flight. C max , AUC, V z /F, and CL/F showed residual changes 3 days post‐flight (R + 3). Supratherapeutic blood levels with standard terrestrial dosing raises concern for inadvertent toxicity in the spaceflight environment, and highlights the value of further pharmacokinetic study of medications commonly included within spaceflight medical systems. Overall, VAMS enabled pharmacokinetic study during spaceflight and could serve as a platform for future pharmacokinetic studies.

The Journal of Clinical PharmacologyVol. 66(8)
Altran (France) (FR), Sterling Research Group (US), Space Micro (United States) (US), SpaceX (United States) (US), Lakewood Regional Medical Center (US), The University of Texas Health Science Center at Houston (US)
Openalex Percentile: Top 10%
Spaceflight effects on biology
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