3.8 Article

Argon pharmacokinetics: a solubility measurement technique

Journal

MEDICAL GAS RESEARCH
Volume 13, Issue 4, Pages 208-211

Publisher

WOLTERS KLUWER MEDKNOW PUBLICATIONS
DOI: 10.4103/2045-9912.351106

Keywords

argon; blood; gas solubility; headspace; noble gas; partition coefficient; pharmacokinetics; quadrupole mass spectrometry

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This paper presents a technique based on mass spectrometry for measuring argon solubility in liquids, including blood, which can be used in pharmacokinetics testing of argon. Results from sensitivity experiments using ambient air, water, and rabbit blood are reported based on a prototype, showing that the system was sensitive to argon during all of the testing. The authors believe that the technique and prototype of the quadrupole mass spectrometer gas analyzer will be capable of inferring argon pharmacokinetics through the analysis of blood samples.
The noble gas argon has demonstrated biological activity that may prove useful as a medical intervention. Pharmacokinetics, the disposition of the drug molecule in the body through time, is fundamental necessary knowledge to drug discovery, development and even post-marketing. The fundamental measurement in pharmacokinetic studies is blood concentration of the molecule (and its metabolites) of interest. While a physiologically based model of argon pharmacokinetics has appeared in the literature, no experimental data have been published. Thus, argon pharmaceutical development requires measurement of argon solubility in blood. This paper reports on the development of a technique based on mass spectrometry for measuring argon solubility in liquids, including blood, to be further employed in pharmacokinetics testing of argon. Based on a prototype, results are reported from sensitivity experiments using ambient air, water and rabbit blood. The key takeaway is that the system was sensitive to argon during all of the testing. We believe the technique and prototype of the quadrupole mass spectrometer gas analyzer will be capable of inferring argon pharmacokinetics through the analysis of blood samples.

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