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<p>Oxime reactivators are a part of the standard treatment for chemical warfare nerve agent exposure. Evaluating oxime candidates of interest in biological samples requires analytical detection methods, but oximes as a class of compounds have historically been difficult to isolate, detect, and analyze using conventional analytical techniques. Our lab previously developed novel extraction and liquid chromatography-tandem mass spectrometry (LC–MS/MS) methods to detect and quantitate 2-PAM, HI-6, HLö-7, and MMB-4 in human acetylcholinesterase knock-in, mouse carboxylesterase knock-out (KIKO) mouse plasma. These methods were validated to meet the Food and Drug Administration bioanalytical method validation requirements under Good Laboratory Practice conditions and then were utilized to analyze pharmacokinetic samples from KIKO mice. However, the future utility of these methods has been limited by the lack of reproducibly filled liquid chromatography (LC) columns. Herein we present an alternative LC column for the analysis of these oximes. Previously validated assay methods for oxime extraction from KIKO mouse plasma were evaluated for performance when analyzed by the new LC–MS/MS methodologies. Assays were evaluated for sensitivity, linearity, precision, accuracy, selectivity, and specificity. The results demonstrate that for 2-PAM, HI-6, and HLö-7, there was no change in assay performance when analyzed with the new LC–MS/MS methodologies. However, while MMB-4 was able to be retained on the new column, the sensitivity and linear range were not maintained from the original method. This study evaluates the potential of this alternative column to address inter-lot variability challenges, ensuring the robustness of oxime analytical methods.</p>

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Development of an Improved LC–MS/MS Assay for the Quantification of Oximes in KIKO Mouse Plasma

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年11月17日

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  • Katie A. Walker,
  • Justin N. Vignola,
  • C. Linn Cadieux,
  • Robert C. diTargiani

摘要

Oxime reactivators are a part of the standard treatment for chemical warfare nerve agent exposure. Evaluating oxime candidates of interest in biological samples requires analytical detection methods, but oximes as a class of compounds have historically been difficult to isolate, detect, and analyze using conventional analytical techniques. Our lab previously developed novel extraction and liquid chromatography-tandem mass spectrometry (LC–MS/MS) methods to detect and quantitate 2-PAM, HI-6, HLö-7, and MMB-4 in human acetylcholinesterase knock-in, mouse carboxylesterase knock-out (KIKO) mouse plasma. These methods were validated to meet the Food and Drug Administration bioanalytical method validation requirements under Good Laboratory Practice conditions and then were utilized to analyze pharmacokinetic samples from KIKO mice. However, the future utility of these methods has been limited by the lack of reproducibly filled liquid chromatography (LC) columns. Herein we present an alternative LC column for the analysis of these oximes. Previously validated assay methods for oxime extraction from KIKO mouse plasma were evaluated for performance when analyzed by the new LC–MS/MS methodologies. Assays were evaluated for sensitivity, linearity, precision, accuracy, selectivity, and specificity. The results demonstrate that for 2-PAM, HI-6, and HLö-7, there was no change in assay performance when analyzed with the new LC–MS/MS methodologies. However, while MMB-4 was able to be retained on the new column, the sensitivity and linear range were not maintained from the original method. This study evaluates the potential of this alternative column to address inter-lot variability challenges, ensuring the robustness of oxime analytical methods.