Department of Chemistry and Biochemistry, South Dakota State University, Brookings, SD 57007, USA.
Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2022 Oct 1;1208:123392. doi: 10.1016/j.jchromb.2022.123392. Epub 2022 Jul 26.
Cyanide, hydrogen sulfide, and methanethiol are common toxic inhalation agents that inhibit mitochondrial cytochrome c oxidase and result in cellular hypoxia, cytotoxic anoxia, apnea, respiratory failure, cardiovascular collapse, seizure and potentially death. While all are occupational gas exposure hazards that have the potential to cause mass casualties from industrial accidents or acts of terrorism, only cyanide has approved antidotes, and each of these has major limitations, including difficult administration in mass-casualty settings. While bisaminotetrazole cobinamide (Cbi(AT)) has recently gained attention because of its efficacy in treating these metabolic poisons, there is no method available for the analysis of Cbi(AT) in any biological matrix. Hence, in this study, a simple and rapid liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated for the analysis of Cbi(AT) in swine plasma. The method is extremely simple, consisting of protein precipitation, separation and drying of the supernatant, reconstitution in an aqueous solvent, and LC-MS/MS analysis. The method produced an LOD of 0.3 μM with a wide dynamic range (2 - 500 μM). Inter- and intraassay accuracies (100 ± 12 % and 100 ± 19 %, respectively) were acceptable and the precision (<12 % and < 9 % relative standard deviation, respectively) was good. The developed method was used to analyze Cbi(AT) from treated swine and the preliminary pharmacokinetic parameters showed impressive antidotal behavior, most notably a long estimated elimination half-life (t = 37.5 h). This simple and rapid method can be used to facilitate the development of Cbi(AT) as a therapeutic against toxic cyanide, hydrogen sulfide and methanethiol exposure.
氰化物、硫化氢和甲硫醇是常见的抑制线粒体细胞色素 c 氧化酶的有毒吸入性物质,导致细胞缺氧、细胞毒性缺氧、呼吸暂停、呼吸衰竭、心血管衰竭、癫痫发作,甚至可能导致死亡。虽然这些都是可能导致工业事故或恐怖主义行为造成大量人员伤亡的职业性气体暴露危害,但只有氰化物有批准的解毒剂,而这些解毒剂都有重大限制,包括在大规模伤亡情况下的给药困难。虽然双氨基四唑联脒(Cbi(AT))最近因其治疗这些代谢性毒物的功效而受到关注,但目前还没有可用于分析任何生物基质中 Cbi(AT)的方法。因此,在这项研究中,开发并验证了一种用于分析猪血浆中 Cbi(AT)的简单快速的液相色谱-串联质谱(LC-MS/MS)方法。该方法非常简单,包括蛋白质沉淀、上清液的分离和干燥、在水性溶剂中复溶以及 LC-MS/MS 分析。该方法的检测限为 0.3 μM,具有较宽的动态范围(2-500 μM)。内、日间准确度(分别为 100 ± 12%和 100 ± 19%)可接受,精密度(分别为<12%和<9%相对标准偏差)良好。所开发的方法用于分析经处理猪的 Cbi(AT),初步药代动力学参数显示出令人印象深刻的解毒作用,特别是估计的消除半衰期较长(t = 37.5 h)。这种简单快速的方法可用于促进 Cbi(AT)作为治疗有毒氰化物、硫化氢和甲硫醇暴露的药物的开发。