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梭曼及其立体异构体在水溶液中的稳定性:毒理学考量

The stability of soman and its stereoisomers in aqueous solution: toxicological considerations.

作者信息

Broomfield C A, Lenz D E, MacIver B

出版信息

Arch Toxicol. 1986 Dec;59(4):261-5. doi: 10.1007/BF00290548.

DOI:10.1007/BF00290548
PMID:3827593
Abstract

The paucity of information regarding the characteristics of soman (pinacolyl methylphosphonofluoridate) in aqueous solution has limited its use as a toxicological or pharmacological reagent. We report here on the stability of soman under conditions in which it may normally be found during use and storage in the laboratory. Solutions of 1 mM soman in normal saline were not hydrolyzed after 5 months of storage at -90 degrees C. Samples that were repeatedly thawed but not allowed to warm to room temperature and then immediately refrozen showed no apparent hydrolysis. Portions of the same solution, stored in the refrigerator just above freezing, exhibited 50% hydrolysis after 150 days. When portions of this solution were stored at 21 degrees C, the time for 50% hydrolysis was in excess of 5 days. This rate of hydrolysis was the same for all four of the soman stereoisomers. In buffered solutions at pH 7.4, 8.0 and 8.6 the half-times were 6.6, 3.2 and 2.2 h at 27 degrees C and 4.8, 1.6 and 1.2 h at 37 degrees C, respectively. Hydrolysis rates were not significantly influenced by the presence of a carbodimide stabilizer in the agent. There is no reason to expect any deviation from a direct correlation between total soman concentration and toxicity.

摘要

有关梭曼(频那基甲基膦酰氟)在水溶液中特性的信息匮乏,限制了其作为毒理学或药理学试剂的应用。我们在此报告梭曼在实验室使用和储存过程中通常会遇到的条件下的稳定性。1 mM梭曼的生理盐水溶液在-90℃储存5个月后未水解。反复解冻但未升温至室温然后立即重新冷冻的样品未显示明显水解。同一溶液的部分样品,储存在略高于冰点的冰箱中,150天后水解50%。当该溶液的部分样品储存在21℃时,50%水解的时间超过5天。所有四种梭曼立体异构体的水解速率相同。在pH值为7.4、8.0和8.6的缓冲溶液中,27℃时的半衰期分别为6.6、3.2和2.2小时,37℃时分别为4.8、1.6和1.2小时。试剂中碳二亚胺稳定剂的存在对水解速率没有显著影响。没有理由预期总梭曼浓度与毒性之间的直接相关性会有任何偏差。

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本文引用的文献

1
The stability of sarin and soman in dilute aqueous solutions and the catalytic effect of acetate ion.沙林和梭曼在稀水溶液中的稳定性及醋酸根离子的催化作用
J Environ Sci Health B. 1981;16(6):713-7. doi: 10.1080/03601238109372290.
2
Detoxification of soman and o-cyclopentyl-s-diethylaminoethyl methylphosphonothioate in vivo.体内梭曼和O-环戊基-S-二乙氨基乙基甲基硫代磷酸酯的解毒作用
Proc West Pharmacol Soc. 1984;27:315-8.
3
Stability of aqueous solutions of sarin and soman: influence of concentration and an equation for determining concentration.
Arch Toxicol. 1992;66(3):204-10. doi: 10.1007/BF01974016.
沙林和梭曼水溶液的稳定性:浓度的影响及浓度测定方程
Bull Environ Contam Toxicol. 1984 Jul;33(1):1-5. doi: 10.1007/BF01625503.
4
Stabilization and gas chromatographic analysis of the four stereoisomers of 1,2,2-trimethylpropyl methylphosphonofluoridate (soman) in rat blood.大鼠血液中1,2,2-三甲基丙基甲基膦酰氟(梭曼)四种立体异构体的稳定性及气相色谱分析
Anal Biochem. 1985 Dec;151(2):242-53. doi: 10.1016/0003-2697(85)90172-1.
5
Recovery of central respiratory function following anticholinesterase intoxication.抗胆碱酯酶中毒后中枢呼吸功能的恢复
Eur J Pharmacol. 1976 Jul;38(1):101-12. doi: 10.1016/0014-2999(76)90206-5.
6
Soman and receptor-ligand interaction in Electrophorus electroplaques.
Biochem Pharmacol. 1977 Feb 15;26(4):337-43. doi: 10.1016/0006-2952(77)90187-3.