Literature DB >> 1497486

Interaction of obidoxime with sarin in aqueous solution.

P G Waser1, C M Alioth-Streichenberg, W H Hopff, R Portmann, W Hofmann, A Niederhauser.   

Abstract

The interaction of obidoxime (Toxogonin) with sarin was shown by different analytical methods. The UV spectrum of obidoxime at pH 7.4 yields two absorption maxima, lambda 1 = 284 nm and lambda 2 = 353 nm. The peak at lambda 2 = 353 nm is representative for the amount of zwitter-ionic obidoxime, i.e. the active form of obidoxime. By addition of sarin, lambda 1 shifts immediately to 278 nm and the intensity at lambda 2 decreases, thus indicating an interaction. TLC and 31P-NMR evidence shows that both mono-phosphonylated and diphosphonylated obidoximes are present. Decomposition of phosphonylated obidoxime in MOPS (3-[N-morpholino] propanesulfonic acid) buffered D2O at pH 7.4 occurs with t1/2 = 13.3 min at 24 degrees C. Decomposition of di-phosphonylated obidoxime is faster. It is suggested that decomposition of di-phosphonylated obidoxime occurs through the mono-phosphonylated form. Formation and decomposition of mono- and di-phosphonylated obidoxime is pH dependent. We conclude that obidoxime exerts a detoxifying effect by capturing free sarin molecules and thus increasing its polarity. Thereby the transition of sarin through the blood-brain barrier is restricted and its renal elimination facilitated.

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Year:  1992        PMID: 1497486     DOI: 10.1007/bf01974017

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  10 in total

1.  ISOPROPYL METHYLPHOSPHONYLATED BISQUATERNARY OXIMES; POWERFUL INHIBITORS OF CHOLINESTERASE.

Authors:  J C LAMB; G M STEINBERG; B E HACKLEY
Journal:  Biochim Biophys Acta       Date:  1964-07-08

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Journal:  Can J Biochem Physiol       Date:  1959-11

3.  Hydrolysis of bis(4-hydroxyiminomethyl-1-pyridiniomethyl)ether dichloride (Toxogonin). I. Decomposition products.

Authors:  I Christenson
Journal:  Acta Pharm Suec       Date:  1968-02

4.  Hydrolysis of bis(4-hydroxyiminomethyl-1-pyridiniomethyl)ether dichloride (Toxogonin). II. Kinetics and equilibrium in acidic solution.

Authors:  I Christenson
Journal:  Acta Pharm Suec       Date:  1968-09

5.  [Reactivation of phosphorylated acetylcholine esterase with oximes: contribution to the study of the reaction course].

Authors:  I Hagedorn; W H Gündel; K Schoene
Journal:  Arzneimittelforschung       Date:  1969-04

6.  Anticholinesterase activity and rate of decomposition of some phosphylated oximes.

Authors:  L P de Jong; D I Ceulen
Journal:  Biochem Pharmacol       Date:  1978-03-15       Impact factor: 5.858

7.  [PHARMACOLOGIC-TOXICOLOGIC STUDIES WITH THE DICHLORIDE OF BIS-(4-HYDROXYIMINOMETHYL-1-PYRIDINIUM-METHYL)-ETHER, A NEW ESTERASE REACTIVATOR].

Authors:  W D ERDMANN; H ENGELHARD
Journal:  Arzneimittelforschung       Date:  1964-01

8.  Hydrolysis of obidoxime chloride (Toxogonin). 3. Kinetics in neutral and alkaline solution.

Authors:  I Christenson
Journal:  Acta Pharm Suec       Date:  1972-09

9.  Studies on the decomposition of the oxime HI 6 in aqueous solution.

Authors:  P Eyer; W Hell; A Kawan; H Klehr
Journal:  Arch Toxicol       Date:  1986-12       Impact factor: 5.153

10.  Studies on the stability and decomposition of the Hagedorn-oxime HLö 7 in aqueous solution.

Authors:  P Eyer; B Ladstetter; W Schäfer; J Sonnenbichler
Journal:  Arch Toxicol       Date:  1989       Impact factor: 5.153

  10 in total

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