Literature DB >> 3196158

Study on the stability of the oxime HI 6 in aqueous solution.

P Eyer1, I Hagedorn, B Ladstetter.   

Abstract

HI 6 (Pyridinium, 1-[[[4-(aminocarbonyl)pyridinio]methoxy]methyl]-2-[(hydro xyimino) methyl]-dichloride is an effective antidote against poisoning with extremely toxic organophosphates. Because of conflicting reports on the stability of HI 6 in aqueous solutions, we studied the factors influencing its stability. HI 6 has been shown to be most stable in acidic solution between pH 2 and 3. At that pH, HI 6 decomposes probably by attack of nucleophiles on the methylene carbon atom of the animal-acetal bond of the "ether bridge". HI 6 decomposition follows first order kinetics. From Arrhenius plots of the decay of HI 6 at various concentrations it became obvious that the rate of decomposition increased with increasing HI 6 concentration with simultaneous decrease in the energy of activation. To decide whether the pyridinium compound itself or its anions are responsible for the enhanced decomposition, we studied the influence of chloride, phosphate and iodide. These anions stimulated the decay of HI 6 at increasing strength; their effect, however, was small as compared to that brought about by the pyridinium oxime itself. Since 1-methylisonicotinamide chloride had virtually no effect in contrast to 1-methylpyridinium-2-aldoxime chloride, we conclude that the oximate anion is responsible for the intermolecular attack on HI 6. At present, we recommend storage of HI 6 at concentrations not exceeding 0.1 M in aqueous solution at pH 2.5 and low temperatures. Under these conditions an apparent shelf-life of 20 years is calculated when HI 6 is stored at 8 degrees C.

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Year:  1988        PMID: 3196158     DOI: 10.1007/bf00570145

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


  7 in total

1.  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

2.  Stability study of HI-6 dichloride in various anticholinergic formulations.

Authors:  N D Brown; R R Gray; M G Stermer-Cox; B P Doctor; I Hagedorn
Journal:  J Chromatogr       Date:  1984-12-19

3.  Efficacy of a combination of acetylcholinesterase reactivators, HI-6 and obidoxime, against tabun and soman poisoning of mice.

Authors:  J G Clement; J D Shiloff; C Gennings
Journal:  Arch Toxicol       Date:  1987       Impact factor: 5.153

4.  HI-6 in man: blood levels, urinary excretion, and tolerance after intramuscular administration of the oxime to healthy volunteers.

Authors:  R Kusić; B Bosković; V Vojvodić; D Jovanović
Journal:  Fundam Appl Toxicol       Date:  1985-12

5.  Formation of cyanide after i.v. administration of the oxime HI 6 to dogs.

Authors:  P Eyer; A Kawan; B Ladstetter
Journal:  Arch Toxicol       Date:  1987       Impact factor: 5.153

6.  Pharmacokinetics and pharmacodynamics of the oxime HI6 in dogs.

Authors:  R Klimmek; P Eyer
Journal:  Arch Toxicol       Date:  1986-12       Impact factor: 5.153

7.  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

  7 in total
  7 in total

1.  Treatment of organophosphate poisoning in pigs: antidote administration by a new binary autoinjector.

Authors:  A Göransson-Nyberg; G Cassel; T Jeneskog; L Karlsson; R Larsson; M Lundström; S A Persson
Journal:  Arch Toxicol       Date:  1995       Impact factor: 5.153

2.  Pharmacokinetics of the oximes HI 6 and HLö 7 in dogs after i.m. injection with newly developed dry/wet autoinjectors.

Authors:  U Spöhrer; H Thiermann; R Klimmek; P Eyer
Journal:  Arch Toxicol       Date:  1994       Impact factor: 5.153

Review 3.  Unequal efficacy of pyridinium oximes in acute organophosphate poisoning.

Authors:  Biljana Antonijevic; Milos P Stojiljkovic
Journal:  Clin Med Res       Date:  2007-03

4.  HLö 7 dimethanesulfonate, a potent bispyridinium-dioxime against anticholinesterases.

Authors:  P Eyer; I Hagedorn; R Klimmek; P Lippstreu; M Löffler; H Oldiges; U Spöhrer; I Steidl; L Szinicz; F Worek
Journal:  Arch Toxicol       Date:  1992       Impact factor: 5.153

5.  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

6.  Targeting acetylcholinesterase: identification of chemical leads by high throughput screening, structure determination and molecular modeling.

Authors:  Lotta Berg; C David Andersson; Elisabet Artursson; Andreas Hörnberg; Anna-Karin Tunemalm; Anna Linusson; Fredrik Ekström
Journal:  PLoS One       Date:  2011-11-30       Impact factor: 3.240

7.  Structure of HI-6*sarin-acetylcholinesterase determined by X-ray crystallography and molecular dynamics simulation: reactivator mechanism and design.

Authors:  Fredrik Ekström; Andreas Hörnberg; Elisabet Artursson; Lars-Gunnar Hammarström; Gunter Schneider; Yuan-Ping Pang
Journal:  PLoS One       Date:  2009-06-18       Impact factor: 3.240

  7 in total

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