The effect of temperature and pH on the deacetylation of diamorphine in aqueous solution and in human plasma

Author:

Barrett David A1,Dyssegaard Astrid L P1,Shaw P Nicholas1

Affiliation:

1. Department of Pharmaceutical Sciences, University Park, University of Nottingham, Nottingham NG7 2RD, UK

Abstract

Abstract The effect of temperature on the kinetics of the deacetylation of diamorphine and 6-monoacetylmorphine was studied in human plasma. Diamorphine was rapidly and quantitatively degraded to 6-monoacetylmorphine with initial half-lives of 354, 18 and 3 min at temperatures of 4, 25 and 37°C, respectively. Further deacetylation to morphine was not detected. In aqueous solution, diamorphine was quantitatively degraded to give 6-monoacetylmorphine as the major product and morphine as a minor product, the rate of deacetylation being dependent on temperature and pH. At pH 4·0 and 5·6 diamorphine had a half-life of greater than 14 days at all temperatures but at alkaline pH diamorphine was rapidly deacetylated. The rate of deacetylation of 6-monoacetylmorphine was consistently slower than that of diamorphine under identical conditions of pH and temperature. A method is described for the rapid stabilization and subsequent assay of diamorphine in plasma which will prevent errors in estimation of the drug due to unwanted hydrolysis.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

Reference16 articles.

1. Determination of morphine and 6-acetylmorphine in plasma by high-performance liquid chromatography with fluorescence detection;Barrett;J. Chromatogr. Biomed. Applic.,1991

2. Stability study of aqueous solutions of diamorphine and morphine using HPLC;Beaumont;Pharm. J.,1982

3. Stability of diamorphine in chloroform water mixture;Cooper;Ibid.,1981

4. Hydrolysis of diamorphine in aqueous solutions;Davey;Ibid.,1969

5. Pharmacokinetics of morphine and its surrogates II: methods of separation of stabilized heroin and its metabolites from hydrolyzing biological fluids and applications to protein binding and red blood cell partition studies;Garrett;J. Pharm. Sci.,1979

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