The influence of plasma butyrylcholinesterase concentration on the in vitro hydrolysis of cocaine in human plasma

In humans, the plasma enzyme butyrylcholinesterase, BChE (EC 3.1.1.8), mediates the in vivo plasma hydrolysis of cocaine to the pharmacologically inactive metabolite ecgonine methyl ester, EME. This enzyme has been purified from human plasma to investigate the potential as a treatment for cocaine in...

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Veröffentlicht in:Biopharmaceutics & drug disposition 1998-07, Vol.19 (5), p.309-314
Hauptverfasser: Browne, Susan P., Slaughter, Elizabeth A., Couch, Richard A., Rudnic, Edward M., McLean, Angus M.
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Sprache:eng
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Zusammenfassung:In humans, the plasma enzyme butyrylcholinesterase, BChE (EC 3.1.1.8), mediates the in vivo plasma hydrolysis of cocaine to the pharmacologically inactive metabolite ecgonine methyl ester, EME. This enzyme has been purified from human plasma to investigate the potential as a treatment for cocaine intoxication. Cocaine (2.1 μg mL−1) was incubated in plasma with a BChE concentration in the normal range (3.02 μg mL−1) and in plasma with enhanced BChE concentrations of 9.14, 20.8 and 37.8 μg mL−1, respectively for time periods up to 120 min. Cocaine and the hydrolytic products, ecgonine methyl ester and ecgonine, were quantified simultaneously by gas chromatography‐mass spectrometry (GC‐MS). The enhancement of plasma BChE concentration resulted in a dramatic increase in the rate of hydrolysis of cocaine. There was a stoichimetric conversion of cocaine to the inactive hydrolysis product, ecgonine methyl ester. Accordingly, the half‐life of cocaine in plasma decreased significantly with enhanced BChE concentration. At plasma BChE concentrations of 3.02, 9.14, 20.8 and 37.8 μg mL−1, half‐life values of 116, 35.8, 21.4 and 9.0 min, respectively were observed. The marked reduction in cocaine half‐life provides evidence supporting the potential therapeutic use of BChE for the treatment of cocaine intoxication. © 1998 John Wiley & Sons, Ltd.
ISSN:0142-2782
1099-081X
DOI:10.1002/(SICI)1099-081X(199807)19:5<309::AID-BDD108>3.0.CO;2-9