Various bispilocarpic acid diesters (double prodrugs of pilocarpine) were synthesized, and their in vitro esterase catalyzed hydrolysis was evaluated in diluted human plasma, rabbit cornea homogenate, and specific butyrylcholinesterase solution. The structural changes greatly affected the rate of en
The influence of plasma butyrylcholinesterase concentration on the in vitro hydrolysis of cocaine in human plasma
β Scribed by Susan P. Browne; Elizabeth A. Slaughter; Richard A. Couch; Edward M. Rudnic; Angus M. McLean
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 179 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0142-2782
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β¦ Synopsis
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 mg mL -1 ) was incubated in plasma with a BChE concentration in the normal range (3.02 mg mL -1 ) and in plasma with enhanced BChE concentrations of 9.14, 20.8 and 37.8 mg 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 mg 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.
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