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Depot preparations of disulfiram: experimental and clinical results
J. Johnsen 1 J. Mørland 2
  1 Incognito Klinikk Apallakkveien 8, N-0956 Oslo and   2 The National Institute of Forensic Toxicology, Box 16 Gaustad, N-0320 Oslo
Copyright 1992 Blackwell Publishing Ltd
KEYWORDS
Disulfiram • implants • sustained-release preparations • review

ABSTRACT

Patient compliance with disulfiram is a troublesome clinical problem. Several strategies have been proposed as a solution to the problem, including subcutaneous implantation of disulfiram. However, well controlled studies of alcoholics and healthy volunteers have failed to discover a pharmacological effect of implanted disulfiram. A major reason for this failure appears to be poor absorption from an inadequate dose. Assessment of new sustained release formulation of depot disulfiram has been found to provoke a mild disulfiram-ethanol reaction (DER). Only a more severe DER would be expected to deter further drinking. If problems with absorption and appropriate dosing of disulfiram can be resolved or a depot preparation of the active metabolite of disulfiram can be prepared, implants might find continued clinical use.


DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1600-0447.1992.tb03311.x About DOI

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