Literature DB >> 6422028

Pharmacokinetic quantitation of naltrexone controlled release from a copolymer delivery system.

R H Reuning, S H Liao, A E Staubus, S B Ashcraft, D A Downs, S E Harrigan, J N Wiley, D L Wise.   

Abstract

Naltrexone release rates from a controlled release delivery system have been quantitated over a time period greater than one month in the monkey. The method requires calibration of the pharmacokinetic parameters of each monkey utilizing an intravenous bolus dose and assay of unchanged naltrexone levels in plasma as a function of time after dosing. Also required are periodic plasma levels of unchanged naltrexone obtained subsequent to administration of the delivery system. Release rates are then calculated as well as the total amount released. Application of the methodology to a biodegradable copolymer naltrexone delivery system in three monkeys showed an initial release rate of 3-8% of the dose per day over the first 3-5 days followed by a slow, rather constant release rate of 1-3% per day from day 5 to the time of the last measurable plasma sample (36-43 days). Comparison of alternative calculation methods using both experimental and simulated plasma naltrexone data verified the accuracy of the release rate calculations. The sum of the calculated total amount of naltrexone released plus the assayed amount remaining in the delivery system after removal from the animal accounted for 91-94% of the administered dose in the two monkeys in which complete data were obtained.

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Year:  1983        PMID: 6422028     DOI: 10.1007/bf01058956

Source DB:  PubMed          Journal:  J Pharmacokinet Biopharm        ISSN: 0090-466X


  13 in total

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Journal:  J Pharmacokinet Biopharm       Date:  1975-02

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5.  New method for calculating the intrinsic absorption rate of drugs.

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6.  Narcotic antagonists: the search for long-acting preparations: introduction.

Authors:  R E Willette
Journal:  Natl Inst Drug Abuse Res Monogr Ser       Date:  1975

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8.  Determination of naloxone and naltrexone as perfluoroalkyl ester derivatives by electron-capture gas-liquid chromatography.

Authors:  R A Sams; L Malspeis
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9.  Development of polylactic/glycolic acid delivery systems for use in treatment of narcotic addiction.

Authors:  A D Schwope; D L Wise; J F Howes
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10.  Continuous intravenous naltrexone effects on morphine self-administration in rhesus monkeys.

Authors:  S E Harrigan; D A Downs
Journal:  J Pharmacol Exp Ther       Date:  1978-02       Impact factor: 4.030

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  1 in total

1.  Disposition of naltrexone after intravenous bolus administration in Wistar rats, low-alcohol-drinking rats and high-alcohol-drinking rats.

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  1 in total

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