4.4 Article

In vitro and in vivo release of naltrexone from biodegradable depot systems

Journal

DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY
Volume 32, Issue 1, Pages 85-94

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/03639040500388466

Keywords

naltrexone; microspheres; tablet; biodegradable system; HPLC poly(D,L-lactide); release in vitro; release in vivo; histopathology

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The aim of this study was to prepare poly(d, l-lactide) (PLA) microspheres containing naltrexone (NTX) by a solvent evaporation method, and to evaluate both in vitro and in vivo release characteristics and histopathological findings of tissue surrounding an implant formulation in rats. This method enabled the preparation of microspheres of regular shape and relatively narrow particle size distribution. The in vitro release profiles of NTX from PLA microspheres showed the release of NTX did not follow zero-order kinetics. An initial burst release was observed, subsequently followed by a nearly constant rate of 0.4% per day after ten days. The cumulative amount of NTX released at the end of 60 days was 80%. Compressed microspheres showed near zero-order sustained release of NTX for 360 days. The plasma NTX levels in rats showed that for compressed microspheres NTX concentrations were constant and exceeded 2 ng/mL for 28 days. Throughout the 28 days of study, the implantations cause a minor inflammatory response, which can be regarded as a normal defence mechanism. The sustained release performance of NTX from the biodegradable depot systems may provide a reliable, convenient, and safe mechanism for the administration of NTX for the long-term treatment of opioid dependence.

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