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Pharmacokinetics of oral zidovudine entrapped in biodegradable nanospheres in rabbits

  • Diana P. Callender
  • , Nalini Jayaprakash
  • , Aaron Bell
  • , Vidmantas Petraitis
  • , Ruta Petratienes
  • , Myrna Candelario
  • , Robert Schaufele
  • , James M. Dunn
  • , Shizuko Sei
  • , Thomas J. Walsh
  • , Frank M. Balis
  • National Institutes of Health
  • Verex Laboratories, Inc.
  • SAIC

Research output: Contribution to journal › Article › peer-review

11 Scopus citations

Abstract

The pharmacokinetic profile of oral zidovudine entrapped in a 50:50 polyactide-coglycolide matrix (nanospheres) was compared to those of standard oral and parenteral zidovudine formulations in rabbits. The bioavailability of zidovudine nanospheres at 50 mg/kg of body weight was 76%, and this dose achieved prolonged exposure to zidovudine compared to standard formulations without an increase in the drug's peak concentration.

Original languageEnglish
Pages (from-to)972-974
Number of pages3
JournalAntimicrobial Agents and Chemotherapy
Volume43
Issue number4
DOIs
StatePublished - Apr 1999

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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