Preparation and characterization of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) microspheres for the sustained release of 5-fluorouracil

  • Gilson Khang*
  • , Sang Wook Kim
  • , Jin Cheol Cho
  • , John M. Rhee
  • , Sung Chul Yoon
  • , Hai Bang Lee
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

Biodegradable microspheres were prepared with poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV, 85:15 by mole ratio of hydroxybutyrate to hydroxyvalerate) by an water-in-oil-in-water (W/O/W), oil-in-water (O/W) and oil-in-oil (O/O) solvent evaporation method for the sustained release of anti-cancer drug, 5-fluorouracil (5-FU) with controlling the fabrication conditions. The shape of microspheres prepared was relatively rough due to highly crystalline property of PHBV and spherical. The efficiency of 5-FU loading into the PHBV microsphere with O/O method was over 80% compared to that 7% for microspheres by O/W method and below 1% for microspheres by a conventional W/O/W method. However, the most desirable release pattern can be achieved from the O/W method due to the cosolvent effect. The effects of preparation conditions such as the type and amount of surfactant, initial amount of loaded drug, the temperature of solvent evaporation, and etc. on the morphology for W/O/W method were investigated. Possible mechanisms of the desirable sustained release pattern for O/W system have been proposed.

Original languageEnglish
Pages (from-to)89-103
Number of pages15
JournalBio-Medical Materials and Engineering
Volume11
Issue number2
StatePublished - 2001

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

Keywords

  • 5-fluorouracil
  • Poly(3-hydroxybutyrate-co-3-hydroxyvalerate)
  • Solvent evaporation methods
  • Sustained release

Quacquarelli Symonds(QS) Subject Topics

  • Materials Science
  • Biological Sciences

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