Effect of hydrophilic polymers on the release of BCNU from BCNU-loaded PLGA wafer

  • Kun An Tae*
  • , Jung Kang Hui
  • , Sik Moon Dae
  • , Soo Lee Jin
  • , Seong Hasoo
  • , Kyo Jeong Je
  • , Khang Gilson
  • , Bang Lee Hai
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU, carmustine) is one of the effective chemotherapeutic agents which has been used clinically for treating malignant glioma. Poly(D,L-lactide-co-glycolide) (PLGA, molecular weight: 20000 g/mole, mole ratio of lactide to glycolide 75:15) is a well known biodegradable polymer used as a drug carrier for drug delivery system. In this study, we investigated the BCNU release behaviour of BCNU-loaded PLGA wafers containing poly (N-vinylpyrrolidone) (PVP) or polyethyleneoxide (PEO) and the effect of hydrophilic polymers incoporated in the wafers. BCNU-loaded PLGA microparticles with or without hydrophilic polymers were prepared by a spray drying method and fabricated into wafers by direct compression. Encapsulation efficiency of BCNU-loaded PLGA microparticles containing PVP and PEO was 85-97% and crystallinity of BCNU encapsulated in PLGA decreased significantly. Initial release amount and release rate of BCNU increased with the increasing PVP or PEO amount. Morphological change and mass loss of wafers during the release test were confirmed that hydration and degradation of PLGA would be facilitated with an increase of hydrophilic polymers.

Original languageEnglish
Pages (from-to)670-679
Number of pages10
JournalPolymer (Korea)
Volume26
Issue number5
StatePublished - 2002.09

Keywords

  • BCNU
  • Brain tumor
  • Hydrophilic polymers
  • Microparticles
  • PLGA
  • Wafers

Quacquarelli Symonds(QS) Subject Topics

  • Materials Science
  • Engineering - Chemical

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