• DocumentCode
    2084148
  • Title

    Biodegradable polylactide microspheres containing anticancer drugs used as injectable drug delivery system

  • Author

    Cao, Tingying ; Gao, Xiangdong ; Gu, Yueqing

  • Author_Institution
    China Pharm. Univ., Nanjing
  • fYear
    2007
  • fDate
    23-27 May 2007
  • Firstpage
    226
  • Lastpage
    229
  • Abstract
    Biodegradable poly(lactic-acid) (PLA ) microspheres containing 5-fluorouracil were prepared by a solid in oil in water emulsion solvent evaporation method. The influences of various preparation parameters, such as polymer concentration, polymer molecular weight, oil-phase volume and PVA concentration in the external water phase on the characteristics of the microspheres and drug release profiles, the in vitro cell inhibition were investigated. It was found that the particle size was 100.25 plusmn 2.50 mum and the drug loading was 8.25%(w/w). The in vitro release profiles of 5-fluorouracil loaded microspheres showed an initial burst release and thereafter the release was relatively slow. The in vitro cell inhibition indicate that the activity of 5-Fu is not weakened during the microspheres fabrication process and the solvent evaporation method is a mild fabrication technique for keeping drug stability.
  • Keywords
    biodegradable materials; cancer; drug delivery systems; drugs; emulsions; evaporation; particle size; polymers; 5-fluorouracil; anticancer drugs; biodegradable poly(lactic-acid) microspheres; drug release profiles; drug stability; in vitro cell inhibition; injectable drug delivery system; microspheres fabrication process; oil-phase volume; particle size; polymer concentration; polymer molecular weight; water emulsion solvent evaporation method; Biodegradable materials; Drug delivery; Fabrication; In vitro; Petroleum; Polymers; Programmable logic arrays; Solids; Solvents; Water; in vitro cell inhibition; in vitro release profiles; microspheres; polylactide;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Complex Medical Engineering, 2007. CME 2007. IEEE/ICME International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-1077-4
  • Electronic_ISBN
    978-1-4244-1078-1
  • Type

    conf

  • DOI
    10.1109/ICCME.2007.4381726
  • Filename
    4381726