화학공학소재연구정보센터
학회 한국고분자학회
학술대회 2003년 가을 (10/10 ~ 10/11, 부경대학교)
권호 28권 2호, p.168
발표분야 의료용 고분자 부문위원회
제목 Preparation of poly(lactic acid)/poly(ethylene glycol)(PLE) nanoparticles and drug release in vitro and in vivo
초록 The polymeric material made with poly(lactic acid)/poly(ethylene glycol)(PLE) were prepared using copolymer of D,L-lactide and poly(ethylene glycol) for application of drug delivery systems. Catalyst made use of stannous octoate. Preparation of nanoparticles by dialysis method and solvent evaporation method that nanoparticle made use of according to solvent of various kinds. Empty particle size preparation by dialysis method and solvent evaporation method were differ greatly(32.4±7.9~535.9±283.7), (33.6±26.4~245.6±136.0), respectively. Moreover, drug loaded particle size were differ greatly(51±4.9~761.9±189.3),(54.8±39.0~832.1±920.3), respectively. Particle size, drug loading, and drug release rate of PLE-2 nanoparticles were slightly changed by the used initial solvents. The degradation behavior of PLE block copolymer nanoparticles has divided three phases, initial rapid degradation phase, stationary phase, and rapid degradation phase until complete degradation. It was suggested that adriamycin release kinetics was dominantly governed by diffusion mechanism at initial burst phase and, after that, both of diffusion and degradation mechanism.
저자 유정준1, 서수원2, 정재승1
소속 1삼성서울병원 의공학과, 2(주)티엔오 휴먼조직공학(연)
키워드 nanoparticle; PLA/PEG copolymer; DDS
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