Park Soo-Jin, Kim Seung-Hak
Advanced Materials Division, Korea Research Institute of Chemical Technology, P.O. Box 107, Yusong, Taejon 305-600, South Korea.
J Colloid Interface Sci. 2004 Mar 15;271(2):336-41. doi: 10.1016/j.jcis.2003.08.067.
In this work, the producing of a biodegradable poly(l-lactide) (PLA)/poly(ethylene glycol) (PEG) microcapsule by emulsion solvent evaporation method was investigated. The effect of PEG segments added to the PLA microcapsules on the degradation, size distribution, and release behavior was studied. According to the results, PLA/PEG copolymer was more hydrophilic than PLA homopolymer, and with lower glass transition temperature. The surface of PLA/PEG microcapsules was not as smooth as that of PLA microcapsules, the mean diameters of prepared PLA and PLA/PEG microcapsules were 40 and 57 microm, respectively. And spherical forms were observed by the image analyzer and the scanning electron microscope (SEM). Drug release from microcapsules was affected by the properties of PLA/PEG copolymers determined by UV-vis spectra. It was found that the drug release rates of the microcapsules were significantly increased with adding of PEG, which explained by increasing hydrophilic groups.
在本研究中,采用乳液溶剂蒸发法制备了可生物降解的聚(L-丙交酯)(PLA)/聚(乙二醇)(PEG)微胶囊。研究了向PLA微胶囊中添加PEG链段对其降解、粒径分布和释放行为的影响。结果表明,PLA/PEG共聚物比PLA均聚物更亲水,且玻璃化转变温度更低。PLA/PEG微胶囊的表面不如PLA微胶囊光滑,制备的PLA和PLA/PEG微胶囊的平均直径分别为40和57微米。通过图像分析仪和扫描电子显微镜(SEM)观察到微胶囊呈球形。通过紫外可见光谱测定的PLA/PEG共聚物的性质会影响微胶囊的药物释放。研究发现,添加PEG后微胶囊的药物释放速率显著提高,这可以通过亲水基团的增加来解释。