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作 者:柴雪[1] 屈铁军[1] 李伟[1] 王蕾[1] 徐波[1] 张亚庆[1]
机构地区:[1]第四军医大学口腔医学院,陕西西安710032
出 处:《牙体牙髓牙周病学杂志》2013年第4期270-274,共5页Chinese Journal of Conservative Dentistry
基 金:国家自然科学基金资助项目(31200738);陕西省社发攻关项目(2011K14-03-07)
摘 要:目的:以牛血清白蛋白(Bull serum albumin,BSA)为模型蛋白,聚乳酸-羟乙酸共聚物(Poly1actic-co-glycolic acid,PLGA)为载体,探索并优化微球的制备工艺。方法:采用复乳溶剂挥发法制备BSA-PLGA微球,激光粒度分析仪测量微球粒径,以微量BCA法测定微球的蛋白含量并计算包封率,进行体外释放,测定微球的24 h累积释放量。探索BSA投药量、外水相PVA(Polyvinyl alcohol)浓度、NaCl浓度及复乳匀质速度对微球包封率、24 h释放量和粒径的影响。结果:通过正交试验,在减少BSA-PLGA微球突释的情况下,兼顾微球粒径大小,通过适当增加BSA的投药量提高BSA-PLGA微球的包封率,得到微球的优化制备条件为BSA投药量10 mg,外水相PVA浓度10 g/L,NaCl浓度50 g/L,复乳的匀质速度10 000 r/min。结论:通过控制不同制备因素,可得到包封率较高、24 h突释量较小,粒径适宜的BSA-PLGA微球。AIM: To optimize the method of preparation of microspheres using bull serum albumin (BSA) as the model protein and poly lactic-co-glycolic acid (PLGA) as the controlled-release carrier. METHODS: The BSA-PLGA microspheres were prepared using a (water-in-oil)-in-water emulsion solvent evaporation technique. Mi- crosphere particle size was measured by laser particle size analyzer. Trace BCA method was used for determination of the protein content in the microspheres. Encapsulating rate was calculated. RESULTS: After various orthogonal tests, it was found that the optimal microsphere preparation condition was with 10 mg BSA, 1% Polyvinyl alcohol (PVA) , 5%NaC1 and at a stirring rate of 10 000 r/min for secondary emulsion . ONCLUSION: The optimized preparation method may produce BSA-PLGA microspheres with increased encapsulation efficiency, reduced 24 h burst release and appropriate particles size.
关 键 词:聚乳酸-羟乙酸共聚物 牛血清白蛋白 正交试验 微球
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