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幽门螺杆菌重组蛋白PLGA微球和PLGA-壳聚糖复合微球的制备及其释放性能研究
引用本文:陈昱作,刘人捷,杨露,李茂圆,索朗斯珠,李婉宜,王保宁. 幽门螺杆菌重组蛋白PLGA微球和PLGA-壳聚糖复合微球的制备及其释放性能研究[J]. 四川大学学报(医学版), 2021, 52(5): 794-798. DOI: 10.12182/20210960208
作者姓名:陈昱作  刘人捷  杨露  李茂圆  索朗斯珠  李婉宜  王保宁
作者单位:四川大学华西基础医学与法医学院 病原生物学系 成都 610041;四川大学华西基础医学与法医学院 病原生物学系 成都 610041;成都市血液中心 成都 610041;西藏农牧学院 林芝 860000;四川大学华西基础医学与法医学院 病原生物学系 成都 610041;西藏农牧学院 林芝 860000
基金项目:四川省科技厅重点研发项目(No. 21ZDYF1885、No. 2021YFS0054),成都市科技局项目(No. 2019-YF05-00298-SN)和西藏农牧学院柔性引进人才项目(No. RXYJ1905)资助
摘    要:目的 制备载有幽门螺杆菌重组蛋白(BIB蛋白)的聚乳酸-羟基乙酸共聚物(poly lactic-co-glycolic acid,PLGA)微球和PLGA-壳聚糖复合微球,优化微球制备参数,并分析两种微球在体外胃、肠液中的释放性能.方法 采用双乳化-溶剂挥发法(W1/O/W2)制备BIB-PLGA微球和BIB-PLGA...

关 键 词:幽门螺杆菌重组蛋白  聚乳酸-羟基乙酸微球  PLGA-壳聚糖复合微球
收稿时间:2020-10-12

Preparation and Release Properties of Helicobacter pylori Recombinant Protein PLGA Microspheres and PLGA-Chitosan Microspheres
CHEN Yu-zuo,LIU Ren-jie,YANG Lu,LI Mao-yuan,LI Wan-yi,WANG Bao-ning. Preparation and Release Properties of Helicobacter pylori Recombinant Protein PLGA Microspheres and PLGA-Chitosan Microspheres[J]. Journal of Sichuan University. Medical science edition, 2021, 52(5): 794-798. DOI: 10.12182/20210960208
Authors:CHEN Yu-zuo  LIU Ren-jie  YANG Lu  LI Mao-yuan  LI Wan-yi  WANG Bao-ning
Affiliation:1.Department of Pathogenic Biology, West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu 610041, China
Abstract:  Objective  To preparethe poly lactic-co-glycolic acid (PLGA) microspheres and PLGA-chitosan microspheres containing Helicobacter pylori recombinant protein, namely the BIB protein, and to explore their optimal preparation parameters and in vitro release performance in gastric and intestinal fluids.  Methods  Double emulsions (water-in-oil-in-water, or W1/O/W2) solvent evaporation method was used to prepare the BIB-PLGA microspheres and the BIB-PLGA-chitosan microspheres. Univariate analysis was done to study the impact of the water-to-oil ratio (W1/O), PLGA mass fraction and PVA concentration on the morphology, particle size, polydispersity index (PDI), encapsulation efficiency (EE), and drug loading (DL) so as to identify the optimal parameters. Bicinchoninic acid (BCA) assay was used to determine the protein concentration and the release efficiency of BIB.  Results   The optimal preparation parameters identified in the study were as follows: W1/O at 1∶2, PLGA mass fraction at 5%, and PVA mass fraction at 0.2%. The BIB-PLGA microspheres were found to be (2.11±0.08) μm in particle size, 0.35±0.18 in PDI, (78.20±1.73)% in EE and (10.58±0.23)% in DL. The BIB-PLGA-chitosan microspheres were (2.28±0.52) μm in particle size, 0.39±0.54 in PDI, and (78.87±1.30)% and (15.50±0.25)% in EE and DL, respectively. Both BIB-PLGA microspheres and BIB-PLGA-chitosan microspheres showed slow-release property in gastric and intestinal fluids in vitro, with BIB-PLGA-chitosan microspheres showing better slow-release performance.  Conclusion  The BIB-PLGA microspheres and BIB-PLGA-chitosan microspheres prepared with the double emulsions solvent evaporation method showed high DL and EE, controllable particle sizes, dispersive appearance, and slow-release property in gastric and intestinal fluids in vitro.
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