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纸质出版日期:2011-6-20,
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张秀梅, 蔡静, 杨亚楠, 陈学思, 谢续明. PLGA/TiO2纳米药物缓释载体的研究[J]. 高分子学报, 2011,(6):653-660.
ZHANG Xiu-Mei, CAI Jing, YANG Ya-Nan, CHEN Xue-Si, XIE Xu-Ming. PREPARATION AND CHARACTERIZATION OF PLGA/TiO2 NANO DRUG DELIBERY CARRIERS[J]. Acta Polymerica Sinica, 2011,(6):653-660.
张秀梅, 蔡静, 杨亚楠, 陈学思, 谢续明. PLGA/TiO2纳米药物缓释载体的研究[J]. 高分子学报, 2011,(6):653-660. DOI: 10.3724/SP.J.1105.2011.10154.
ZHANG Xiu-Mei, CAI Jing, YANG Ya-Nan, CHEN Xue-Si, XIE Xu-Ming. PREPARATION AND CHARACTERIZATION OF PLGA/TiO2 NANO DRUG DELIBERY CARRIERS[J]. Acta Polymerica Sinica, 2011,(6):653-660. DOI: 10.3724/SP.J.1105.2011.10154.
首先利用硅烷偶联剂(KH550)对纳米二氧化钛表面进行预处理
得到氨基改性的二氧化钛
然后与带有高活性端基的丙交酯-乙交酯共聚物(PLGA)反应
制备纳米药物缓释载体PLGA/TiO2有机-无机杂化材料.通过核磁(1H-NMR)、傅里叶变换红外光谱仪(FTIR)、热重分析(TGA)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)等测试方法对杂化材料的结构与形貌进行表征.结果表明
PLGA成功接枝到了TiO2纳米粒子的表面
平均接枝量为14%左右
与纯纳米TiO2粒子相比
杂化材料的分散性得到较好的改善
无明显团聚现象
并对模型药牛血清蛋白(BSA)表现出较好的吸附能力
吸附量由43.3%提高到81.3%.然后采用水包油包固体(S/O/W)乳化法以PLGA为载体分别包裹上述含药纳米TiO2粒子和杂化粒子
比较两者的载药量和包封率
发现后者的载药量和包封率显著提高分别为14.6%和96%
且微球表面光滑
体外释放中突释较小.
A novel biodegradable PLGA/TiO2 organic-inorganic hybrid nano-material was prepared by the reaction between activated carboxyl-terminated PLGA
which was synthesized by PLGA and succinic anhydride with TEA as catalyzer
and amino-terminated TiO2 nano-particles which were modified by amino propyltriethoxysilane (KH550).The structure and morphology of the materials were characterized by Fourier transform infrared spectroscopy (FTIR)
1H nuclear magnetic resonance (1H-NMR)
thermogravimetic analysis (TGA)
environmental scanning electron microscopy (ESEM) and transmission electron microscopy (TEM) methods.The results showed that the PLGA was grafted successfully on the surface of nano scale TiO2 particles with 14% average grafting; PLGA/TiO2 hybrid nano-material dispersed uniformly in BSA aqueous solution without obvious aggregation and showed a better adsorptivity (81.3%) to model drug BSA as compared with that(43.3%) of pure TiO2 nanoparticles.Different kinds of the nanopaticles containing proteins BSA (TiO2-BSA and PLGA/TiO2-BSA) were loaded into polymer microspheres with PLGA as carrier by the solid-in-oil-in-water emulsion method.The drug loading content
entrapment efficiency and drug release in vitro of different drug containing microspheres were tested.The results indicated that the microspheres of PTB/P showed smooth morphologies
high entrapment efficiency 96% and drug loading content 14.6% and decreased burst effect of drug
compared with TB/P microspheres.
纳米二氧化钛PLGA有机-无机杂化药物缓释
TiO2 nano-particlesPLGAOrganic-inorganic hybridDrug control release
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