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通过共组装路线合成表面改性介孔材料及其药物释放性能。

Synthesis of surface modified mesoporous materials via co-assemble route and their drug release properties.

作者信息

Wang Yi, Zhu Jun, Han Jie, Guo Rong

机构信息

School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, 225002, Jiangsu, PR China.

出版信息

J Nanosci Nanotechnol. 2009 Nov;9(11):6700-9. doi: 10.1166/jnn.2009.1351.

DOI:10.1166/jnn.2009.1351
PMID:19908587
Abstract

A series of mesostructured Mn-MCM-41 composites were synthesized via a co-assembly route with tetraethylorthosilicate (TEOS) and manganese sulfate (MnSO4) as silica and manganese sources, respectively. And a model drug of cephanone was introduced via physical adsorption process into the channels of mesoporous silica, which could be used as the Mn-MCM-41 type mesoporous silica-based drug controlled-release delivery system. XRD, TEM, FT-IR, EDS and N2 adsorption-desorption were used to characterize the structural and textural properties of Mn-MCM-41 composites. The investigations showed that the addition of a small amount of manganese species was favorable for the long-range ordered structure of the mesoporous composites, whereas the ordered mesostructure was partially or completely distorted when the loaded manganese increased. The characterizations of cephanone loaded Mn-MCM-41 and in vitro release studies showed that the in vitro releases of cephanone in the ordered mesoporous materials follow an anomalous non-Fick's transport, and the impregnated manganese species had great influences on the release rate of cephanone from mesopores.

摘要

通过共组装路线,分别以正硅酸乙酯(TEOS)和硫酸锰(MnSO4)作为硅源和锰源,合成了一系列介孔结构的Mn-MCM-41复合材料。通过物理吸附过程将头孢酮模型药物引入介孔二氧化硅的孔道中,其可作为基于Mn-MCM-41型介孔二氧化硅的药物控释递送系统。采用XRD、TEM、FT-IR、EDS和N2吸附-脱附对Mn-MCM-41复合材料的结构和织构性质进行了表征。研究表明,少量锰物种的加入有利于介孔复合材料的长程有序结构,而当负载的锰增加时,有序介孔结构会部分或完全扭曲。负载头孢酮的Mn-MCM-41的表征及体外释放研究表明,头孢酮在有序介孔材料中的体外释放遵循非菲克反常传输,且浸渍的锰物种对头孢酮从介孔中的释放速率有很大影响。

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