An implantable sol-gel derived titania-silica carrier system for the controlled release of anticonvulsants

被引:29
作者
Lopez, T.
Manjarrez, J.
Rembao, D.
Vinogradova, E.
Moreno, A.
Gonzalez, R. D.
机构
[1] Univ Autonoma Metropolitana Iztapalapa, Dept Chem, Mexico City 09340, DF, Mexico
[2] Inst Nacl Neurol & Neurocirurg MVS, Dept Neurophysiol & Neuropathol, Mexico City 14269, DF, Mexico
[3] Tulane Univ, Dept Chem & Biomol Engn, New Orleans, LA USA
关键词
sol-gel titania; biocompatibility; sodic phenytoine; valproic acid; epilepsy; controlled release; porosity;
D O I
10.1016/j.matlet.2006.02.017
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A sol-gel derived titania-silica reservoir has been synthesized and characterized. These materials can be used as an implantable carrier for controlled anticonvulsant delivery (sodium phenytoine and valproic acid). Xerogel characteristics, biocompatibility and in vitro release properties were obtained. FT-IR and UV-Vis spectroscopy were used to obtain information regarding the interaction between anticonvulsants and the mesoporous titania-silica ceramic. For the in vitro biocompatibility study, titania-silica reservoirs were surgically implanted into the basolateral amygdale of a rat. Following an implantation for a period of 8 months, the structure of the brain parenchyma and reservoir interface appears to be preserved. There was no evidence of inflammation or gross tissue reaction. Phenytoine was slowly released in vitro from the binary TiO2-SiO, xerogel over a period of 500 h. We envision that this sol-gel derived titania-silica system might play a significant role in the development of a new generation of controlled release biomaterials. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:2903 / 2908
页数:6
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