Pore structures in an implantable sol-gel titania ceramic device used in controlled drug release applications: A modeling study

被引:19
|
作者
Peterson, Aaron
Lopez, Tessy
Islas, Emma Ortiz
Gonzalez, Richard D. [1 ]
机构
[1] Tulane Univ, Dept Chem & Biomol Engn, New Orleans, LA 70118 USA
[2] Metropolitan Autonomous Univ Rectoria Gen, Mexico City 14387, DF, Mexico
[3] Natl Inst Neurol & Neurosurg MVS, Mexico City 14269, DF, Mexico
关键词
epilepsy controlled drug release; implantable devices; pore structures; titania;
D O I
10.1016/j.apsusc.2006.12.094
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Several process variables, which may be helpful in optimizing the rate at which drugs are released from implantable, sol-gel titania devices have been identified in this study. The controlled rate of drug release is compared for two different anticonvulsant drugs, valproic acid and sodic phenytoin. Contrary to what one might expect, when the concentration is increased in the titania reservoir the rate of initial drug delivery decreases. This is a desirable result, because it may reduce the danger of a high initial discharge., which may harm the epileptic rat. The structure of the porous structure within the titania network has been studied using a generalized form of the BET equation which considers only n layers. In general, following an initial discharge, the rate at which the drug is released will increase with the increasing concentration. Pore mouth blocking can present a problem. However, this problem tends to disappear following the initial discharge. The extent of drug loading is a useful variable parameter, which can be adjusted in order to deliver the amount of drug required in a given application. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:5767 / 5771
页数:5
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