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
相关论文
共 26 条
  • [21] Monolithic polydimethylsiloxane-modified silica composites prepared by a low-temperature sol-gel micromolding technique for controlled-drug release
    Prokopowicz, Magdalena
    Szewczyk, Adrian
    Lunio, Rafal
    Sawicki, Wieslaw
    REACTIVE & FUNCTIONAL POLYMERS, 2017, 114 : 136 - 145
  • [22] Influence of a SiO2-CaO-P2O5 sol-gel glass on the bioactivity and controlled release of ceramic/polymer/antibiotic mixed materials
    Arcos, D
    Peña, J
    Vallet-Regí, M
    CHEMISTRY OF MATERIALS, 2003, 15 (21) : 4132 - 4138
  • [23] Antibacterial modification of an injectable, biodegradable, non-cytotoxic block copolymer-based physical gel with body temperature-stimulated sol-gel transition and controlled drug release
    Wang, Xiaowen
    Hu, Huawen
    Wang, Wenyi
    Lee, Ka I.
    Gao, Chang
    He, Liang
    Wang, Yuanfeng
    Lai, Chuilin
    Fei, Bin
    Xin, John H.
    COLLOIDS AND SURFACES B-BIOINTERFACES, 2016, 143 : 342 - 351
  • [24] Raman study of the chemical and thermal degradation of As-received and sol-gel embedded Nicalon and Hi-Nicalon SiC fibres used in ceramic matrix composites
    Karlin, S
    Colomban, P
    JOURNAL OF RAMAN SPECTROSCOPY, 1997, 28 (04) : 219 - 228
  • [25] Hyperbranched Copolymers Forming Polymersome-like Structures Used for Encapsulation and Controlled Release of α-Tocopherol Succinate (TOS): Drug Transport Modeling
    Sengupta, Srijoni
    Ray, Preetam Guha
    Dhara, Santanu
    Bandyopadhyay, Abhijit
    ACS APPLIED BIO MATERIALS, 2021, 4 (12): : 8236 - 8247
  • [26] Novel Sol-Gel Route to Prepare Eu3+-Doped 80SiO2-20NaGdF4 Oxyfluoride Glass-Ceramic for Photonic Device Applications
    Cruz, Maria Eugenia
    Tran, Thi Ngoc Lam
    Chiasera, Alessandro
    Duran, Alicia
    Fernandez, Joaquin
    Balda, Rolindes
    Castro, Yolanda
    NANOMATERIALS, 2023, 13 (05)