Chitosan macroporous asymmetric membranes-Preparation, characterization and transport of drugs

被引:49
作者
Santos, D. E. S. [1 ]
Neto, C. G. T. [1 ]
Fonseca, J. L. C. [1 ]
Pereira, M. R. [1 ]
机构
[1] Univ Fed Rio Grande do Norte, Dept Quim, BR-59078970 Natal, RN, Brazil
关键词
Chitosan; Silica gel; Macroporous; Permeability;
D O I
10.1016/j.memsci.2008.07.050
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Chitosan macroporous membranes with asymmetric morphology were obtained by using an inorganic porogen agent (SiO2). Chitosan/silica ratios used were 1:1, 1:3, and 1:5 w/w. A methodology to obtain asymmetric membranes with control of porosity and average pore size was proposed. The porous membranes were obtained taking advantage of the opposite solubility characteristics of chitosan and silica (4-20 mu m). The membranes were characterized by SEM and water sorption capacity. The porosity was calculated by the relationship between dense and macroporous membranes. The SEM images of both surfaces and cross-section of the membranes confirmed their asymmetric morphology. Using a double-cell method, the permeability coefficients of two model drugs (sodium sulfamerazine and sulfametoxipyridazine) were determined. The effects of porous layer, drug type, concentration and temperature were evaluated. The results revealed that the increase in porosity results in significant differences in permeability and that the effects of drug concentration and bath temperature become less pronounced as porosity increases. The mass transport was analyzed in terms of pore-flow mechanism and the solution-diffusion mechanism. The results showed that the methodology was very efficient to yield asymmetric membranes with good mechanical resistance, control of porous size and dense layer thickness and that these membranes can potentially be used to the transport of drugs. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:362 / 370
页数:9
相关论文
共 33 条
[1]   Using NaCl particles as porogen to prepare a highly adsorbent chitosan membranes [J].
Chao, An-Chong ;
Yu, Shu-Huei ;
Chuang, Guo-Syong .
JOURNAL OF MEMBRANE SCIENCE, 2006, 280 (1-2) :163-174
[2]   Novel fabrication of open-pore chitin matrixes [J].
Chow, KS ;
Khor, E .
BIOMACROMOLECULES, 2000, 1 (01) :61-67
[3]   Formation and characterization of chitosan membranes [J].
Clasen, C. ;
Wilhelms, T. ;
Kulicke, W. -M. .
BIOMACROMOLECULES, 2006, 7 (11) :3210-3222
[4]  
Connor E. E., 1998, Primary Care Update for Ob/Gyns, V5, P32, DOI 10.1016/S1068-607X(97)00121-2
[5]  
Crank J., 1975, The Mathematics of Diffusion, V1
[6]   Natural polymers for gene delivery and tissue engineering [J].
Dang, Jiyoung M. ;
Leong, Kam W. .
ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (04) :487-499
[7]   Endotoxin removal from solutions of F(ab′)2 fragments of equine antibodies against snake venom using macroporous chitosan membrane [J].
de Freitas, SS ;
Machado, RL ;
de Arruda, EJ ;
Santana, CC ;
Bueno, SMA .
JOURNAL OF MEMBRANE SCIENCE, 2004, 234 (1-2) :67-73
[8]   Chitosan-poly(acrylic acid) polyelectrolyte complex membranes: preparation, characterization and permeability studies [J].
De Oliveira, H. C. L. ;
Fonseca, J. L. C. ;
Pereira, M. R. .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2008, 19 (02) :143-160
[9]   Electrolyte diffusion in a chitosan membrane [J].
de Vasconcelos, CL ;
Rocha, ANL ;
Pereira, MR ;
Fonseca, JLC .
POLYMER INTERNATIONAL, 2001, 50 (03) :309-312
[10]   Biological properties of the chitosan-gelatin sponge wound dressing [J].
Deng, Chun-Mei ;
He, Lan-Zhen ;
Zhao, Ming ;
Yang, Dan ;
Liu, Yi .
CARBOHYDRATE POLYMERS, 2007, 69 (03) :583-589