In vitro drug release rates from asymmetric-membrane tablet coatings: Prediction of phase-inversion dynamics

被引:21
作者
Altinkaya, SA [1 ]
Yenal, H [1 ]
机构
[1] Izmir Inst Technol, Dept Chem Engn, TR-35437 Izmir, Turkey
关键词
asymmetric-membrane; phase-inversion; statistical design; cellulose acetate; theophylline;
D O I
10.1016/j.bej.2005.09.009
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Most of the control led-release systems developed for drug delivery applications depend on membrane technology. The dense structure of some membranes used in control led-release systems can excessively prolong the release of drug due to the low permeability of the coating to drug. To increase the drug release rate, asymmetric-membrane tablet coatings were prepared by a phase-inversion technique using cellulose acetate/acetone/water solution. The roles of the composition of the membrane solution and the evaporation condition on the release rate of drug were determined using in vitro dissolution and morphological studies and predicted phase diagrams. Results show that drug release from asymmetric-membrane based tablet coatings is primarily governed by the dynamics of the phase-inversion process with zero-order or near-zero-order release easily achievable. In an attempt to derive an empirical expression for the release rate of drug as a function of composition of the coating solution, a statistical experimental design was used. Good fit of the experimental data by the empirical expression was obtained. In addition, the predictive capability of the model equation was also found to be satisfactory. Analysis of the significance of each term in the expression indicates that the cellulose acetate:acetone ratio has the most significant influence on the release rate of theophylline. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:131 / 139
页数:9
相关论文
共 32 条
[1]   Membrane formation by dry-cast process model validation through morphological studies [J].
Altinkaya, SA ;
Yenal, H ;
Ozbas, B .
JOURNAL OF MEMBRANE SCIENCE, 2005, 249 (1-2) :163-172
[2]   Modeling of asymmetric membrane formation by dry-casting method [J].
Altinkaya, SA ;
Ozbas, B .
JOURNAL OF MEMBRANE SCIENCE, 2004, 230 (1-2) :71-89
[3]  
Baker R.W., 1987, U.S. Patent, Patent No. [4,687,660, 4687660]
[4]   Effects of fabrication conditions on the structure and function of membranes formed from poly (acrylonitrile-vinylchloride) [J].
Broadhead, KW ;
Tresco, PA .
JOURNAL OF MEMBRANE SCIENCE, 1998, 147 (02) :235-245
[5]  
Cardinal JR, 1997, US Patent, Patent No. [5,612,059, 5612059]
[6]   The effect of polymeric additives on the structure and permeability of poly(vinyl alcohol) asymmetric membranes [J].
Chuang, WY ;
Young, TH ;
Chiu, WY ;
Lin, CY .
POLYMER, 2000, 41 (15) :5633-5641
[7]   Effect of coagulation media on membrane formation and vapor permeation performance of novel aromatic polyamide membrane [J].
Fan, SC ;
Wang, YC ;
Li, CL ;
Lee, KR ;
Liaw, DJ ;
Huang, HP ;
Lai, JY .
JOURNAL OF MEMBRANE SCIENCE, 2002, 204 (1-2) :67-79
[8]   ASYMMETRIC-MEMBRANE TABLET COATINGS FOR OSMOTIC DRUG-DELIVERY [J].
HERBIG, SM ;
CARDINAL, JR ;
KORSMEYER, RW ;
SMITH, KL .
JOURNAL OF CONTROLLED RELEASE, 1995, 35 (2-3) :127-136
[9]   Effects of shear rate and forced convection residence time on asymmetric polysulfone membranes structure and gas separation performance [J].
Ismail, AF ;
Ng, BC ;
Rahman, WAWA .
SEPARATION AND PURIFICATION TECHNOLOGY, 2003, 33 (03) :255-272
[10]   Captopril gastrointestinal therapeutic system coated with cellulose acetate pseudolatex: evaluation of main effects of several formulation variables [J].
Khan, MA ;
Sastry, SV ;
Vaithiyalingam, SR ;
Agarwal, V ;
Nazzal, S ;
Reddy, IK .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 193 (02) :147-156