Modelling drug release from inert matrix systems: From moving-boundary to continuous-field descriptions

被引:71
作者
Frenning, Goran [1 ]
机构
[1] Uppsala Univ, Dept Pharm, SE-75123 Uppsala, Sweden
基金
瑞典研究理事会;
关键词
Drug release; Mathematical modelling; Matrix systems; Monolithic systems; Moving-boundary descriptions; Continuous-field descriptions; FINITE-ELEMENT-ANALYSIS; SLOWLY DISSOLVING DRUGS; DIFFUSIONAL RELEASE; THEORETICAL-ANALYSIS; POLYMER DEGRADATION; MATHEMATICAL-MODEL; BIOACTIVE AGENTS; DELIVERY-SYSTEMS; SOLUTE RELEASE; PARTICLE-SIZE;
D O I
10.1016/j.ijpharm.2010.11.030
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this review is to provide a comprehensive overview of mathematical procedures that can be used to describe the release of drugs from inert matrix systems. The review focuses on general principles rather than particular applications. The inherent multiscale nature of the drug-release process is pointed out and multiscale modelling is exemplified for inert porous matrices. Although effects of stagnant layers and finite volumes of release media are briefly discussed, the systematic analysis is restricted to systems under sink conditions. When the initial drug loading exceeds the drug solubility in the matrix, Higuchi-type moving-boundary descriptions continue to be highly valuable for obtaining approximate analytical solutions, especially when coupled with integral balance methods. Continuous-field descriptions have decisive advantages when numerical solutions are sought. This is because the mathematical formulation reduces to a diffusion equation with a nonlinear source term, valid over the entire matrix domain. Solutions can thus be effortlessly determined for arbitrary geometries using standard numerical packages. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:88 / 99
页数:12
相关论文
共 105 条
[1]  
Abramowitz M, 1965, Handbook of Mathematical Functions
[2]  
[Anonymous], 1994, Applications of Percolation Theory
[3]   COMPUTER-SIMULATIONS OF CATALYST DEACTIVATION .1. MODEL FORMULATION AND VALIDATION [J].
ARBABI, S ;
SAHIMI, M .
CHEMICAL ENGINEERING SCIENCE, 1991, 46 (07) :1739-1747
[4]   DIFFUSION-MODEL FOR DRUG RELEASE FROM SUSPENSIONS .1. THEORETICAL CONSIDERATIONS [J].
AYRES, JW ;
LINDSTROM, FT .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1977, 66 (05) :654-662
[5]   A problem for drug release from 2D polymeric systems [J].
Blagoeva, R. ;
Nedev, A. .
MECHANICS RESEARCH COMMUNICATIONS, 2008, 35 (05) :344-349
[6]  
BONNY JD, 1991, PHARM ACTA HELV, V66, P160
[7]  
BONNY JD, 1993, EUR J PHARM BIOPHARM, V39, P31
[8]   Simulation and parametric study of a film-coated controlled-release pharmaceutical [J].
Borgquist, P ;
Zackrisson, G ;
Nilsson, B ;
Axelsson, A .
JOURNAL OF CONTROLLED RELEASE, 2002, 80 (1-3) :229-245
[9]   Implications of regular solution theory on the release mechanism of catanionic mixtures from gels [J].
Bramer, Tobias ;
Frenning, Goran ;
Grasjo, Johan ;
Edsman, Katarina ;
Hansson, Per .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2009, 71 (02) :214-225
[10]   Percolative drug diffusion from cylindrical matrix systems with unsealed boundaries [J].
Brohede, U. ;
Valizadeh, S. ;
Stromme, M. ;
Frenning, G. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 96 (11) :3087-3099