Probabilistic methods for drug dissolution. Part 2. Modelling a soluble binary drug delivery system dissolving in vitro

被引:21
作者
Barat, Ana [1 ]
Ruskin, Heather J. [1 ]
Crane, Martin [1 ]
机构
[1] Dublin City Univ, Sch Comp, Dublin 9, Ireland
关键词
modelling; drug delivery systems; dissolution; design and experiment; multicomponent soluble compacts; Monte Carlo; cellular automata;
D O I
10.1016/j.simpat.2006.03.003
中图分类号
TP39 [计算机的应用];
学科分类号
081203 [计算机应用技术]; 0835 [软件工程];
摘要
The objective of this work is to use direct Monte Carlo techniques in simulating drug delivery from compacts of complex composition, taking into consideration the special features of the in vitro dissolution environment. The paper focuses on simulating a binary system, consisting of poorly soluble drug, dispersed in a matrix of highly soluble acid excipient. At dissolution, the acid excipient develops certain mechanisms, based on local pH modifications of the medium, which strongly influence drug release. Our model directly accounts for such effects as local interactions of the dissolving components, development of wall roughness at the solid-liquid interface, moving concentration boundary layer and mass transport by advection. Results agree with experimental data and have demonstrated that when modelling dissolution in vitro, special attention must be paid to including the particular conditions of the dissolution environment. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:857 / 873
页数:17
相关论文
共 24 条
[1]
Stochastic modeling of controlled-drug release [J].
Chen, XY ;
Chen, WY ;
Hikal, AH ;
Shen, BC ;
Fan, LT .
BIOCHEMICAL ENGINEERING JOURNAL, 1998, 2 (03) :161-177
[2]
Chopard B, 1998, CELLULAR AUTOMATA MO, V01
[3]
Modeling and comparison of dissolution profiles [J].
Costa, P ;
Manuel, J ;
Lobo, S .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 13 (02) :123-133
[4]
Cranck J., 1975, MATH DIFFUSION, Vsecond
[5]
CRANE M, 2004, SIMULATION MODELLING
[6]
CRANE M, 2004, SIMUL MODEL PRACT TH, P12
[7]
MODELING MONOMER RELEASE FROM BIOERODIBLE POLYMERS [J].
GOPFERICH, A ;
LANGER, R .
JOURNAL OF CONTROLLED RELEASE, 1995, 33 (01) :55-69
[8]
Erosion of composite polymer matrices [J].
Gopferich, A .
BIOMATERIALS, 1997, 18 (05) :397-403
[9]
PREDICTING THE DISSOLUTION RATE OF IBUPROFEN-ACIDIC EXCIPIENT COMPRESSED MIXTURES IN REACTIVE MEDIA [J].
HEALY, AM ;
CORRIGAN, OI .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1992, 84 (02) :167-173
[10]
The influence of excipient particle size, solubility and acid strength on the dissolution of an acidic drug from two-component compacts [J].
Healy, AM ;
Corrigan, OI .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1996, 143 (02) :211-221