Mathematical modelling of variable porosity coatings for controlled drug release

被引:12
作者
McGinty, Sean [1 ]
King, David [1 ]
Pontrelli, Giuseppe [2 ]
机构
[1] Univ Glasgow, Div Biomed Engn, Glasgow, Lanark, Scotland
[2] CNR, Ist Applicaz Calcolo, Rome, Italy
基金
英国工程与自然科学研究理事会;
关键词
Drug delivery; Controlled release; Porous materials; Variable porosity; Mathematical modelling; Partial differential equations; MULTILAYER MATRIX TABLETS; DIFFUSION; TRANSPORT;
D O I
10.1016/j.medengphy.2017.04.006
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In this paper we investigate the extent to which variable porosity drug-eluting coatings can provide better control over drug release than coatings where the porosity is constant throughout. In particular, we aim to establish the potential benefits of replacing a single-layer with a two-layer coating of identical total thickness and initial drug mass. In our study, what distinguishes the layers (other than their individual thickness and initial drug loading) is the underlying microstructure, and in particular the effective porosity and the tortuosity of the material. We consider the effect on the drug release profile of varying the initial distribution of drug, the relative thickness of the layers and the relative resistance to diffusion offered by each layer's composition. Our results indicate that the contrast in properties of the two layers can be used as a means of better controlling the release, and that the quantity of drug delivered in the early stages can be modulated by varying the distribution of drug across the layers. We conclude that microstructural and loading differences between multi-layer variable porosity coatings can be used to tune the properties of the coating materials to obtain the desired drug release profile for a given application. (C) 2017 The Author(s). Published by Elsevier Ltd on behalf of IPEM.
引用
收藏
页码:51 / 60
页数:10
相关论文
共 18 条
[1]   Modeling the transport of drugs eluted from stents: physical phenomena driving drug distribution in the arterial wall [J].
Bozsak, Franz ;
Chomaz, Jean-Marc ;
Barakat, Abdul I. .
BIOMECHANICS AND MODELING IN MECHANOBIOLOGY, 2014, 13 (02) :327-347
[2]   Modulation of the dissolution profiles from Geomatrix(R) multi-layer matrix tablets containing drugs of different solubility [J].
Conte, U ;
Maggi, L .
BIOMATERIALS, 1996, 17 (09) :889-896
[3]  
Cussler E L., 2009, Diffusion: Mass Transfer in Fluid Systems
[4]   Two- and three-layer tablet drug delivery systems for oral sustained release of soluble and poorly soluble drugs [J].
Efentakis, M. ;
Naseef, H. ;
Vlachou, M. .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2010, 36 (08) :903-916
[5]   Combined drug release from biodegradable bilayer coating for endovascular stents [J].
Gagliardi, M. ;
Silvestri, D. ;
Cristallini, C. ;
Guadagni, M. ;
Crifaci, G. ;
Giusti, P. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2010, 93B (02) :375-385
[6]   A controlled antibiotic release system to prevent orthopedic-implant associated infections: An in vitro study [J].
Gimeno, Marina ;
Pinczowski, Pedro ;
Perez, Marta ;
Giorello, Antonella ;
Angel Martinez, Miguel ;
Santamaria, Jesus ;
Arruebo, Manuel ;
Lujan, Lluis .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2015, 96 :264-271
[7]  
Grathwohl P., 1998, Diffusion in Natural Porous Media: Contaminant Transport, Sorption/Desorption and Dissolution Kinetics
[8]   Metallic implant drug/device combinations for controlled drug release in orthopaedic applications [J].
Lyndon, Jessica A. ;
Boyd, Ben J. ;
Birbilis, Nick .
JOURNAL OF CONTROLLED RELEASE, 2014, 179 :63-75
[9]   A general model of coupled drug release and tissue absorption for drug delivery devices [J].
McGinty, Sean ;
Pontrelli, Giuseppe .
JOURNAL OF CONTROLLED RELEASE, 2015, 217 :327-336
[10]   A decade of modelling drug release from arterial stents [J].
McGinty, Sean .
MATHEMATICAL BIOSCIENCES, 2014, 257 :80-90