Recent Developments in Skin Mimic Systems to Predict Transdermal Permeation

被引:23
作者
Waters, Laura J. [1 ]
机构
[1] Univ Huddersfield, Sch Appl Sci, Dept Pharm, Huddersfield HD1 3DH, W Yorkshire, England
关键词
In vitro; measurement; permeation; skin; transdermal; BIOPARTITIONING MICELLAR CHROMATOGRAPHY; MEMBRANE-PERMEABILITY ASSAY; IN-VITRO DIFFUSION; DRUG-DELIVERY; SYNTHETIC MEMBRANES; HAIRLESS MOUSE; TOPICAL APPLICATION; STATIONARY-PHASE; ARTIFICIAL SKIN; STRATUM-CORNEUM;
D O I
10.2174/1381612821666150428124733
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In recent years there has been a drive to create experimental techniques that can facilitate the accurate and precise prediction of transdermal permeation without the use of in vivo studies. This review considers why permeation data is essential, provides a brief summary as to how skin acts as a natural barrier to permeation and discusses why in vivo studies are undesirable. This is followed by an in-depth discussion on the extensive range of alternative methods that have been developed in recent years. All of the major 'skin mimic systems' are considered including: in vitro models using synthetic membranes, mathematical models including quantitative structure-permeability relationships (QSPRs), human skin equivalents and chromatographic based methods. All of these model based systems are ideally trying to achieve the same end-point, namely a reliable in vitro-in vivo correlation, i.e. matching non-in vivo obtained data with that from human clinical trials. It is only by achieving this aim, that any new method of obtaining permeation data can be acknowledged as a potential replacement for animal studies, for the determination of transdermal permeation. In this review, the relevance and potential applicability of the various models systems will also be discussed.
引用
收藏
页码:2725 / 2732
页数:8
相关论文
共 105 条
[11]   Physicochemical determinants of linear alkylbenzene sulfonate (LAS) disposition in skin exposed to aqueous cutting fluid mixtures [J].
Baynes, RE ;
Brooks, JD ;
Barlow, BM ;
Riviere, JE .
TOXICOLOGY AND INDUSTRIAL HEALTH, 2002, 18 (05) :237-248
[12]   Effect of chemical interactions in pentachlorophenol mixtures on skin and membrane transport [J].
Baynes, RE ;
Brooks, JD ;
Mumtaz, M ;
Riviere, JE .
TOXICOLOGICAL SCIENCES, 2002, 69 (02) :295-305
[13]   In vitro 3D Full-Thickness Skin-Equivalent Tissue Model Using Silk and Collagen Biomaterials [J].
Bellas, Evangelia ;
Seiberg, Miri ;
Garlick, Jonathan ;
Kaplan, David L. .
MACROMOLECULAR BIOSCIENCE, 2012, 12 (12) :1627-1636
[14]  
Benson H.A., 2012, TRANSDERMAL TOPICAL
[15]   LIMITATIONS OF HAIRLESS MOUSE SKIN AS A MODEL FOR INVITRO PERMEATION STUDIES THROUGH HUMAN-SKIN - HYDRATION DAMAGE [J].
BOND, JR ;
BARRY, BW .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1988, 90 (04) :486-489
[16]   Human skin equivalents are an excellent tool to study the effect of moisturizers on the water distribution in the stratum corneum [J].
Bouwstra, J. A. ;
Nahmoed, N. ;
Groenink, H. W. W. ;
Ponec, M. .
INTERNATIONAL JOURNAL OF COSMETIC SCIENCE, 2012, 34 (06) :560-566
[17]  
Bouwstra J.A., 2010, OPEN DERMATOL J, V4, P10
[18]   Metabolically Competent Human Skin Models: Activation and Genotoxicity of Benzo[a]pyrene [J].
Brinkmann, Joep ;
Stolpmann, Kristin ;
Trappe, Susanne ;
Otter, Timo ;
Genkinger, Doris ;
Bock, Udo ;
Liebsch, Manfred ;
Henkler, Frank ;
Hutzler, Christoph ;
Luch, Andreas .
TOXICOLOGICAL SCIENCES, 2013, 131 (02) :351-359
[19]   Artificial skin in perspective: concepts and applications [J].
Brohem, Carla A. ;
da Silva Cardeal, Laura B. ;
Tiago, Manoela ;
Soengas, Maria S. ;
de Moraes Barros, Silvia B. ;
Maria-Engler, Silvya S. .
PIGMENT CELL & MELANOMA RESEARCH, 2011, 24 (01) :35-50
[20]   An evaluation of the potential of linear and nonlinear skin permeation models for the prediction of experimentally measured percutaneous drug absorption [J].
Brown, Marc B. ;
Lau, Chi-Hian ;
Lim, Sian T. ;
Sun, Yi ;
Davey, Neail ;
Moss, Gary P. ;
Yoo, Seon-Hie ;
De Muynck, Christian .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2012, 64 (04) :566-577