The effect of formulations and experimental conditions on in vitro human skin permeation-Data from updated EDETOX database

被引:32
|
作者
Samaras, Eleftherios G. [1 ,2 ]
Riviere, Jim E. [3 ]
Ghafourian, Taravat [1 ,2 ]
机构
[1] Univ Kent, Medway Sch Pharm, Chatham ME4 4TB, Kent, England
[2] Univ Greenwich, Chatham ME4 4TB, Kent, England
[3] N Carolina State Univ, Ctr Chem Toxicol Res & Pharmacokinet, Raleigh, NC 27695 USA
关键词
QSAR; Skin; Dermal; Permeation; Absorption; In vitro; Decision tree; Finite dosing; Occlusion; Hydration; STRUCTURE-PERMEABILITY RELATIONSHIP; VIVO PERCUTANEOUS-ABSORPTION; COMPLEX CHEMICAL-MIXTURES; PENETRATION ENHANCERS; STRATUM-CORNEUM; RISK-ASSESSMENT; DIFFUSION CELL; DRUG-DELIVERY; BENZOIC-ACID; MULTICENTER;
D O I
10.1016/j.ijpharm.2012.05.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In vitro methods are commonly used in order to estimate the extent of systemic absorption of chemicals through skin. Due to the wide variability of experimental procedures, types of skin and data analytical methods, the resulting permeation measures varies significantly between laboratories and individuals. Inter-laboratory and inter-individual variations with the in vitro measures of skin permeation lead to unreliable extrapolations to in vivo situations. This investigation aimed at a comprehensive assessment of the available data and development of validated models for in vitro skin flux of chemicals under various experimental and vehicle conditions. Following an exhaustive literature review, the human skin flux data were collated and combined with those from EDETOX database resulting in a dataset of a total of 536 flux reports. Quantitative structure-activity relationship techniques combined with data mining tools were used to develop models incorporating the effects of permeant molecular structure, properties of the vehicle, and the experimental conditions including the membrane thickness, finite/infinite exposure, skin pre-hydration and occlusion. The work resulted in statistically valid models for estimation of the skin flux from varying experimental conditions, including relevant real-world mixture exposure scenarios. The models indicated that the most prominent factors influencing flux values were the donor concentration, lipophilicity, size and polarity of the penetrant, and the melting and boiling points of the vehicle, with skin occlusion playing significant role in a non-linear way. The models will aid assessment of the utility of dermal absorption data collected under different conditions with broad implications on transdermal delivery research. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:280 / 291
页数:12
相关论文
共 50 条
  • [21] In Vitro Evaluation of Sunscreen Safety: Effects of the Vehicle and Repeated Applications on Skin Permeation from Topical Formulations
    Montenegro, Lucia
    Turnaturi, Rita
    Parenti, Carmela
    Pasquinucci, Lorella
    PHARMACEUTICS, 2018, 10 (01):
  • [22] Permeation of topically applied caffeine through human skin - a comparison of in vivo and in vitro data
    Trauer, Sindy
    Patzelt, Alexa
    Otberg, Nina
    Knorr, Fanny
    Rozycki, Christel
    Balizs, Gabor
    Buettemeyer, Rolf
    Linscheid, Michael
    Liebsch, Manfred
    Lademann, Juergen
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2009, 68 (02) : 181 - 186
  • [23] Interrelation of permeation and penetration parameters obtained from in vitro experiments with human skin and skin equivalents
    Wagner, H
    Kostka, KH
    Lehr, CM
    Schaefer, UF
    JOURNAL OF CONTROLLED RELEASE, 2001, 75 (03) : 283 - 295
  • [24] 2-STEP EXTRAPOLATION FROM INVITRO ANIMAL SKIN PERMEATION DATA TO INVIVO HUMAN-SKIN PERMEATION
    SATO, K
    SUGIBAYASHI, K
    MORIMOTO, Y
    JOURNAL OF PHARMACEUTICAL SCIENCES, 1987, 76 (11) : S295 - S295
  • [25] Modelling of drug permeation in human skin in vitro from finite dose applications
    Vieira, R.
    Lane, M. E.
    Hadgraft, J.
    Anissimov, Y.
    Watkinson, A. C.
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2010, 62 (10) : 1287 - 1288
  • [26] In vitro evaluation of the permeation through reconstructed human epidermis of essentials oils from cosmetic formulations
    Gabbanini, S.
    Lucchi, E.
    Carli, M.
    Berlini, E.
    Minghetti, A.
    Valgimigli, L.
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2009, 50 (03) : 370 - 376
  • [27] Triclosan: release from transdermal adhesive formulations and in vitro permeation across human epidermal membranes
    Chedgzoy, P
    Winckle, G
    Heard, CM
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 235 (1-2) : 229 - 236
  • [28] DRUG PERMEATION THROUGH HUMAN-SKIN .1. EFFECT OF STORAGE-CONDITIONS OF SKIN
    SWARBRICK, J
    LEE, G
    BROM, J
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1982, 78 (01) : 63 - 66
  • [29] Effect of chemical enhancers and iontophoresis on thiocolchicoside permeation across rabbit and human skin in vitro
    Artusi, M
    Nicoli, S
    Colombo, P
    Bettini, R
    Sacchi, A
    Santi, P
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 93 (10) : 2431 - 2438
  • [30] Assessment of in vitro skin permeation and accumulation of phenolic acids from honey and honey-based pharmaceutical formulations
    Nowak, Anna
    Muzykiewicz-Szymanska, Anna
    Peruzynska, Magdalena
    Kucharska, Edyta
    Kucharski, Lukasz
    Jakubczyk, Karolina
    Niedzwiedzka-Rystwej, Paulina
    Stefanowicz-Hajduk, Justyna
    Drozdzik, Marek
    Majtan, Juraj
    BMC COMPLEMENTARY MEDICINE AND THERAPIES, 2025, 25 (01)