Improving the applicability of (Q)SARs for percutaneous penetration in regulatory risk assessment

被引:29
作者
Bouwman, T. [1 ]
Cronin, M. T. D. [2 ]
Bessems, J. G. M. [1 ]
van de Sandt, J. J. M. [1 ]
机构
[1] TNO Qual Life, Dept Food & Chem Risk Anal, NL-3700 AJ Zeist, Netherlands
[2] Liverpool John Moores Univ, Sch Pharm & Chem, Liverpool L3 5UX, Merseyside, England
关键词
dermal absorption; risk assessment; REACH; (Q)SAR; quantitative structure-activity relationships;
D O I
10.1177/0960327107085829
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 [卫生毒理学];
摘要
The new regulatory framework REACH (Registration, Evaluation, and Authorisation of Chemicals) foresees the use of non-testing approaches, such as read-across, chemical categories, structure-activity relationships (SARs) and quantitative structure-activity relationships (QSARs). Although information on skin absorption data are not a formal requirement under REACH, data on dermal absorption are an integral part of risk assessment of substances/products to which man is predominantly exposed via the dermal route. In this study, we assess the present applicability of publicly available QSARs on skin absorption for risk assessment purposes. We explicitly did not aim to give scientific judgments on individual QSARs. A total of 33 QSARs selected from the public domain were evaluated using the OECD (Organisation for Economic Co-operation and Development) Principles for the Validation of (Q)SAR Models. Additionally, several pragmatic criteria were formulated to select QSARs that are most suitable for their use in regulatory risk assessment. Based on these criteria, four QSARs were selected. The predictivity of these QSARs was evaluated by comparing their outcomes with experimentally derived skin absorption data (for 62 compounds). The predictivity was low for three of four QSARs, whereas one model gave reasonable predictions. Several suggestions are made to increase the applicability of QSARs for skin absorption for risk assessment purposes.
引用
收藏
页码:269 / 276
页数:8
相关论文
共 41 条
[1]
Human skin permeation and partition: General linear free-energy relationship analyses [J].
Abraham, MH ;
Martins, F .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 93 (06) :1508-1523
[2]
Algorithms for skin permeability using hydrogen bond descriptors: the problem of steroids [J].
Abraham, MH ;
Martins, F ;
Mitchell, RC .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1997, 49 (09) :858-865
[3]
THE FACTORS THAT INFLUENCE SKIN PENETRATION OF SOLUTES [J].
ABRAHAM, MH ;
CHADHA, HS ;
MITCHELL, RC .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1995, 47 (01) :8-16
[4]
QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIPS FOR SKIN PERMEABILITY [J].
BARRATT, MD .
TOXICOLOGY IN VITRO, 1995, 9 (01) :27-37
[5]
A SIMPLE METHOD FOR ESTIMATING DERMAL ABSORPTION OF CHEMICALS IN WATER [J].
BROWN, SL ;
ROSSI, JE .
CHEMOSPHERE, 1989, 19 (12) :1989-2001
[6]
A simple, predictive, structure-based skin permeability model [J].
Buchwald, P ;
Bodor, N .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2001, 53 (08) :1087-1098
[7]
Investigation of the mechanism of flux across human skin in vitro by quantitative structure-permeability relationships [J].
Cronin, MTD ;
Dearden, JC ;
Moss, GP ;
Murray-Dickson, G .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 1999, 7 (04) :325-330
[8]
CRONIN MTD, 2005, DERMAL ABSORPTION MO
[9]
Dearden J. C., 2000, Journal of Pharmacy and Pharmacology, V52, P221
[10]
New tools and approaches for predicting skin permeability [J].
Degim, I. Tuncer .
DRUG DISCOVERY TODAY, 2006, 11 (11-12) :517-523