Recent advances in predicting skin permeability of hydrophilic solutes.

Chen, L, Han, L and Lian, G (2013) Recent advances in predicting skin permeability of hydrophilic solutes. Adv Drug Deliv Rev, 65 (2). pp. 295-305.

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Abstract

Understanding the permeation of hydrophilic molecules is of relevance to many applications including transdermal drug delivery, skin care as well as risk assessment of occupational, environmental, or consumer exposure. This paper reviews recent advances in modeling skin permeability of hydrophilic solutes, including quantitative structure-permeability relationships (QSPR) and mechanistic models. A dataset of measured human skin permeability of hydrophilic and low hydrophobic solutes has been compiled. Generally statistically derived QSPR models under-estimate skin permeability of hydrophilic solutes. On the other hand, including additional aqueous pathway is necessary for mechanistic models to improve the prediction of skin permeability of hydrophilic solutes, especially for highly hydrophilic solutes. A consensus yet has to be reached as to how the aqueous pathway should be modeled. Nevertheless it is shown that the contribution of aqueous pathway can constitute to more than 95% of the overall skin permeability. Finally, future prospects and needs in improving the prediction of skin permeability of hydrophilic solutes are discussed.

Item Type:	Article
Authors :	Name Email ORCID Chen, L UNSPECIFIED UNSPECIFIED Han, L UNSPECIFIED UNSPECIFIED Lian, G g.lian@surrey.ac.uk UNSPECIFIED
Date :	February 2013
Identification Number :	https://doi.org/10.1016/j.addr.2012.05.001
Uncontrolled Keywords :	Administration, Cutaneous, Drug Delivery Systems, Humans, Hydrophobic and Hydrophilic Interactions, Models, Theoretical, Permeability, Pharmaceutical Preparations, Quantitative Structure-Activity Relationship, Skin, Skin Absorption
Related URLs :	Author
Depositing User :	Symplectic Elements
Date Deposited :	17 May 2017 13:04
Last Modified :	17 May 2017 15:08
URI:	http://epubs.surrey.ac.uk/id/eprint/837854

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