Quantitative structure-activity relationships (QSARs) for the prediction of skin permeation of exogenous chemicals
Patel H., ten Berge W., and Cronin M.T. Quantitative structure-activity relationships (QSARs) for the prediction of skin permeation of exogenous chemicals. Chemosphere 48 (2002) 603-613
Algorithms for skin permeability using hydrogen bond descriptors: the problem of steroids
Abraham M.H., Martins F., and Mitchell R.C. Algorithms for skin permeability using hydrogen bond descriptors: the problem of steroids. J. Pharm. Pharmacol. 49 (1997) 858-865
Prediction of human skin permeability using a combination of molecular orbital calculations and artificial neural network
Lim C.W., Fujiwara S., Yamashita F., and Hashida M. Prediction of human skin permeability using a combination of molecular orbital calculations and artificial neural network. Biol. Pharm. Bull. 25 (2002) 361-366
Drug permeation through human skin: theory and in vitro experimental measurement
Michaels A.S., Chandrasekaran S.K., and Shaw J.E. Drug permeation through human skin: theory and in vitro experimental measurement. AIChE J. 21 (1975) 985-996
Evaluation of solute permeation through the stratum corneum: lateral bilayer diffusion as the primary transport mechanism
Johnson M.E., Blankschtein D., and Langer R. Evaluation of solute permeation through the stratum corneum: lateral bilayer diffusion as the primary transport mechanism. J. Pharm. Sci. 86 (1997) 1162-1172
A theoretical analysis of permeation of small hydrophobic solutes across the stratum corneum based on scaled particle theory
Mitragotri S. A theoretical analysis of permeation of small hydrophobic solutes across the stratum corneum based on scaled particle theory. J. Pharm. Sci. 91 (2002) 744-752
Membrane solubility parameter and in situ release of theophylline
Adjei A., Newburger J., Stavchansky S., and Martin A. Membrane solubility parameter and in situ release of theophylline. J. Pharm. Sci. 73 (1984) 742-745