Quantitative structure-permeability relationships (QSPRs) for percutaneous absorption

Toxicology in Vitro

Volumn 16, Issue 3, 2002, Pages 299-317

  Moss, G P ^a   Dearden, J C ^a   Patel, H ^a   Cronin, M T D ^a  

^a LIVERPOOL JOHN MOORES UNIVERSITY   (United Kingdom)

Author keywords

Hydrophobicity; In vitro methodology; Molecular size; QSAR; Skin

Indexed keywords

ALDOSTERONE; CORTICOSTERONE; CORTISONE; CORTODOXONE; DEOXYCORTICOSTERONE; ESTRADIOL; ESTRIOL; ESTRONE; HYDROCORTISONE; HYDROXYPROGESTERONE; PREGNENOLONE DERIVATIVE; PROGESTERONE; TESTOSTERONE; OCTANOL; WATER; XENOBIOTIC AGENT;

AQUEOUS SOLUTION; BIOAVAILABILITY; BIOTECHNOLOGY; HUMAN; HYDROPHOBICITY; IN VITRO STUDY; MEDICAL LITERATURE; METHODOLOGY; MOLECULAR SIZE; MOLECULAR WEIGHT; NONHUMAN; PARTITION COEFFICIENT; QUANTITATIVE STRUCTURE ACTIVITY RELATION; REVIEW; RISK ASSESSMENT; SKIN ABSORPTION; SKIN PENETRATION; SKIN PERMEABILITY; ANIMAL; CHEMISTRY; INTRADERMAL DRUG ADMINISTRATION; METABOLISM; ORGAN CULTURE TECHNIQUE; SKIN; SOLUBILITY;

ADMINISTRATION, CUTANEOUS; ANIMALS; HUMANS; HYDROPHOBICITY; MOLECULAR WEIGHT; OCTANOLS; ORGAN CULTURE TECHNIQUES; QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP; SKIN; SKIN ABSORPTION; SOLUBILITY; WATER; XENOBIOTICS;

EID: 0036096659     PISSN: 08872333     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-2333(02)00003-6     Document Type: Short Survey

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