Simple rules defining the potential of compounds for transdermal delivery or toxicity

Pharmaceutical Research

Volumn 21, Issue 6, 2004, Pages 1047-1054

  Magnusson, Beatrice M ^a   Pugh, W John ^b   Roberts, Michael S ^a  

^a UNIVERSITY OF QUEENSLAND   (Australia)

^b CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

multivariate data analysis; quantitative structure activity relationships; transdermal absorption

Indexed keywords

DRUG;

ARTICLE; CONTROLLED STUDY; DRUG DELIVERY SYSTEM; DRUG PENETRATION; DRUG SOLUBILITY; FEASIBILITY STUDY; HUMAN; HUMAN CELL; HYDROGEN BOND; MELTING POINT; MOLECULAR WEIGHT; PARTITION COEFFICIENT; PHYSICAL CHEMISTRY; PRIORITY JOURNAL; SKIN PENETRATION; TOXICITY TESTING;

ADMINISTRATION, CUTANEOUS; DRUG EVALUATION, PRECLINICAL; HUMANS; HYDROGEN BONDING; MATERIALS TESTING; MOLECULAR WEIGHT; SKIN; SKIN ABSORPTION; SOLUBILITY; TOXICITY TESTS; TRANSITION TEMPERATURE; VEHICLES;

EID: 3042764452     PISSN: 07248741     EISSN: None     Source Type: Journal    
DOI: 10.1023/B:PHAM.0000029295.38564.e1     Document Type: Article

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