Effect of bilayer disruption on transdermal transport of low-molecular weight hydrophobic solutes

Pharmaceutical Research

Volumn 18, Issue 7, 2001, Pages 1018-1023

  Mitragotri, S ^a  

^a University of California   (United States)

Author keywords

Chemical enhancer; Diffusion; Enhancers; Modeling; Scaled particle theory; Transdermal

Indexed keywords

DRUG CARRIER; UNCLASSIFIED DRUG; ALDOSTERONE; CORTICOSTERONE; LIDOCAINE; NAPHTHOL DERIVATIVE; TESTOSTERONE;

ARTICLE; BILAYER MEMBRANE; DIFFUSION COEFFICIENT; DRUG DELIVERY SYSTEM; DRUG PENETRATION; DRUG UPTAKE; HYDROPHOBIC DRUG; HYDROPHOBICITY; LIPID BILAYER; MATHEMATICAL COMPUTING; MATHEMATICAL MODEL; MEMBRANE DAMAGE; MOLECULAR WEIGHT; NONHUMAN; PARTICLE RADIATION; PARTITION COEFFICIENT; PREDICTION; PRIORITY JOURNAL; SKIN ABSORPTION; SKIN PERMEABILITY; STRATUM CORNEUM; THEORY; BIOLOGICAL MODEL; CHEMISTRY; DIFFUSION; DRUG EFFECT; INTRADERMAL DRUG ADMINISTRATION; METABOLISM; PARTICLE SIZE; PERMEABILITY; SKIN; SOLUTION AND SOLUBILITY; TRANSPORT AT THE CELLULAR LEVEL;

ADMINISTRATION, CUTANEOUS; ALDOSTERONE; BIOLOGICAL TRANSPORT; CORTICOSTERONE; DIFFUSION; HYDROPHOBICITY; LIDOCAINE; LIPID BILAYERS; MODELS, BIOLOGICAL; MOLECULAR WEIGHT; NAPHTHOLS; PARTICLE SIZE; PERMEABILITY; SKIN; SOLUTIONS; TESTOSTERONE;

EID: 0034741916     PISSN: 07248741     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1010952731205     Document Type: Article

References (25)

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