Effect of surfactant concentration on transdermal lidocaine delivery with linker microemulsions

International Journal of Pharmaceutics

Volumn 392, Issue 1-2, 2010, Pages 274-284

  Yuan, Jessica S ^a   Yip, Alice ^a   Nguyen, Nga ^a   Chu, Jacquelene ^a   Wen, Xiao Yan ^b   Acosta, Edgar J ^a  

^a UNIVERSITY OF TORONTO   (Canada)

^b ST MICHAEL'S HOSPITAL   (Canada)

Author keywords

Lidocaine; Mass balance; Mechanism; Model; Partition; Transdermal

Indexed keywords

LIDOCAINE; PHOSPHATIDYLCHOLINE; SURFACTANT;

ANIMAL TISSUE; ARTICLE; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG ABSORPTION; DRUG FORMULATION; DRUG PENETRATION; DRUG SOLUBILITY; DRUG TRANSPORT; FLUORESCENCE ANALYSIS; FLUORESCENCE MICROSCOPY; HYDROPHOBICITY; IN VITRO STUDY; MICROEMULSION; NONHUMAN; PARTICLE SIZE; PARTITION COEFFICIENT; PRIORITY JOURNAL; SKIN; SKIN PERMEABILITY; SKIN STRUCTURE; SWINE;

ADMINISTRATION, CUTANEOUS; ANESTHETICS, LOCAL; ANIMALS; DRUG CARRIERS; EMULSIONS; HEXOSES; LECITHINS; LIDOCAINE; MYRISTATES; OCTANOIC ACIDS; PARTICLE SIZE; PHASE TRANSITION; SKIN; SKIN ABSORPTION; SURFACE-ACTIVE AGENTS; SWINE;

EID: 77952741003     PISSN: 03785173     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2010.03.051     Document Type: Article

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