Interfacial properties of most monofluorinated bile acids deviate markedly from the natural congeners: Studies with the Langmuir-Pockels surface balance

Journal of Lipid Research

Volumn 46, Issue 3, 2005, Pages 571-581

  Kauffman, John M ^a,b   Pellicciari, Roberto ^c   Carey, Martin C ^a,b  

^a HARVARD MEDICAL SCHOOL   (United States)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

^c UNIVERSITY OF PERUGIA   (Italy)

Author keywords

Bulk solubility; Condensation; Farnesoid X receptor; Orientation; Phosphatidylcholine; Pressure area isotherm; Spectroscopic imaging

Indexed keywords

2 OLEOYL 1 PALMITOYLPHOSPHATIDYLCHOLINE; 6ALPHA FLUOROCHENODEOXYCHOLIC ACID; 7ALPHA FLUOROHYODEOXYCHOLIC ACID; 7ALPHA FLUOROMUROCHOLIC ACID; BILE ACID; CHENODEOXYCHOLIC ACID; CHOLIC ACID DERIVATIVE; HYODEOXYCHOLIC ACID; PHOSPHATIDYLCHOLINE; UNCLASSIFIED DRUG; URSODEOXYCHOLIC ACID; 1-PALMITOYL-2-OLEOYLPHOSPHATIDYLCHOLINE; FLUORINE; WATER;

ANALYTIC METHOD; ARTICLE; CHEMICAL INTERACTION; CHEMICAL MODIFICATION; COMPARATIVE STUDY; CONCENTRATION (PARAMETERS); FLUORINATION; ISOTHERM; MOLECULAR MODEL; MOLECULAR STABILITY; PHASE TRANSITION; POLYMERIZATION; PRIORITY JOURNAL; SURFACE PROPERTY; AIR; CHEMICAL STRUCTURE; CHEMISTRY;

AIR; BILE ACIDS AND SALTS; FLUORINE; MODELS, MOLECULAR; PHOSPHATIDYLCHOLINES; SURFACE PROPERTIES; WATER;

EID: 24144501155     PISSN: 00222275     EISSN: 15397262     Source Type: Journal    
DOI: 10.1194/jlr.M400439-JLR200     Document Type: Article

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