The role of drug hydrophobicity in β-cyclodextrin complexes

Journal of Molecular Liquids

Volumn 155, Issue 2-3, 2010, Pages 103-108

  Al Omari, Mahmoud M ^a   El Barghouthi, Musa I ^b   Zughul, Mohammad B ^c   Davies, J Eric D ^d   Badwan, Adnan A ^a  

^a JORDANIAN PHARMACEUTICAL MANUFACTURING COMPANY   (Jordan)

^b HASHEMITE UNIVERSITY   (Jordan)

^c UNIVERSITY OF JORDAN   (Jordan)

^d LANCASTER UNIVERSITY   (United Kingdom)

Author keywords

Cyclodextrin; Free energy; Hydrophobic effect; Phase solubility diagram

Indexed keywords

CELECOXIB; COMPLEX FORMATIONS; COMPLEX STABILITY; DIPYRIDAMOLE; DRIVING FORCES; DRUG SOLUBILITY; FEXOFENADINE; HYDROPHOBIC CHARACTER; HYDROPHOBIC EFFECT; INTERACTING MOLECULES; KETOTIFEN; LINEAR CORRELATION; PHASE SOLUBILITY; QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIPS; RISPERIDONE; SILDENAFIL; STRUCTURAL FACTOR; THEORETICAL APPROACH; THREE-DIMENSIONAL STRUCTURE;

DRUG INTERACTIONS; FREE ENERGY; SLOPE STABILITY; SOLUBILITY; THIOPHENE;

HYDROPHOBICITY;

EID: 77956263690     PISSN: 01677322     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molliq.2010.05.018     Document Type: Article

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