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Drug Development and Industrial Pharmacy

Volumn 26, Issue 3, 2000, Pages 253-259

Study of omeprazole-γ-cyclodextrin complexation in the solid state

(6) Arias, M J a Moyano, J R a Munoz P a Gines J M a Justo, A b Giordano, F c

a UNIVERSITY OF SEVILLE (Spain)

b CSIC (Spain)

c UNIVERSITY OF PARMA (Italy)

Author keywords

CD; Dissolution rate; DSC; Inclusion complex; Omeprazole; PXRD

Indexed keywords

GAMMA CYCLODEXTRIN; OMEPRAZOLE;

ARTICLE; COMPLEX FORMATION; CONTROLLED STUDY; CRYSTAL STRUCTURE; DIFFERENTIAL SCANNING CALORIMETRY; DISSOLUTION; DRUG FORMULATION; DRUG RELEASE; DRUG SOLUBILITY; FREEZE DRYING; INFRARED SPECTROSCOPY; PRECIPITATION; SCANNING ELECTRON MICROSCOPY; SURFACE PROPERTY; X RAY POWDER DIFFRACTION;

ANTI-ULCER AGENTS; CHEMISTRY, PHARMACEUTICAL; CYCLODEXTRINS; HUMANS; OMEPRAZOLE; SOLUBILITY;

EID: 0034028738 PISSN: 03639045 EISSN: None Source Type: Journal
DOI: 10.1081/DDC-100100353 Document Type: Article

Times cited : (45)

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