Physicochemical characterization and in vitro dissolution behavior of nicardipine–cyclodextrins inclusion compounds

Author:

Fernandes Catarina M,Teresa Vieira M,B. Veiga Francisco J

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference28 articles.

1. Solubilization and interaction of naproxen with cyclodextrins in aqueous solution and in the solid state;Bettinetti;Farmaco,1989

2. Studies of cyclodextrin inclusion complexes. I. The salbutamol–cyclodextrin complex as studied by phase solubility and DSC;Cabral Marques;Int. J. Pharm.,1990

3. Improvement in solubility and dissolution rate of 1,2-dithiole-3-thiones upon complexation with β-cyclodextrin and its hydroxypropyl and sulfobutyl ether-7 derivatives;Dollo;J. Pharm. Sci.,1999

4. Physicochemical characteristics of carbamazepine–β-cyclodextrin inclusion compounds and carbamazepine–PEG solid dispersions;El-Nahhas;Pharmazie,1996

5. Inclusion complexation of glibenclamide with 2-hydroxypropyl-β-cyclodextrin in solution and in solid state;Esclusa-Dı́az;Eur. J. Pharm. Sci.,1994

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