Brazilian Journal of Chemical Engineering · 2008 · 55 citations · 9 references
PharmacyPharmaceuticsPharmacologyBioavailabilityDissolution TestingStructure-activity RelationshipsDrug SolubilityHerbicide SolubilitySolubility EnhancementSolubility OptimizationAbsorbance SpectroscopyComplex Formation EquilibriumHighly Soluble DrugsLow SolubilityMacromolecular Complex FormationSolubilitySolubility DeterminationSolubility Equilibrium
A high dosage of albendazole (ABZ) is required for treating systemic helminthe infections because of its low solubility. Aiming at increasing ABZ solubility, complexation with beta-cyclodextrin (β-CD) using aqueous and acetic acid solutions as ABZ solubilizer was studied. In aqueous β-CD, complexation increased solubility 53.4 times, giving a complex equilibrium constant of 1266 L mol-1 with a maximum ABZ concentration of 276 µmol L-1 for 16.3 mmol L-1 β-CD. For complexation in 1.05 mol L-1 acetic acid, UV absorbance spectra and ¹H-NMR analysis confirmed complex formation. The UV absorbance of ABZ/acid acetic/β-CD solutions was modeled by the formation of two complexes with molar ratios 1:1 and 1:2 ABZ:β-CD. When neutralized with NaOH these solutions did not form precipitates only for the ABZ:β-CD molar ratios of 1:8 and 1:10, showing that ABZ solubility could be increased 306 times. Results show that high β-CD molar ratios hold ABZ in solution by complexation enhanced by the acetate anion.
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T. Higuchi, A Connors · 1965 · 2.5K citations
Cyclodextrins in the Pharmaceutical Field
Otto Bekers, Esther V. Uijtendaal, Jos H. Beijnen et al. · Drug Development and Industrial Pharmacy · 1991 · 220 citations
Metabolism of albendazole in cattle, sheep, rats and mice.
Robert J. Gyurik, Alice Chow, B Zaber et al. · Drug Metabolism and Disposition · 1981 · 128 citations