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J Pharm Sci ; 72(10): 1215-7, 1983 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-6644576

RESUMO

The formation of an inclusion compound by beta-cyclodextrin with hydrocortisone has been studied by proton magnetic resonance (1H-NMR) and phase solubility analysis. The magnitude of the chemical shifts of the interior and exterior beta-cyclodextrin protons in the presence of hydrocortisone indicated that hydrocortisone is included within the beta-cyclodextrin cavity and probably interacts with protons on the edge of the torus. The overall stoichiometry of the inclusion compound was not a single, simple relationship, but was unusual in that it was variable and apparently dependent on the relative amounts of hydrocortisone and beta-cyclodextrin in the system.


Assuntos
Ciclodextrinas/análise , Dextrinas/análise , Hidrocortisona/análise , Amido/análise , beta-Ciclodextrinas , Química Farmacêutica , Espectroscopia de Ressonância Magnética , Conformação Molecular , Solubilidade , Termodinâmica
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