Inclusion Complexes of Cyclodextrins with Cinnamic Acid Derivatives: Dissolution and Thermal Behavior

36Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

Abstract

Typical Bs type phase solubility diagrams were obtained for α- and β-cyclodextrins (a-CyD and β-CyD) with methyl cinnamate, ethyl cinnamate, and cinnamaldehyde in water at 25°. Solid complexes for a- and β-CyDs with three guest molecules were obtained and their molar ratios were found to be 2:1 (a-CyD/guest molecule) and 1: 1 (β-CyD/guest molecule), respectively. In sharp contrast, apparent stability constant (Kc' x2018;) and dissolution rate ' x2018;)of a-CyD complexes were larger than those of β-CyD complexes. The thermal gravimetric analysis thermogram showed that the volatility of the guest molecule was lowered by the formation of CyD inclusion complex. © 1979, The Pharmaceutical Society of Japan. All rights reserved.

Cite

CITATION STYLE

APA

Uekama, K., Hirayama, F., Esaki, K., & Inoue, M. (1979). Inclusion Complexes of Cyclodextrins with Cinnamic Acid Derivatives: Dissolution and Thermal Behavior. Chemical and Pharmaceutical Bulletin, 27(1), 76–79. https://doi.org/10.1248/cpb.27.76

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free