Please use this identifier to cite or link to this item:
http://repositorio.ufla.br/jspui/handle/1/33261
Title: | Formation of β-Cyclodextrin inclusion compound with doxycycline: a theoretical approach |
Keywords: | Doxycycline Tetracycline Doxiciclina Tetraciclina |
Issue Date: | 16-Jan-2018 |
Publisher: | Elsevier |
Citation: | PERARO, C. R.; ANCONI, A. C. S. A.; ANCONI, C. P. A. Formation of β-Cyclodextrin inclusion compound with doxycycline: a theoretical approach. Chemical Physics Letters, Amsterdam, v. 692, p. 140-145, 16 Jan. 2018. |
Abstract: | Recently, the inclusion compound formed by doxycycline and modified CD was investigated. In the inclusion compound, the unstable site of doxycycline was protected by the hydrophobic CD cavity. However, the guest arrangement inside CD cavity has not identified. In some situations, the correlation between protons of the guest and host in a 2D-ROESY experiment can be compatible with head and tail spatial arrangements. In the present work, the most stable guest spatial arrangement for the inclusion of doxycycline into β-CD was evaluated at B97-D/6-311++(2d,p) level of theory. For sake of comparison, tetracycline inclusion compound was also studied. |
URI: | https://www.sciencedirect.com/science/article/pii/S000926141731103X#! http://repositorio.ufla.br/jspui/handle/1/33261 |
Appears in Collections: | DQI - Artigos publicados em periódicos |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.