Supramolecular self-assembly of β-cyclodextrin: an effective carrier of the antimicrobial agent chlorhexidine
The supramolecular assembly between chlorhexidine and cyclomaltoheptaose (β-cyclodextrin, βCD) was characterized using NMR spectroscopy ( 1H, T 1, and ROESY), ESIMS and ITC. NMR data suggest the formation of high ordered complexes. ESIMS and ITC allowed the confirmation of the average stoichiometry...
Saved in:
Published in: | Carbohydrate research Vol. 342; no. 15; pp. 2286 - 2296 |
---|---|
Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Netherlands
Elsevier Ltd
05-11-2007
|
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The supramolecular assembly between chlorhexidine and cyclomaltoheptaose (β-cyclodextrin, βCD) was characterized using NMR spectroscopy (
1H,
T
1, and ROESY), ESIMS and ITC. NMR data suggest the formation of high ordered complexes. ESIMS and ITC allowed the confirmation of the average stoichiometry as 1:4 and the thermodynamic data, also obtained by ITC, showed that the assembly is strongly stabilized by short distance interactions, but suffers a strong, opposite effect of entropy reduction. The antimicrobial activity of 1:1, 1:2, 1:3, and 1:4 Clx/βCD molar ratio mixtures was investigated in aqueous solution and after incorporation into mucoadhesive gels. These were used to determine the initial and the long-term antimicrobial activity, respectively, toward
Actinobacillus actinomycetemcomitans (
A.a.) (Y4-FDC) and
Enterococcus faecalis (
E.f.) (ATCC 14508) strains. The results showed that
A.a. and
E.f. were more susceptible to the 1:4 molar ratio mixture in either solution or gel (
p
<
0.05). |
---|---|
ISSN: | 0008-6215 1873-426X |
DOI: | 10.1016/j.carres.2007.05.002 |