Novel anti-microbial host-guest complexes based on cationic β-cyclodextrin polymers and triclosan/butylparaben

被引:27
作者
Guan, Yong [1 ]
Qian, Liying [1 ,2 ]
Xiao, Huining [1 ,2 ]
机构
[1] Univ New Brunswick, Dept Chem Engn, Fredericton, NB E3B 5A3, Canada
[2] S China Univ Technol, State Key Lab Pulp & Paper Engn, Guangzhou, Peoples R China
关键词
antibiotics; anti-microbial activity; cationic beta-cyclodextrin polymers; host-guest systems; NMR;
D O I
10.1002/marc.200700505
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The preparation of novel cationic beta-cyclodextrin polymers (CP beta Ms) and its complexes with butylparaben and triclosan were reported in this paper. FT-IR and two-dimensional (2D) H-1-H-1 gradient correlated spectroscopy (gCOSY) NMR spectra confirmed that the antibiotics could be included inside the lipophilic cavities of CP beta CDs. The water solubility of the antibiotics was improved significantly after cl inclusion with CP beta CDs. The results also suggest that it was easier for butylparaben, which had relatively small molecular size, to form the complexes with CP beta CDs than triclo san. Due to the targeting effect after the inclusion with cationic CP beta CDs, the anti-microbial activity of butylparaben was also enhanced substantially. However, similar im provement was not obvious for triclosan.
引用
收藏
页码:2244 / 2248
页数:5
相关论文
共 18 条
[11]   Thermoanalytical and spectroscopic characterization of beta-cyclodextrin/ketoprofen inclusion complexes [J].
Marini, A ;
Berbenni, V ;
Bruni, G ;
Mustarelli, P ;
Giordano, F ;
Villa, M .
JOURNAL OF INCLUSION PHENOMENA AND MOLECULAR RECOGNITION IN CHEMISTRY, 1995, 22 (03) :221-234
[12]  
MIZUBA S, 1987, J IND MICROBIOL, V1, P63
[13]   Characterization of physicochemical properties of naproxen systems with amorphous β-cyclodextrin-epichlorohydrin polymers [J].
Mura, P ;
Faucci, MT ;
Maestrelli, F ;
Furlanetto, S ;
Pinzauti, S .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2002, 29 (06) :1015-1024
[14]   Improved anti-inflammatory properties for naproxen with cyclodextrin-grafted polyssaccharides [J].
Ramirez, Hector L. ;
Cao, Roberto ;
Fragoso, Alex ;
Torres-Labandeira, Juan J. ;
Dominguez, Amalia ;
Schacht, Etienne H. ;
Banos, Maysa ;
Villalonga, Reynaldo .
MACROMOLECULAR BIOSCIENCE, 2006, 6 (07) :555-561
[15]   Rapid test for distinguishing membrane-active antibacterial agents [J].
Singh, Maya Prakash .
JOURNAL OF MICROBIOLOGICAL METHODS, 2006, 67 (01) :125-130
[16]   Development of a new colloidal drug carrier from chemically-modified cyclodextrins: Nanospheres and influence of physicochemical and technological factors on particle size [J].
Skiba, M ;
Duchene, D ;
Puisieux, F ;
Wouessidjewe, D .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1996, 129 (1-2) :113-121
[17]   Introduction and general overview of cyclodextrin chemistry [J].
Szejtli, J .
CHEMICAL REVIEWS, 1998, 98 (05) :1743-1753
[18]   Enantiomeric separation of enzymatic hydrolysis products of dihydropyrimidinone methyl ester with cationic cyclodextrin by capillary electrophoresis [J].
Wang, F ;
Loughlin, T ;
Dowling, T ;
Bicker, G ;
Wyvratt, J .
JOURNAL OF CHROMATOGRAPHY A, 2000, 872 (1-2) :279-288