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
[1]  
[Anonymous], PHARMACEUTICALS
[2]   Investigation of the triamterene-beta-cyclodextrin system prepared by co-grinding [J].
Arias, MJ ;
Moyano, JR ;
Gines, JM .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 153 (02) :181-189
[3]   Effect of inclusion complexation with cyclodextrins on photostability of nifedipine in solid state [J].
Bayomi, MA ;
Abanumay, KA ;
Al-Angary, AA .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 243 (1-2) :107-117
[4]   Cyclodextrins in polymer synthesis:: Free radical copolymerization of methylated β-cyclodextrin complexes of hydrophobic monomers with N-isopropylacrylamide in aqueous medium [J].
Casper, P ;
Glöckner, P ;
Ritter, S .
MACROMOLECULES, 2000, 33 (12) :4361-4364
[5]   INTERACTION OF CYCLODEXTRIN-CONTAINING POLYMERS WITH FLUORESCENT COMPOUNDS [J].
HARADA, A ;
FURUE, M ;
NOZAKURA, S .
MACROMOLECULES, 1977, 10 (03) :676-681
[6]   Decrease in skin permeation and antibacterial effect of parabens by a polymeric additive, poly(2-methacryloyloxyethyl phosphorylcholine-co-butylmetacrylate) [J].
Hasegawa, T ;
Kim, S ;
Tsuchida, M ;
Issiki, Y ;
Kondo, S ;
Sugibayashi, K .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2005, 53 (03) :271-276
[7]   Investigation of cyclodextrin inclusion compounds using FT-IR and Raman spectroscopy [J].
Lamcharfi, E ;
Kunesch, G ;
Meyer, C ;
Robert, B .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 1995, 51 (11) :1861-1870
[8]   Drug carrier systems based on water-soluble cationic β-cyclodextrin polymers [J].
Li, JS ;
Xiao, HN ;
Li, JH ;
Zhong, YP .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 278 (02) :329-342
[9]   NB2001, a novel antibacterial agent with broad-spectrum activity and enhanced potency against β-lactamase-producing strains [J].
Li, Q ;
Lee, JY ;
Castillo, R ;
Hixon, MS ;
Pujol, C ;
Doppalapudi, VR ;
Shepard, HM ;
Wahl, GM ;
Lobl, TJ ;
Chan, MF .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (05) :1262-1268
[10]   Cyclodextrins and their pharmaceutical applications [J].
Loftsson, Thorsteinn ;
Duchene, Dominique .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 329 (1-2) :1-11