Synthesis and antimicrobial activities of new water-soluble bis-quaternary ammonium methacrylate polymers

被引:154
作者
Dizman, B
Elasri, MO
Mathias, LJ
机构
[1] Univ So Mississippi, Dept Polymer Sci, Hattiesburg, MS 39406 USA
[2] Univ So Mississippi, Dept Biol Sci, Hattiesburg, MS 39406 USA
关键词
antimicrobial; quaternary ammonium; water-soluble polymers; biopolymers; NMR;
D O I
10.1002/app.20872
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
New methacrylate monomers containing pendant quaternary ammonium moieties based on 1,4-diazabicyclo-[2.2.2]-octane (DABCO) were synthesized. The DABCO group contains either a butyl or a hexyl pendant group comprising the hydrophobic segment of the monomers and one tether group to the methacrylate moiety. The monomers were homopolymerized in water by using 2,2'azobis-(2-methylpropionamide) dihydrochloride (V-50) as an initiator. The monomers and polymers were characterized by elemental analysis, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), FTIR, and C-13-NMR. The antimicrobial activities of the corresponding small molecules (bis-quaternary ammonium monocarboxylates) and polymers were investigated against Staphylococcus aureus and Escherichia coli. Although the small molecules did not show any antimicrobial activity, the polymers were moderately effective against both Gram-positive and Gram-negative bacteria. The minimum inhibitory concentration (MIC) values of the polymers with butyl and hexyl hydrocarbon chains against S. aureus and E. coli were found to be 250 and 62.5 mug/mL, respectively. The minimum bactericidal concentration (MBC) value for the polymer with the butyl group was higher than 1 mg/mL, whereas the MBC value for the polymer with hexyl group was found to be 62.5 mug/mL. Thus, an increase of the alkyl chain length from 4 to 6 significantly increased the antimicrobial activity of the polymer. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:635 / 642
页数:8
相关论文
共 44 条
[1]   Preparation and investigation of antibacterial carbohydrate-based surfaces [J].
Abel, T ;
Cohen, JI ;
Engel, R ;
Filshtinskaya, M ;
Melkonian, A ;
Melkonian, K .
CARBOHYDRATE RESEARCH, 2002, 337 (24) :2495-2499
[2]  
[Anonymous], 1990, J BIOACT COMPAT POL, DOI DOI 10.1177/088391159000500104
[3]   ESTER DERIVATIVES OF ALPHA-HYDROXYMETHYLACRYLATES - ITACONATE ISOMERS GIVING HIGH-MOLECULAR-WEIGHT POLYMERS [J].
AVCI, D ;
KUSEFOGLU, SH ;
THOMPSON, RD ;
MATHIAS, LJ .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1994, 32 (15) :2937-2945
[4]  
Borman S, 2002, CHEM ENG NEWS, V80, P36, DOI 10.1021/cen-v080n023.p036
[5]  
Borman S, 2001, CHEM ENG NEWS, V79, P13, DOI 10.1021/cen-v079n021.p013a
[6]  
BROUGHTON RM, 1998, NATL TEXTILE CTR ANN, P347
[7]  
BROWN GE, 1999, POSTHARVEST FLORIDA
[8]  
COHEN JI, 2002, 223 ACS NAT M ORL FL
[9]  
Gabrielska J., 1994, TENSIDE SURFACT DET, V31, P296, DOI [10.1515/tsd-1994-310505, DOI 10.1515/TSD-1994-310505]
[10]   Characterization of novel antimicrobial peptoids [J].
Goodson, B ;
Ehrhardt, A ;
Ng, S ;
Nuss, J ;
Johnson, K ;
Giedlin, M ;
Yamamoto, R ;
Moos, WH ;
Krebber, A ;
Ladner, M ;
Giacona, MB ;
Vitt, C ;
Winter, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (06) :1429-1434