Biocidal activity of hydantoin-containing polyurethane polymeric surface modifiers

被引:40
作者
Grunzinger, Stephen J.
Kurt, Pinar
Brunson, Kennard M.
Wood, Lynn
Ohman, Dennis E.
Wynne, Kenneth J.
机构
[1] Virginia Commonwealth Univ, Dept Chem & Life Sci Engn, Richmond, VA 23284 USA
[2] Virginia Commonwealth Univ, Dept Microbiol & Immunol, Richmond, VA 23284 USA
[3] McGuire Vet Affairs Med Ctr, Richmond, VA 23249 USA
基金
美国国家科学基金会;
关键词
antimicrobial coatings; hydantoin; poly(oxetanes);
D O I
10.1016/j.polymer.2007.06.010
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
preparation of a new hydantoin-containing polyurethane surface modifier has been enabled by the development of a hydantoin-oxetane monomer that co-polymerizes to polyoxetane telechelics by ring-opening polymerization. After solution blending the hydantoin-containing polymer surface modifiers (2 wt%) with a conventional polyurethane, coating a substrate, and treating with dilute hypochlorite (bleach), the surfaces were challenged with Gram -ve Pseudonionas aeruginosa and Gram +ve Staphylococcus aureits in AATCC-100 'sandwich' and aerosol spray tests. Thirty-minute spray tests were used to establish concentrations at which overchallenges of the contact-kill surfaces occurred. These tests confirmed that no biocide release occurred under the test conditions. The spray test showed unambiguously the improved efficacy of biocidal action for a surface modifier with 5 mol% sernifluorinated content compared to the non-fluorinated version. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4653 / 4662
页数:10
相关论文
共 49 条
[1]   Novel antimicrobial N-halamine polymer coatings generated by emulsion polymerization [J].
Eknoian, MW ;
Worley, SD ;
Bickert, J ;
Williams, JF .
POLYMER, 1999, 40 (06) :1367-1371
[2]   Contrasting nanoseale surface morphologies of polyurethanes containing polyoxetane soft blocks with random and block segmer sequences [J].
Fujiwara, T ;
Wynne, KJ .
MACROMOLECULES, 2004, 37 (23) :8491-8494
[3]   Synthesis and characterization of novel Amphiphilic telechelic polyoxetanes [J].
Fujiwara, T ;
Makal, U ;
Wynne, KJ .
MACROMOLECULES, 2003, 36 (25) :9383-9389
[4]   Microdomain morphology of poly(urethane urea) multiblock copolymers [J].
Garrett, JT ;
Siedlecki, CA ;
Runt, J .
MACROMOLECULES, 2001, 34 (20) :7066-7070
[5]   Polyurethanes from novel 1,3-propyleneoxide co-telechelics having pendant hydantoin and methoxymethyl groups [J].
Grunzinger, Stephen J. ;
Wynne, Kenneth J. .
POLYMER, 2006, 47 (11) :4230-4237
[6]   BIOCIDAL POLYMERS ACTIVE BY CONTACT .4. POLYURETHANES BASED ON POLYSILOXANES WITH PENDANT PRIMARY ALCOHOLS AND QUATERNARY AMMONIUM GROUPS [J].
HAZZIZALASKAR, J ;
HELARY, G ;
SAUVET, G .
JOURNAL OF APPLIED POLYMER SCIENCE, 1995, 58 (01) :77-84
[7]  
Ho T., 1994, POLYM ADVAN TECHNOL, V6, P25
[8]   Assessment of a silver-coated barrier dressing for potential use with skin grafts on excised burns [J].
Holder, IA ;
Durkee, P ;
Supp, AP ;
Boyce, ST .
BURNS, 2003, 29 (05) :445-448
[9]   MOLECULAR-WEIGHT DEPENDENCE AND END-GROUP EFFECTS ON THE SURFACE-TENSION OF POLY(DIMETHYLSILOXANE) [J].
JALBERT, C ;
KOBERSTEIN, JT ;
YILGOR, I ;
GALLAGHER, P ;
KRUKONIS, V .
MACROMOLECULES, 1993, 26 (12) :3069-3074
[10]  
Ji Q., 2000, POLYM PREPR, V41, P346