journal article·2014-10-13

Biocidal Polymers: Preparation and Antimicrobial Assessment of Immobilized Onium Salts onto Modified Chitosan

Mohamed H. El-Newehy, El-Refaie Kenawy, Salem S. Al-Deyab

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Abstract

Abstract New derivatives of chitosan were synthesized by modification of chitosan (CTS) either with chloroacetyl chloride or with bromoacetyl chloride. The haloacetylated chitosan derivatives were quaternized by reaction with triethyl amine and triphenyl phosphine. The quaternized new derivatives of chitosan were tested against Gram-negative bacteria the Gram-positive bacteria Staphylococcus aureus, and the fungi by the cut plug method and viable cell counting methods. The results showed that the new chitosan derivatives have stronger antimicrobial activities than the chitosan itself. The examination of the treated cells by TEM showed complete discharge of cellular cytoplasm which led to the death of the cells. Keywords: Biologically active polymerschitosanonium saltsquaternary salts Notes Color versions of one or more of the figures in the article can be found online at www.tandfonline.com/gpom.
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OpenAlex topics: Antimicrobial agents and applications · Nanocomposite Films for Food Packaging · Marine Biology and Environmental Chemistry

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References (28)

Show source-provided references
1. 10.1080/03602559.2012.69868710.1080/03602559.2012.698687 ↗
2. 10.1080/00914037.2012.71914010.1080/00914037.2012.719140 ↗
3. 10.1080/03602559.2012.76267310.1080/03602559.2012.762673 ↗
4. 10.1080/00914037.2011.55780310.1080/00914037.2011.557803 ↗
5. 10.1080/15685551.2013.77130610.1080/15685551.2013.771306 ↗
6. 10.1016/j.progpolymsci.2011.08.00510.1016/j.progpolymsci.2011.08.005 ↗
7. 10.1002/pola.1032510.1002/pola.10325 ↗
8. 10.1016/j.carbpol.2007.06.02710.1016/j.carbpol.2007.06.027 ↗
9. 10.1016/S0079-6700(01)00007-710.1016/S0079-6700(01)00007-7 ↗
10. 10.1016/0144-8617(83)90012-710.1016/0144-8617(83)90012-7 ↗
11. 10.1016/S1381-5148(00)00038-910.1016/S1381-5148(00)00038-9 ↗
12. 10.1007/s11814-012-0154-510.1007/s11814-012-0154-5 ↗
13. 10.1016/j.carres.2005.05.00910.1016/j.carres.2005.05.009 ↗
14. 10.1007/s10118-010-8239-210.1007/s10118-010-8239-2 ↗
15. 10.1016/j.biomaterials.2008.07.03410.1016/j.biomaterials.2008.07.034 ↗
16. 10.1016/j.jscs.2011.03.01510.1016/j.jscs.2011.03.015 ↗
17. 10.1007/s00706-009-0197-410.1007/s00706-009-0197-4 ↗
18. 10.1016/j.progpolymsci.2006.06.00110.1016/j.progpolymsci.2006.06.001 ↗
19. 10.1177/088391150504965510.1177/0883911505049655 ↗
20. 10.1002/app.3304610.1002/app.33046 ↗
21. Pridham T. G. · Phytopathology · 1956 · 46 · 568
22. Shadomy S. · 1985
23. 10.1002/jps.260065011510.1002/jps.2600650115 ↗
24. Ardenne M. · Elektrochemie · 1940 · 46 · 270
25. 10.1016/S0168-3659(97)00126-010.1016/S0168-3659(97)00126-0 ↗
26. 10.1021/bm061150q10.1021/bm061150q ↗
27. 10.1016/j.ijfoodmicro.2010.09.01210.1016/j.ijfoodmicro.2010.09.012 ↗
28. 10.1016/j.eurpolymj.2010.03.00110.1016/j.eurpolymj.2010.03.001 ↗