scholarly journals The synthesis of polymeric dual-functional antimicrobial surface based on poly(2-methyl-2-oxazoline)

2015 ◽  
Vol 19 (1) ◽  
pp. 12 ◽  
Author(s):  
Bidhari Pidhatika ◽  
Ekaterina Rakhmatullina

There is a high interest in the development of antimicrobial coatings to fi ght bacterial infections.We present the development of dual-functional antimicrobial surface, in which a biopassive platform wasfunctionalized with bioactive compounds on the surface, using a graft copolymer system poly(L-lysine)-graftpoly(2-methyl-2-oxazoline)-quarternery ammonium compound (PLL-g-PMOXA-QAC). Alkyne functionalitywas introduced to the PMOXA chain at α-terminus by initiating the living cationic polymerization of 2-methyl-2-oxazoline with a propargylic-initiator. The reaction was terminated with carboxy derivative-terminator thatallows grafting of the polymeric chain from the β-terminus to poly(L-lysine) (PLL) backbone, resulting in graftcopolymer alkynyl PLL-g-PMOXA. The conjugation between alkynyl PLL-g-PMOXA and QAC was thenperformed using click reaction. The chemical structures of the polymers were characterized by MALDI-TOFspectrometry and NMR spectroscopy. The results demonstrate that we have successfully synthesized PLL-g-PMOXA-QAC copolymer with grafting density (number of lysine/number of PMOXA) of 0.33. The resultingPLL-g-PMOXA-QAC copolymer was then immobilized onto carboxylated tissue cultured polystyrene (TCPS)surface and exposed to bacteria solution to test its dual-functional properties. Preliminary live-and-deadbacteria study indicates dual-functionality of the PLL-g-PMOXA-QAC-coated surface.

Biomolecules ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 72 ◽  
Author(s):  
Jin Motoyanagi ◽  
Minh Nguyen ◽  
Tomonari Tanaka ◽  
Masahiko Minoda

Polymer particles modified with carbohydrates on their surfaces are of significant interest, because their specific recognition abilities to biomolecules are valuable for developing promising materials in biomedical fields. Carbohydrate-decorated core-shell polymer particles are expected to be efficiently prepared by dispersion polymerization using a glycopolymer-based amphiphilic macromonomer as both a polymeric steric stabilizer and a monomer. To create glycopolymer-type macromonomers, we propose a new strategy combining living cationic polymerization of an alkynyl-functionalized vinyl ether (VE), and the click reaction for the preparation of glycopolymers having a polymerizable terminal group, and investigate their dispersion copolymerization with styrene for generating carbohydrate-decorated polymer particles. This study deals with (i) the synthesis of block copolymer-type amphiphilic macromonomers bearing a methacryloyl group at the α-terminus, and pendant alkynyl groups by living cationic polymerization of alkynyl-substituted VE (VEEP), (ii) the derivatization of maltose-carrying macromonomers by click chemistry of the pendant alkynyl groups of the precursor macromonomers with maltosyl azide without any protecting/deprotecting processes, and (iii) the preparation of maltose-decorated (Mal-decorated) polymer particles through the dispersion copolymerization of glycopolymer-type macromonomers with styrene in polar media. Moreover, this study concerns the specific interactions of the resultant polymer particles with the lectin concanavalin A (Con A).


1987 ◽  
Vol 18 (2) ◽  
Author(s):  
Toshinobu Higashimura ◽  
Yasuhisa Kishimoto ◽  
Sadahito Aoshima

1994 ◽  
Vol 31 (11) ◽  
pp. 1609-1618 ◽  
Author(s):  
Mitsuo Sawamoto ◽  
Hajime Shohi ◽  
Hiroe Sawamoto ◽  
Hiroji Fukui ◽  
Toshinobu Higashimura

2015 ◽  
Vol 88 (12) ◽  
pp. 461-465
Author(s):  
Mineto UCHIYAMA ◽  
Kotaro SATOH ◽  
Masami KAMIGAITO

Sign in / Sign up

Export Citation Format

Share Document