Effect of hydrophilic groups on the bioactivity of antimicrobial polymers
文献信息
Phuong Pham, Susan Oliver, Edgar H. H. Wong, Cyrille Boyer
Antimicrobial polymers have recently been investigated as potential treatments to combat multidrug-resistant pathogens. A typical antimicrobial polymer consists of cationic groups that allow the polymers to adsorb onto negatively charged bacterial membranes and hydrophobic groups that insert into and disrupt the bilipid membrane. Recently, with the introduction of ternary polymer systems, neutral hydrophilic groups have been added to modulate hydrophobic/hydrophilic balance more easily. Although numerous studies have examined the effect of active components (cationic and hydrophobic groups) of antimicrobial polymers on their bioactivity, limited studies focus on hydrophilic groups. Therefore, in this study, we developed a series of statistical amphiphilic ternary polymers to systematically investigate the effect of hydrophilic groups on antibacterial activity and biocompatibility. The results revealed that, unlike the hydrophobic groups that directly disrupt the cell membrane, the hydrophilic groups have an indirect but important impact on bioactivity through tuning of the hydrophobic/hydrophilic balance and global hydrophobicity, leading to a change in the aqueous characteristics of the polymers. Therefore, in antimicrobial polymer design, an appropriate hydrophobic/hydrophilic balance as well as the structural features of the hydrophilic group, such as length, flexibility, and hydrophilicity of the hydrophilic chain, are key determinants that can be optimised to maximise biocompatibility without negatively impacting antibacterial effect.
期刊推荐
相关文献
Transition-metal free direct C–H functionalization of quinoxalin-2(1H)-ones with oxamic acids leading to 3-carbamoyl quinoxalin-2(1H)-ones
Jin-Wei Yuan, Jun-Liang Zhu, Hu-Lin Zhu, Fang Peng, Liang-Yu Yang, Pu Mao, Shou-Ren Zhang, Yan-Chun Li, Ling-Bo Qu
DOI: 10.1039/C9QO01322A
The decarboxylative C–H heteroarylation of azoles catalysed by nickel catalysts to access unsymmetrical biheteroaryls
Ke Yang, Mengjie Song, Zhiyan Ma, Yi Li, Zhengyi Li, Xiaoqiang Sun
DOI: 10.1039/C9QO01073D
Merging photochemistry with electrochemistry in organic synthesis
Yi Yu, Peng Guo, Jun-Song Zhong, Yaofeng Yuan, Ke-Yin Ye
DOI: 10.1039/C9QO01193E
Catalytic asymmetric 1,4-type Friedel–Crafts (hetero)arylations of 1-azadienes: the highly enantioselective syntheses of chiral hetero-triarylmethanes
Cheng-Jie Wang, Qi-Qiong Yang, Mei-Xin Wang, Yun-Han Shang, Xin-Yu Tong, Yu-Hua Deng, Zhihui Shao
DOI: 10.1039/C9QO01391A
Asymmetric total synthesis of nodulisporiviridin E
Yang Ji, Zhengyuan Xin, Yingbo Shi, Haibing He
DOI: 10.1039/C9QO01278H
Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles
G. Surendra Reddy, Dhevalapally B. Ramachary
DOI: 10.1039/C9QO00864K
Enzymatic triggering of C–ON bond homolysis of alkoxyamines
Gérard Audran, Lionel Bosco, Paul Brémond, Natacha Jugniot, Sylvain R. A. Marque, Philippe Massot, Tataye Moussounda Moussounda Koumba, Elodie Parzy, Angélique Rivot, Eric Thiaudière, Pierre Voisin, Carina Wedl, Toshihide Yamasaki
DOI: 10.1039/C9QO00899C
Bistachybotrysins L–V, bioactive phenylspirodrimane dimers from the fungus Stachybotrys chartarum
Jimei Liu, Xiaona Jia, Jinlian Zhao, Jiamin Feng, Minghua Chen, Ridao Chen, Kebo Xie, Dawei Chen, Yan Li, Dan Zhang, Ying Peng, Shuyi Si, Jungui Dai
DOI: 10.1039/C9QO01284B
您可能还喜欢
什么是5-Fluoro-4-iodo-2-methylaniline(CAS号:307306-08-7)?
5-氟-4-碘-2-甲氨基苯属于芳香族化合物,其分子式为C8H7FN2I。该化合物具有一定的反应活性,在有机合成和药物化学领域有一定的应用。
4-氟-3-硝基三氟甲苯(CAS号:367-86-2)通常如何合成?
4-氟-3-硝基三氟甲苯通常通过将三氟甲基苯在酸性条件下催化氧化为三氟甲基硝基苯,然后进行氟化反应得到目标化合物。该过程需要使用催化剂,如三氟乙酸,反应产率较高...
6-氯-9-(2,3,5-三苯甲酰氧基-2-C-甲基-beta-D-呋喃核糖基)-9H-嘌呤(CAS号:205171-05-7)的物理化学性质是什么?
该化合物为白色至类白色晶体,分子量约为1046.95。它在水中几乎不溶,在有机溶剂如乙腈和甲醇中具有一定的溶解性。该化合物具有良好的化学稳定性和生物活性。
如何储存6-氟喹啉-4-羧酸(CAS号:220844-73-5)?
6-氟喹啉-4-羧酸应储存在阴凉、干燥、通风良好的地方,避免阳光直射。储存在密闭容器中,避免与空气中的水分接触。储存温度应控制在室温以下,避免高温。
(2S,2'S,3S,3'S)-3,3'-di-tert-butyl-4,4'-bis(2,6-dimethoxyphenyl)-2,2',3,3'-tetrahydro-2,2'-bibenzo[d][1,3]oxaphosphole(CAS号:1435940-21-8)通常如何合成?
该化合物通常通过芳香族化合物的亲核取代反应合成,首先将2,6-二甲氧基苯基引入到双环结构中,然后通过特定条件下的还原或氧化反应引入二叔丁基。反应过程中使用了钯作...
如何储存KY02111(CAS号:1118807-13-8)?
KY02111应储存于阴凉、干燥、通风良好的地方,避免阳光直射和高温环境。应使用合适的密闭容器储存,并确保容器密封良好,防止水分和潮气进入。在储存期间,应注意检...
如何储存4-(4-氯苯氧基)丁酸乙酯(CAS号:59227-79-1)?
4-(4-氯苯氧基)丁酸乙酯应储存在阴凉、干燥、通风良好的地方,远离火源和热源。避免阳光直射,防止容器破裂导致泄漏。储存时应保持容器密封,避免与空气中的水蒸气接...
4-庚基苯乙酮(CAS号:37593-03-6)安全吗?
4-庚基苯乙酮相对安全,但在使用和储存时仍需注意。应避免吸入其蒸气,避免皮肤接触,使用时需佩戴防护眼镜和手套。储存时应远离火源和热源,保持容器密封,放置于阴凉、...
什么是乙基2-氨基-4-(3-溴苯基)噻吩-3-羧酸乙酯(CAS号:438218-48-5)?
乙基2-氨基-4-(3-溴苯基)噻吩-3-羧酸乙酯是一种有机化合物,分子式为C16H12BrN2O2S。它是一种含有噻吩环、氨基、溴苯基和羧酸酯结构的化合物。这...
什么是(9ci)-2-氨基-6-甲基-苯甲酰胺(CAS号:1885-31-0)?
(9ci)-2-氨基-6-甲基-苯甲酰胺是一种化学化合物,其英文名称为2-Amino-6-methylbenzamide,CAS号为1885-31-0。该化合物...
来源期刊
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.











![N-[(E)-Phenylmethylene]benzenesulfonamide structure N-[(E)-Phenylmethylene]benzenesulfonamide structure](https://cnstatic.chemtradehub.com/structs/139/13909-34-7-8167.webp)


