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聚乙二醇化壳聚糖涂层的防污活性:侧链长度和包封的ZnO/Ag纳米颗粒的影响。

Antifouling activity of PEGylated chitosan coatings: Impacts of the side chain length and encapsulated ZnO/Ag nanoparticles.

作者信息

Yu Dongkun, Ye Fei, Dobretsov Sergey, Dutta Joydeep

机构信息

Functional NanoMaterials Group, Department of Applied Physics, School of Engineering Sciences, KTH Royal Institute of Technology, Hannes Alfvéns väg 12, 114 19 Stockholm, Sweden.

Functional NanoMaterials Group, Department of Applied Physics, School of Engineering Sciences, KTH Royal Institute of Technology, Hannes Alfvéns väg 12, 114 19 Stockholm, Sweden.

出版信息

Int J Biol Macromol. 2024 Nov;281(Pt 1):136316. doi: 10.1016/j.ijbiomac.2024.136316. Epub 2024 Oct 5.

Abstract

PEGylation is regarded as a common antifouling strategy and the effect is normally linked with surface hydrophilicity of the coatings. Herein, the biopolymer chitosan (CS) was grafted by polyethylene glycol (PEG) of different chain lengths (molecular weight 200, 4 k and 100 k Da) to verify if the hydrophilicity of CS-PEG coatings is crucial in determining antifouling activities and if PEG chain length influences biofouling in marine environment. Properties of copolymers such as melting points and crystallinity are affected by grafting PEG. The water contact angle (WCA) of CS-PEG coatings increases with the chain length of grafted PEG, from 27° to 58°. Photocatalyst of zinc oxide-silver (ZnO/Ag) was also studied and its embedment (2 % to CS-PEG) renders the surface of CS-PEG coatings more hydrophobic with WCA increased from 52° to 86°. Antibacterial, anti-diatom, and anti-biofilm activities of the coatings were evaluated in natural sea water. The bacterial density on CS-PEG coatings was dramatically reduced to 4 × 10 compared to the control of 7 × 10 ind/mm, and further to 2 × 10 for CS-PEG-ZnO/Ag coatings. CS-PEG coatings also strongly inhibit diatoms (120-200 ind/mm), but the inclusion of ZnO/Ag did not obviously enhance such effect (50-150 ind/mm). The findings provide useful insights for designing polymer-based antifouling coatings.

摘要

聚乙二醇化被视为一种常见的防污策略,其效果通常与涂层的表面亲水性有关。在此,生物聚合物壳聚糖(CS)被不同链长(分子量200、4k和100kDa)的聚乙二醇(PEG)接枝,以验证CS-PEG涂层的亲水性在决定防污活性方面是否至关重要,以及PEG链长是否会影响海洋环境中的生物污损。接枝PEG会影响共聚物的熔点和结晶度等性能。CS-PEG涂层的水接触角(WCA)随着接枝PEG链长的增加而增大,从27°增至58°。还研究了氧化锌-银(ZnO/Ag)光催化剂,将其嵌入(占CS-PEG的2%)会使CS-PEG涂层表面更疏水,WCA从52°增至86°。在天然海水中评估了涂层的抗菌、抗硅藻和抗生物膜活性。与对照的7×10 ind/mm相比,CS-PEG涂层上的细菌密度大幅降至4×10,而CS-PEG-ZnO/Ag涂层的细菌密度进一步降至2×10。CS-PEG涂层也强烈抑制硅藻(120 - 200 ind/mm),但加入ZnO/Ag并没有明显增强这种效果(50 - 150 ind/mm)。这些发现为设计基于聚合物的防污涂层提供了有用的见解。

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