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New biobased non-ionic hyperbranched polymers as environmentally friendly antibacterial additives for biopolymers

机译:新的Biobased非离子超支化聚合物是生物聚合物的环保抗菌添加剂

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The aim of this research was to develop new biobased non-ionic polymeric additives with significant bacterial inhibition and low leaching potential, so that they can be used to produce biopolymer materials for various applications such as biomedical devices, surgical textile, or food packaging. Two new non-ionic hyperbranched polymers (HBPs) were prepared by a facile solvent-free polymerization of an AB2monomer derived from naturally existing molecular building blocks 2-phenylethanol, isatin, and anisole. The molecular structures and thermal properties of the obtained HBPs were characterized by GPC, NMR, FTIR, HRMS, MALDI-TOF, TGA and DSC analyses. Disk diffusion tests revealed that the two obtained HBPs showed more significant antibacterial activity against 9 different food and human pathogenic bacteria, compared with small molecular antibiotics. The maximal antibacterial effect of HBPs was achieved at 2 ae g per disk (or 0.1 mg mL-1), which was significantly lower (similar to 1/15) compared to the linear antibacterial polymer chitosan. Such enhanced antibacterial properties can be attributed to the unique highly branched structures and effectively amplified functionalities of HBPs. Finally, the prepared HBPs were added into natural polymers cellulose and polyhydroxybutyrate (PHB), and the resulting biopolymer films showed no significant leakage after being merged in water for 5 days. This was in sharp contrast to the biopolymer films containing a small model compound, which leaked out significantly under the same conditions. To our knowledge, this is the first report on non-ionic bio-based dendritic macromolecules with significant bacteria inhibition and low leakage.
机译:该研究的目的是开发具有显着细菌抑制和低浸出潜力的新型生物化的非离子聚合物添加剂,使得它们可用于生产用于各种应用的生物聚合物材料,例如生物医学装置,手术纺织品或食品包装。通过衍生自天然现有的分子结构块2-苯基乙醇,isatin和苯甲醚的AB2聚体的无溶剂的聚合来制备两种新的非离子超支化聚合物(HbPs)。通过GPC,NMR,FTIR,HRMS,MALDI-TOF,TGA和DSC分析表征所得HBP的分子结构和热性能。盘扩散试验显示,与小分子抗生素相比,两种获得的HBPS对9种不同的食物和人致病细菌显示出更明显的抗菌活性。与线性抗菌聚合物壳聚糖相比,每盘(或0.1mg ML-1)以每盘(或0.1mg ml-1)的2 AE G(或0.1mg ml-1)实现最大抗菌作用。这种增强的抗菌性质可归因于独特的高度分支结构,并有效扩增HBP的功能。最后,将制备的HBP加入天然聚合物纤维素和多羟基丁酸盐(PHB)中,并且所得的生物聚合物膜在水中合并5天后没有显着渗漏。这与含有小型模型化合物的生物聚合物膜鲜明对比,这在相同条件下显着泄漏。据我们所知,这是第一份关于非离子生物生物的树突式大分子的报告,具有显着的细菌抑制和低渗漏。

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