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In situ synthesis of polyamidoamine/β-cyclodextrin/silver nanocomposites on polyester fabric tailoring drug delivery and antimicrobial properties

机译:原位合成聚酰胺胺/β-环糊精/银纳米复合材料对涤纶织物剪裁药物递送和抗菌性质

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摘要

Here, the polyester fabric was modified using polyamidoamine/beta-cyclodextrin (beta-CD)/silver nanocomposites to make a fabric with antibacterial and drug delivery properties. The aminolysis of polyester fabric with polyamidoamine led to the possible stable linkages with (beta-CD)/Ag composites. The drug absorption and release behavior of the fabrics investigated in the water and phosphate buffer solutions confirming the maximum drug absorption of 16.9% after 24 h in which 45% of the loaded drug was slowly released in the buffer solution after 3 h. The synthesized nanocomposites on the fabric were detected by FESEM images and EDX mapping showed various percentages and distribution of the used elements. Also, FTIR analysis displayed some changes in the chemical structure of the functional groups. The XRD pattern of beta-CD/Ag nanocomposite suggested a peak at 2 theta = 44.6 degrees with the calculated crystal size of 9.5 nm. The tensile strength unremarkably decreased according to the mechanical testing. Further, the treated fabrics indicated 100, 100 and 99% microbial reduction against E. coli, S. aureus and C. albican. Moreover, the cytotoxicity of the fabric against fibroblast cell was studied through MTT test. Based on the obtained results, it can suggest that the new modified polyester fabric can be used in drug delivery system.
机译:这里,使用聚酰胺胺/β-环糊精(β-CD)/银纳米复合材料改性聚酯织物以使织物具有抗菌和药物递送性能。聚酰胺胺的聚酯织物的氨基溶解于可能的稳定连接(β-CD)/ Ag复合材料。在水和磷酸盐缓冲溶液中研究的织物的药物吸收和释放行为证实在24小时后的最大药物吸收为16.9%,其中在3小时后在缓冲溶液中缓慢释放45%的负载药物。通过FeSEM图像检测织物上的合成纳米复合材料,EDX映射显示了所用元件的各种百分比和分布。此外,FTIR分析显示了官能团化学结构的一些变化。 β-CD / Ag纳米复合材料的XRD图案表明,计算出晶粒尺寸为9.5nm的峰值= 44.6度。根据机械测试,拉伸强度不起一体地降低。此外,处理过的织物指示为100,100和99%的微生物减少对大肠杆菌,金黄色葡萄球菌和抗糖醛糖。此外,通过MTT试验研究了织物对成纤维细胞细胞的细胞毒性。基于所得的结果,它可以表明新型改性聚酯织物可用于药物输送系统。

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