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壳聚糖-刺槐豆胶/二氧化硅@载银纳米复合材料的羟基磷灰石矿化及其抗菌活性评价。

Hydroxyapatite mineralization on chitosan-tragacanth gum/silica@silver nanocomposites and their antibacterial activity evaluation.

机构信息

Organic Polymer Chemistry Research Laboratory, Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111, Islamic Republic of Iran.

Organic Polymer Chemistry Research Laboratory, Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111, Islamic Republic of Iran.

出版信息

Int J Biol Macromol. 2020 May 15;151:909-923. doi: 10.1016/j.ijbiomac.2020.02.167. Epub 2020 Feb 19.

Abstract

The goal of this research was the fabrication of chitosan (CT)-tragacanth gum (TG)/SiO nanocomposite as a potential use in tissue engineering. For the antibacterial activity induction and stabilization of SiO nanoparticles (NPs) in the polymer matrix, SiO and green synthesized Ag NPs were hybrid with SiO/Ag. Then, the obtained hybrids were inserted into the CT-TG blend, separately. The ultrasonic waves were applied, and the films were subsequently constructed by the solution casting technique. Finally, the CT-TG/SiO nanocomposites and CT-TG/SiO@Ag nanocomposite films were studied by the variant techniques. The in-vitro bioactivity examination all samples was performed in a simulated body fluid. It was observed that hydroxyapatite was grown more on the surface of the CT-TG/SiO@Ag (1/1) nanocomposite film in comparison to the other specimens, due to its high surface area and the presence of many specific functional groups. Furthermore, the antibacterial activity assessment of the all samples were performed against Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria via well diffusion method. The higher inhibition zone diameters for the CT-TG/SiO@Ag (1/1) nanocomposite film against both bacteria were observed in the presence of aqueous solution of acetic acid 1% v/v (11 and 13 mm) and deionized water (18 and 20 mm), respectively.

摘要

本研究的目的是制备壳聚糖(CT)-荆豆胶(TG)/SiO 纳米复合材料,将其作为组织工程的潜在用途。为了在聚合物基质中诱导和稳定 SiO 纳米颗粒(NPs)的抗菌活性,将 SiO 和绿色合成的 Ag NPs 与 SiO/Ag 杂化。然后,将得到的杂化物分别插入 CT-TG 共混物中。应用超声波,然后通过溶液浇铸技术构建薄膜。最后,通过各种技术研究 CT-TG/SiO 纳米复合材料和 CT-TG/SiO@Ag 纳米复合材料薄膜。所有样品的体外生物活性测试均在模拟体液中进行。观察到 CT-TG/SiO@Ag(1/1)纳米复合材料薄膜表面生长的羟基磷灰石比其他样品更多,这是由于其高比表面积和存在许多特定的功能基团。此外,通过琼脂扩散法对所有样品进行了针对革兰氏阴性(大肠杆菌)和革兰氏阳性(金黄色葡萄球菌)细菌的抗菌活性评估。在 1%v/v 乙酸水溶液(11 和 13 毫米)和去离子水(18 和 20 毫米)存在下,观察到 CT-TG/SiO@Ag(1/1)纳米复合材料薄膜对两种细菌的抑制圈直径更大。

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