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Facile In Situ Preparation and In Vitro Antibacterial Activity of PDMAEMA-Based Silver-Bearing Copolymer Micelles

机译:PDMAEMA基含银共聚物胶束的便捷原位制备和体外抗菌活性

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摘要

Well-defined polymer micelles with core-shell structure are good delivery platform for stabilizing silver nanoparticles (AgNPs) in the field of antimicrobials targeting diseases. The rational construction of the polymer structure, an efficient, facile, and green preparation approach, and comprehensive exploration of the derived AgNPs are necessary, such as size, particle stability, antibacterial activity, and other properties. Herein, we designed and assessed the in vitro antimicrobial activity of AgNPs-decorated copolymer micelles with different copolymer topologies. First, linear or four-arm star triblock copolymers with the similar molecular weight and degree of polymerization were obtained, which consisted of DMAEMA for in situ reduction of silver ions to form AgNPs without external reducing agent. HEMA and PEGMA in micellar shell gave an enhanced stability of AgNPs during blood circulation. The combination of computational modeling and experimental results indicated that both types of micelles could fabricate AgNPs with monodisperse and spherical morphology. Star copolymer micelles stabilized AgNPs had smaller average size, better stability, and higher antibacterial activity than those with linear structure, which may due to higher stability of micelles from star copolymers. Furthermore, the cytotoxicity evaluation test showed that the achieved linear or star copolymers micelles stabilized AgNPs had good biocompatibility. This work provides a facile and universal approach in the rational design of micelles stabilized AgNPs with suitable topology for fighting against a wide range of bacterial infections.Electronic supplementary materialThe online version of this article (10.1186/s11671-019-3074-z) contains supplementary material, which is available to authorized users.
机译:定义明确的具有核-壳结构的聚合物胶束是在靶向疾病的抗菌剂领域稳定银纳米颗粒(AgNP)的良好传递平台。聚合物结构的合理构建,高效,便捷和绿色的制备方法以及对衍生的AgNP的全面探索是必要的,例如尺寸,颗粒稳定性,抗菌活性和其他特性。在这里,我们设计和评估了具有不同共聚物拓扑结构的AgNPs装饰的共聚物胶束的体外抗菌活性。首先,获得了具有相似分子量和聚合度的线性或四臂星形三嵌段共聚物,该共聚物由DMAEMA组成,用于在不使用外部还原剂的情况下原位还原银离子以形成AgNP。胶束壳中的HEMA和PEGMA在血液循环过程中提高了AgNP的稳定性。计算模型和实验结果的结合表明,两种类型的胶束都可以制备具有单分散和球形形态的AgNP。星形共聚物胶束稳定的AgNPs比线性结构的胶束具有更小的平均尺寸,更好的稳定性和更高的抗菌活性,这可能是由于星形共聚物胶束的稳定性更高。此外,细胞毒性评估测试表明,所获得的线性或星形共聚物胶束稳定的AgNPs具有良好的生物相容性。这项工作为胶束稳定的AgNPs的合理设计提供了一种简便而通用的方法,该AgNPs具有合适的拓扑结构可以抵抗各种细菌感染。电子补充材料本文的在线版本(10.1186 / s11671-019-3074-z)包含补充信息资料,可供授权用户使用。

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