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制备血清包裹的银纳米粒子,用于选择性杀死微生物细胞而不损伤宿主细胞。

Preparation of serum capped silver nanoparticles for selective killing of microbial cells sparing host cells.

机构信息

Department of Microbiology, Institute of Post-Graduate Medical Education and Research, Calcutta, 700020, India.

Department of Signal Transduction and Biogenic Amines, Chittaranjan National Cancer Institute, Calcutta, 700026, India.

出版信息

Sci Rep. 2021 Jun 2;11(1):11610. doi: 10.1038/s41598-021-91031-7.

Abstract

Following access into the cell, colloidal silver nanoparticles exhibit generalized cytotoxic properties, thus appear as omnipotent microbicidal, but not suitable for systemic use unless are free of toxic effects on host cells. The AgNP-Serum-18 when prepared from silver nitrate, using dextrose as reducing and group-matched homologous serum as a stabilizing agent, selective endocytosis, and oxidative stress-dependent bio-functional damages to the host are mostly eliminated. For their bio-mimicking outer coat, there is the least possibility of internalization into host cells or liberation of excess oxidants in circulation following interaction with erythrocytes or vascular endothelial cells. The presence of infection-specific antibodies in the serum can make such nano-conjugates more selective. A potent antimicrobial action and a wide margin of safety for mammalian cells in comparison with very similar PVA-capped silver nanoparticles have been demonstrated by the in-vitro challenge of such nanoparticles on different microbes, human liver cell-line, and in-vivo study on mice model. This may open up wide-range therapeutic prospects of colloidal nanoparticles.

摘要

进入细胞后,胶态银纳米粒子表现出普遍的细胞毒性,因此看起来像是万能的杀菌物质,但除非对宿主细胞没有毒性作用,否则不适合全身使用。当用葡萄糖作为还原剂,用与被结合物同源的血清作为稳定剂,从硝酸银中制备出 AgNP-Serum-18 时,对宿主的选择性内吞作用以及依赖于氧化应激的生物功能损伤大多被消除。由于其具有仿生的外壳,与红细胞或血管内皮细胞相互作用后,纳米复合物进入宿主细胞或释放过多的氧化剂的可能性最小。血清中存在感染特异性抗体可以使这些纳米缀合物更具选择性。与非常相似的 PVA 封端的银纳米粒子相比,这种纳米粒子在不同微生物、人肝癌细胞系以及小鼠模型中的体内研究中表现出强大的抗菌作用和对哺乳动物细胞的宽安全范围。这可能为胶态纳米粒子开辟广泛的治疗前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f74e/8172638/a6cc58aefb17/41598_2021_91031_Fig1_HTML.jpg

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