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7,8-二羟基黄酮功能化金纳米粒子靶向.的精氨酸酶

7,8-dihydroxyflavone-functionalized gold nanoparticles target the arginase enzyme of .

机构信息

Department of Biotechnology, National Institute of Pharmaceutical Education & Research (NIPER), Hajipur, 844102, India.

Department of Chemistry, Indian Institute of Technology, Patna, 801106, India.

出版信息

Nanomedicine (Lond). 2021 Sep;16(21):1887-1903. doi: 10.2217/nnm-2021-0161. Epub 2021 Aug 16.

Abstract

To analyze the efficacy and possible mechanism of action of 7,8-dihydroxyflavone (DHF) and DHF synthesized gold nanoparticles (GNPs) against the parasite . GNPs were synthesized using DHF and characterized by dynamic light scattering, ζ potential, Fourier transform infrared spectroscopy, transmission electron microscopy and x-ray diffraction. The efficacy of DHF and DHF-GNP were tested against sensitive and drug-resistant parasites. GNP uptake was measured on macrophages by atomic absorption spectroscopy. DHF and DHF-GNP (∼35 nm) were equally effective against sensitive and drug-resistant strains and inhibited the arginase activity of parasites. Increased IFN-γ and reduced IL-12 cytokine response showed a Th1/Th2-mediated cell death in macrophages. The low cytotoxicity and high biological activity of DHF-GNP may be useful for chemotherapy of leishmaniasis.

摘要

分析 7,8-二羟基黄酮(DHF)和 DHF 合成的金纳米颗粒(GNPs)对寄生虫的疗效和可能作用机制。使用 DHF 合成 GNPs 并通过动态光散射、ζ 电位、傅里叶变换红外光谱、透射电子显微镜和 X 射线衍射进行表征。测试了 DHF 和 DHF-GNP 对敏感和耐药寄生虫的疗效。通过原子吸收光谱法测量巨噬细胞中 GNP 的摄取量。DHF 和 DHF-GNP(∼35nm)对敏感和耐药株均有效,并抑制寄生虫的精氨酸酶活性。增加的 IFN-γ 和减少的 IL-12 细胞因子反应表明巨噬细胞中存在 Th1/Th2 介导的细胞死亡。DHF-GNP 的低细胞毒性和高生物活性可能对利什曼病的化疗有用。

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