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首页> 外文期刊>Medical Microbiology and Immunology >Antimicrobial and antibiofilm activity of curcumin-silver nanoparticles with improved stability and selective toxicity to bacteria over mammalian cells
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Antimicrobial and antibiofilm activity of curcumin-silver nanoparticles with improved stability and selective toxicity to bacteria over mammalian cells

机译:姜黄素 - 银纳米粒子的抗菌和抗菌剂活性,具有改善稳定性和对哺乳动物细胞的细菌的稳定性和选择性毒性

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摘要

Antibiotic resistance has necessitated search for new antibacterials for combating threat of pathogenic bacteria. Though chemically synthesized silver nanoparticles are a well-known antimicrobial agent, they are toxic to human cells at higher concentrations. Hence in the present study, curcumin-silver nanoparticles (Cur-AgNPs) of size 25-35 nm, were synthesized using curcumin, a phytochemical. These nanoparticles were effective against both Gram positive and Gram-negative bacteria and were less toxic to human keratinocytes. They had very low total silver content and high stability. The antibacterial activity of Cur-AgNPs, as studied by minimum inhibitory concentration (MIC = 5 mg/L), time kill kinetics and post agent effect, was better than silver nanoparticles (AgNPs, size ae 35 nm, MIC = 20 mg/L). The inhibitory effect of Cur-AgNPs on biofilm formation was also ae 20% more than AgNPs as demonstrated by live-dead imaging and scanning electron microscopy. The cytotoxic test to skin keratinocytes (HaCaT) showed that Cur-AgNPs were toxic at a concentration of 156 mg/L which is much higher than the bacterial MIC (selective toxicity). They also showed anti-inflammatory effect on human macrophages (THP1) by reducing secretion of pro-inflammatory cytokines IL-6 and TNF-alpha as compared to chemically synthesized AgNPs.
机译:抗生素抗性已经需要寻找用于打击致病性细菌威胁的新抗菌。虽然化学合成的银纳米颗粒是众所周知的抗微生物剂,但它们在较高浓度下对人细胞有毒。因此,在本研究中,使用姜黄素,植物化学化合成曲霉菌 - 银纳米颗粒(Cur-angnps)的大小25-35nm。这些纳米颗粒对革兰氏阳性和革兰氏阴性细菌有效,对人角蛋白细胞的毒性较小。它们总银含量和高稳定性非常低。通过最小抑制浓度(MIC = 5mg / L)研究的Cur-agnps的抗菌活性,时间杀死动力学和后药物效果,优于银纳米颗粒(AgNP,尺寸AE 35nm,MIC = 20 mg / L. )。 Cur-agnps对生物膜形成的抑制作用也是20%的20%而不是通过活死的成像和扫描电子显微镜证明的agnps。对皮肤角蛋白细胞(HACAT)的细胞毒性试验表明,Cur-agnps以156mg / L的浓度毒性远高于细菌MIC(选择性毒性)。与化学合成的AgNP相比,它们还通过减少促炎细胞因子IL-6和TNF-α的分泌而对人巨噬细胞(THP1)表现出抗炎作用。

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