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富含熊果酸的水溶性且无细胞毒性的纳米颗粒对肠球菌的疗效

Efficacy of Ursolic Acid-Enriched Water-Soluble and Not Cytotoxic Nanoparticles against Enterococci.

作者信息

Schito Anna Maria, Caviglia Debora, Piatti Gabriella, Zorzoli Alessia, Marimpietri Danilo, Zuccari Guendalina, Schito Gian Carlo, Alfei Silvana

机构信息

Department of Surgical Sciences and Integrated Diagnostics (DISC), University of Genoa, Viale Benedetto XV, 6, 16132 Genoa, Italy.

Stem Cell Laboratory and Cell Therapy Center, IRCCS Istituto Giannina Gaslini, via Gerolamo Gaslini 5, 16147 Genoa, Italy.

出版信息

Pharmaceutics. 2021 Nov 21;13(11):1976. doi: 10.3390/pharmaceutics13111976.

Abstract

Ursolic acid (UA), a pentacyclic triterpenoid acid found in many medicinal plants and aromas, is known for its antibacterial effects against multi-drug-resistant (MDR) Gram-positive bacteria, which seriously threaten human health. Unfortunately, UA water-insolubility, low bioavailability, and systemic toxicity limit the possibilities of its application in vivo. Consequently, the beneficial activities of UA observed in vitro lose their potential clinical relevance unless water-soluble, not cytotoxic UA formulations are developed. With a nano-technologic approach, we have recently prepared water-soluble UA-loaded dendrimer nanoparticles (UA-G4K NPs) non-cytotoxic on HeLa cells, with promising physicochemical properties for their clinical applications. In this work, with the aim of developing a new antibacterial agent based on UA, UA-G4K has been tested on different strains of the genus, including marine isolates, toward which UA-G4K has shown minimum inhibitory concentrations (MICs) very low (0.5-4.3 µM), regardless of their resistance to antibiotics. Time-kill experiments, in addition to confirming the previously reported bactericidal activity of UA against , also established it for UA-G4K. Furthermore, cytotoxicity experiments on human keratinocytes revealed that nanomanipulation of UA significantly reduced the cytotoxicity of UA, providing UA-G4K NPs with very high LD (96.4 µM) and selectivity indices, which were in the range 22.4-192.8, depending on the enterococcal strain tested. Due to its physicochemical and biological properties, UA-G4K could be seriously evaluated as a novel oral-administrable therapeutic option for tackling difficult-to-treat enterococcal infections.

摘要

熊果酸(UA)是一种在许多药用植物和香料中发现的五环三萜酸,以其对多重耐药(MDR)革兰氏阳性菌的抗菌作用而闻名,这些细菌严重威胁人类健康。不幸的是,UA的水不溶性、低生物利用度和全身毒性限制了其在体内应用的可能性。因此,除非开发出水溶性且无细胞毒性的UA制剂,否则在体外观察到的UA的有益活性将失去其潜在的临床相关性。通过纳米技术方法,我们最近制备了对HeLa细胞无细胞毒性的水溶性载UA树枝状聚合物纳米颗粒(UA-G4K NPs),其具有有望用于临床应用的理化性质。在这项工作中,为了开发一种基于UA的新型抗菌剂,对UA-G4K在该属的不同菌株上进行了测试,包括海洋分离株,UA-G4K对这些菌株显示出极低的最低抑菌浓度(MICs)(0.5-4.3 µM),无论它们对抗生素的耐药性如何。时间杀菌实验除了证实先前报道的UA对[具体细菌]的杀菌活性外,还确定了UA-G4K的杀菌活性。此外,对人角质形成细胞的细胞毒性实验表明,对UA进行纳米操作可显著降低其细胞毒性,使UA-G4K NPs具有非常高的半数致死剂量(LD,96.4 µM)和选择性指数,根据测试的肠球菌菌株不同,选择性指数在22.4-192.8范围内。由于其理化和生物学特性,UA-G4K可作为一种新型的口服治疗选择,用于应对难治性肠球菌感染,值得认真评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb3c/8625572/39e448ecf7d3/pharmaceutics-13-01976-g001.jpg

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