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

被引:9
|
作者
Schito, Anna Maria [1 ]
Caviglia, Debora [1 ]
Piatti, Gabriella [1 ]
Zorzoli, Alessia [2 ]
Marimpietri, Danilo [2 ]
Zuccari, Guendalina [3 ]
Schito, Gian Carlo [1 ]
Alfei, Silvana [3 ]
机构
[1] Univ Genoa, Dept Surg Sci & Integrated Diagnost DISC, Viale Benedetto XV 6, I-16132 Genoa, Italy
[2] IRCCS Ist Giannina Gaslini, Stem Cell Lab & Cell Therapy Ctr, Via Gerolamo Gaslini 5, I-16147 Genoa, Italy
[3] Univ Genoa, Dept Pharm, Viale Cembrano 4, I-16148 Genoa, Italy
关键词
fourth-generation polyester-based lysine-modified dendrimer; physical encapsulation; ursolic acid (UA); Gram-positive MDR isolates; MICs; time-kill experiments; cytotoxicity on human keratinocytes; ANTIMICROBIAL ACTIVITY; OLEANOLIC ACID; ANTIBACTERIAL ACTIVITY; SALVIA-OFFICINALIS; DELIVERY; SOLUBILITIES; EXTRACTION; RESISTANCE; MICROBIOTA; CORRUGATA;
D O I
10.3390/pharmaceutics13111976
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 Enterococcus genus, including marine isolates, toward which UA-G4K has shown minimum inhibitory concentrations (MICs) very low (0.5-4.3 mu M), regardless of their resistance to antibiotics. Time-kill experiments, in addition to confirming the previously reported bactericidal activity of UA against E. faecium, 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 LD50 (96.4 mu M) 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.
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页数:21
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