Department of Pharmacy, University of Genoa, 16148 Genoa, Italy.
Department of Surgical Sciences and Integrated Diagnostics (DISC), University of Genoa, 16132 Genoa, Italy.
Int J Mol Sci. 2024 Feb 27;25(5):2761. doi: 10.3390/ijms25052761.
Organic ammonium and phosphonium salts exert excellent antimicrobial effects by interacting lethally with bacterial membranes. Particularly, quaternary ammonium lipids have demonstrated efficiency both as gene vectors and antibacterial agents. Here, aiming at finding new antibacterial devices belonging to both classes, we prepared a water-soluble quaternary ammonium lipid () and a phosphonium salt () by designing a synthetic path where would be an intermediate to achieve . All synthesized compounds were characterized by Fourier-transform infrared spectroscopy and Nuclear Magnetic Resonance. Additionally, potentiometric titrations of NH groups and were performed to further confirm their structure by determining their experimental molecular weight. The antibacterial activities of and were assessed first against a selection of multi-drug-resistant clinical isolates of both Gram-positive and Gram-negative species, observing remarkable antibacterial activity of both compounds against Gram-positive isolates of and genus. Further investigations on a wider variety of strains of these species confirmed the remarkable antibacterial effects of and (MICs = 4-16 and 4-64 µg/mL, respectively), while 24 h-time-killing experiments carried out with on different isolates evidenced a bacteriostatic behavior. Moreover, both compounds and , at the lower MIC concentration, did not show significant cytotoxic effects when exposed to HepG2 human hepatic cell lines, paving the way for their potential clinical application.
有机铵盐和鏻盐通过与细菌膜发生致命相互作用而表现出优异的抗菌效果。特别是,季铵脂质作为基因载体和抗菌剂都表现出了效率。在这里,我们旨在寻找属于这两类的新型抗菌设备,设计了一条合成路线,使 成为合成 的中间体,从而制备了一种水溶性季铵脂质()和一种鏻盐()。所有合成的化合物都通过傅里叶变换红外光谱和核磁共振进行了表征。此外,还进行了 NH 基团的电位滴定实验和 ,通过确定其实验分子量进一步证实了它们的结构。首先评估了 和 对一系列耐多药的革兰氏阳性和革兰氏阴性临床分离株的抗菌活性,观察到这两种化合物对 和 属的革兰氏阳性分离株具有显著的抗菌活性。对这些物种的更多菌株进行的进一步研究证实了 和 (MIC 分别为 4-16 和 4-64 µg/mL)具有显著的抗菌作用,而用 对不同 的 分离株进行的 24 小时时程杀菌实验表明其具有抑菌作用。此外,当以较低的 MIC 浓度暴露于 HepG2 人肝细胞系时,化合物 和 均没有表现出明显的细胞毒性作用,为它们的潜在临床应用铺平了道路。