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用于药物制剂的双重功能表面活性剂:表面活性和抗菌 1-甲苯烷基双胍衍生物的情况。

Dual function surfactants for pharmaceutical formulations: The case of surface active and antibacterial 1-tolyl alkyl biguanide derivatives.

机构信息

Chemistry Interdisciplinary Project (CHIP), School of Pharmacy, University of Camerino, Via Madonna delle Carceri, Camerino, 62032, Italy.

Microbiology Unit, School of Pharmacy, University of Camerino, via Gentile III da Varano, Camerino, 62032, Italy.

出版信息

Int J Pharm. 2024 Aug 15;661:124388. doi: 10.1016/j.ijpharm.2024.124388. Epub 2024 Jun 24.

DOI:10.1016/j.ijpharm.2024.124388
PMID:38925239
Abstract

One interesting field of research in the view of developing novel surfactants for pharmaceutical and cosmetic applications is the design of amphiphiles showing further bioactive properties in addition to those commonly displayed by surface-active compounds. We propose here the chemical synthesis, and characterization of 1-o-tolyl alkyl biguanide derivatives, having different lengths of the hydrocarbon chain (C3, C6, and C10), and showing surface active and antibacterial/disinfectant activities toward both Gram-positive and Gram-negative bacteria. Both surface active properties in terms of critical micelle concentration (CMC) and surface tension at CMC (γCMC), as well as the antimicrobial activity in terms of minimum inhibitory concentrations (MICs), were strongly dependent on the length of the hydrocarbon chain. Particularly, the C6 and C10 derivatives have a good ability to decrease surface tension (γCMC <40 mN/m) at low concentrations (CMC < 12 mM) and a satisfactory antibacterial effect (MIC values between 0.230 and 0.012 mM against S. aureus strains and between 0.910 and 0.190 against P.aeruginosa strains). Interestingly, these compounds showed a disinfectant activity at the tested concentrations that was comparable to that of the reference compound chlorhexidine digluconate. All these results support the possible use of these amphiphilic compounds as antibacterial agents and disinfectants in pharmaceutical or cosmetic formulations.

摘要

一个有趣的研究领域是开发新型表面活性剂用于药物和化妆品应用,在这个领域中,除了通常表现出表面活性化合物的性质外,设计具有其他生物活性的两亲物是很有意义的。在这里,我们提出了 1- 对甲苯基烷基双胍衍生物的化学合成和表征,这些衍生物具有不同长度的碳氢链(C3、C6 和 C10),表现出表面活性和抗革兰氏阳性和革兰氏阴性细菌的抗菌/消毒活性。临界胶束浓度(CMC)和 CMC 时的表面张力(γCMC)的表面活性性质,以及最低抑菌浓度(MIC)的抗菌活性,都强烈依赖于碳氢链的长度。特别是 C6 和 C10 衍生物具有在低浓度(CMC < 12 mM)下降低表面张力(γCMC < 40 mN/m)的良好能力,并且具有令人满意的抗菌作用(MIC 值介于 0.230 和 0.012 mM 之间,对金黄色葡萄球菌菌株有效,介于 0.910 和 0.190 mM 之间,对铜绿假单胞菌菌株有效)。有趣的是,这些化合物在测试浓度下表现出与参考化合物葡萄糖酸氯己定相当的消毒活性。所有这些结果都支持这些两亲性化合物在药物或化妆品制剂中作为抗菌剂和消毒剂的可能用途。

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