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基于精氨酸的 Gemini 阳离子表面活性剂的生物学特性。

Biological properties of arginine-based gemini cationic surfactants.

作者信息

Pérez Lourdes, García Maria Teresa, Ribosa Isabel, Vinardell Maria Pilar, Manresa Angeles, Infante Maria Rosa

机构信息

Department of Tecnología de Tensioactivos, Instituto de Investigaciones Quimicas y Ambientales de Barcelona-Centro Superior de Investigaciones Cientificas, Spain.

出版信息

Environ Toxicol Chem. 2002 Jun;21(6):1279-85.

Abstract

Biological properties of novel gemini (double-chain/double-head) cationic surfactants, Nalpha,Nomega-bis(Nalpha-acylarginine)alpha,omega-alkylendiamides, so-called bis(Args), are reported. The effect of both the alkyl (10 and 12 carbon atoms) and the spacer chain (from 2-10 methylene groups) of bis(Args) on their antimicrobial activity, acute toxicity on Daphnia magna and Photobacterium phosphoreum, and aerobic biodegradability is studied. These surfactants constitute a novel class of chemicals of low toxicity with excellent surface properties and considerable antimicrobial activity. The aquatic toxicity of these compounds is lower than that of the conventional Monoquats. As regards the biodegradation test, the molecules with a spacer chain < or =6 methylene groups can be considered as ready biodegradable. The increase of hydrophobicity in the bis(Args) is a negative structural parameter for their environmental behavior.

摘要

报道了新型双子(双链/双头)阳离子表面活性剂Nα,Nω-双(Nα-酰基精氨酸)α,ω-亚烷基二酰胺,即所谓的双(精氨酸)的生物学特性。研究了双(精氨酸)的烷基(10和12个碳原子)和间隔链(2至10个亚甲基)对其抗菌活性、对大型溞和发光杆菌的急性毒性以及需氧生物降解性的影响。这些表面活性剂构成了一类新型的低毒化学品,具有优异的表面性能和相当可观的抗菌活性。这些化合物的水生毒性低于传统的单季铵盐。关于生物降解试验,间隔链≤6个亚甲基的分子可被视为易于生物降解。双(精氨酸)中疏水性的增加对其环境行为而言是一个负面的结构参数。

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