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首页> 外文期刊>Journal of Colloid and Interface Science >Synthesis, characterization and comparative evaluation of phenoxy ring containing long chain gemini imidazolium and pyridinium amphiphiles
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Synthesis, characterization and comparative evaluation of phenoxy ring containing long chain gemini imidazolium and pyridinium amphiphiles

机译:含长链双子座咪唑鎓和吡啶鎓两亲物的苯氧基环的合成,表征和比较评价

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摘要

Two series of phenoxy ring containing long chain imidazolium and pyridinium based gemini amphiphiles have been synthesized from renewable cardanol oil having different spacers (i. e. S(CH_2)_nS, where n is 2, 3, 4 & 6). Critical micelle concentration (cmc) of these new gemini amphiphiles has been determined by conductivity method. Further, these new cationic amphiphiles have been evaluated for their DNA binding capability by agarose gel electrophoresis, ethidium bromide exclusion experiments and transmission electron microscopy (TEM). The cytotoxicity of these new amphiphiles have been evaluated by MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. Comparative studies of these phenoxy ring containing long chain gemini imidazolium amphiphiles and their pyridinium analogues depicted low cmc values of the later but greater DNA interaction capability and low cytotoxicity of the former series of amphiphiles.
机译:已从具有不同间隔基(即S(CH_2)_nS,其中n为2、3、4和6)的可再生腰果酚油合成了两个系列的含苯氧基环的长链咪唑鎓和吡啶鎓基双亲两亲物。这些新的双子座两亲物的临界胶束浓度(cmc)已通过电导法测定。此外,已经通过琼脂糖凝胶电泳,溴化乙锭排除实验和透射电子显微镜(TEM)对这些新型阳离子两亲物的DNA结合能力进行了评估。这些新的两亲物的细胞毒性已通过MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物)分析进行了评估。对这些含有苯氧基环的长链双子座咪唑鎓两亲物及其吡啶鎓类似物的比较研究表明,后者的cmc值较低,但前两亲的DNA相互作用能力较高,细胞毒性较低。

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