Design, synthesis and properties investigation of N-acylation lysine based derivatives

被引:1
|
作者
Shi, Ting-Ting [1 ,2 ]
Fang, Zheng [1 ]
Zeng, Wen-Bo [1 ]
Yang, Zhao [3 ]
He, Wei [1 ]
Guo, Kai [1 ,4 ]
机构
[1] Nanjing Tech Univ, Coll Biotechnol & Pharmaceut Engn, Nanjing 211816, Jiangsu, Peoples R China
[2] Bengbu Med Coll, Dept Chem, Bengbu 233030, Peoples R China
[3] China Pharmaceut Univ, Sch Engn, 639 Longmian Ave, Nanjing 211198, Jiangsu, Peoples R China
[4] Nanjing Tech Univ, State Key Lab Mat Oriented Chem Engn, Nanjing 211816, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
AMINO-ACID SURFACTANTS; AGGREGATION PROPERTIES; BIOLOGICAL-PROPERTIES; CATIONIC SURFACTANTS; IONIC LIQUIDS; MICELLIZATION; AMPHIPHILES; ADSORPTION; BEHAVIOR;
D O I
10.1039/c9ra00213h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amino acid-based compounds have attracted attention as environmentally friendly bio-based materials. Our group has recently developed a novel family of N-acylation lysine based derivatives. We introduced long chain acyl groups at the N position selectively by a new synthetic route that avoided the process of amino protection and deprotection. Sodium N-octanamide lysine (C8), sodium N-capramide lysine (C10) and sodium N-lauramide lysine (C12) can self-assemble into vesicles spontaneously. As a result, not only do they have potential in drug delivery system but also they may be used as bio-based surfactants applied in cosmetics and other industries.
引用
收藏
页码:7587 / 7593
页数:7
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