摘要
在保留C2-NH2抗菌活性基团的基础上,以DCC为脱水剂制备了具有双抑菌活性中心的水杨酸低聚壳聚糖酯(SEC),并对其抑菌活性进行了研究。结果显示,SEC最佳合成反应条件为:n(低聚壳聚糖)∶n(水杨酸)∶n(DCC)=1∶4∶4,冰浴条件下酯化反应48 h,产物酯化度接近73%。该条件下制备的壳聚糖衍生物对各种常见菌的抑制效果明显增强,而且抑菌范围变宽。
Retaining the amine group and taking N,N'-dicyclohexylcarbodiimide(DCC) as a dehydration agent,a salicylic ester of chitooligosaccharide(SEC) with two antibacterial active sites was synthesized and its antibacterial and antifungal activities were studied.The experimental results showed that the optimum reaction conditions were: n(chitooligosaccharide)∶n(salicylic acid)∶n(DCC)=1∶4∶4 and reacting for 48 h in ice bath.The esterification degree of SEC prepared under this condition could reach 72%,and it has high efficiency and broad anti-bacterial activity.
出处
《化学世界》
CAS
CSCD
北大核心
2011年第3期155-158,161,共5页
Chemical World
基金
北京市教委项目资助(KM201011417007)
关键词
低聚壳聚糖
DCC法
酯化
抑菌
chitooligosaccharide(CTS)
DCC
esterification
anti-bacterial function