胶束
两亲性
两性离子
自组装
疏水效应
肽
氢键
静电学
材料科学
化学
纳米技术
作者
Rui Zhang,Logan D. Morton,Josiah D. Smith,Fabio Gallazzi,Tommi A. White,Bret D. Ulery
出处
期刊:ACS Biomaterials Science & Engineering
[American Chemical Society]
日期:2018-04-24
卷期号:4 (7): 2330-2339
被引量:36
标识
DOI:10.1021/acsbiomaterials.8b00300
摘要
Hydrophobically driven self-assembly is a well-understood principle that has been shown to facilitate micelle formation. Although quite useful, the library of structures accessible is limited to only a few simplistic geometric configurations that are suboptimal for complex applications. It is believed that other physical phenomena like hydrogen bonding and electrostatic interactions can be exploited to complement hydrophobic interactions allowing for the design of structurally complex, aggregated micelles. To test this theory, ABC triblock peptide amphiphiles comprising an application-specific peptide, a zwitterion-like peptide, and a hydrophobic lipid were synthesized for which block sequence modifications and order changes were used to investigate their impact on micelle formation. The results provide significant evidence that both hydrophobic and electrostatic driving forces influence the formation of complex micellar structures. Specifically, hydrophobic self-assembly facilitates individual micelle fo...
科研通智能强力驱动
Strongly Powered by AbleSci AI