共 62 条
Stable Emulsions Formed by Self-Assembly of Interfacial Networks of Dipeptide Derivatives
被引:128
作者:
Bai, Shuo
[1
]
Pappas, Charalampos
[1
]
Debnath, Sisir
[1
]
Frederix, Pim W. J. M.
[1
]
Leckie, Joy
[1
]
Fleming, Scott
[1
]
Ulijn, Rein V.
[1
,2
]
机构:
[1] Univ Strathclyde, Dept Pure & Appl Chem, WestCHEM, Glasgow G1 1XL, Lanark, Scotland
[2] CUNY, ASRC, New York, NY 10031 USA
来源:
基金:
欧洲研究理事会;
关键词:
dipeptide;
self-assembly;
emulsion;
interface;
microcapsules;
OIL-IN-WATER;
FMOC-DIPHENYLALANINE;
SUPRAMOLECULAR ORDER;
ENZYME CATALYSIS;
DRUG-DELIVERY;
BETA-SHEETS;
NANOPARTICLES;
MICROCAPSULES;
DROPLETS;
HYDROGEL;
D O I:
10.1021/nn501909j
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
We demonstrate the use of dipeptide amphiphiles that, by hand shaking of a biphasic solvent system for a few seconds, form emulsions that remain stable for months through the formation of nanofibrous networks at the organic/aqueous interface. Unlike absorption of traditional surfactants, the interfacial networks form by self-assembly through a-stacking interactions and hydrogen bonding. Altering the dipeptide sequence has a dramatic effect on the properties of the emulsions formed, illustrating the possibility of tuning emulsion properties by chemical design. The systems provide superior long-term stability toward temperature and salts compared to with sodium dodecyl sulfate (SDS) and can be enzymatically disassembled causing on-demand demulsification under mild conditions. The interfacial networks facilitate highly tunable and stable encapsulation and compartmentalization with potential applications in cosmetics, therapeutics, and food industry.
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页码:7005 / 7013
页数:9
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