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Protection/Deprotection of Surface Activity and Its Applications in the Controlled Release of Liposomal Contents
Author(s) -
Xueshu Li,
Yan Zhao
Publication year - 2012
Publication title -
langmuir
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.042
H-Index - 333
eISSN - 1520-5827
pISSN - 0743-7463
DOI - 10.1021/la2050702
Subject(s) - dithiothreitol , chemistry , ethylene glycol , cationic polymerization , micelle , aqueous solution , liposome , surface tension , reducing agent , polymer chemistry , combinatorial chemistry , thiol , alkyne , organic chemistry , catalysis , biochemistry , physics , quantum mechanics , enzyme
The micelles of two tripropargylammonium-functionalized cationic surfactants were cross-linked by a disulfide-containing diazido cross-linker in the presence of Cu(I) catalysts. With multiple residual alkyne groups on the surface, the resulting surface cross-linked micelles (SCMs) were postfunctionalized by reaction with 2-azidoethanol and an azido-terminated poly(ethylene glycol), respectively, via the alkyne-azide click reaction. The water-soluble nanoparticles obtained had low surface activity due to the buried hydrophobic tails. Cleavage of the disulfide cross-links by dithiothreitol (DTT) exposed the hydrophobic tails and resumed surface activity of the "caged" surfactants within 2 min after DTT addition. The controlled breakage of the SCMs was used to lower the surface tension of aqueous solutions and trigger the release of liposomal contents on demand.

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