Chemical encoding of amphiphilic copolymers for a dual controlled release from their assemblies
Literature Information
Publication Date
2014-10-16
DOI
10.1039/C4PY01159G
Impact Factor
5.582
Authors
Li-Ping Lv, Yi Zhao, Katharina Landfester, Daniel Crespy
View Original
Abstract
Amphiphilic random copolymers are designed to bear a corrosion inhibitor as cleavable side group, which can be released upon activation by chemical reduction. Polymer nanoparticles are obtained by self-assembly of the copolymers in water. A model dye is encapsulated in the nanoparticles and its release is triggered by reductive cleavage of the copolymer, leading hence to the co-release of the corrosion inhibitor. The present system has the advantage that the cleaved units are functional payloads.
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Source Journal
Polymer Chemistry
CiteScore:
8.6
Self-citation Rate:
7.3%
Articles per Year:
457
Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.
Recommended Compounds
![N-[(1-Ethyl-2-pyrrolidinyl)methyl]-2-hydroxy-5-sulfamoylbenzamide structure](https://static.chemtradehub.com/structs/673/67381-52-6-877f.webp "N-[(1-Ethyl-2-pyrrolidinyl)methyl]-2-hydroxy-5-sulfamoylbenzamide structure")
N-[(1-Ethyl-2-pyrrolidinyl)methyl]-2-hydroxy-5-sulfamoylbenzamide
CAS Number:
67381-52-6
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Molecular Formula:
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