Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/19833
Title: Interfacial thiol-isocyanate reactions for functional nanocarriers: a facile route towards tunable morphologies and hydrophilic payload encapsulation
Authors: KUYPERS, Soren 
PRAMANIK, Sumit 
D'OLIESLAEGER, Lien 
REEKMANS, Gunter 
PETERS, Martijn 
D'HAEN, Jan 
VANDERZANDE, Dirk 
JUNKERS, Tanja 
ADRIAENSENS, Peter 
ETHIRAJAN, Anitha 
Issue Date: 2015
Publisher: ROYAL SOC CHEMISTRY
Source: CHEMICAL COMMUNICATIONS, 51 (87), p. 15858-15861
Abstract: Functional nanocarriers were synthesized using an in situ inverse miniemulsion polymerization employing thiol-isocyanate reactions at the droplet interface to encapsulate hydrophilic payloads. The morphology of the nanocarriers is conveniently tunable by varying the reaction conditions and the dispersions are easily transferable to the aqueous phase.
Notes: [Kuypers, Soren; Pramanik, Sumit Kumar; D'Olieslaeger, Lien; D'Haen, Jan; Ethirajan, Anitha] Hasselt Univ, Inst Mat Res IMO, B-3590 Diepenbeek, Belgium. [Kuypers, Soren; Pramanik, Sumit Kumar; Reekmans, Gunter; Peters, Martijn; Vanderzande, Dirk; Junkers, Thomas; Adriaensens, Peter; Ethirajan, Anitha] Hasselt Univ, Inst Mat Res, Organ & Biopolymer Chem, B-3590 Diepenbeek, Belgium. [D'Haen, Jan; Vanderzande, Dirk; Junkers, Thomas; Adriaensens, Peter] IMEC, Associated Lab IMOMEC, B-3590 Diepenbeek, Belgium.
Document URI: http://hdl.handle.net/1942/19833
ISSN: 1359-7345
e-ISSN: 1364-548X
DOI: 10.1039/c5cc05258k
ISI #: 000363262400028
Rights: This journal is © The Royal Society of Chemistry 2015
Category: A1
Type: Journal Contribution
Validations: ecoom 2016
Appears in Collections:Research publications

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