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Siloxane surfactants in polymer nanoparticles formulation
Author(s) -
Racles Carmen,
Hamaide Thierry,
Ioanid Aurelia
Publication year - 2006
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.1051
Subject(s) - chemistry , dynamic light scattering , polymer , polymer chemistry , chemical engineering , hydrodynamic radius , nanoparticle , siloxane , micelle , hydrosilylation , caprolactone , glass transition , polysulfone , copolymer , organic chemistry , aqueous solution , catalysis , engineering
Abstract Carbohydrate‐modified cyclosiloxanes were synthesized by hydrosilylation reactions of protected allyl‐monosaccharides and subsequent deprotection with a gel‐type ion exchanger. They were characterized by 1 H and 13 C‐NMR, FT‐IR, GPC and surface tension measurements. These compounds, as well as other water soluble, carboxylate‐based siloxanes were tested as stabilizers in nanoparticle formulations, with polydimethylsiloxane (PDMS), poly(ε‐caprolactone) (PCL) and UDEL polysulfone (PSF) as polymer cores. Owing to their low critical micelle concentrations (cmc), small amounts of surfactants were required. The particle size and granulometric distribution were measured by dynamic light scattering (DLS). Electron microscopy confirmed the DLS results and revealed aggregation phenomena in dry state, depending on the polymer core. In the tested conditions, the glass transition temperature of the polymer seems to be the driving force for the stability of dry nanoparticles. Copyright © 2006 John Wiley & Sons, Ltd.