Journal of Polymer Science Part A Polymer Chemistry · 2008 · 30 citations · 15 references
Natural SciencesChemistryMaterials SciencePolymer ChemistryPolymer EngineeringPolymer MaterialsFree-radical PolymerizationPolymer CharacterizationPolymer StructurePolymer SynthesisPolymerization ChemistryPolymerization ProcessesControlled PolymerizationControlled Radical PolymerizationCyclodextrin Polymer ChemistryPropagation Reactions
Abstract A straightforward synthesis of amphiphilic β‐cyclodextrin‐poly(4‐acryloylmorpholine) (β‐CD‐PACM) polymers of controlled molecular weight, consisting of the radical polymerization of 4‐acryloylmorpholine in the presence of 6‐deoxy‐6‐mercapto‐β‐cyclodextrin (β‐CD‐SH) as chain‐transfer agent, has been established. These derivatives carry a single β‐cyclodextrin (β‐CD) moiety at one terminus and their average molecular weight is in the order of 10 4 . Thus, their β‐CD content is ∼ 10% by weight. No evidence of un‐functionalized PACM was found in the final products. The chain‐transfer constant ( C T ) of β‐CD‐SH was found to be 1.30 by independently determining the reaction constants of both chain‐transfer and propagation reactions. This ensures that the molecular weight, hence the β‐CD content of the polymers, does not significantly vary with conversion. These β‐CD‐PACM polymers are highly soluble in water as well as in several organic solvents such as chloroform and lower alcohols. They proved capable of solubilizing in water poorly soluble drugs such as 9‐[(2‐hydroxyethoxy)methyl]guanine (Acyclovir) and of gradually releasing them in aqueous systems. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1607–1617, 2008
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Maël Bathfield, Franck D’Agosto, Roger Spitz et al. · Journal of the American Chemical Society · 2006 · 172 citations
Natural Sciences, Biotechnology, Pharmaceutical Biotechnology +17
Oddone Schiavon, Paolo Caliceti, Paolo Ferruti et al. · Il Farmaco · 2000 · 101 citations