Polymer Chemistry · 2012 · 40 citations · 56 references
Natural SciencesMaterials EngineeringMaterials ScienceDrug DeliveryPolymer ChemistryPolymer MaterialsChiral RecognitionChiral SeparationCircular Dichroism SpectroscopyControlled Release MechanismsDrug EncapsulationOptical PolymersChiral AffinityChiral Separation By AdsorptionControlled Release MicrospheresMicrosphere DeliveryMicrospheresOptical ActivityOptical CharacterizationSuspension Polymerization
A new class of chiral microspheres (μm in size) was prepared via suspension polymerization. The microspheres were constituted by optically active helical substituted polyacetylenes, which render the microspheres with considerable optical activity according to CD and UV-vis spectroscopy measurements. The chiral microspheres exhibited large oil-absorbency (ca. 70 g g−1 toward CHCl3). The presence of helical polymer chains enabled the microspheres to show remarkable chiral recognition and chiral adsorption ability: the maximum adsorption toward D- and L-menthol was 90 and 25 wt%, respectively. More interestingly, the microspheres also demonstrated remarkable chirally controlled release ability: under similar conditions, the release of L- and D-menthol was 95 and 65 wt%, respectively. The present chiral microspheres open new possibilities for developing materials used for enantiomeric drug release.
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Functional polymer microspheres
Haruma Kawaguchi · Progress in Polymer Science · 2000 · 945 citations
The Macromolecular Route to Chiral Amplification
Mark M. Green, Ji‐Woong Park, Takahiro Sato et al. · Angewandte Chemie International Edition · 1999 · 748 citations
Jacky W. Y. Lam, Ben Zhong Tang · Accounts of Chemical Research · 2005 · 725 citations