Publication | Closed Access
Glycosaminoglycan Mimetic Biomaterials. 4. Synthesis of Sulfated Lactose-Based Glycopolymers That Exhibit Anticoagulant Activity
98
Citations
20
References
2002
Year
Macromolecular ChemistryGlycosaminoglycan Mimetic BiomaterialsEngineeringGlycobiologyPolysaccharideBiomedical EngineeringThrombin TimesSulfated Lactose-based GlycopolymersPolymersThrombin InhibitionPolymer ChemistryExhibit Anticoagulant ActivityGlycosylationSynthetic MacromoleculeNatural PolymerBiochemistryBiomolecular EngineeringBiomanufacturingPolymer ScienceCyanoxyl Persistent RadicalsMedicinePolymer ReactionCarbohydrate-protein InteractionPolymer Synthesis
Cyanoxyl persistent radicals can be used as chain-growth moderators of the statistical copolymerization of a variety of monomers. We report herein the preparation of fully sulfated lactose-based glycopolymers by cyanoxyl (.OC[triple bond]N)-mediated free-radical polymerization of acrylamide derivatized glycomonomers in good yield (60-80%) and low polydispersity (1.1 < M(w)/M(n) < 1.6). Prolongation of the activated partial thromboplastin time (aPTT) was observed, and structure-activity relationships were defined. Specifically, the anticoagulant effect varied in response to both polymer molecular weight and the density of pendant sulfated lactose units. Nonetheless, measured thrombin times were only modestly prolonged suggesting that the observed anticoagulant effect is not primarily related to direct thrombin inhibition.
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