Self-Assembly of Maltoheptaose-block-polycaprolactone Copolymers: Carbohydrate-Decorated Nanoparticles with Tunable Morphology and Size in Aqueous Media
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文摘
This paper describes the systematic investigation into the aqueous self-assembly of a series of block copolymers (BCPs) consisting of maltoheptaose (MH; as the A block) and poly(ε-caprolactone) (PCL; as the B block), i.e., linear AB-type diblock copolymers with varied PCL molecular weights (MH-b-PCL(2.5k,3.3k,5k,10k)), ABy-type (y = 2, MH-b-(PCL5k)2; y = 3, MH-b-(PCL3.3k)3), A2B2-type ((MH)2-b-(PCL5k)2), and AxB-type miktoarm star polymers (x = 2, (MH)2-b-PCL10k; x = 3, (MH)3-b-PCL10k), which had been precisely synthesized via the combination of the living ring-opening polymerization and click reaction. Under similar conditions, the nanoprecipitation method was employed to self-assemble them in an aqueous medium. Imaging and dynamic light scattering techniques indicated the successful formation of the carbohydrate-decorated nanoparticles via self-assembly. The MH-b-PCLs formed regular core–shell micellar nanoparticles with the hydrodynamic radius (Rh) of 17–43 nm. MH-b-(PCL5k)2 and MH-b-(PCL3.3k)3, which have an NPCL comparable to MH-b-PCL10k, were found to form large compound micelles with relatively large radii (Rh of 49 and 56 nm, respectively). On the other hand, (MH)2-b-(PCL5k)2, (MH)2-b-PCL10k, and (MH)3-b-PCL10k predominantly formed the regular core–shell micellar nanoparticles (Rh = 29–39 nm) with a size smaller than that of MH-b-PCL10k (Rh = 43 nm).

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