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Multiblock Copolymers toward Segmentation-Driven Morphological Transition
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DOI：10.1021/acs.macromol.0c00374.png)
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Abstract
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Conventional methods for controlling self-assembly are generally based on the change in hydrophilic/hydrophobic volume fraction of diblock or triblock copolymers, which suffer from low structural diversity and limited chemical tunability. Inspired by nature, segmented multiblock copolymers (MBCs) offer unparalleled opportunities for engineering of biomimetic nanomaterials with tailored properties. However, the self-assembly of MBCs remains largely unexplored and poorly understood. In this study, we report a segmentation-mediated self-assembly strategy to manipulate the morphology of protein-mimic responsive MBCs by facilely altering the block numbers while holding the amphiphilicity constant. In particular, we found that an increased number of nearly alternating biodegradable poly(epsilon-caprolactone) and hydrophilic polyethylene glycol segments drives micelle-to-worm-to-vesicle transition. Moreover, the L-cystine residue-enriched interlayer of assemblies enables a depolymerization-induced morphology reversion, resulting in a redox-hyper-responsive property and ultrafast intracellular drug release. Both experimental and computational results provide a new insight into the self-assembly of macromolecules and propose a convenient approach to the construction of smart nanoassemblies with controlled architectures.
Keywords:
DIBLOCK COPOLYMER
CELLULAR INTERNALIZATION
CYLINDRICAL MICELLES
POLYMER VESICLES
NANOPARTICLES
GLYCOL)
AMPHIPHILES
ASSEMBLIES
DELIVERY
RELEASE
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