Multiblock Copolymers toward Segmentation-Driven Morphological Transition
journal contributionposted on 2020-07-07, 14:40 authored by Yi Zheng, Chuang Weng, Cheng Cheng, Jinling Zhao, Rui Yang, Qin Zhang, Mingming Ding, Hong Tan, Qiang Fu
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(ε-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.
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chemical tunabilityl-cystine residue-enriched interlayerultrafast intracellular drug releasepolyethylene glycol segments drives...block numbersMBCtriblock copolymersmultiblock copolymersdepolymerization-induced morphology...redox-hyper-responsive propertybiomimetic nanomaterialsSegmentation-Driven Morphological T...Multiblock Copolymerssegmentation-mediated self-assembly...