Zeng Haoxiang, Liang Xiaoli, Roberts Derrick A, Gillies Elizabeth R, Müllner Markus
Key Centre for Polymers and Colloids, School of Chemistry, The University of Sydney, 2006, Sydney, NSW, Australia.
Department of Chemistry and Department of Chemical and Biochemical Engineering, The University of Western Ontario, N6A 5B7, London, Ontario, Canada.
Angew Chem Int Ed Engl. 2024 Mar 22;63(13):e202318881. doi: 10.1002/anie.202318881. Epub 2024 Feb 22.
Polymer nanodiscs, especially with stimuli-responsive features, represent an unexplored frontier in the nanomaterial landscape. Such 2D nanomaterials are considered highly promising for advanced biomedicine applications. Herein, we designed a rod-coil copolymer architecture based on an amphiphilic, tadpole-like bottlebrush copolymer, which can directly self-assemble into core-shell nanodiscs in an aqueous environment. As the bottlebrush side chains are made of amorphous, UV-responsive poly(ethyl glyoxylate) (PEtG) chains, they can undergo rapid end-to-end self-immolation upon light irradiation. This triggered nanodisc disassembly can be used to boost small molecule release from the nanodisc core, which is further aided by a morphological change from discs to spheres.
聚合物纳米盘,尤其是具有刺激响应特性的纳米盘,代表了纳米材料领域中尚未探索的前沿领域。这类二维纳米材料被认为在先进生物医学应用方面极具前景。在此,我们基于一种两亲性、蝌蚪状刷状共聚物设计了一种棒-线圈共聚物结构,该共聚物能在水性环境中直接自组装成核壳纳米盘。由于刷状侧链由无定形、对紫外线有响应的聚乙醛酸乙酯(PEtG)链构成,光照时它们能快速进行端到端的自裂解。这种引发的纳米盘解体可用于促进小分子从纳米盘核心释放,从盘状到球状的形态变化进一步助力了这一过程。