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Reversibly Switching Bilayer Permeability and Release Modules of Photochromic Polymersomes Stabilized by Cooperative Noncovalent Interactions

机译:通过合作非共价相互作用稳定的光致变色聚合物囊泡的可逆转换双层渗透性和释放模块

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摘要

We report on the fabrication of photochromic polymersomes exhibiting photoswitchable and reversible bilayer permeability from newly designed poly(ethylene oxide)-b-PSPA (PEO-b-PSPA) diblock copolymers, where SPA is spiropyran (SP)-based monomer containing a unique carbamate linkage. Upon self-assembling into polymersomes, SP moieties within vesicle bilayers undergo reversible phototriggered isomerization between hydrophobic spiropyran (SP, λ_2 > 450 run irradiation) and zwitterionic merocyanine (MC, λ_1 < 420 nm irradiation) states. For both SP and MC polymersomes, their microstructures are stabilized by multiple cooperative noncovalent interactions including hydrophobic, hydrogen bonding, π-π stacking, and paired electrostatic (zwitterionic) interactions, with the latter two types being exclusive for MC polymersomes. Control experiments using analogous block copolymers of hydrophobic SP monomer with a carbonate linkage (SPO) and conventional spiropyran methacrylate monomer (SPMA) containing a single ester functionality were then conducted, revealing that carbamate-incurred hydrogen bonding interactions in PEO-b-PSPA are crucial for polymersome stabilization in the zwitterionic MC state. Moreover, reversible phototriggered SP-to-MC polymersome transition is accompanied by membrane polarity and permeability switching from being nonimpermeable to selectively permeable toward noncharged, charged, and zwitterionic small molecule species below critical molar masses. Intriguingly, UV-actuated MC polymersomes possess two types of release modules: (1) sustained release upon short UV irradiation duration by taking advantage of the unexpectedly slow spontaneous MC-to-SP transition kinetics (t_(1/2) > 20 h) under dark conditions; (2) on-demand and switchable release under alternated UV-vis light irradiation. We further demonstrate photoswitchable spatiotemporal release of 4',6-diamidino-2-phenylindole (DAPL cell nuclei-staining dye) within living HeLa cells.
机译:我们报道了由新设计的聚(环氧乙烷)-b-PSPA(PEO-b-PSPA)二​​嵌段共聚物制备的光致变色聚合物体的光可转换和可逆双层渗透性,其中SPA是基于螺吡喃(SP)的单体,其中含有独特的氨基甲酸酯连锁。自组装成聚合物小体后,囊泡双层中的SP部分在疏水性螺吡喃(SP,λ_2> 450 nm辐照)和两性离子花菁(MC,λ_1<420 nm辐照)状态之间经历可逆的光引发异构化。对于SP和MC聚合物囊泡,它们的微结构通过多种协同非共价相互作用(包括疏水,氢键,π-π堆积和成对的静电(两性离子)相互作用)得以稳定,后两种类型是MC聚合物囊泡所独有的。然后进行了具有疏水性的具有碳酸酯键的SP单体的类似嵌段共聚物和含有单酯官能团的常规螺吡喃甲基丙烯酸酯单体(SPMA)的对照实验,发现在PEO-b-PSPA中氨基甲酸酯引起的氢键相互作用至关重要。用于两性离子MC态的多聚体稳定。此外,可逆的光触发SP-MC聚合物囊泡的转变伴随着膜极性和渗透性的切换,从不可渗透变为选择性渗透,直至低于临界摩尔质量的不带电荷,带电和两性离子小分子物质。有趣的是,紫外线驱动的MC聚合物囊泡具有两种类型的释放模块:(1)通过利用出乎意料的缓慢的自发MC到SP转变动力学(t_(1/2)> 20 h),在短的紫外线照射时间下持续释放在黑暗的条件下(2)在交替的紫外线可见光照射下按需和可切换释放。我们进一步证明在生活中的HeLa细胞内4',6-diamidino-2-phenylindole(DAPL细胞核染色染料)的光开关时空释放。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2015年第48期|15262-15275|共14页
  • 作者单位

    CAS Key Laboratory of Soft Matter Chemistry, Hefei National Laboratory for Physical Sciences at the Microscale, iChem (Collaborative Innovation Center of Chemistry for Energy Materials), Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, China;

    CAS Key Laboratory of Soft Matter Chemistry, Hefei National Laboratory for Physical Sciences at the Microscale, iChem (Collaborative Innovation Center of Chemistry for Energy Materials), Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, China;

    CAS Key Laboratory of Soft Matter Chemistry, Hefei National Laboratory for Physical Sciences at the Microscale, iChem (Collaborative Innovation Center of Chemistry for Energy Materials), Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, China;

    Engineering and Materials Science Experiment Center, University of Science and Technology of China, Hefei, Anhui 230027, China;

    Engineering and Materials Science Experiment Center, University of Science and Technology of China, Hefei, Anhui 230027, China;

    Engineering and Materials Science Experiment Center, University of Science and Technology of China, Hefei, Anhui 230027, China;

    CAS Key Laboratory of Soft Matter Chemistry, Hefei National Laboratory for Physical Sciences at the Microscale, iChem (Collaborative Innovation Center of Chemistry for Energy Materials), Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:09:50

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