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螺吡喃与苯并吡喃部分的甲基丙烯酸酯的合成及其聚合物膜的疏水性和细胞黏附性的控制。

Synthesis of spiropyran with methacrylate at the benzopyran moiety and control of the water repellency and cell adhesion of its polymer film.

机构信息

Division of Materials Science, Graduate School of Science and Technology, Nara Institute of Science and Technology, 8916-5 Takayama-cho, Ikoma, Nara 630-0192, Japan.

出版信息

J Mater Chem B. 2020 Feb 19;8(7):1489-1495. doi: 10.1039/c9tb02733e.

Abstract

Stimuli-responsive materials have been actively researched over the past few decades. Among such materials, spiropyran is one of the most attractive compounds because the structure and polarity of the material are dramatically changed after photo irradiation, unlike other materials. In this work, we designed and synthesized a spiropyran derivative (SpMA) with a methacryloyl group on the nitrobenzene ring of a spiropyran skeleton. The UV spectra of the newly synthesized SpMA showed the photo-isomerization of spiropyran. The maximum absorption wavelength (λmax) of SpMA was 616 nm in n-hexane, a nonpolar solvent, although λmax of SpMA was 532 nm in methanol, a polar protic solvent, which resulted in an 84 nm blue-shift. SpMA was successfully polymerized by ruthenium (Ru)-catalyzed living radical polymerization. Poly(SpMA) (PSpMA) was then spin-coated on a PET substrate in order to control the surface properties of water repellency and cell adhesion. The water repellency was decreased approximately 10° under UV irradiation, because of the polarity change of PSpMA caused by photo-isomerization from the spiropyran (SP) type to the merocyanine (MC) type. In addition, NIH3T3 cells were spread only on 6% of the surface of the PSpMA thin film after UV irradiation compared with no UV irradiation. The polarity change of PSpMA by photo-isomerization is also believed to be the reason for this behavior. As a result, we successfully synthesized a photo-controllable cell culture scaffold.

摘要

刺激响应材料在过去几十年中得到了积极的研究。在这些材料中,螺吡喃是最吸引人的化合物之一,因为与其他材料不同,材料的结构和极性在光照射后会发生剧烈变化。在这项工作中,我们设计并合成了一种螺吡喃衍生物(SpMA),其硝基苯环上带有一个丙烯酰基。新合成的 SpMA 的紫外光谱显示出螺吡喃的光致异构化。SpMA 在非极性溶剂正己烷中的最大吸收波长(λmax)为 616nm,尽管在极性质子溶剂甲醇中 λmax 为 532nm,导致 84nm 的蓝移。SpMA 成功地通过钌(Ru)催化的活性自由基聚合聚合。然后将聚(SpMA)(PSpMA)旋涂在 PET 基底上,以控制表面的疏水性和细胞黏附性。由于光致异构化从螺吡喃(SP)型到内消旋体(MC)型引起的 PSpMA 的极性变化,在紫外光照射下,疏水性降低了约 10°。此外,与未辐照相比,NIH3T3 细胞仅在 PSpMA 薄膜的 6%表面上展开。光致异构化引起的 PSpMA 极性变化也被认为是这种行为的原因。结果,我们成功合成了一种光可控的细胞培养支架。

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