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Developing a Silk Fibroin Composite Film to Scavenge and Probe H2O2 Associated with UV-Excitable Blue Fluorescence

机译:开发丝素蛋白复合膜以清除和探测与紫外线激发的蓝色荧光有关的H2O2

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摘要

A silk fibroin composite film that can simultaneously scavenge and probe H O in situ was developed for possibly examining local concentrations of H O for biomedical applications. A multi-functional composite film (GDES) that consists of graphene oxide (G), a photothermally responsive element that was blended with polydopamine (PDA, D)/horseradish peroxidase (HRP, E) (or DE complex), and then GDE microaggregates were coated with silk fibroin (SF, S), a tyrosine-containing protein. At 37 °C, the H O -scavenging ability of a GDES film in solution at approximately 7.5 × 10 μmol H O /mg film was the highest compared with those of S and GS films. The intensities of UV-excitable blue fluorescence of a GDES film linearly increased with increasing H O concentrations from 4.0 μM to 80 μM at 37 °C. Interestingly, after a GDES film scavenged H O , the UV-excitable blue fluorescent film could be qualitatively monitored by eye, making the film an eye-probe H O sensor. A GDES film enabled to heat H O -containing samples to 37 °C or higher by the absorption of near-IR irradiation at 808 nm. The good biocompatibility of a GDES film was examined according to the requirements of ISO-10993-5. Accordingly, a GDES film was developed herein to scavenge and eye-probe H O in situ and so it has potential for biomedical applications.
机译:开发了一种可以同时清除和探测H O的丝素蛋白复合膜,可用于检查生物医学应用中H O的局部浓度。多功能复合膜(GDES),由氧化石墨烯(G),与聚多巴胺(PDA,D)/辣根过氧化物酶(HRP,E)(或DE配合物)混合而成的光热响应元素,然后由GDE微聚集体组成用丝蛋白(SF,S),一种含酪氨酸的蛋白包被。在37°C下,与S和GS膜相比,溶液中GDES膜的H O清除能力最高,约为7.5×10μmolH O / mg膜。在37°C下,随着H O浓度从4.0μM增加到80μM,GDES膜的紫外线激发蓝色荧光强度呈线性增加。有趣的是,在清除GDES膜的H O之后,可以用肉眼定性监视可紫外线激发的蓝色荧光膜,从而使该膜成为H-探头传感器。通过吸收808 nm的近红外辐射,GDES膜能够将含H O的样品加热到37°C或更高。根据ISO-10993-5的要求检查了GDES膜的良好生物相容性。因此,本文开发了GDES膜以原位清除和探测H O,因此在生物医学应用中具有潜力。

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