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Cellulose hydrogel is a novel carbon‑source and doping‑material‑carrier to prepare fluorescent carbon dots for intracellular bioimaging

机译:纤维素水凝胶是一种新型的碳源和掺杂材料载体,可制备用于细胞内生物成像的荧光碳点

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Carbon dots (CDs) is considered as a potential candidate for biological labeling due to its excellent biocompatibility,and element-doping was usually used to improve its labeling brightness. Thus, the carbon source with material-carriedfunction will be of importance to produce the element-doped CDs. In present work, cellulose hydrogel was used bothas the carbon source and the doping-material-carrier to obtain the N-doped CDs. The groups in so-obtained CDs weremeasured by means of ultraviolent-visible spectrophotometer (UV–Vis), Fourier infrared spectroscopy (FT-IR), and X-rayphotoelectron spectroscopy. The microstructure of CDs was observed by means of high-resolution transmission electronmicroscope. The fluorescence quantum yield (QY) of the CDs was detected, and the labeling brightness on living cells wassubsequently investigated. Finally, the influence of element-doping on the cytotoxicity was measured. The experimentalresults showed that Cellulose hydrogel is a nice carbon source and doping-material-carrier to produce fine N-doped CDsdue to its distinct spatial network structure. The carried NaOH and urea in cellulose hydrogel significantly improved theQY of the CDs from 0.0542 ± 0.0030 to the maximum 0.1965 ± 0.0013. For the same kind of CDs, the smaller the particlesize is, the higher the QY value is. The CDs immobilized in the cytoplasm of the living cells, and contributed to a nonspecificfluorescent labeling. The labeling brightness is both the QY value of the CDs and the uptake rate of the livingcells dependent. For the same cell line, the QY of CDs and the labeling brightness of living cells are significantly linearcorrelated. The cytotoxicity of CDs is low enough for a long-time observation on living cells.
机译:碳点(CD)由于其出色的生物相容性,被认为是生物标记的潜在候选者,通常使用元素掺杂来提高其标记亮度。因此,碳源带有物质功能对于生产掺杂元素的CD至关重要。在目前的工作中,纤维素水凝胶作为碳源和掺杂材料载体,得到N掺杂的CD。如此获得的CD中的组是通过紫外可见分光光度计(UV-Vis),傅立叶红外光谱(FT-IR)和X射线进行测量光电子能谱。 CDs的微观结构通过高分辨率透射电子观察显微镜。检测CD的荧光量子产率(QY),活细胞上的标记亮度为随后进行了调查。最后,测量了元素掺杂对细胞毒性的影响。实验性结果表明,纤维素水凝胶是良好的碳源和掺杂材料的载体,可以生产出精细的N掺杂CD。由于其独特的空间网络结构。纤维素水凝胶中携带的NaOH和尿素显着改善了CD的QY从0.0542±0.0030到最大0.1965±0.0013。对于相同类型的CD,颗粒越小尺寸越大,QY值越高。 CD固定在活细胞的细胞质中,并导致非特异性荧光标记。标签的亮度既是CD的QY值,也是活体的吸收率细胞依赖性。对于同一细胞系,CD的QY和活细胞的标记亮度呈线性关系相关的。 CD的细胞毒性很低,无法长期观察活细胞。

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