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Microwave-assisted ultra-fast synthesis of carbon quantum dots from linter: Fluorescence cancer imaging and human cell growth inhibition properties

机译:来自LINTER的微波辅助超快速合成碳量子点:荧光癌症成像和人细胞生长抑制性能

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The water dispersed-fluorescent carbon quantum dots (CDs) were synthesized using microwave-assisted hydrothermal process in the closed system from the waste cotton linter as a new carbon source. This method provided an ultra-fast, more effective, economical and easier synthesis for cancer-imaging applications compared to the other methods presented in literature. The morphological and optical properties of the hydrothermally produced carbon quantum dots were characterized by using FT-IR, transmission electron microscopy (TEM), SEM, EDX, UV-vis and fluorescent spectrophotometry techniques. An emission peak was observed at 420 nm when the CDs were excited at 376 nm. CDs were calculated to have an average particle diameter of 10.14 nm by TEM. In order to determine the usability of the CDs in cell imaging, two different concentrations (50 mu L/mL and 100 mu L/mL) of the CDs colloidal solution were applied to a human mesothelioma cell line, H2452, and human umbilical vein endothelial cells (HUVEC) for varying durations. While the fluorescent photos revealed that 2 h of exposure was sufficient for the cells to take the C-dots in and higher concentrations appeared brighter in the wavelengths studied (red channel (excitation/emission 586/646 nm), blue channel (390/446 nm) and the green channel (482/532 nm)), cell viability and proliferation assays indicated that the material was cytotoxic against the both cell lines and inhibited the cell growth in a time- and dose- dependent manner.
机译:使用微波辅助水热处理在封闭系统中从废棉兰棉作为新的碳源合成水分散荧光碳量子点(CDS)。与文献中呈现的其他方法相比,该方法提供了对癌症成像应用的超快速,更有效,更容易的合成。通过使用FT-IR,透射电子显微镜(TEM),SEM,EDX,UV-VI和荧光分光光度法,表征了水热产生的碳量子点的形态学和光学性质。当Cds在376nm激发时,在420nm下观察到发射峰。计算CD以通过TEM的平均粒径为10.14nm。为了确定CD在细胞成像中CD的可用性,将CDS胶体溶液的两种不同的浓度(50μmL/ ml和100μl/ ml)施加到人的间皮瘤细胞系,H2452和人脐静脉内皮内用于不同持续时间的细胞(HUVEC)。虽然荧光照片显示出2小时足以使细胞采用C点,并且在研究的波长(红色通道(激发/发射586/646nm),蓝色通道(390/446)中出现更高的浓度NM)和绿色通道(482/532nm),细胞活力和增殖测定表明,该材料是对两种细胞系细胞毒性,并以时间和剂量依赖性的方式抑制细胞生长。

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