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Amino acid functionalized blue and phosphorous-doped green fluorescent carbon dots as bioimaging probe

机译:氨基酸功能化的蓝磷掺杂绿色荧光碳点作为生物成像探针

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摘要

Amino acid functionalized carbon dots (CDs) were synthesized in a simple and cost effective bottom up approach. Citric acid was used as the source of the carbon core and three amino acids L-isoleucine, L-valine and glycine were used for the surface fabrication of CDs to produce CDiso, CDval and CDgly, respectively. Interestingly these CDs were found to fluoresce with a blue emission. Doping of phosphorus to these CDs (PCDs) tuned the photoemission properties and produced green emitting PCDs. The doping of phosphorous (P) to these CDs improved their fluorescence intensity as well as quantum yields. Both doped and non-doped CDs were characterized by spectroscopic and microscopic techniques. These highly stable CDs were biocompatible in nature and did not exhibit any photobleaching property over a long span of time even under UV exposure. Subsequently, these CDs were exploited as an excellent bioimaging probe. Importantly CDs and PCDs illuminated cells in two completely different spectral regions blue and green, respectively in accordance with their fluorescence spectral behaviour. Hence, amino acid functionalized carbon dots based bioimaging probes with different fluorescence characteristics were developed that are widely applicable for cellular imaging in both blue and green spectral regions.
机译:氨基酸官能化碳点(CD)以简单且经济高效的自下而上的方法合成。柠檬酸用作碳核的来源,L-异亮氨酸,L-缬氨酸和甘氨酸的三个氨基酸用于CD的表面制备,分别生产CDiso,CDval和CDgly。有趣的是,发现这些CD发出蓝色荧光。向这些CD(PCD)掺入磷可调节光发射特性并产生绿色发光PCD。将磷(P)掺杂到这些CD可以改善其荧光强度以及量子产率。掺杂和未掺杂的CD都通过光谱和显微镜技术进行了表征。这些高度稳定的CD本质上具有生物相容性,即使在暴露于紫外线下,也不会长时间显示任何光漂白特性。随后,这些CD被用作优秀的生物成像探针。重要的是,CD和PCD分别根据它们的荧光光谱行为,照亮了两个完全不同的光谱区域蓝色和绿色的细胞。因此,开发了具有不同荧光特性的基于氨基酸功能化碳点的生物成像探针,其广泛适用于蓝色和绿色光谱区域中的细胞成像。

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