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Near-infrared quantum dots based fluorescent assay of Cu~(2+) and in vitro cellular and in vivo imaging

机译:基于Cu〜(2+)的近红外量子点荧光测定及体外细胞和体内成像

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Compared to visible light, near infrared (N1R) light is attractive for the development of novel assay method because it can provide deeper imaging penetration and lower fluorescence background and scattering intensity. In this paper, near infrared (NIR) quantum dots (QDs) were synthesized under a convenient and mild condition, afterwards applied to highly sensitive detection of Cu~(2+) and monitoring the change of Cu~(2+) concentration through in vitro and in vivo fluorescent imaging. The quenching of NIR light was resulted from the aggregation of NIR QDs induced by the competitive binding between 3-mercaptopropionic acid (MPA)and the Cu~(2+) present in the solution. A low detection limit of 5 × 10~(-8) M and a broad linear detection range from 1 × 10~(-7) to 5 × 10~(-5) M could be realized in this strategy for the quantitative evaluation of Cu~(2+). This NIR QDs based sensor possess high selectivity, rapid response and excellent photostability. Furthermore, the great potential of this NIR nanosensor has also been fully proved by the in vitro cellular imaging and in vivo imaging.
机译:与可见光相比,近红外(N1R)光对于新型测定方法的发展具有吸引力,因为它可以提供更深的成像穿透力和更低的荧光背景和散射强度。本文在方便温和的条件下合成了近红外(NIR)量子点(QDs),然后用于高灵敏度检测Cu〜(2+),并通过红外监测Cu〜(2+)浓度的变化。体外和体内荧光成像。 NIR光的猝灭是由溶液中存在的3-巯基丙酸(MPA)与Cu〜(2+)之间的竞争性结合引起的NIR QD聚集引起的。该策略可实现5×10〜(-8)M的低检测限和从1×10〜(-7)到5×10〜(-5)M的宽线性检测范围,用于定量评估。铜〜(2+)。这种基于NIR QDs的传感器具有高选择性,快速响应和出色的光稳定性。此外,该NIR纳米传感器的巨大潜力也已通过体外细胞成像和体内成像得到了充分证明。

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