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Application of a cation-exchange reaction of CuS nanoparticles and fluorescent copper nanoparticles in a DNA biosensor

机译:CuS纳米粒子和荧光铜纳米粒子的阳离子交换反应在DNA生物传感器中的应用

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摘要

A novel detection method based on the cation-exchange reaction of CuS nanoparticles (CuS NPs) combined with poly T-templated fluorescent Cu nanoparticles (Cu NPs) was developed. First, CuS NPs-magnetic bead conjugates were prepared through the hybridization of DNA. Competition with target DNA resulted in the release of CuS NPs, and exonuclease III catalysis could lead to recycling of the target DNA. Then, the CuS NPs released into the supernatant were subjected to a cation-exchange reaction after the addition of AgNO _(3) . The obtained Cu ~(2+) could form fluorescent Cu NPs using poly T DNA as a template. The fluorescence intensity of the Cu NPs could be used to determine the concentration of the target DNA. To further increase the detection sensitivity, two types of DNA decorated magnetic beads were used. After Exo III digestion for two cycle processes, more CuS NPs entered the supernatant. Hence, a stronger fluorescence intensity was found after the cation-exchange reaction and the formation of fluorescent Cu NPs. The developed method is convenient and low cost with good sensitivity and selectivity.
机译:基于CuS纳米颗粒(CuS NPs)与聚T模板荧光Cu纳米颗粒(Cu NPs)的阳离子交换反应,开发了一种新的检测方法。首先,通过DNA杂交制备CuS NPs-磁珠共轭物。与靶标DNA的竞争导致CuS NP的释放,核酸外切酶III催化可导致靶标DNA的回收。然后,在添加AgNO_(3)之后,释放到上清液中的CuS NPs进行阳离子交换反应。得到的Cu〜(2+)可以以poly T DNA为模板形成荧光Cu NP。 Cu NPs的荧光强度可用于确定目标DNA的浓度。为了进一步提高检测灵敏度,使用了两种类型的DNA装饰磁珠。经过Exo III消化两个循环过程后,更多的CuS NP进入上清液。因此,在阳离子交换反应和形成荧光铜纳米颗粒之后发现了更强的荧光强度。该方法简便,成本低,灵敏度和选择性好。

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