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Dual-spectra encoded suspension array using reversed-phase microemulsion UV curing and electrostatic self-assembling

机译:使用反相微乳液UV固化和静电自组装的双光谱编码悬浮阵列

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摘要

The rapid growth of demand for high-throughput multiplexed biochips from modern biotechnology has led to growing interest in suspension array based on multi-channel encoded microbeads. We prepare dual-spectra encoded PEGDA microbeads (DSEPM) by reversed-phase microemulsion UV curing method and layer-by-layer electrostatic self-assembly method. Excitation of the synthesized DSEPM results in two spectra, including fluorescence spectra from quantum dots and laser induced breakdown spectra from nanoparticles with specific elements. With further surface modification and bio-probes grafting, we use DSEPM to carry a series of detection experiments of biomolecules. The adsorption experiment to two types of anti-IgG in mixture sample has demonstrated the availability of DSEPM in multiplexing. Then, the contrast experiment has verified the specificity of DSEPM in detection. Finally, we carry out the concentration gradient experiment and obtain the response curve to show the performance of DSEPM in quantitative analysis. The results indicate our method provide an effective way to improve multiplexed biochips with more coding capacity, accuracy and stability.
机译:现代生物技术对高通量多重生物芯片的需求迅速增长,导致人们对基于多通道编码微珠的悬浮阵列的兴趣日益增长。我们通过反相微乳液紫外光固化方法和逐层静电自组装方法制备了双光谱编码的PEGDA微珠(DSEPM)。合成DSEPM的激发产生两个光谱,包括来自量子点的荧光光谱和来自具有特定元素的纳米粒子的激光诱导击穿光谱。经过进一步的表面修饰和生物探针接枝,我们使用DSEPM进行了一系列生物分子检测实验。混合物样品中两种类型抗IgG的吸附实验证明了DSEPM在多路复用中的可用性。然后,对比实验验证了DSEPM在检测中的特异性。最后,我们进行了浓度梯度实验并获得了响应曲线,以显示DSEPM在定量分析中的性能。结果表明我们的方法提供了一种有效的方法来改进具有更多编码能力,准确性和稳定性的多路复用生物芯片。

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