He Qinghua, Li Dongmei, He Yonghong, Guan Tian, Zhang Yilong, Shen Zhiyuan, Chen Xuejing, Liu Siyu, Lu Bangrong, Ji Yanhong
Tsinghua University, Department of Physics, Beijing, China.
Tsinghua University, Shenzhen Key Laboratory for Minimal Invasive Medical Technologies, Institute of, China.
J Biomed Opt. 2017 Sep;22(9):1-7. doi: 10.1117/1.JBO.22.9.097003.
A laser-induced breakdown spectroscopy and fluorescence spectroscopy-coupled optical system is reported to demodulate digitally encoded suspension array in fluoroimmunoassay. It takes advantage of the plasma emissions of assembled elemental materials to digitally decode the suspension array, providing a more stable and accurate recognition to target biomolecules. By separating the decoding procedure of suspension array and adsorption quantity calculation of biomolecules into two independent channels, the cross talk between decoding and label signals in traditional methods had been successfully avoided, which promoted the accuracy of both processes and realized more sensitive quantitative detection of target biomolecules. We carried a multiplexed detection of several types of anti-IgG to verify the quantitative analysis performance of the system. A limit of detection of 1.48×10-10 M was achieved, demonstrating the detection sensitivity of the optical demodulation system.
据报道,一种激光诱导击穿光谱和荧光光谱耦合的光学系统可用于在荧光免疫分析中对数字编码的悬浮阵列进行解调。它利用组装的元素材料的等离子体发射来对悬浮阵列进行数字解码,从而对目标生物分子提供更稳定、准确的识别。通过将悬浮阵列的解码过程和生物分子的吸附量计算分离到两个独立的通道中,成功避免了传统方法中解码信号与标记信号之间的串扰,提高了两个过程的准确性,并实现了对目标生物分子更灵敏的定量检测。我们对几种抗IgG进行了多重检测,以验证该系统的定量分析性能。实现了1.48×10-10 M的检测限,证明了该光学解调系统的检测灵敏度。