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1. 中国科学院 长春光学精密机械与物理研究所,吉林 长春,中国,130033
2. 中国科学院大学 北京,中国,100049
3. 中国科学院 苏州生物医学工程技术研究所,江苏 苏州,中国,215163
4. 南洋理工大学 仿生传感器科学中心 新加坡,637553
5. 浙江大学 光电信息工程学系,浙江 杭州,310027
收稿日期:2014-06-11,
修回日期:2014-08-09,
纸质出版日期:2015-03-25
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何皓, 张涛, 姚佳等. 多孔分子印迹膜修饰的表面等离子体共振微囊藻毒素LR检测传感器[J]. 光学精密工程, 2015,23(3): 723-728
HE Hao, ZHANG Tao, YAO Jia etc. Surface plasmon resonance sensor coated with poriferous MIPs for microcystin-LR detection[J]. Editorial Office of Optics and Precision Engineering, 2015,23(3): 723-728
何皓, 张涛, 姚佳等. 多孔分子印迹膜修饰的表面等离子体共振微囊藻毒素LR检测传感器[J]. 光学精密工程, 2015,23(3): 723-728 DOI: 10.3788/OPE.20152303.0723.
HE Hao, ZHANG Tao, YAO Jia etc. Surface plasmon resonance sensor coated with poriferous MIPs for microcystin-LR detection[J]. Editorial Office of Optics and Precision Engineering, 2015,23(3): 723-728 DOI: 10.3788/OPE.20152303.0723.
开发了一种多孔分子印迹膜修饰的表面等离子体共振(SPR)传感器
用于快速检测水中微囊藻毒素LR。研究了利用该传感器检测微囊藻毒素LR的方法。首先
通过原位聚合法在SPR传感芯片的裸金表面合成了微囊藻毒素LR的多孔分子印迹膜
制备出可以特异性捕获微囊藻毒素LR的SPR传感芯片。然后
利用Kretschmann棱镜耦合结构
构建了基于Kretschmann结构的波长调制型表面等离子体共振传感器。最后
通过检测不同浓度的微囊藻毒素LR溶液以及干扰物质微囊藻毒素RR溶液
研究了该传感器的测量范围、特异性等参数。结果表明
该传感器对于微囊藻毒素LR的检测灵敏度很高
可实现微囊藻毒素LR的定量检测
动态测量达2.1×10
-9
~1×10
-6
mol/L。另外
传感器对于干扰物质微囊藻毒素RR无明显信号响应
表明传感器对于微囊藻毒素LR具有很好的特异性检测能力。
A novel surface plasmon resonance (SPR) sensor coated with poriferous molecularly imprinted polymers (MIPs)was developed to detect the trace microcystin-LR in water. The method to detect the trace microcystin-LR in water was explored. Firstly
the in situ self-assembly method was used to synthesize a poriferous thin MIPs film on the gold-plated glass. The SPR chip to specifically capture the microcystin-LR was obtained. Then
based on the typical Kretschmann prism coupling structure
a new type of SPR sensor based on wavelength interrogation was constructed by utilizing the MIPs coated gold-plated glass as the sensing chip. The sensor was used to detect different concentration of microcystin-LR solutions and microcystin-RR solutions and to obtain its measuring ranges and specificity parameters. The result indicates that the sensor is sensitive to microcystin-LR and completes a quantitative determination with a dynamic measure range of 2.1×10
-9
—1×10
-6
mol/L. Moreover
the sensor did not have obvious response to microcystin-RR
the analogues of microcystin-LR. It means that the sensor has special selectivity to recognize the microcystin-LR.
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