Design and Implementation of a Dual-Region Self-Referencing Fiber-Optic Surface Plasmon Resonance Biosensor

被引:13
|
作者
Bello, Valentina [1 ,2 ]
Vandezande, Wouter [3 ]
Daems, Devin [2 ]
Lammertyn, Jeroen [2 ]
机构
[1] Univ Pavia, Dept Elect Comp & Biomed Engn, Dept Biosyst, I-27100 Pavia, Italy
[2] Katholieke Univ Leuven, Fac Biosci Engn, Dept Biosyst, MeBioS Biosensor Grp, B-3001 Leuven, Belgium
[3] Katholieke Univ Leuven, Ctr Membrane Separat Adsorpt Catalysis & Spect Sus, Dept Microbial & Mol Syst, B-3001 Leuven, Belgium
基金
欧盟地平线“2020”;
关键词
surface plasmon resonance; fiber-optic biosensor; dual-region biosensor; aptamer-based bioassay; high-resolution melting assay; REFRACTIVE-INDEX; SPR SENSOR; SENSITIVITY; EXCITATION; SILVER;
D O I
10.1021/acssensors.2c01362
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The need for self-referencing is extremely important in the field of biosensing. In this manuscript, we report on the study, design, and validation of a dual-region self-referencing fiber-optic surface plasmon resonance biosensor. One region is intended to measure and monitor the binding events of the biological sample under test, while the other one is designed to be used as a reference channel to compensate for external factors, such as bulk refractive index modifications and temperature oscillations, that can negatively affect the biomolecular interaction measurement. Two different configurations for the biosensor probe are presented and investigated here, both theoretically and experimentally. First, the theoretical performance of the proposed biosensor probes, in terms of surface plasmon resonance wavelength shift, was simulated using a numerical model. Afterward, they were experimentally validated in sucrose-water solutions and showed a response to refractive index and temperature changes with sensitivities up to 2000 nm/RIU and 1.559 nm/degrees C, respectively. Finally, an aptamer-based bioassay and a high-resolution melting assay were successfully implemented on the two proposed configurations, demonstrating the feasibility of analyzing the binding events and measuring other external signal modifications simultaneously using the same biosensor probe.
引用
收藏
页码:3360 / 3368
页数:9
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