An Optofluidic Guided-Mode Resonance Platform for Binding Kinetics Applications

被引:0
|
作者
Avci, Meryem Beyza [1 ]
Kocer, Furkan [1 ]
Yildirim-Tirgil, Nimet [2 ]
Chananonnawathorn, Chanunthorn [3 ]
Lertvanithphol, Tossaporn [3 ]
Horprathum, Mati [3 ]
Waiwijit, Uraiwan [3 ]
Boonruang, Sakoolkan [3 ]
Tantiwanichapan, Khwanchai [3 ]
Cetin, Arif E. [1 ,4 ]
机构
[1] Izmir Biomed & Genome Ctr, TR-35340 Izmir, Turkiye
[2] Ankara Yildirim Beyazit Univ, Dept Biomed Engn, TR-06010 Ankara, Turkiye
[3] Natl Elect & Comp Technol Ctr NECTEC, Optoelectrochem Sensing Res Team OEC, Spectroscop & Sensing Devices Res Grp SSDRG, Pathum Thani 12120, Thailand
[4] Dokuz Eylul Univ, Izmir Int Biomed & Genome Inst, TR-35340 Izmir, Turkiye
关键词
Binding dynamics; guided mode resonance (GMR); label-free biosensing; nanotechnology; optofluidic; REFRACTIVE-INDEX SENSOR; INDUCED TRANSPARENCY; OPTICAL BIOSENSOR; LIGHT; SENSITIVITY;
D O I
10.1109/JSEN.2024.3515653
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Guided mode resonance (GMR) sensors have emerged as transformative tools in sensing technology, offering exceptional sensitivity, selectivity, and real-time, label-free detection capabilities across diverse applications, including medical diagnostics and environmental monitoring. Their miniaturization potential, cost-effective manufacturing, and wide dynamic range make GMR sensors highly versatile and commercially attractive. In this study, we present an optofluidic GMR platform tailored for real-time analysis of biomolecular interactions without the need for optical labels. The platform integrates a custom-built inverted microscopy system, a high-resolution multispectrometer setup with a spectral resolution of 0.15 nm, and an automated multipump fluid control system, enabling precise and efficient monitoring of binding kinetics between biomolecules. Key outcomes include a refractive index sensitivity of 201.73 nm/RIU and a demonstrated detection limit of 0.15 ng/mL for IgG protein, emphasizing the platform's suitability for highly sensitive biodetection applications. Additionally, the automated flow methodology enhances efficiency and reproducibility by streamlining chip preparation, ligand/analyte incubation, and postexperiment cleaning, minimizing manual intervention and human error. The self-cleaning feature ensures contamination-free operation, facilitating seamless multiuse experiments. Furthermore, we determined the association constant during the binding of protein A/G and IgG, underscoring the platform's applicability to real-time binding kinetics studies. These results establish our optofluidic GMR platform as a robust and precise tool for advancing the understanding of complex biomolecular processes.
引用
收藏
页码:4481 / 4493
页数:13
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