Label-free optical and electrical immunoassays based on lyotropic chromonic liquid crystals: Implications of real-time detection and kinetic analysis

被引:6
|
作者
Shaban, Hassanein [1 ,2 ]
Hsieh, Jui-Teng [1 ]
Lee, Mon-Juan [3 ,4 ]
Lee, Wei [1 ]
机构
[1] Natl Yang Ming Chiao Tung Univ, Inst Imaging & Biomed Photon, Coll Photon, Tainan 711010, Taiwan
[2] British Univ Egypt, Fac Engn, Dept Basic Sci, Cairo 11837, Egypt
[3] Chang Jung Christian Univ, Dept Med Sci Ind, Tainan 711301, Taiwan
[4] Chang Jung Christian Univ, Dept Biosci Technol, Tainan 711301, Taiwan
来源
关键词
Lyotropic chromonic liquid crystal; Azo dye; Sunset yellow; Label-free immunosensor; Real-time monitoring; Dielectric spectroscopy; CANCER ANTIGEN 125; CARBON DOTS; CA125; CELLS; ANTIBODY; GREEN;
D O I
10.1016/j.bios.2022.115011
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Conventional liquid crystal (LC)-based biosensors utilize predominantly thermotropic LCs as the signaltransducing media, which are less environmentally sustainable compared with lyotropic counterparts. In this study, the nematic phase of the anionic azo dye sunset yellow (SSY), a type of lyotropic chromonic liquid crystals (LCLCs), was employed in the optical and electrical biosensing of bovine serum albumin (BSA) and the cancer biomarker CA125. The optical response observed under a polarizing optical microscope was quantified by image analysis, taking advantage of the specific absorption of SSY. The electrical response derived from the dielectric spectra of SSY provided a new alternative for quantitative bioassay based on nematic LCLCs. The limit of detection (LOD) of the optical and electrical protein assay was -10-11- and -10-10-g/ml BSA, respectively, whereas that of the optical and electrical immunoassay was 5.97 x 10-11 and 6.02 x 10-12 g/ml for CA125, respectively. Moreover, real-time monitoring and kinetic analysis, which are hardly achievable for the hydrophobic thermotropic LCs, were demonstrated by dispersing CA125 in nematic SSY and subsequently recording the optical response over time during the specific binding between CA125 and the immobilized anti-CA125 antibody. Results from this study further the potential of nematic LCLCs in biosensing, especially in dielectric and real-time detection.
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页数:7
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