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基于溶致变色各向异性液晶的肿瘤标志物 CA125 的无标记检测与光谱定量分析。

Label-Free Detection and Spectrometrically Quantitative Analysis of the Cancer Biomarker CA125 Based on Lyotropic Chromonic Liquid Crystal.

机构信息

Institute of Imaging and Biomedical Photonics, College of Photonics, National Yang Ming Chiao Tung University, Guiren District, Tainan 71150, Taiwan.

Department of Basic Science, Faculty of Engineering, The British University in Egypt, El Sherouk City 11837, Egypt.

出版信息

Biosensors (Basel). 2021 Aug 11;11(8):271. doi: 10.3390/bios11080271.

Abstract

Compared with thermotropic liquid crystals (LCs), the biosensing potential of lyotropic chromonic liquid crystals (LCLCs), which are more biocompatible because of their hydrophilic nature, has scarcely been investigated. In this study, the nematic phase, a mesophase shared by both thermotropic LCs and LCLCs, of disodium cromoglycate (DSCG) was employed as the sensing mesogen in the LCLC-based biosensor. The biosensing platform was constructed so that the LCLC was homogeneously aligned by the planar anchoring strength of polyimide, but was disrupted in the presence of proteins such as bovine serum albumin (BSA) or the cancer biomarker CA125 captured by the anti-CA125 antibody, with the level of disturbance (and the optical signal thus produced) predominated by the amount of the analyte. The concentration- and wavelength-dependent optical response was analyzed by transmission spectrometry in the visible light spectrum with parallel or crossed polarizers. The concentration of CA125 can be quantified with spectrometrically derived parameters in a linear calibration curve. The limit of detection for both BSA and CA125 of the LCLC-based biosensor was superior or comparable to that of thermotropic LC-based biosensing techniques. Our results provide, to the best of our knowledge, the first evidence that LCLCs can be applied in spectrometrically quantitative biosensing.

摘要

与热致液晶 (LCs) 相比,溶致变色液晶 (LCLCs) 的生物传感潜力尚未得到充分研究,因为 LCLCs 的亲水性使其具有更好的生物相容性。在本研究中,我们将二钠色甘酸 (DSCG) 的向列相用作基于 LCLC 的生物传感器中的传感介晶,向列相是热致 LCs 和 LCLCs 共有的中间相。该生物传感平台的构建方式是,聚酰亚胺的平面锚定强度使 LCLC 均匀排列,但在存在蛋白质(如牛血清白蛋白 (BSA))或被抗 CA125 抗体捕获的癌症标志物 CA125 的情况下会被破坏,其干扰程度(以及由此产生的光学信号)主要取决于分析物的含量。通过在可见光光谱中使用平行或交叉偏光器进行透射光谱分析,研究了浓度和波长依赖性的光学响应。可以通过光谱衍生参数在线性校准曲线上定量 CA125 的浓度。基于 LCLC 的生物传感器对 BSA 和 CA125 的检测限优于或可与基于热致 LC 的生物传感技术相媲美。据我们所知,我们的研究结果首次提供了证据,表明 LCLCs 可应用于光谱定量生物传感。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf8e/8394883/041e9d94d49f/biosensors-11-00271-g001.jpg

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