Graduate Institute of Biomedical Optomechatronics; Graduate Institute of Nanomedicine and Medical Engineering; International PhD Program in Biomedical Engineering; Graduate Institute of Biomedical Materials and Tissue Engineering; School of Biomedical Engineering; College of Biomedical Engineering, Taipei Medical University, Taipei, Taiwan.
Department of Orthopedics, Taipei Medical University-Shuang Ho Hospital, New Taipei City, Taiwan.
Int J Nanomedicine. 2021 Feb 4;16:763-773. doi: 10.2147/IJN.S285125. eCollection 2021.
The sensitive interfacial interaction of liquid crystals (LC) holds potential for precision biosensors. In the past, the developments of LC biosensors were limited by the complicated manufacturing process, which hinders commercialization and wider applications of such devices. In this report, we demonstrate the first nano-structural polymeric stabilized-cholesteric LC (PSCLC) thin films to be a new label-free biosensing technology.
The transmission spectra of PSCLC devices were measured by the fiber-optic spectrometer with high-resolution. In addition, a smartphone was set on the stage, and the camera of smartphone was placed and aligned with a set of lenses embedded in the designed stage. To decrease the chromatic and spherical aberrations, an achromatic lens set composition, consisting of both dual-convex lens and concave-plane lens, was applied for measuring and imaging the PSCLC texture. The average and the estimated standard deviation (SD) were used to present quantitative experimental results. The test BSA was immobilized and fulfilled by the ceramic silicon-constructed DMOAP-coated glass in aqueous BSA solutions at 1 mg/mL, 1 µg/mL, and 1 ng/mL.
The fabrication process of PSCLC is much simplified compared to previous LC biosensors. The color of PSCLC biosensor altered with the BSA concentration, making detection result easy to read. The detection limit of 1 ng/mL is achieved for label-free PSCLC biosensor. The PSCLC biosensor was able to successfully detect due to the albumin concentration's alteration, with a linear range of 1 ng/mL-2 mg/mL. Thus, the label-free-proposed design-integrated nanoscale PSCLCs smartphone-based biosensor could successfully detect BSA in a preclinical urine sample.
Finally, we propose a design to integrate the PSCLC biosensor with a smartphone. The PSCLC owns potential for high performance, low cost for detecting various disease biomarkers in home use. Owing to its great potential for high performance and low cost, the PSCLC biosensors can be used as a label-free point-of-care for detecting various disease biomarkers for patients in care homes.
液晶(LC)的敏感界面相互作用具有成为精密生物传感器的潜力。过去,LC 生物传感器的发展受到复杂制造工艺的限制,这阻碍了此类设备的商业化和更广泛的应用。在本报告中,我们展示了第一个纳米结构聚合物稳定胆甾相液晶(PSCLC)薄膜,作为一种新的无标记生物传感技术。
通过光纤光谱仪以高分辨率测量 PSCLC 器件的透射光谱。此外,将智能手机置于台上,将智能手机的摄像头放置并与嵌入设计台的一组镜头对齐。为了减少色差和球差,应用了由双凸透镜和凹面镜组成的消色差透镜组来测量和成像 PSCLC 纹理。使用平均值和估计标准偏差(SD)来呈现定量实验结果。测试 BSA 通过陶瓷硅构建的 DMOAP 涂覆玻璃在 1mg/mL、1μg/mL 和 1ng/mL 的水溶液中的 BSA 溶液中固定和完成。
与以前的 LC 生物传感器相比,PSCLC 的制造工艺大大简化。PSCLC 生物传感器的颜色随 BSA 浓度的变化而变化,使检测结果易于读取。实现了无标记 PSCLC 生物传感器的检测限为 1ng/mL。PSCLC 生物传感器能够成功检测到白蛋白浓度的变化,线性范围为 1ng/mL-2mg/mL。因此,无标记-提出的设计-集成纳米 PSCLCs 智能手机生物传感器能够成功地检测到临床前尿液样本中的 BSA。
最后,我们提出了一种将 PSCLC 生物传感器与智能手机集成的设计。PSCLC 具有高性能、低成本的潜力,可用于家庭使用检测各种疾病生物标志物。由于其高性能和低成本的巨大潜力,PSCLC 生物传感器可用作无标记的即时护理点,用于检测疗养院患者的各种疾病生物标志物。