Liang Jie, Tong William G
Department of Chemistry and Biochemistry, San Diego State University, San Diego 92182, California, United States.
ACS Omega. 2023 Aug 16;8(34):31030-31039. doi: 10.1021/acsomega.3c02845. eCollection 2023 Aug 29.
The carbohydrate antigen 19-9 (CA 19-9) is the most commonly used biomarker in the clinical diagnosis of pancreatic cancer. Multiphoton nonlinear laser wave-mixing spectroscopy is presented as an ultrasensitive detection method for CA 19-9. Wave mixing is an optical absorption-based method, and hence, one can detect CA 19-9 without labels in their native form using compact ultraviolet (UV) lasers or labeled samples using a visible laser. The wave-mixing signal exhibits a quadratic dependence on the sample concentration, and hence, it is an ideal sensor to monitor small changes in the sample. Wave mixing has inherent advantages over other absorption-based detection methods, including short optical path length (micrometer-thin samples instead of 1 cm cuvette) and excellent spatial resolution (micrometer probe). Since the laser wave-mixing probe volume is small (picoliter), it is convenient to interface to microfluidics or capillary-based electrophoresis systems to enhance chemical specificity. Our wave-mixing detectors could be configured as portable battery-powered devices suitable for field use. Laser wave-mixing spectroscopy offers enhanced selectivity levels for protein detection when coupled with capillary electrophoresis (CE). We report a concentration detection limit of 0.16 U/mL, and a corresponding mass detection limit of 1.2 × 10 U, and these detection limits are better than those of chemiluminescence- or ELISA- based methods.
碳水化合物抗原19-9(CA 19-9)是胰腺癌临床诊断中最常用的生物标志物。多光子非线性激光波混频光谱法被提出作为一种用于检测CA 19-9的超灵敏检测方法。波混频是一种基于光吸收的方法,因此,使用紧凑型紫外(UV)激光器可以直接检测天然形式的CA 19-9,使用可见激光器则可以检测标记样品。波混频信号对样品浓度呈二次依赖性,因此,它是监测样品微小变化的理想传感器。与其他基于吸收的检测方法相比,波混频具有固有优势,包括光程长度短(微米级薄样品而非1厘米比色皿)和出色的空间分辨率(微米级探针)。由于激光波混频探针体积小(皮升),便于与微流控或毛细管电泳系统连接以提高化学特异性。我们的波混频探测器可以配置为适合现场使用的便携式电池供电设备。当与毛细管电泳(CE)结合时,激光波混频光谱法对蛋白质检测具有更高的选择性。我们报告的浓度检测限为0.16 U/mL,相应的质量检测限为1.2×10 U,这些检测限优于基于化学发光或酶联免疫吸附测定的方法。