College of Biological and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 211816, PR China; College of Food and Pharmaceutical Engineering, Nanjing Normal University, Nanjing 210023, PR China.
College of Food and Pharmaceutical Engineering, Nanjing Normal University, Nanjing 210023, PR China.
Spectrochim Acta A Mol Biomol Spectrosc. 2023 Feb 5;286:121961. doi: 10.1016/j.saa.2022.121961. Epub 2022 Oct 13.
A portable instrument-free detection method for lipopolysaccharide (LPS) analysis was developed based on dual-emission ratiometric fluorescence sensing system. Herein, red-emitting Au nanoclusters (Au NCs) were as reference probe, while blue-emitting fluorescent silica quantum dots (Si QDs) were as response probe. Additionally, the aptamer of LPS was covalently grafted to the surface of Si QDs in order to specific recognize the LPS. According to the changes of fluorescence intensityratio (FL ratio, I/I) with the concentrations of LPS, the linear equation was fitted with the range of 50-3000 ng/mL, and the limit of detection (LOD) was 29.3 ng/mL. As a practical application, this method was employed to analyze LPS in normal saline with the recovery rate of 97.7-103.8 %. The color picker platform in the smartphone was used to transform the detection picture to the process of Red, Green and Blue (RGB) for visual detection of LPS. The low-cost and easy-carry method reported here presents broad merits for the visually quantitative detection of LPS.
基于双发射比率荧光传感系统,开发了一种用于脂多糖(LPS)分析的便携式无仪器检测方法。在此,红色发射的金纳米簇(Au NCs)用作参考探针,而蓝色发射的荧光硅量子点(Si QDs)用作响应探针。此外,LPS 的适体被共价接枝到 Si QDs 的表面,以特异性识别 LPS。根据荧光强度比(FL 比,I/I)随 LPS 浓度的变化,拟合出 50-3000ng/mL 的线性方程,检测限(LOD)为 29.3ng/mL。作为实际应用,该方法用于分析生理盐水中的 LPS,回收率为 97.7-103.8%。智能手机中的拾色器平台用于将检测图像转换为红、绿、蓝(RGB)的过程,用于 LPS 的可视化检测。这里报道的低成本、便于携带的方法为 LPS 的可视化定量检测提供了广泛的优势。