Slug-Flow Microextraction Mass Spectrometry for Enhanced Detection of Analytes in Human Tear Fluids using Noninvasive Microsampling and Nanoelectrospray Ionization via a Capillary.
Songbin DongNing ZhangMan YiJianfeng ZhangDandan DiJiewei DengLei LiBin HuPublished in: Analytical chemistry (2023)
In vivo noninvasive sampling and sensitive analysis of human tear fluids at the microliter level is an important but challenging task in investigating eye health. In this work, capillary microsampling coupled with slug-flow microextraction mass spectrometry (SFME-MS) was developed for enhanced detection of analytes in human tear fluids. As low as 1.0 μL of human tear fluid could be directly sampled using a capillary, and extraction/spray solvent was then loaded into the capillary to perform slug-flow microextraction and direct nanoelectrospray ionization (nESI) of analytes. All analytical procedures, including tear microsampling, microextraction, and ionization of analytes, were performed using a capillary. Enhanced detection of therapeutic drugs and disease biomarkers in human tear fluids was successfully demonstrated. Acceptable analytical performances including sensitivity, reproducibility, and quantitation were obtained. It is found that the use of SFME could improve the nESI-MS detection of trace analytes over 100-fold that depends on the chemical properties of analytes. Overall, this study showed that SFME-nESI-MS is a highly effective method for enhanced detection of trace analytes in tear fluids and is expected to be a potentially powerful tool in significant biological and clinical applications.
Keyphrases
- mass spectrometry
- gas chromatography
- liquid chromatography
- endothelial cells
- high performance liquid chromatography
- ms ms
- ionic liquid
- loop mediated isothermal amplification
- multiple sclerosis
- liquid chromatography tandem mass spectrometry
- induced pluripotent stem cells
- epithelial mesenchymal transition
- tandem mass spectrometry
- high resolution
- healthcare
- simultaneous determination
- risk assessment
- real time pcr
- solid phase extraction
- drug delivery
- climate change
- signaling pathway
- human health
- health promotion
- drug induced