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Ultrasensitive Detection and Separation of Pancreatic Cancer Biomarker CA 19-9 Using a Multiphoton Laser Wave-Mixing Detector Interfaced to Capillary Electrophoresis
[Image: see text] 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-base...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10468764/ https://www.ncbi.nlm.nih.gov/pubmed/37663511 http://dx.doi.org/10.1021/acsomega.3c02845 |
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author | Liang, Jie Tong, William G. |
author_facet | Liang, Jie Tong, William G. |
author_sort | Liang, Jie |
collection | PubMed |
description | [Image: see text] 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(–8) U, and these detection limits are better than those of chemiluminescence- or ELISA- based methods. |
format | Online Article Text |
id | pubmed-10468764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104687642023-09-01 Ultrasensitive Detection and Separation of Pancreatic Cancer Biomarker CA 19-9 Using a Multiphoton Laser Wave-Mixing Detector Interfaced to Capillary Electrophoresis Liang, Jie Tong, William G. ACS Omega [Image: see text] 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(–8) U, and these detection limits are better than those of chemiluminescence- or ELISA- based methods. American Chemical Society 2023-08-16 /pmc/articles/PMC10468764/ /pubmed/37663511 http://dx.doi.org/10.1021/acsomega.3c02845 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Liang, Jie Tong, William G. Ultrasensitive Detection and Separation of Pancreatic Cancer Biomarker CA 19-9 Using a Multiphoton Laser Wave-Mixing Detector Interfaced to Capillary Electrophoresis |
title | Ultrasensitive
Detection and Separation of Pancreatic
Cancer Biomarker CA 19-9 Using a Multiphoton Laser Wave-Mixing
Detector Interfaced to Capillary Electrophoresis |
title_full | Ultrasensitive
Detection and Separation of Pancreatic
Cancer Biomarker CA 19-9 Using a Multiphoton Laser Wave-Mixing
Detector Interfaced to Capillary Electrophoresis |
title_fullStr | Ultrasensitive
Detection and Separation of Pancreatic
Cancer Biomarker CA 19-9 Using a Multiphoton Laser Wave-Mixing
Detector Interfaced to Capillary Electrophoresis |
title_full_unstemmed | Ultrasensitive
Detection and Separation of Pancreatic
Cancer Biomarker CA 19-9 Using a Multiphoton Laser Wave-Mixing
Detector Interfaced to Capillary Electrophoresis |
title_short | Ultrasensitive
Detection and Separation of Pancreatic
Cancer Biomarker CA 19-9 Using a Multiphoton Laser Wave-Mixing
Detector Interfaced to Capillary Electrophoresis |
title_sort | ultrasensitive
detection and separation of pancreatic
cancer biomarker ca 19-9 using a multiphoton laser wave-mixing
detector interfaced to capillary electrophoresis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10468764/ https://www.ncbi.nlm.nih.gov/pubmed/37663511 http://dx.doi.org/10.1021/acsomega.3c02845 |
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