Acoustic Wave Sensor Detection of an Ovarian Cancer Biomarker with Antifouling Surface Chemistry

Ovarian cancer (OC) must be detected in its early stages when the mortality rate is the lowest to provide patients with the best chance of survival. Lysophosphatidic acid (LPA) is a critical OC biomarker since its levels are elevated across all stages and increase with disease progression. This pape...

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Автори: Katharina Davoudian, Sandro Spagnolo, Edmund Chan, Tibor Hianik, Michael Thompson
Формат: Стаття
Мова:English
Опубліковано: MDPI AG 2024-12-01
Серія:Sensors
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Онлайн доступ:https://www.mdpi.com/1424-8220/24/24/7884
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author Katharina Davoudian
Sandro Spagnolo
Edmund Chan
Tibor Hianik
Michael Thompson
author_facet Katharina Davoudian
Sandro Spagnolo
Edmund Chan
Tibor Hianik
Michael Thompson
author_sort Katharina Davoudian
collection DOAJ
description Ovarian cancer (OC) must be detected in its early stages when the mortality rate is the lowest to provide patients with the best chance of survival. Lysophosphatidic acid (LPA) is a critical OC biomarker since its levels are elevated across all stages and increase with disease progression. This paper presents an LPA assay based on a thickness shear mode acoustic sensor with dissipation monitoring that involves a new thiol molecule 3-(2-mercaptoethanoxy)propanoic acid (HS-MEG-COOH). HS-MEG-COOH is an antifouling linker that provides (a) antifouling properties for gold substrates and (b) linking ability via its terminal carboxylic acid functional group. The antifouling ability of HS-MEG-COOH was tested in whole human serum. The new molecule was applied to the LPA assay in conjunction with a spacer molecule, 2-(2-mercaptoethoxy)ethan-1-ol (HS-MEG-OH), in a 1:1 <i>v</i>/<i>v</i> ratio. HS-MEG-COOH was covalently linked to gelsolin–actin, a protein complex probe that dissociates due to LPA-binding. LPA was detected in phosphate-buffered saline and undiluted human serum and achieved a low limit of detection (1.0 and 0.7 μM, respectively) which was below the concentration of LPA in healthy individuals. The antifouling properties of HS-MEG-COOH and the detection of LPA demonstrate the ability of the sensor to successfully identify the early-stage OC biomarker in undiluted human serum.
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spelling doaj.art-51a0b8fce28042e6b500da41c1a38d162024-12-27T14:52:20ZengMDPI AGSensors1424-82202024-12-012424788410.3390/s24247884Acoustic Wave Sensor Detection of an Ovarian Cancer Biomarker with Antifouling Surface ChemistryKatharina Davoudian0Sandro Spagnolo1Edmund Chan2Tibor Hianik3Michael Thompson4Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, ON M5S 3H6, CanadaFaculty of Mathematics, Physics and Informatics, Comenius University, Mlynská dolina F1, 842 48 Bratislava, SlovakiaDepartment of Chemistry, University of Toronto, 80 St. George Street, Toronto, ON M5S 3H6, CanadaFaculty of Mathematics, Physics and Informatics, Comenius University, Mlynská dolina F1, 842 48 Bratislava, SlovakiaDepartment of Chemistry, University of Toronto, 80 St. George Street, Toronto, ON M5S 3H6, CanadaOvarian cancer (OC) must be detected in its early stages when the mortality rate is the lowest to provide patients with the best chance of survival. Lysophosphatidic acid (LPA) is a critical OC biomarker since its levels are elevated across all stages and increase with disease progression. This paper presents an LPA assay based on a thickness shear mode acoustic sensor with dissipation monitoring that involves a new thiol molecule 3-(2-mercaptoethanoxy)propanoic acid (HS-MEG-COOH). HS-MEG-COOH is an antifouling linker that provides (a) antifouling properties for gold substrates and (b) linking ability via its terminal carboxylic acid functional group. The antifouling ability of HS-MEG-COOH was tested in whole human serum. The new molecule was applied to the LPA assay in conjunction with a spacer molecule, 2-(2-mercaptoethoxy)ethan-1-ol (HS-MEG-OH), in a 1:1 <i>v</i>/<i>v</i> ratio. HS-MEG-COOH was covalently linked to gelsolin–actin, a protein complex probe that dissociates due to LPA-binding. LPA was detected in phosphate-buffered saline and undiluted human serum and achieved a low limit of detection (1.0 and 0.7 μM, respectively) which was below the concentration of LPA in healthy individuals. The antifouling properties of HS-MEG-COOH and the detection of LPA demonstrate the ability of the sensor to successfully identify the early-stage OC biomarker in undiluted human serum.https://www.mdpi.com/1424-8220/24/24/7884lysophosphatidic acidgelsolinactinovarian cancerantifouling linkerthickness shear mode
spellingShingle Katharina Davoudian
Sandro Spagnolo
Edmund Chan
Tibor Hianik
Michael Thompson
Acoustic Wave Sensor Detection of an Ovarian Cancer Biomarker with Antifouling Surface Chemistry
Sensors
lysophosphatidic acid
gelsolin
actin
ovarian cancer
antifouling linker
thickness shear mode
title Acoustic Wave Sensor Detection of an Ovarian Cancer Biomarker with Antifouling Surface Chemistry
title_full Acoustic Wave Sensor Detection of an Ovarian Cancer Biomarker with Antifouling Surface Chemistry
title_fullStr Acoustic Wave Sensor Detection of an Ovarian Cancer Biomarker with Antifouling Surface Chemistry
title_full_unstemmed Acoustic Wave Sensor Detection of an Ovarian Cancer Biomarker with Antifouling Surface Chemistry
title_short Acoustic Wave Sensor Detection of an Ovarian Cancer Biomarker with Antifouling Surface Chemistry
title_sort acoustic wave sensor detection of an ovarian cancer biomarker with antifouling surface chemistry
topic lysophosphatidic acid
gelsolin
actin
ovarian cancer
antifouling linker
thickness shear mode
url https://www.mdpi.com/1424-8220/24/24/7884
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AT edmundchan acousticwavesensordetectionofanovariancancerbiomarkerwithantifoulingsurfacechemistry
AT tiborhianik acousticwavesensordetectionofanovariancancerbiomarkerwithantifoulingsurfacechemistry
AT michaelthompson acousticwavesensordetectionofanovariancancerbiomarkerwithantifoulingsurfacechemistry