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Grant: Research Tools and Instruments

University of Windsor

$149,940.00

Electrochemical Surface Enhanced Raman Spectroscopy Platform for Disease Detection and Physicochemical Characterization

FY 2024-25

Summary
The requested instrumentation is for two technologies, Raman spectroscopy and electrochemistry, which we will combine as a single research platform. Raman uses a laser to provide a unique signal for every type of molecule based on molecular vibrations. This "vibrational fingerprint" allows easy identification of a sample, but the downside of Raman is that its signal is weak for low concentration samples. This problem is solved by a method called surface-enhanced Raman spectroscopy (SERS), which typically boosts the signal by at least a million-fold and often more. SERS occurs when the analyte molecule is on or near or gold or silver nanoparticles (NPs) and the laser is focussed on them. Concentrated NP paste is often dried on a surface, and the NPs can be modified to capture a target molecule. The signal boost in SERS makes it a popular technique for scientists and engineers who research new ways to diagnose diseases with low concentration biomarkers. A less commonly researched variation of SERS is called electrochemical SERS (EC-SERS). In this method, the NPs are dried on an electrode, it is exposed to an analyte, immersed in an electrolyte solution, and then a voltage is applied while recording SERS. EC-SERS has many benefits, including boosting the signal even more than traditional SERS and controlling how molecules interact with the NPs. For example, a positively charged molecule could be brought closer to a negatively charged surface. This is important because all SERS signals require the molecule to be very close to the NPs (10 nm or less). As another example, unwanted molecules that interfere with the signal can be removed from the surface. A classic case is negatively charged citrate, which is left over from making NPs and stuck on their surface. It is best to remove the citrate, as it creates an interfering signal. I am requesting funding for an EC-SERS platform. I am a new assistant professor and early career researcher with expertise in EC-SERS, but we do not have the instruments. With them, I can drive innovation and train the next generation of scientists with expertise in healthcare diagnostics. My research goal is to develop the EC-SERS platform for early disease detection. We will start with the fundamentals of this underexplored technology, but as practical examples, we will work on detecting molecules that provide early warning for prostate and ovarian cancers. My other area of research expertise is DNA nanotechnology, which can use specially designed DNA to capture target molecules. By chemically modifying NPs with DNA and drying them on a disposable material, we will use EC-SERS to detect molecules found in urine that can help with earlier diagnosis of these cancers. Research students trained on EC-SERS will gain highly employable skills in spectroscopy, electrochemistry, nanomaterials, DNA chemistry, safety using biofluids and lasers, and experience in clinical collaboration, all in the context of making a biomedical device.
Program
Research Tools and Instruments
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
RTI-2025-00715
Name nom
Harroun, Scott
Department département
Chemistry and Biochemistry
Organization id
37
Institution établissement
University of Windsor
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2024
Competition year année de concours
2025
Award amount
149940
Program id
RTI
Program name en
Research Tools and Instruments
Program name fr
Outils et instruments de recherche
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1604
Committee name en
Chemistry (RTI)
Committee name fr
Chimie (OIR)
Area of application code
1102
Area of application group en
Health, education and social services
Area of application group fr
Santé publique, éducation et services sociaux
Area of application en
Biomedical engineering
Area of application fr
Génie biomédical
Research subject code
3505
Research subject group en
Analytical chemistry
Research subject group fr
Chimie analytique
Research subject en
Analytical spectroscopy
Research subject fr
Spectroscopie analytique
Field of research list names en
Not available
Field of research list names fr
Non disponible
Socioeconomic objective list names en
Not available
Socioeconomic objective list names fr
Non disponible
Application title
Electrochemical Surface Enhanced Raman Spectroscopy Platform for Disease Detection and Physicochemical Characterization
Keywords
surface-enhanced raman spectroscopy (sers); electrochemistry; biomedical diagnostics; biosensors; gold and silver nanoparticles; dna aptamer; dna nanotechnology; biomarkers of disease; cancer detection; point-of-care devices
Application summary
The requested instrumentation is for two technologies, Raman spectroscopy and electrochemistry, which we will combine as a single research platform. Raman uses a laser to provide a unique signal for every type of molecule based on molecular vibrations. This "vibrational fingerprint" allows easy identification of a sample, but the downside of Raman is that its signal is weak for low concentration samples. This problem is solved by a method called surface-enhanced Raman spectroscopy (SERS), which typically boosts the signal by at least a million-fold and often more. SERS occurs when the analyte molecule is on or near or gold or silver nanoparticles (NPs) and the laser is focussed on them. Concentrated NP paste is often dried on a surface, and the NPs can be modified to capture a target molecule. The signal boost in SERS makes it a popular technique for scientists and engineers who research new ways to diagnose diseases with low concentration biomarkers. A less commonly researched variation of SERS is called electrochemical SERS (EC-SERS). In this method, the NPs are dried on an electrode, it is exposed to an analyte, immersed in an electrolyte solution, and then a voltage is applied while recording SERS. EC-SERS has many benefits, including boosting the signal even more than traditional SERS and controlling how molecules interact with the NPs. For example, a positively charged molecule could be brought closer to a negatively charged surface. This is important because all SERS signals require the molecule to be very close to the NPs (10 nm or less). As another example, unwanted molecules that interfere with the signal can be removed from the surface. A classic case is negatively charged citrate, which is left over from making NPs and stuck on their surface. It is best to remove the citrate, as it creates an interfering signal. I am requesting funding for an EC-SERS platform. I am a new assistant professor and early career researcher with expertise in EC-SERS, but we do not have the instruments. With them, I can drive innovation and train the next generation of scientists with expertise in healthcare diagnostics. My research goal is to develop the EC-SERS platform for early disease detection. We will start with the fundamentals of this underexplored technology, but as practical examples, we will work on detecting molecules that provide early warning for prostate and ovarian cancers. My other area of research expertise is DNA nanotechnology, which can use specially designed DNA to capture target molecules. By chemically modifying NPs with DNA and drying them on a disposable material, we will use EC-SERS to detect molecules found in urine that can help with earlier diagnosis of these cancers. Research students trained on EC-SERS will gain highly employable skills in spectroscopy, electrochemistry, nanomaterials, DNA chemistry, safety using biofluids and lasers, and experience in clinical collaboration, all in the context of making a biomedical device.