Publication | Closed Access
Microfluidic Electrochemical Sensor for Cerebrospinal Fluid and Blood Dopamine Detection in a Mouse Model of Parkinson’s Disease
102
Citations
43
References
2020
Year
EngineeringAnalytical MicrosystemsNeurophysiological BiomarkersOrgan-on-a-chipBiomedical EngineeringNeurochipSocial SciencesMicrofluidic Electrochemical SensorBiosensing SystemsNeurologyClinical ChemistryMicrofluidicsMouse ModelNew Microfluidic DeviceBiomedical AnalysisDecreased DopamineDopamineDopamine ResearchNeurodegenerative DiseasesBiomedical SensorsNeuroengineeringNeurophysiologyCellular NeuroscienceBiomedical DiagnosticsDopaminergic NeuronsBlood Dopamine DetectionLab-on-a-chipNeuroscienceBrain ElectrophysiologyElectrophysiologyElectroanalytical Sensor
Parkinson's disease (PD) is a progressive neurodegenerative disorder involving dopaminergic neurons from the substantia nigra. The loss of dopaminergic neurons results in decreased dopamine (DA) release in the striatum and thus impaired motor functions. DA is one of the key neurotransmitters monitored for the diagnosis and during the progression and treatment of PD. Therefore, sensitive and selective DA detection methods are of high clinical relevance. In this study, a new microfluidic device utilized for electrochemical DA detection is reported. The microfluidic sensing device operates in the range of 0.1-1000 nM DA requiring only ∼2.4 μL sample volume, which corresponds to detectable 240 amol of DA. Using this sensor, we were able to monitor the changes in DA levels in cerebrospinal fluid and plasma of a mouse model of PD and following the treatment of drug l-3,4-dihydroxyphenylalanine.
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