| Literature DB >> 32786441 |
Mehmet Senel1, Esma Dervisevic2, Sammy Alhassen1, Muamer Dervisevic3,4, Amal Alachkar1, Victor J Cadarso2,5, Nicolas H Voelcker3,4,5.
Abstract
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.Entities:
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Year: 2020 PMID: 32786441 DOI: 10.1021/acs.analchem.0c02032
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986