| Literature DB >> 34145703 |
Jong-Min Moon1, Hazhir Teymourian1, Ernesto De la Paz1, Juliane R Sempionatto1, Kuldeep Mahato1, Thitaporn Sonsa-Ard1, Nickey Huang1, Katherine Longardner2, Irene Litvan2, Joseph Wang1.
Abstract
Levodopa (L-Dopa) is the "gold-standard" medication for symptomatic therapy of Parkinson disease (PD). However, L-Dopa long-term use is associated with the development of motor and non-motor complications, primarily due to its fluctuating plasma levels in combination with the disease progression. Herein, we present the first example of individualized therapeutic drug monitoring for subjects upon intake of standard L-Dopa oral pill, centered on dynamic tracking of the drug concentration in naturally secreted fingertip sweat. The touch-based non-invasive detection method relies on instantaneous collection of fingertip sweat on a highly permeable hydrogel that transports the sweat to a biocatalytic tyrosinase-modified electrode, where sweat L-Dopa is measured by reduction of the dopaquinone enzymatic product. Personalized dose-response relationship is demonstrated within a group of human subjects, along with close pharmacokinetic correlation between the finger touch-based fingertip sweat and capillary blood samples.Entities:
Keywords: Levodopa; Parkinson disease; biosensor; phamacokinetics; therapeutic drug monitoring
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Year: 2021 PMID: 34145703 PMCID: PMC8373796 DOI: 10.1002/anie.202106674
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 16.823