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A bacterial cellulose-based LiSrVO(4):Eu(3+) nanosensor platform for smartphone sensing of levodopa and dopamine: point-of-care diagnosis of Parkinson's disease

Among the catecholamines, dopamine (DA) is essential in regulating multiple aspects of the central nervous system. The level of dopamine in the brain correlates with neurological diseases such as Parkinson's disease (PD). However, dopamine is unable to cross the blood–brain barrier (BBB). There...

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Autores principales: Mahdavi, Mohammad, Emadi, Hamid, Nabavi, Seyed Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496915/
https://www.ncbi.nlm.nih.gov/pubmed/37705795
http://dx.doi.org/10.1039/d3na00297g
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author Mahdavi, Mohammad
Emadi, Hamid
Nabavi, Seyed Reza
author_facet Mahdavi, Mohammad
Emadi, Hamid
Nabavi, Seyed Reza
author_sort Mahdavi, Mohammad
collection PubMed
description Among the catecholamines, dopamine (DA) is essential in regulating multiple aspects of the central nervous system. The level of dopamine in the brain correlates with neurological diseases such as Parkinson's disease (PD). However, dopamine is unable to cross the blood–brain barrier (BBB). Therefore, levodopa (LD) is used to restore normal dopamine levels in the brain by crossing the BBB. Thus, the control of LD and DA levels is critical for PD diagnosis. For this purpose, LiSr(0.0985)VO(4):0.015Eu(3+) (LSV:0.015Eu(3+)) nanoplates were synthesized by the microwave-assisted co-precipitation method, and have been employed as an optical sensor for the sensitive and selective detection of catecholamines. The synthesized LSV:0.015Eu(3+) nanoplates emitted red fluorescence with a high quantum yield (QY) of 48%. By increasing the LD and DA concentrations, the fluorescence intensity of LSV:0.015Eu(3+) nanoplates gradually decreased. Under optimal conditions, the linear dynamic ranges were 1–40 μM (R(2) = 0.9972) and 2–50 μM (R(2) = 0.9976), and the detection limits (LOD) were 279 nM, and 390 nM for LD and DA, respectively. Herein, an instrument-free, rapid quantification visual assay was developed using a paper-based analytical device (PAD) with LSV:0.015Eu(3+) fixed on the bacterial cellulose nanopaper (LEBN) to determine LD and DA concentrations with ease of operation and low cost. A smartphone was coupled with the PAD device to quantitatively analyze the fluorescence intensity changes of LSV:0.015Eu(3+) using the color recognizer application (APP). In addition, the LSV:0.015Eu(3+) nanosensor showed acceptable repeatability and was used to analyze real human urine, blood serum, and tap water samples with a recovery of 96–107%.
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spelling pubmed-104969152023-09-13 A bacterial cellulose-based LiSrVO(4):Eu(3+) nanosensor platform for smartphone sensing of levodopa and dopamine: point-of-care diagnosis of Parkinson's disease Mahdavi, Mohammad Emadi, Hamid Nabavi, Seyed Reza Nanoscale Adv Chemistry Among the catecholamines, dopamine (DA) is essential in regulating multiple aspects of the central nervous system. The level of dopamine in the brain correlates with neurological diseases such as Parkinson's disease (PD). However, dopamine is unable to cross the blood–brain barrier (BBB). Therefore, levodopa (LD) is used to restore normal dopamine levels in the brain by crossing the BBB. Thus, the control of LD and DA levels is critical for PD diagnosis. For this purpose, LiSr(0.0985)VO(4):0.015Eu(3+) (LSV:0.015Eu(3+)) nanoplates were synthesized by the microwave-assisted co-precipitation method, and have been employed as an optical sensor for the sensitive and selective detection of catecholamines. The synthesized LSV:0.015Eu(3+) nanoplates emitted red fluorescence with a high quantum yield (QY) of 48%. By increasing the LD and DA concentrations, the fluorescence intensity of LSV:0.015Eu(3+) nanoplates gradually decreased. Under optimal conditions, the linear dynamic ranges were 1–40 μM (R(2) = 0.9972) and 2–50 μM (R(2) = 0.9976), and the detection limits (LOD) were 279 nM, and 390 nM for LD and DA, respectively. Herein, an instrument-free, rapid quantification visual assay was developed using a paper-based analytical device (PAD) with LSV:0.015Eu(3+) fixed on the bacterial cellulose nanopaper (LEBN) to determine LD and DA concentrations with ease of operation and low cost. A smartphone was coupled with the PAD device to quantitatively analyze the fluorescence intensity changes of LSV:0.015Eu(3+) using the color recognizer application (APP). In addition, the LSV:0.015Eu(3+) nanosensor showed acceptable repeatability and was used to analyze real human urine, blood serum, and tap water samples with a recovery of 96–107%. RSC 2023-08-15 /pmc/articles/PMC10496915/ /pubmed/37705795 http://dx.doi.org/10.1039/d3na00297g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Mahdavi, Mohammad
Emadi, Hamid
Nabavi, Seyed Reza
A bacterial cellulose-based LiSrVO(4):Eu(3+) nanosensor platform for smartphone sensing of levodopa and dopamine: point-of-care diagnosis of Parkinson's disease
title A bacterial cellulose-based LiSrVO(4):Eu(3+) nanosensor platform for smartphone sensing of levodopa and dopamine: point-of-care diagnosis of Parkinson's disease
title_full A bacterial cellulose-based LiSrVO(4):Eu(3+) nanosensor platform for smartphone sensing of levodopa and dopamine: point-of-care diagnosis of Parkinson's disease
title_fullStr A bacterial cellulose-based LiSrVO(4):Eu(3+) nanosensor platform for smartphone sensing of levodopa and dopamine: point-of-care diagnosis of Parkinson's disease
title_full_unstemmed A bacterial cellulose-based LiSrVO(4):Eu(3+) nanosensor platform for smartphone sensing of levodopa and dopamine: point-of-care diagnosis of Parkinson's disease
title_short A bacterial cellulose-based LiSrVO(4):Eu(3+) nanosensor platform for smartphone sensing of levodopa and dopamine: point-of-care diagnosis of Parkinson's disease
title_sort bacterial cellulose-based lisrvo(4):eu(3+) nanosensor platform for smartphone sensing of levodopa and dopamine: point-of-care diagnosis of parkinson's disease
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496915/
https://www.ncbi.nlm.nih.gov/pubmed/37705795
http://dx.doi.org/10.1039/d3na00297g
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