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  5. Screen printed 3D microfluidic paper-based and modifier-free electroanalytical device for clozapine sensing
 
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2024
Zweitveröffentlichung
Artikel
Verlagsversion

Screen printed 3D microfluidic paper-based and modifier-free electroanalytical device for clozapine sensing

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Hauptpublikation
D4AN01136H.pdf
CC BY 3.0 Unported
Format: Adobe PDF
Size: 3.41 MB
TUDa URI
tuda/12694
URN
urn:nbn:de:tuda-tuprints-286500
DOI
10.26083/tuprints-00028650
Autor:innen
Ghanbari, Mohammad Hossein ORCID 0000-0003-0951-8028
Biesalski, Markus ORCID 0000-0001-6662-0673
Friedrich, Oliver ORCID 0000-0003-2238-2049
Etzold, Bastian J. M. ORCID 0000-0001-6530-4978
Kurzbeschreibung (Abstract)

The increasing demand in healthcare for accessible and cost-effective analytical tools is driving the development of reliable platforms to the customization of therapy according to individual patient drug serum levels, e.g. of anti-psychotics in schizophrenia. A modifier-free microfluidic paper-based electroanalytical device (μPED) holds promise as a portable, sensitive, and affordable solution. While many studies focus on the working electrode catalysts, improvements by engineering aspects e.g. of the electrode arrangement are less reported. In our study, we demonstrate the enhanced capabilities of the 3D electrode layout of μPED compared to 2D μPED arrangements. We especially show that screen printing can be employed to prepare 3D μPEDs. We conducted a comparison of different 2D and 3D electrode arrangements utilizing cyclic voltammetry in [Fe(CN)₆]³⁻/⁴⁻, along with square-wave voltammetry for clozapine (CLZ) sensing. Our findings reveal that the utilization of the 3D μPED leads to an increase in both the electrochemically active surface area and the electron transfer rate. Consequently, this enhancement contributes to improve sensitivity in the CLZ sensing. The 3D μPED clearly outperforms the 2D μPED arrangement in terms of signal strength. With the 3D μPED under the optimized conditions, a linear dose–response for a concentration range from 7.0 to 100 μM was achieved. The limit of detection and sensitivity was determined to be 1.47 μM and 1.69 μA μM⁻¹ cm⁻², respectively. This evaluation is conducted in the context of detection and determination of CLZ in a human blood serum sample. These findings underscore the potential of the 3D μPED for future applications in pharmacokinetic analyses and clinical tests to personalize the management of schizophrenia.

Sprache
Englisch
Fachbereich/-gebiet
07 Fachbereich Chemie > Ernst-Berl-Institut > Fachgebiet Makromolekulare Chemie > Makromolekulare Chemie und Papierchemie
DDC
500 Naturwissenschaften und Mathematik > 540 Chemie
Institution
Universitäts- und Landesbibliothek Darmstadt
Ort
Darmstadt
Titel der Zeitschrift / Schriftenreihe
Analyst
Startseite
5411
Endseite
5422
Jahrgang der Zeitschrift
149
Heftnummer der Zeitschrift
22
ISSN
1364-5528
Verlag
The Royal Society of Chemistry
Ort der Erstveröffentlichung
Cambridge
Publikationsjahr der Erstveröffentlichung
2024
Verlags-DOI
10.1039/d4an01136h
PPN
53245216X

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