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Updated: Jun 11, 2025

Fabrication of Three-dimensional Paper-based Microfluidic Devices for Immunoassays
Published on: March 9, 2017
Screen printed 3D microfluidic paper-based and modifier-free electroanalytical device for clozapine sensing
Mohammad Hossein Ghanbari1,2, Markus Biesalski2, Oliver Friedrich3
1Friedrich-Alexander-Universität Erlangen-Nürnberg, Power-To-X Technologies, 90762 Fürth, Germany. bastian.etzold@fau.de.
A novel 3D microfluidic paper-based electroanalytical device (μPED) enhances drug monitoring. This 3D μPED improves sensitivity and signal strength for personalized clozapine therapy in schizophrenia patients.
Area of Science:
- Electrochemistry
- Analytical Chemistry
- Materials Science
Background:
- Accessible and affordable analytical tools are crucial for personalized medicine, particularly for monitoring drug serum levels like anti-psychotics in schizophrenia.
- Microfluidic paper-based electroanalytical devices (μPEDs) offer a portable and sensitive platform, but engineering aspects like electrode arrangement are less explored.
Purpose of the Study:
- To investigate the impact of 3D electrode arrangements in modifier-free μPEDs compared to 2D arrangements.
- To demonstrate the feasibility of using screen printing for fabricating 3D μPEDs.
- To evaluate the performance of 3D μPEDs for clozapine (CLZ) sensing in human blood serum.
Main Methods:
- Fabrication of 2D and 3D microfluidic paper-based electroanalytical devices (μPEDs) using screen printing.
- Electrochemical characterization using cyclic voltammetry with [Fe(CN)6]3-/4- redox probe.
- Quantitative analysis of clozapine (CLZ) using square-wave voltammetry.
Main Results:
- The 3D μPED configuration significantly increased electrochemically active surface area and electron transfer rates compared to 2D designs.
- Screen printing was successfully employed to create the 3D μPED.
- The 3D μPED demonstrated superior signal strength for CLZ sensing.
- Optimized 3D μPED achieved a limit of detection of 1.47 μM for CLZ in human blood serum, with a linear range from 7.0 to 100 μM.
Conclusions:
- 3D electrode arrangement in μPEDs enhances electrochemical performance, leading to improved sensitivity for drug monitoring.
- Screen-printable 3D μPEDs represent a promising, cost-effective platform for personalized therapeutic drug monitoring.
- This technology holds potential for pharmacokinetic analysis and clinical applications in managing schizophrenia treatment.
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