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Updated: Mar 9, 2026

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Published on: August 4, 2023
Single Drop Electroanalysis and Interfacial Interactions: Sensitivity versus Limit of Detection†
Charuksha Walgama1, Matthew Gallman1, Sadagopan Krishnan1
1C. Walgama, M. Gallman, S. Krishnan, Department of Chemistry, Oklahoma State University, Stillwater, OK, USA 74078.
This study introduces a novel electroanalytical method using modified screen-printed electrodes for detecting pharmaceutical compounds. The technique offers high sensitivity and a wide dynamic range for analyzing acetaminophen, nicotine, and other vital substances.
Area of Science:
- Electrochemistry
- Materials Science
- Analytical Chemistry
Background:
- Screen-printed electrodes (SPEs) are versatile platforms for electrochemical sensing.
- Carboxylated multiwalled carbon nanotubes (MWCNT-COOH) offer unique surface properties for analyte interaction.
- Accurate quantification of pharmaceutical compounds in complex matrices remains a challenge.
Purpose of the Study:
- To develop a sensitive and reliable single-drop electroanalytical method for detecting pharmaceutically relevant compounds.
- To investigate the role of MWCNT-COOH surface modifications in enhancing analyte detection.
- To validate the method's applicability to real-world pharmaceutical samples.
Main Methods:
- Utilizing screen-printed electrodes (SPEs) modified with carboxylated multiwalled carbon nanotubes (MWCNT-COOH).
- Performing single-drop electroanalytical measurements for acetaminophen, nicotine, ascorbic acid, and NADH.
- Analyzing the influence of polar and nonpolar interactions on sensitivity and detection limits.
Main Results:
- Achieved highly sensitive detection of target analytes within a single drop of solution.
- Demonstrated a wide dynamic range attributed to combined polar/nonpolar interactions with MWCNT-COOH.
- Showcased excellent recovery rates when applying the method to commercial pharmaceutical samples.
Conclusions:
- The developed single-drop electroanalytical method using MWCNT-COOH modified SPEs is effective for sensitive and accurate quantification of key pharmaceutical compounds.
- Analyte interaction with the sensor surface, involving both polar and nonpolar forces, critically influences sensitivity and detection limits.
- This approach holds significant promise for rapid, on-site analysis of pharmaceuticals in various real-world applications.
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