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<ArticleSet>
<Article>
<Journal>
<PublisherName>OICC Press</PublisherName>
<JournalTitle>Iranian Journal of Catalysis</JournalTitle>
<Issn>2345-4865</Issn>
<Volume>15</Volume>
<Issue>3</Issue>
<PubDate PubStatus="epublish">
<Year>2025</Year>
<Month>09</Month>
<Day>30</Day>
</PubDate>
</Journal>
<ArticleTitle>Synthesis of MXene as a Modifier of Screen-Printed Carbon Electrode for the Measurement of Clonazepam as an Anesthetic Drug</ArticleTitle>
<VernacularTitle></VernacularTitle>
<FirstPage></FirstPage>
<LastPage></LastPage>
<ELocationID EIdType="doi">10.57647/j.ijc.2025.1503.29</ELocationID>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>Mahbobe</FirstName>
<LastName>Eghbali</LastName>
<Affiliation>School of Medicine, Kashan University of Medical Sciences, Kashan, Iran</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Esmail</FirstName>
<LastName>Sohouli</LastName>
<Affiliation>Department of Chemistry, Faculty of Science, Electrochemical Sensors Research Laboratory, Shahid Rajaee Teacher Training University, Lavizan, Tehran, Iran</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Amin</FirstName>
<LastName>Moradi-hsanabad</LastName>
<Affiliation>Autoimmune diseases research center, Kashan University of Medical Sciences, Kashan, Iran</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Gholamreza</FirstName>
<LastName>Mostafai</LastName>
<Affiliation>Department of Environmental Health, School of Health Kashan University of Medical Sciences, Kashan, Iran</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Mehdi</FirstName>
<LastName>Rahiminasarabadi</LastName>
<Affiliation>Institute of Electronic and Sensor Materials, TU Bergakademie, Freiberg, Germany</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Reza</FirstName>
<LastName>Hosseiniara</LastName>
<Affiliation>Research Center for Biochemistry and Nutrition in Metabolic Diseases, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, Iran</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Maryam</FirstName>
<LastName>Akbari</LastName>
<Affiliation>Department of Surgery, School of Medicine, Kashan University of Medical Sciences, Kashan, Iran</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Amir Hossein</FirstName>
<LastName>Mohammadi</LastName>
<Affiliation>Research Center for Biochemistry and Nutrition in Metabolic Diseases, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, Iran</Affiliation>
<Identifier Source="ORCID">https://orcid.org/0000-0003-4157-3588</Identifier>
</Author>
<Author>
<FirstName>Ali</FirstName>
<LastName>Sobhani nasab</LastName>
<Affiliation>Physiology Research Center, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, Iran</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
</AuthorList>
<PublicationType>Journal Article</PublicationType>
<History>
<PubDate PubStatus="received">
<Year>2025</Year>
<Month>09</Month>
<Day>30</Day>
</PubDate>
</History>
<Abstract>Benzodiazepines are psychoactive compounds with sedative, hypnotic, anti-anxiety, anticonvulsant, muscle relaxant, and anti-inflammatory effects. The increasing use of benzodiazepine anesthetics in recent years highlights the importance of analyzing these drugs in biological fluids to ensure therapeutic effectiveness, monitor concentrations, identify toxic levels, minimize negative effects, and enhance understanding of their function in biological matrices. In this study, we present the fabrication and electrochemical assessment of a novel sensing platform with high sensitivity to the drug clonazepam (CLZP). The synthesized electrode modifier, comprising MXE, was characterized using Fourier transform infrared spectrometry, scanning electron microscopy, and XRD techniques. The electrode modifier was applied to a screen-printed carbon electrode surface using the drop-casting method. The modification of the electrode with the proposed nanocomposite led to an increase in the current observed during the reduction of clonazepam and a decrease in the peak potential required for reduction. This enhancement in the electrochemical response to clonazepam reduction suggests a synergistic effect between MXE and the screen-printed carbon electrode. In optimal circumstances, the developed sensor displayed a direct relationship between the reduction peak current and CLZP concentrations within the 1 to 100 μM range, achieving a detection limit of 0.3 μM. The sensor was successfully employed for the accurate measurement of CLZP in human serum and pharmaceutical samples, demonstrating excellent sensitivity, enduring stability, and consistent reproducibility.
Highlights
·       A novel MXE-based sensor was developed for the sensitive electrochemical detection of clonazepam.
·       The SPE/MXE platform demonstrated excellent conductivity, stability, and biocompatibility for CLZP analysis.
·       The fabricated sensor showed a wide linear detection range (1–100 µM) and a low detection limit (0.3 µM).
·       The method was successfully applied for the quantification of CLZP in pharmaceutical tablets and human serum samples.
·       This approach provides a fast, cost-effective, and reliable strategy for the real-time monitoring of anesthetic drugs.</Abstract>
<ObjectList>
<Object Type="keyword">
<Param Name="value">Anesthetic drugs</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Benzodiazepine</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Clonazepam</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Magzen</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Printed carbon electrode</Param>
</Object>
</ObjectList>
</Article>
</ArticleSet>