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dc.contributor.authorSamanci, Seyda Nur
dc.contributor.authorKaya, S. Irem
dc.contributor.authorUnal, Mehmet Altay
dc.contributor.authorOzkan, Sibel A.
dc.date.accessioned2025-12-28T16:39:53Z
dc.date.available2025-12-28T16:39:53Z
dc.date.issued2025
dc.identifier.issn1618-2642
dc.identifier.issn1618-2650
dc.identifier.urihttps://doi.org/10.1007/s00216-025-06261-9
dc.identifier.urihttps://hdl.handle.net/20.500.12933/2183
dc.description.abstractAn advantageous electrochemical sensor was designed and fabricated for the sensitive and selective analysis of abacavir, an antiviral agent, by integrating the molecularly imprinted polymer (MIP) strategy and nanomaterial-based performance enhancement. The molecular imprinting was achieved on the glassy carbon electrode (GCE) surface through photopolymerization, using acrylamide (ACR) as the functional monomer and abacavir (ABC) as the template drug, and the system was computationally designed. Amine-functionalized multi-walled carbon nanotubes (MWCNT-NH2) were incorporated into the polymeric network as a supporter to improve binding efficiency, active surface area, and porosity. The successfully formed MIP and specific recognition capability were verified through electrochemical and microscopic characterizations using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR) methods. A systematic optimization procedure was followed to design an efficient MIP sensor. As a result, the ACR-ABC/MWCNT-NH2@MIP/GCE sensor exhibited a linear response in the range of 0.2 and 1 pM for standard solution and serum sample (corresponding correlation coefficient value of 0.999), with the corresponding limit of detection (LOD) values of 26.5 fM and 8.04 fM. In both solutions, good RSD% values (1.23% and 1.48%) were obtained, confirming the sensor's repeatability performance. Detailed selectivity tests validated the sensor's high affinity to ABC in the presence of structurally and pharmaceutically related drugs (lamivudine, zidovudine, tenofovir, etc.). The relative imprinting factor (IF') values were found to be higher than 2 for each compound. The ACR-ABC/MWCNT-NH2@MIP/GCE sensor's sensitive and selective determination performance was further validated in serum and tablet samples, providing reliable recovery results (98.99-102.01%). Additionally, the Analytical GREEnness Metric Approach (AGREE), the Analytical Greenness Metric for Sample Preparation (AGREEprep), the Blue Applicability Grade Index (BAGI), and the Analytical Greenness Assessment Tool for Molecularly Imprinted Polymer Synthesis (AGREEMIP) tools were utilized to assess sensor's green profile. The ACR-ABC/MWCNT-NH2@MIP/GCE sensor demonstrated its potential to provide a selective, reliable, low-cost, and efficient analytical tool for ABC analysis.
dc.description.sponsorshipScientific and Technological Research Council of Turkiye (TUBITAK) [BIDEB/2211-A]
dc.description.sponsorshipSeyda Nur Samanci thanks the financial support from the Scientific and Technological Research Council of Turkiye (TUBITAK) under the BIDEB/2211-A Ph.D. Scholarship Program.
dc.language.isoen
dc.publisherSpringer Heidelberg
dc.relation.ispartofAnalytical And Bioanalytical Chemistry
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAbacavir
dc.subjectMolecularly imprinted polymer
dc.subjectElectrochemical sensor
dc.subjectNanomaterial
dc.titleEco-friendly nanoscale recognition: a MIP-based electrochemical sensor for selective determination of abacavir in pharmaceutical and serum samples
dc.typeArticle
dc.departmentAfyonkarahisar Sağlık Bilimleri Üniversitesi
dc.identifier.doi10.1007/s00216-025-06261-9
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.department-temp[Samanci, Seyda Nur; Ozkan, Sibel A.] Ankara Univ, Fac Pharm, Dept Analyt Chem, Ankara, Turkiye; [Samanci, Seyda Nur] Ankara Univ, Grad Sch Hlth Sci, Ankara, Turkiye; [Samanci, Seyda Nur] Afyonkarahisar Hlth Sci Univ, Fac Pharm, Dept Analyt Chem, Afyon, Turkiye; [Kaya, S. Irem] Univ Hlth Sci, Gulhane Fac Pharm, Dept Analyt Chem, Ankara, Turkiye; [Unal, Mehmet Altay] Ankara Univ, Stem Cell Inst, Ankara, Turkiye
dc.identifier.pmid41390585
dc.identifier.scopus2-s2.0-105024889984
dc.identifier.scopusqualityN/A
dc.identifier.wosWOS:001637501800001
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.snmzKA_WoS_20251227


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