Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/10737
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dc.contributor.authorTIMAKWE, SAPOKAZIen_US
dc.contributor.authorMatoetoe, Mangakaen_US
dc.date.accessioned2026-08-25T08:50:46Z-
dc.date.available2026-08-25T08:50:46Z-
dc.date.issued2025-
dc.identifier.citationTimakwe, S & Matoetoe, M. 2025. Silver nanoclay human albumin serum composite electrochemical biosensor for quantification of zidovudine in tablets. Pharmaceutical Research, 42:2157-2167. [https://doi.org/10.1007/s11095-025-03954-9]en_US
dc.identifier.issn1573-904X (Online)-
dc.identifier.urihttp://hdl.handle.net/11189/10737-
dc.description.abstractObjective This work aims to develop an electrochemical biosensor for the analysis of zidovudine (ZDV) in commercial tablets. Method The biosensor utilised silver nanoclay composites (AgNCs) together with drop-coated Human Serum Albumin (HSA) on a glassy carbon electrode (GCE/AgNCs/HSA). The electrochemical properties of the GCE/AgNCs/HSA were studied using cyclic voltammetry (CV) and analysed using the Randles–Sevcik equation. Procedurally, optimised differential pulse voltammetry (DPV) technique in 1 M PBS, pH 7.04, was used to determine analytical parameters of the methods, validation, and study of commercial tablets. Results The optimum procedural conditions used were -0.4 V to -1 V potential range, 0.0405 V step potential, 0.075 V modulation amplitude, 0.01 s modulation time, and 0.25 s interval time. GCE/AgNCs/HSA film’s electrochemical properties obtained were a diffusion coefficient (D) of 1.55 × 10–11 cm2.s-1, a heterogeneous rate constant (Ks) of 3.40 × 10–6 cm.s1, with two electrons. The calibration graph linear range was from 0.12 to 6.98 μM with a low limit of detection (LOD) of 0.3 μM, and 1.0 μM limit of quantification (LOQ). Method validation showed an acceptable %RSD for reproducibility and repeatability. The sensor was stable over 10 days and remained unaffected by the presence of the interferences studied. The commercial study of 300 mg commercial tablets was found to be 301.3 mg with 1.9% RSD, which is in agreement with the tablet's stated amount. Conclusion The development of the GCE/AgNCs/HSA biosensor was successful and efficiently used to quantify ZDV in tablets.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofPharmaceutical Researchen_US
dc.subjectBiosensorsen_US
dc.subjectHuman serum albuminen_US
dc.subjectSilver nanoclay composites en_US
dc.subjectZidovudineen_US
dc.titleSilver nanoclay human albumin serum composite electrochemical biosensor for quantification of zidovudine in tabletsen_US
dc.identifier.doihttps://doi.org/10.1007/s11095-025-03954-9-
dc.typeArticleen_US
Appears in Collections:Appsc - Journal Articles (DHET subsidised)
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