Journals / Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü Dergisi / 2020 / Cilt: 24 - Sayı: 1

Clay-Protein Nanocomposite Based Electrochemical Sensor for the Determination of Ascorbic Acid

Pages
80–89
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Real sample analysis was performed with drug samples and the recovery values ranged from 94.64% to 111.2%.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:This paper describes sensitive ascorbic acid (AA) determination on montmorillonite clay and silk protein sericinnanocomposite(MMT-Ser NC) modified pencil graphite electrode (PGE) for the first time.
📊
Key Findings & Data:As a result of the characterization studies, it was determined that the sericin was successfully converged with the montmorillonite structure, and that the MMT-Ser NCs were homogeneous and uniform, with the size of 150 nm and zeta potentials of approximately -27.6 mV.
💡
Conclusion & Impact:Real sample analysis was performed with drug samples and the recovery values ranged from 94.64% to 111.2%.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

This paper describes sensitive ascorbic acid (AA) determination on montmorillonite clay and silk protein sericinnanocomposite(MMT-Ser NC) modified pencil graphite electrode (PGE) for the first time. Nanocomposite structures were synthesized by desolvation technique and cross-linked with glutaraldehyde (GA). The synthesized MMT-Ser NC was evaluated by various methods. As a result of the characterization studies, it was determined that the sericin was successfully converged with the montmorillonite structure, and that the MMT-Ser NCs were homogeneous and uniform, with the size of 150 nm and zeta potentials of approximately -27.6 mV. MMT-Ser NCmodified electrodes were evaluated by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM).Under the optimized conditions, working linear range for the modified sensor was found as 10-1000 μM with square wave voltammetry and the limit of detection (LOD) was found as 8 μM. The relative standard deviation for reproducibility was calculated as % 4.82 (n=6). Real sample analysis was performed with drug samples and the recovery values ranged from 94.64% to 111.2%.

🔖

Cite This Article

AKBAL, O., BOLAT, G., ABACI, S. (2020). Clay-Protein Nanocomposite Based Electrochemical Sensor for the Determination of Ascorbic Acid. Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü Dergisi, Cilt: 24 - Sayı: 1, 80–89. https://ajindex.com/articles/309891

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (1)

  1. Padayatty,S.J., Katz, A., Wang, Y., Eck, P., Kwon, O., Lee, J.H., Chen, S., Corpe, C., Dutta, A., Dutta, S.K., Levine, M.2003. Vitamin C as an antioxidant: evaluation of its role in disease prevention. Journal of the American College of Nutrition, 22(1), 18–35. [2]Pisoschi, A.M., Pop, A., Serban, A.I., Fafaneata, C.2014. Electrochemical methods for ascorbic acid determination.ElectrochimicaActa, 121, 443–460. [3]Arrigoni, O., De Tullio, M.C.2002. Ascorbic acid: much more than just an antioxidant. Biochimica et Biophysica Acta, 1569(2), 1–9. [4]Bradshaw, M.P., Barril, C., Clark, A.C., Prenzler, P.D., Scollary, G.R.2011. Ascorbic acid: A review of its chemistry and reactivity in relation to a wine environment. Critical Reviews in Food Science and Nutrition, 51(6), 479–98. [5]Erdurak-Kiliç, C.S., Uslu, B., Dogan, B., Ozgen, U., Ozkan, S.A., Coskun, M.2006. Anodic voltammetric behavior of ascorbic acid and its selective determination in pharmaceutical dosage forms and some Rosa species of Turkey. Journal of Analytical Chemistry, 61(11), 1113–20. [6]Levine, M., Rumsey, S.C., Daruwala, R., Park, J.B., WangY.1999. Criteria and Recommendations for Vitamin C Intake. JAMA, 281(15), 1415. [7]Kumar, S.A., Lo, P.H., Chen, S.M.2008. Electrochemical selective determination of ascorbic acid at redox active polymer modified electrode derived from direct blue 71. Biosensors and Bioelectronics, 24(4), 518–23. [8]Pisoschi, A.M., Cheregi, M.C., Danet, A.F.2009. Total antioxidant capacity of some commercial fruit juices: Electrochemical and spectrophotometrical approaches. Molecules, 14(1), 480–93. [9]Kabasakalis, V., Siopidou, D., Moshatou, E.2000. Ascorbic acid content of commercial fruit juices and its rate of loss upon storage. Food Chemistry, 70(3), 325–28. [10]Versari, A., Mattioli, A., Parpinello, G.P., Galassi, S.2004. Rapid analysis of ascorbic and isoascorbic acids in fruit juice by capillary electrophoresis. Food Control, 15(5), 355–58. [11]Koncki, R., Lenarczuk, T., Głab, S.1999. Disposable integrated cuvette test for quantitative determination of vitamin C in pharmaceutical products. Analytica Chimica Acta, 379(1–2), 69–74. [12]Arya, S.P., Mahajan, M., Jain, P.2000. Non-spectrophotometric methods for the determination of Vitamin C. Analytica Chimica Acta, 417(1), 1–14. [13]Lykkesfeldt, J.2000. Determination of ascorbic acid and dehydroascorbic acid in biological samples by high-performance liquid chromatography using subtraction methods: Reliable reduction with