Journals / Cumhuriyet Science Journal / 2021 / Cilt: 42 - Sayı: 3

Sensitive electrochemical determination of Cefpirome in human urine using differential pulse voltammetry

Pages
593–598
Publication Date
2022-10-12
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)

Cefpirome was electrochemically determined at the linear range between 2-200 μM, and the detection limit was found as 0.167 μM in pH 4.7 acetate buffer solution.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Cefpirome, which is a fourth-generation cephalosporin, was analyzed for the first time at a glassy carbon electrode using differential pulse voltammetry in this novel method.
📊
Key Findings & Data:Cefpirome was electrochemically determined at the linear range between 2-200 μM, and the detection limit was found as 0.167 μM in pH 4.7 acetate buffer solution.
💡
Conclusion & Impact:As a result, a simple, sensitive, reproducible, no time-consuming, and more environmentally friendly method was developed when compared to the literature studies.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Cefpirome, which is a fourth-generation cephalosporin, was analyzed for the first time at a glassy carbon electrode using differential pulse voltammetry in this novel method. Different experimental conditions were optimized, such as pH and electrolyte type, to achieve a high peak current. Under the optimum conditions, the oxidation of cefpirome exhibited diffusion- controlled process depending on pH. Cefpirome was electrochemically determined at the linear range between 2-200 μM, and the detection limit was found as 0.167 μM in pH 4.7 acetate buffer solution. Analysis results showed that the proposed electrochemical method could be used for the determination of cefpirome in human urine samples. A linear relationship has been obtained in the concentration range of 2-10 μM. At the same time, the detection limit was found as 0.101 μM for cefpirome in human urine. Moreover, to check the selectivity of the proposed method, the effect of some interference species, including ascorbic acid, uric acid, dopamine, glucose, Na+, K+, Ca+2, NO3 - , have also been investigated. As a result, a simple, sensitive, reproducible, no time-consuming, and more environmentally friendly method was developed when compared to the literature studies.

🔖

Cite This Article

ERKMEN, C., PALABIYIK, B. B., USLU, B. (2022). Sensitive electrochemical determination of Cefpirome in human urine using differential pulse voltammetry. Cumhuriyet Science Journal, Cilt: 42 - Sayı: 3, 593–598. https://ajindex.com/articles/477525

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (8)

  1. Nawaz M., Arayne M. S., Sultana N., Abbas H. F., Investigation of interaction studies of Cefpirome with ACE-Inhibitors in various buffers, Spectrochim. Acta - Part A Mol. Biomol. Spectrosc., 137 (2015) 1050–1054
  2. Kong X. X., Jiang J. L., Qiao B., Liu H., Cheng J. S., Yuan Y. J., The biodegradation of Cefuroxime, Cefotaxime and Cefpirome by the Synthetic Consortium with Probiotic Bacillus Clausii and investigation of their potential biodegradation pathways, Sci. Total Environ., 651 (2019) 271–280
  3. Zalewski P., Skibiński R., Szymanowska- Powałowska D., Piotrowska H., Kozak M., Pietralik Z., Bednarski W., Cielecka-Piontek J., The Radiolytic Studies of Cefpirome Sulfate in the solid state, J. Pharm. Biomed. Anal., 118 (2016) 410–416
  4. Jain R., Vikas, Voltammetric Determination of Cefpirome at Multiwalled Carbon Nanotube modified Glassy Carbon Sensor based electrode in bulk form and Pharmaceutical formulation, Colloids Surfaces B. Biointerfaces, 87(2) (2011) 423– 426
  5. Hong Y. H., Xu X. L., Li W. Q., Xu B. Z., Wu H. Q., Cheng Y., Chen H., Zhang B. S., Zhang F., A high-accuracy screening method of 44 Cephalosporins in meat using liquid Chromatography Quadrupole-Orbitrap hybrid mass spectrometry, Anal. Methods, 9(46) (2017) 6534–6548 [6] Li W., Shen H., Hong Y., Zhang Y., Yuan F., Zhang F., Simultaneous determination of 22 Cephalosporins drug residues in Pork Muscle using liquid Chromatography-Tandem mass spectrometry, J. Chromatogr. B. Anal. Technol. Biomed. Life Sci., 1022 (2016) 298– 307
  6. Zalewski, P., Skibiński R., Cielecka-Piontek J., Bednarek-Rajewska K., Development and validation of stability-indicating HPLC method for determination of Cefpirome Sulfate, Acta Pol. Pharm., 71(5) (2014) 731- 736
  7. Breilh D., Lavallee C., Fratta A., Ducint D., Cony-Makhoul P., Saux M. C., Determination of Cefepime and Cefpirome in human serum by high-performance liquid Chromatography using an ultrafiltration for antibiotics serum extraction, J. Chromatogr. B Biomed. Sci. Appl., 734(1) (1999) 121–127
  8. Kearns G.L., Johnson V.A., Hendry I.R., Wells T.G., Microanalytical high- performance liquid Chromatographic assay for Cefpirome in human milk and Urine, J. Chromatogr., 574(2) (1992) 356-60. [10]Elghobashy M. R., Bebawy L. I., Abbas S. S., and Shokry R. F., Stability-indicating HPLC and RP-TLC determination of Cefpirome Sulfate with kinetic study, Chromatographia, 76 (17–18) (2013) 1141–1151. [11]Watanabe E., Review of Sample Preparation Methods for