Disposable cerium oxide/graphene nanosheets based sensor for monitoring acebutolol in environmental samples and bio-fluids

被引:18
作者
Selvi S.V. [1 ]
Nataraj N. [1 ]
Chen T.-W. [1 ,2 ,3 ]
Chen S.-M. [1 ]
Balu P. [5 ]
Liu X. [4 ]
机构
[1] Electroanalysis and Bioelectrochemistry Lab, Department of Chemical Engineering and Biotechnology, National Taipei University of Technology, No. 1, Section 3, Chung-Hsiao East Road, Taipei
[2] Research and Development Center for Smart Textile Technology, National Taipei University of Technology, No.1, Section 3, Chung-Hsiao East Road, Taipei
[3] Department of Materials, Imperial College London, London
[4] Key Laboratory of Education Ministry for Soft Chemistry and Functional Materials, Nanjing University of Science and Technology, Nanjing
[5] Department of Biotechnology, School of Life Science, Vels Institute of Science, Technology and Advanced Studies, Chennai, Tamilnadu
关键词
Conducting substrate; Environmental pollution; Human urine; Metal Oxide-Graphene nanosheets; River water;
D O I
10.1016/j.jece.2022.107182
中图分类号
学科分类号
摘要
The production and utilization of medicines strives to be an essential factor in the modern world in treatment, diagnosis and prevention. On the other hand, the medical discharge and the unmetabolized drugs all turns out into environmental polluting agents. The demand for detecting and solving these issues are essential. Herein, we report an electrochemical sensor for quantifying β-adrenoreceptor blocker acebutolol (ACT) in environmental and biological samples. Cerium oxide (CeO2) was implied with graphene nanosheets (GNS) as highly conducting material for electrochemically detecting ACT. The structural and morphological studies were studied and electrochemical analysis were also performed to efficiently study oxidation mechanism of ACT at CeO2/GNS interface. Electrochemical impedance spectroscopy (EIS) proved the higher conducting behavior of CeO2/GNS. Moreover, CeO2/GNS/SPCE holds higher surface area with more edge sites facilitating the electro-oxidation of ACT. The linear range of detecting ACT was in the range of 0.039 μM to 486.6 μM. The limit of detection was found to be 0.007 μM with the sensitivity about 27.3 μAμM−1cm−2. The real samples like river water and urine samples were utilized for real time detection of ACT. Thus, the fabricated electrode with more efficiency and higher conducting property will enhance the real time sensing of ACT in environmental and biological samples. © 2022 Elsevier Ltd
引用
收藏
相关论文
共 36 条
[1]  
To M.H., Hadi P., Hui C.W., Lin C.S.K., McKay G., Mechanistic study of atenolol, acebutolol and carbamazepine adsorption on waste biomass derived activated carbon, J. Mol. Liq., 241, pp. 386-398, (2017)
[2]  
Shi W., Chu Y., Xia M., Wang F., Fu C., The adsorption performance and micro-mechanism of MoS2/montmorillonite composite to atenolol and acebutolol: adsorption experiments and a novel visual study of interaction, Ecotoxicol. Environ. Saf., 213, (2021)
[3]  
Tay K.S., Madehi N., Ozonation of acebutolol in aqueous solution: ozonation by-products and degradation pathway, Sep. Purif. Technol., 135, pp. 48-63, (2014)
[4]  
Chen T.W., Kumar J.V., Chen S.M., Mutharani B., Karthik R., Nagarajan E.R., Muthuraj V., Rational construction of novel rose petals-like yttrium molybdate nanosheets: a Janus catalyst for the detection and degradation of cardioselective β-blocker agent acebutolol, Chem. Eng. J., 359, pp. 1472-1485, (2019)
[5]  
Ayad M.M., Abdellatef H.E., El-Henawee M.M., El-Sayed H.M., Spectrophotometric and spectrofluorimetric methods for analysis of acyclovir and acebutolol hydrochloride, Spectrochim. Acta - Part A Mol. Biomol. Spectrosc., 66, pp. 106-110, (2007)
[6]  
Radha A., Singh A., Sharma L., Thakur K.K., Molecular interactions of acebutolol hydrochloride to human serum albumin: a combined calorimetric, spectroscopic and molecular modelling approach, Mater. Today Proc., 44, pp. 1700-1706, (2021)
[7]  
Lin A.Y.C., Lin C.A., Tung H.H., Chary N.S., Potential for biodegradation and sorption of acetaminophen, caffeine, propranolol and acebutolol in lab-scale aqueous environments, J. Hazard. Mater., 183, pp. 242-250, (2010)
[8]  
Muta K., Fukami T., Nakajima M., A proposed mechanism for the adverse effects of acebutolol: CES2 and CYP2C19-mediated metabolism and antinuclear antibody production, Biochem. Pharmacol., 98, pp. 659-670, (2015)
[9]  
Rakibe U., Tiwari R., Mahajan A., Rane V., Wakte P., LC and LC–MS/MS studies for the identification and characterization of degradation products of acebutolol, J. Pharm. Anal., 8, pp. 357-365, (2018)
[10]  
Abdellatef H.E., El-Henawee M.M., El-Sayed H.M., Ayad M.M., Spectrophotometric and spectrofluorimetric methods for analysis of tramadol, acebutolol and dothiepin in pharmaceutical preparations, Spectrochim. Acta - Part A Mol. Biomol. Spectrosc., 65, pp. 1087-1092, (2006)