A hybrid nanocomposite of CeO2-ZnO-chitosan as an enhanced sensing platform for highly sensitive voltammetric determination of paracetamol and its degradation product p-aminophenol

被引:30
作者
Almandil, Noor B. [1 ]
Ibrahim, Mohamed [1 ]
Ibrahim, Hossieny [2 ]
Kawde, Abdel-Nasser [3 ]
Shehatta, Ibrahim [4 ]
Akhtar, Sultan [5 ]
机构
[1] Imam Abdulrahman Bin Faisal Univ, Inst Res & Med Consultat, Dept Clin Pharm Res, POB 1982, Dammam 31441, Saudi Arabia
[2] Assiut Univ, Fac Sci, Chem Dept, Assiut, Egypt
[3] King Fahd Univ Petr & Minerals, Coll Sci, Chem Dept, Dhahran 31261, Saudi Arabia
[4] Imam Abdulrahman Bin Faisal Univ, Basic & Appl Sci Res Ctr BASRC, POB 1982, Dammam 31441, Saudi Arabia
[5] Imam Abdulrahman Bin Faisal Univ, Inst Res & Med Consultat, Electron Microscopy Unit, POB 1982, Dammam 31441, Saudi Arabia
关键词
PHARMACEUTICAL FORMULATIONS; ELECTROCHEMICAL SENSOR; GOLD NANOPARTICLES; COMPOSITE FILM; SPECTROPHOTOMETRIC DETERMINATION; ELECTRODE; ACETAMINOPHEN; BIOSENSOR; 4-AMINOPHENOL; SAMPLES;
D O I
10.1039/c9ra01587f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For the determination of paracetamol (PAR) and its primary degradation product (p-aminophenol, PAP) a highly selective electrochemical sensor was fabricated. A glassy carbon microspheres paste electrode (GCMPE) was modified with a CeO2-ZnO-chitosan hybrid nanocomposite (CeO2-ZnO-CS) which was characterized by X-ray diffraction and transmission electron microscopy. The CeO2-ZnO-CS/GCMPE was characterized by scanning electron microscopy, and cyclic voltammetry. The modified GCMPE exhibits excellent electrocatalytic activity for the determination of PAR and PAP separately or simultaneously, typically at working potentials of 0.38 and 0.09 V vs. Ag/AgCl. The square wave voltammetric response in solutions of near-neutral pH value increases linearly in the 20 nM to 1.8 M PAR concentration range, and the lower LOD is 0.86 nM. The sensor is shown to enable the determination of PAR even in the presence of a 180-fold excess of PAP. PAR and PAP can also be simultaneously determined, and the LODs for PAR and PAP are 0.98 nM and 9.5 nM, respectively. The results agreed well with data obtained using other electrodes. The sensor is reproducible and stable over eight weeks, and interference by biologically essential compounds is negligible. The method was applied to the determination of PAR in pharmaceutical formulations and in spiked blood serum and urine samples. The relative standard deviations ranged from 97.5 to 102.0%.
引用
收藏
页码:15986 / 15996
页数:11
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