<p>The purpose of this research is to explain the voltammetric evaluation of aprepitant (APT) using the boron-doped diamond (BDD) electrode with an anionic surfactant media. The APT was measured by cyclic voltammetry in a 0.1&#xa0;mol L<sup>− 1</sup> H<sub>2</sub>SO<sub>4</sub> solution, revealing adsorption and diffusion-controlled processes. The oxidation peaks were well-defined at + 1.5&#xa0;V (vs. Ag/AgCl). The addition of sodium dodecyl sulfate (an anionic surfactant) in the selected supporting electrolyte significantly increased the oxidation peak currents of APT. To determine APT in a 0.1&#xa0;mol L<sup>− 1</sup> H<sub>2</sub>SO<sub>4</sub> solution, a linear relationship was observed under the optimized experimental conditions, including 1.0 × 10<sup>− 4</sup> mol L<sup>− 1</sup> SDS at an accumulation potential of + 1.5&#xa0;V (vs. Ag/AgCl) for 30&#xa0;s under open-circuit conditions. The linear concentration was discovered by applying 1.0 to 25.0&#xa0;µg mL<sup>− 1</sup> (1.87 × 10<sup>− 6</sup> − 4.68 × 10<sup>− 5</sup> mol L<sup>− 1</sup>) as well as the detection limit 0.19&#xa0;µg mL<sup>− 1</sup> (3.56 × 10<sup>− 7</sup> mol L<sup>− 1</sup>). The established technology was successfully utilized to measure APT in pharmaceutical formulations and urine samples. Our research indicates that this is the first non-modified electroanalytical method for voltammetric APT detection to be identified.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

A Sensitive Electroanalytical Approach for Aprepitant Quantification in Pharmaceutical Formulations and Urine Samples at A Boron-Doped Diamond Electrode: The Role of Anionic Surfactant Media

  • Hemn A.H. Barzani,
  • Hoshyar Saadi Ali,
  • Seerwan Hamadameen Sulaiman,
  • Yavuz Yardım

摘要

The purpose of this research is to explain the voltammetric evaluation of aprepitant (APT) using the boron-doped diamond (BDD) electrode with an anionic surfactant media. The APT was measured by cyclic voltammetry in a 0.1 mol L− 1 H2SO4 solution, revealing adsorption and diffusion-controlled processes. The oxidation peaks were well-defined at + 1.5 V (vs. Ag/AgCl). The addition of sodium dodecyl sulfate (an anionic surfactant) in the selected supporting electrolyte significantly increased the oxidation peak currents of APT. To determine APT in a 0.1 mol L− 1 H2SO4 solution, a linear relationship was observed under the optimized experimental conditions, including 1.0 × 10− 4 mol L− 1 SDS at an accumulation potential of + 1.5 V (vs. Ag/AgCl) for 30 s under open-circuit conditions. The linear concentration was discovered by applying 1.0 to 25.0 µg mL− 1 (1.87 × 10− 6 − 4.68 × 10− 5 mol L− 1) as well as the detection limit 0.19 µg mL− 1 (3.56 × 10− 7 mol L− 1). The established technology was successfully utilized to measure APT in pharmaceutical formulations and urine samples. Our research indicates that this is the first non-modified electroanalytical method for voltammetric APT detection to be identified.