Pre-concentration and Sensitive Determination of Propranolol and Metoprolol Using Dispersive Solid-Phase Microextraction and High-Performance Liquid Chromatography in Biological, Wastewater, and Pharmaceutical Samples
محل انتشار: نشریه متدهای شیمیایی، دوره: 6، شماره: 10
سال انتشار: 1401
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 174
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شناسه ملی سند علمی:
JR_CHM-6-10_003
تاریخ نمایه سازی: 11 مرداد 1401
چکیده مقاله:
Determination of drugs at environmental and biological samples is a critical issue for controlling the effects of a drug on human health and environmental pollution. In the present study, a dispersive solid phase microextraction mode was developed for the preconcentration and cleanup of low amounts of propranolol and metoprolol before their determination with a high-performance liquid chromatography diode array detector. Carboxyl functionalized single-walled carbon nanotubes supported by magnetic nanoparticles (Fe۳O۴@SWCNT-COOH) were synthesized as a sorbent using a chemical procedure. Various factors affecting the microextraction method such as pH, donor phase volume, extraction desorption time, sorbent quantity solvent type and volume, and stirring rate were evaluated along with improving efficiency. The dynamic linear range of the method for the propranolol and metoprolol determination was ۰.۱-۲۳۴ and ۰.۲-۱۸۷ mg L-۱ with a determination correlation coefficient (R۲) of ۰.۹۹۸۹ and ۰.۹۹۸۴, respectively. Besides, the enrichment factor for the determination of propranolol and metoprolol were ۲۸۳.۱ and ۲۷۸.۷, respectively. Limit of detection (LOD) and limit of quantification (LOQ) were turn down by ۰.۰۶ and ۰.۲ for the analyte determination, correspondingly. Intraday and inter-day RSD% were determined for five times to determine propranolol and metoprolol at a concentration of ۲.۰ ng.mL-۱ and were lower than ۳.۲۶ and ۴.۲۹%, respectively. Determination of propranolol and metoprolol in hospital wastewater, human urine and plasma samples indicated that this proposed method can be employed to analyze the actual samples without the significant matrix effects with a recovery range of ۹۱.۰-۹۷.۲% and an RSD of less than ۵.۴۹%.
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نویسندگان
Bagher Farhadi
Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran
Mahmoud Ebrahimi
Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran
Ali Morsali
Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran
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