Development of a deep eutectic solvent-based ultrasound-assisted homogenous liquid-liquid microextraction method for simultaneous extraction of daclatasvir and sofosbuvir from urine samples

Development of a deep eutectic solvent-based ultrasound-assisted homogenous liquid-liquid microextraction method for simultaneous extraction of daclatasvir and sofosbuvir from urine samples


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نویسندگان: ابوالقاسم جویبان , محمدرضا افشار مقدم , مریم خوب نسب جعفری

کلمات کلیدی: Homogenous liquid–liquid microextraction Deep eutectic solvent Urine High performance liquid chromatography–diode array detector

نشریه: 18344 , 114254 , 204 , 2021

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نویسنده ثبت کننده مقاله محمدرضا افشار مقدم
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات ایمنی غذا و دارو
کد مقاله 76428
عنوان فارسی مقاله Development of a deep eutectic solvent-based ultrasound-assisted homogenous liquid-liquid microextraction method for simultaneous extraction of daclatasvir and sofosbuvir from urine samples
عنوان لاتین مقاله Development of a deep eutectic solvent-based ultrasound-assisted homogenous liquid-liquid microextraction method for simultaneous extraction of daclatasvir and sofosbuvir from urine samples
ناشر 5
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت

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An ultrasound-assisted homogenous liquid–liquid microextraction method using a new deep eutectic solvent was proposed for the extraction of daclatasvir and sofosbuvir from urine. The analytes were determined by high performance liquid chromatography–diode array detector. The deep eutectic solvent was prepared bymixing p-aminophenol with tetrabutyl ammoniumchloride.It was used in the extraction procedure as an extraction solvent. The amine group in structure ofthe prepared deep eutectic solventled to its various solubility in different pHs. In this method, urine sample was placed in a glass test tube and then mixed with sodium chloride and its temperature adjusted at 50 ◦C. Then, the deep eutectic solvent was dissolved in the solution by manually shaking. In the following, an ammonia solution was added to the solution and the mixture was sonicated for 4 min. After centrifugation, an aliquat of the sedimented phase was injected into the determination system. Low limits of detection (daclatasvir 1.0 and sofosbuvir 1.3 g/L) and quantification (daclatasvir 3.3 and sofosbuvir 4.0 g/L), high enrichment factor (daclatasvir 96 and sofosbuvir 90) and extraction recovery (daclatasvir 96 and sofosbuvir 90 %), and good percision (relative standard deviation ≤9.3 %) were obtained. The introduced method was successfully applied in the determination of daclatasvir and sofosbuvir concentrations in urine samples.

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نویسنده نفر چندم مقاله
ابوالقاسم جویباناول
محمدرضا افشار مقدمپنجم
مریم خوب نسب جعفریچهارم

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JPBA-Daclatasvir-2021.pdf1400/05/064755467دانلود