Development of green sodium sulfate‐induced solidification of floating organic droplets–dispersive liquid phase microextraction method: Application to extraction of four antidepressants
Development of green sodium sulfate‐induced solidification of floating organic droplets–dispersive liquid phase microextraction method: Application to extraction of four antidepressants
نویسندگان: محمدرضا افشار مقدم , محبوب نعمتی
کلمات کلیدی: deep eutectic solvent, GC–MS, SFO–DLPME, tricyclic antidepressants, urine
نشریه: 4726 , 33 , 33 , 2019
| نویسنده ثبت کننده مقاله |
محمدرضا افشار مقدم |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
مرکز تحقیقات ایمنی غذا و دارو |
| کد مقاله |
69572 |
| عنوان فارسی مقاله |
Development of green sodium sulfate‐induced solidification of floating organic droplets–dispersive liquid phase microextraction method: Application to extraction of four antidepressants |
| عنوان لاتین مقاله |
Development of green sodium sulfate‐induced solidification of floating organic droplets–dispersive liquid phase microextraction method: Application to extraction of four antidepressants |
| ناشر |
5 |
| آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ |
خیر |
| عنوان نشریه (خارج از لیست فوق) |
|
| نوع مقاله |
Short Communication |
| نحوه ایندکس شدن مقاله |
ایندکس شده سطح یک – ISI - Web of Science |
| آدرس لینک مقاله/ همایش در شبکه اینترنت |
|
| Sodium sulfate‐induced deep eutectic solvent–based solidification of floating organic
droplets–dispersive liquid phase microextraction was developed prior to gas
chromatography–mass spectrometry. In this method, a mixture of Na2SO4 solution
(as phase separation agent and disperser) containing menthol–decanoic acid was rapidly injected into an alkaline aqueous solution containing Na2SO4. The solution was
placed in an ice bath and the menthol–decanoic acid solvent was solidified on the surface of the solution. Under the optimal conditions, the enrichment factors and extraction recoveries were 122–147 and 74–89%, respectively. Finally, an aliquot of the
collected organic phase was removed and mixed with acetonitrile and injected into
the separation system. The limits of detection and lower limits of quantification were
obtained at the ranges of 13–25 and 24–41 ng L−1
, respectively. The relative standard
deviations of the proposed method were ≤11% for intra‐ and inter‐day precisions at
four concentrations. |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| Biomedical-TCA-2019.pdf | 1398/08/06 | 242479 | دانلود |