Simultaneous derivatization and lighter-than-water air-assisted liquid–liquid microextraction using a homemade device for the extraction and preconcentration of some parabens in different samples

Simultaneous derivatization and lighter-than-water air-assisted liquid–liquid microextraction using a homemade device for the extraction and preconcentration of some parabens in different samples


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دانشگاه علوم پزشکی تبریز
دانشگاه علوم پزشکی تبریز

نویسندگان: محمدرضا افشار مقدم , علی اکبر علیزاده نبیل

کلمات کلیدی: Air-assisted liquid–liquid microextraction; Gas chromatography; Derivatization; Parabens; Preservatives

نشریه: 55358 , 15 , 41 , 2018

اطلاعات کلی مقاله
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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 70639
عنوان فارسی مقاله Simultaneous derivatization and lighter-than-water air-assisted liquid–liquid microextraction using a homemade device for the extraction and preconcentration of some parabens in different samples
عنوان لاتین مقاله Simultaneous derivatization and lighter-than-water air-assisted liquid–liquid microextraction using a homemade device for the extraction and preconcentration of some parabens in different samples
ناشر 4
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ خیر
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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Simultaneous derivatization and air-assisted liquid–liquid microextraction using an organic solvent lighter than water has been developed for the extraction of some parabens in different samples with the aid of a newly designed device for collecting the extractant. For this purpose, the sample solution is transferred into a glass test tube and a few microliters of acetic anhydride (as a derivatization agent) and p-xylene (as an extraction solvent) are added to the solution. After performing the procedure, the homemade device consists of an inverse funnel with a capillary tube placed into the tube. In this step, the collected extraction solvent and a part of the aqueous solution are transferred into the device and the organic phase indwells in the capillary tube of the device. Under the optimal conditions, limits of detection and quantification for the analytes were obtained in the ranges of 0.90–2.7 and 3.0–6.1 ng mL−1 , respectively. The enrichment and enhancement factors were in the ranges of 370–430 and 489–660, respectively. The method precision, expressed as the relative standard deviation, was within the ranges of 4–6% (n=6) and 4–9% (n=4) for intra- and inter-day precisions, respectively. The proposed method was successfully used for the determination of methyl-, ethyl-, and propyl parabens in cosmetic, hygiene, and food samples, and personal care products.

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نویسنده نفر چندم مقاله
محمدرضا افشار مقدمسوم
علی اکبر علیزاده نبیلچهارم

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