Application of new N- and S-doped amorphous carbon in D-mSPE and its combination with deep eutectic solvent-based DLLME for the extraction of some mycotoxins from soymilk

Application of new N- and S-doped amorphous carbon in D-mSPE and its combination with deep eutectic solvent-based DLLME for the extraction of some mycotoxins from soymilk


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نویسندگان: آناهید رضایی فر , محبوب نعمتی , محمدرضا افشار مقدم , فرزانه لطفی پور بناب

کلمات کلیدی: Aflatoxin, soymilk

نشریه: 1985 , 4604 , 13 , 2021

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 77188
عنوان فارسی مقاله Application of new N- and S-doped amorphous carbon in D-mSPE and its combination with deep eutectic solvent-based DLLME for the extraction of some mycotoxins from soymilk
عنوان لاتین مقاله Application of new N- and S-doped amorphous carbon in D-mSPE and its combination with deep eutectic solvent-based DLLME for the extraction of some mycotoxins from soymilk
ناشر 5
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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A new amorphous carbon-based dispersivemicro solid-phase extraction method was developed for the extraction and preconcentration of several mycotoxins from soymilk samples. The extracted analytes were concentrated by a deep eutectic solvent-based dispersive liquid–liquid microextraction method, and then, quantified by a high-performance liquid chromatography-fluorescence detector. The sorbent was prepared from b-cyclodextrin and methionine under mild conditions. The sorbent was doped by N and S, which improved its physicochemical properties. The optimization and validation of the method were performed using the “one-variable-at-a-time” method and International Council Harmonization guideline, respectively. Under the optimal conditions, low limits of detection and quantifications in the ranges of 0.08–0.56 and 0.27–1.9 ng L1 were obtained, respectively. Also, intra- (n ¼ 6) and inter-day (n ¼ 6) precisions showed an acceptable repeatability of the present work as they were in the ranges of 3.9–6.2 and 4.6–8.9% at a concentration of 3 ng L1 of each analyte, respectively. Finally, the proposed method was performed on different soymilk samples marketed in Tabriz city, and aflatoxin B1 was found in all samples. One soymilk was contaminated by ochratoxin A.

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نویسنده نفر چندم مقاله
آناهید رضایی فراول
محبوب نعمتیسوم
محمدرضا افشار مقدمچهارم
فرزانه لطفی پور بنابپنجم

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Rezaeefar-Analytical methods-2021.pdf1400/08/07791160دانلود