کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1241760 1495777 2016 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Microwave-assisted enzymatic hydrolysis followed by extraction with restricted access nanocomposites for rapid analysis of glucocorticoids residues in liver tissue
ترجمه فارسی عنوان
هیدرولیز آنزیمی با کمک مایکروویو و سپس استخراج با نانوکامپوزیت های دسترسی محدود برای تجزیه و تحلیل سریع باقی مانده های گلوکوکورتیکوئید در بافت کبدی
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• Microwave-assisted enzymatic hydrolysis and RAM-SPE were combined.
• C8-functionalized hydrophobic interior pore-walls for extraction of glucocorticoids.
• Different enzymatic hydrolysis influencing factors were optimized.
• Different extraction conditions were optimized.

We developed a novel, simple and fast method for the determination of glucocorticoids residues in liver tissue by combining microwave-assisted enzymatic hydrolysis and restricted access matrix dispersive solid phase extraction (RAM-dSPE) followed with liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis. Firstly, microwave-assisted enzymatic hydrolysis was introduced in order to obtain a maximum amount of unconjugated parent drug in a short time (8 s), while the traditional method commonly needs 4–12 h. Secondly, further cleanup was carried out by RAM-dSPE based on the graphene@mSiO2-C8 nanomaterials which were synthesized by coating mesoporous silica onto hydrophilic graphene nano-sheets through a surfactant-mediated co-condensation sol-gel process. The enzymatic hydrolysis influencing factors (pH of the buffer, microwave radiation power, incubation time) and the experimental conditions of RAM-dSPE (sorbents amount, type and volume of the elution solvent, adsorption and desorption time) were optimized. Three glucocorticoids (prednisolone (PREL), betamethasone (BE) and dexamethasone (DE)) were selected as models to evaluate the feasibility of the method. According to the results, the developed method provided low detection limit (S/N=3) of 0.01–0.05 μg kg−1 and good linearity range of 0.25–800 μg kg−1 (R2>0.996) for glucocorticoids. The limit of quantification (S/N=10) range from 0.03 to 0.19 μg kg−1. Compared with other traditional methods, the developed method could provide similar or even better results in a greatly reduced analysis time.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Talanta - Volume 159, 1 October 2016, Pages 155–162
نویسندگان
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