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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Electrospun NiFe layered double hydroxide/Nylon 6 composite nanofibers as a sorbent for micro solid phase extraction by packed sorbent of non-steroidal anti-inflammatory drugs in human blood
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Electrospun NiFe layered double hydroxide/Nylon 6 composite nanofibers as a sorbent for micro solid phase extraction by packed sorbent of non-steroidal anti-inflammatory drugs in human blood

机译:Electrom淘nife层叠双氢氧化物/尼龙6复合纳米纤维作为用于微固相萃取的吸附剂,通过人体血液中的非甾体抗炎药的包装吸附剂

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In the present work, NiFe layered double hydroxide (LDH)/Nylon 6 composite nanofibers were prepared by electrospinning method and used as a new sorbent for the extraction and measurement of nonsteroidal anti-inflammatory drugs (naproxen, mefenamic acid, and diclofenac) in whole blood samples. The method is based on micro solid phase extraction (mu SPE) by packed sorbent followed by HPLC-UV analysis. Effective parameters on the extraction efficiency were optimized using a central composite design (CCD). In order to characterize the sorbent, Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), field emission scanning electron microscopy (FESEM), energy dispersive X-ray analysis (EDX) and elemental mapping were applied. The method was fully validated based on linearity, limits of detection (LOD) and quantification (LOQ), precision, and recovery. Under the optimal conditions, LOD values were found to be 25 ng mL(-1) for naproxen and diclofenac and 15 ng mL -1 for mefenamic acid. A seven-point calibration curve was obtained in the range of 75-2000 ng mL(-1) for naproxen and diclofenac and 50-2000 for mefenamic acid. The method showed good linearity with coefficients of determination, r(2) > 0.9962, for the three drugs. In the entire analytical range, the relative standard deviations (RSD%) were less than 8.1%. Finally, the efficiency of the method was investigated for the analysis of the target analytes in human blood samples, and the recoveries were obtained in the range of 90.7-109.8%. (C) 2019 Elsevier B.V. All rights reserved.
机译:另外,在本工作中,由NiFe层状双氢氧化物(LDH)/通过电纺丝方法制备的并且用作用于提取和非甾体抗炎药(萘普生,甲灭酸,和双氯芬酸)在整个测量一个新的吸附剂尼龙6个复合纳米纤维血液样本。该方法是基于微固相萃取(SPE亩)通过吸附剂填充,随后通过HPLC-UV分析。使用中央复合设计(CCD)对提取效率有效的参数进行了优化。为了表征吸附剂,傅里叶变换红外光谱(FTIR),热重量分析(TGA),场发射扫描电子显微镜(FESEM),施加的能量色散X射线分析(EDX)和元素的映射。该方法是基于线性充分验证,检测(LOD)和定量限(LOQ),精度和恢复的限制。在此条件下,发现LOD值是25毫微克毫升(-1),萘普生和双氯芬酸和15纳克毫升-1甲芬那酸。在75-2000每mL(-1)为萘普生和双氯芬酸和50-2000对于甲芬那酸的范围内进行,得到七点校准曲线。该方法表现出良好的线性关系确定的系数,R(2)> 0.9962,对于三种药物。在整个分析范围,相对标准偏差(RSD%)均小于8.1%。最后,该方法的效率进行了研究用于人类血液样品中的目标分析物的分析,并且在90.7-109.8%的范围内,得到的回收率。 (c)2019 Elsevier B.v.保留所有权利。

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