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首页> 外文期刊>Analytica chimica acta >Determination of clenbuterol in urine using headspace solid phase microextraction or liquid-liquid-liquid microextraction
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Determination of clenbuterol in urine using headspace solid phase microextraction or liquid-liquid-liquid microextraction

机译:顶空固相微萃取或液-液-液微萃取法测定尿中盐酸克伦特罗

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摘要

Headspace solid phase microextraction (HS-SPME) and liquid-liquid-liquid microextraction with automated movement of the acceptor phase (LLLME/AMAP) techniques are described for the extraction of clenbuterol (CB) in urine.HS-SPME technique involves the extraction of the drug by SPME fibre in a headspace mode with a cooling device at the upper part of the vial to cool the headspace of the vial where the fiber is suspended.This cooling effect will enhance the absorption of analytes by the fiber.As the cooling system is surrounding the vial,the headspace will also be cooled in addition to the cooling of the fiber.After extraction the derivatization of the extracted drug with hexamethyldisilazane (HMDS) was performed by suspending the fiber in the headspace of another vial saturated with the vapor of HMDS.This derivatized compound was analyzed by gas chromatography with mass spectrometric detection (GC/MS).LLLME/AMAP technique involves the extraction of CB,a basic drug,from an alkaline solution into the organic solvent residing in the pores of the hollow fiber and then back extracted into the acidic acceptor solution inside the lumen of the hollow fiber.The acceptor solution was repeatedly moved in and out of the hollow fibre assisted by a syringe pump.This repeated movement provides fresh acceptor phase to come in-contact with the organic phase and thus improving the efficiency of extraction.Quantification was performed using high performance liquid chromatography with ultraviolet (HPLC/UV) detection.In both the techniques,experimental parameters have been studied to achieve greater sensitivity.Linearity was observed over the range of 1-1000 ng ml~(-1) (R~2 = 0.9990) and 50-3000 ng ml~(-1) (R~2 = 0.9956) with detection limits of 0.23 ng ml~(-1) and 3.9 ng ml~(-1),respectively,for HS-SPME-GC/MS and LLLME/AMAP-HPLC/UV method.R.S.D.values of 3.9% (HS-SPME-GC/MS) and 5.8% (LLLME/AMAP-HPLC/UV) indicated good precision of the techniques.Absolute recovery was found to be 0.007% and 18%,respectively,for HS-SPME-GC/MS and LLLME-HPLC/UV methods.Finally,the techniques have been applied for the analysis of CB in urine samples.No effort has been made to compare the method with official method.
机译:描述了顶空固相微萃取(HS-SPME)和具有受体相自动移动的液-液-液微萃取技术(LLLME / AMAP),用于尿液中盐酸克伦特罗(CB)的提取。通过SPME纤维在顶空模式下使用药水,在小瓶的上部装有冷却装置,以冷却小瓶中悬浮纤维的顶空,这种冷却效果将增强纤维对分析物的吸收。围绕小瓶,除纤维冷却外,顶部空间也将被冷却。萃取后,将六氟二硅氮烷(HMDS)衍生的药物通过将纤维悬浮在另一个充满水蒸气的小瓶的顶部空间进行衍生化。 HMDS。该衍生化合物通过气相色谱-质谱检测(GC / MS)进行分析。LLLME/ AMAP技术涉及从碱性溶液中提取碱性药物CB。进入残留在中空纤维孔中的有机溶剂,然后再抽回中空纤维内腔内部的酸性受体溶液中。在注射泵的帮助下,将受体溶液反复移入和移出中空纤维。重复移动可提供新鲜的受主相,使其与有机相接触,从而提高了萃取效率。使用高效液相色谱-紫外检测(HPLC / UV)进行定量。在这两种技术中,均研究了实验参数在1-1000 ng ml〜(-1)(R〜2 = 0.9990)和50-3000 ng ml〜(-1)(R〜2 = 0.9956)的范围内观察到线性对于HS-SPME-GC / MS和LLLME / AMAP-HPLC / UV法,分别为0.23 ng ml〜(-1)和3.9 ng ml〜(-1).RSD值为3.9%(HS-SPME-GC / MS)和5.8%(LLLME / AMAP-HPLC / UV)表示该技术具有良好的精密度,绝对回收率为0.007分别为HS-SPME-GC / MS和LLLME-HPLC / UV方法的%和18%。最后,该技术已用于尿液样品中CB的分析。方法。

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