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首页> 外文期刊>Daru Journal of pharmaceutical sciences. >Quantitative analysis of piroxicam using temperature-controlled ionic liquid dispersive liquid phase microextraction followed by stopped-flow injection spectrofluorimetry
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Quantitative analysis of piroxicam using temperature-controlled ionic liquid dispersive liquid phase microextraction followed by stopped-flow injection spectrofluorimetry

机译:控温离子液体分散液相微萃取-停流注射荧光光谱法定量分析吡罗昔康

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Background Piroxicam (PXM) belongs to the wide class of non-steroidal anti-inflammatory drugs ( NSAIDs ). PXM has been widely applied in the treatment of rheumatoid arthritis, gonarthrosis, osteoarthritis, backaches, neuralgia, mialgia. In the presented work, a green and benign sample pretreatment method called temperature-controlled ionic liquid dispersive liquid phase microextraction (TCIL-DLPME) was followed with stopped-flow injection spectrofluorimetry (SFIS) for quantitation of PXM in pharmaceutical formulations and biological samples. Methods Temperature-controlled ionic liquid dispersive liquid phase microextraction (TCIL-DLPME) was applied as an environmentally friendly sample enrichment method to extract and isolate PXM prior to quantitation. Dispersion of 1-hexyl-3-methylimidazolium hexafluorophosphate ([Hmim][PF6]) ionic liquid (IL) through the sample aqueous solution was performed by applying a relatively high temperature. PXM was extracted into the extractor, and after phase separation, PXM in the final solution was determined by stopped-flow injection spectrofluorimetry (SFIS). Results and Major Conclusion Different factors affecting the designed method such as IL amount, diluting agent, pH and temperature were investigated in details and optimized. The method provided a linear dynamic range of 0.2-150 μg l-1, a limit of detection (LOD) of 0.046 μg l-1 and a relative standard deviation (RSD) of 3.1%. Furthermore, in order to demonstrate the analytical applicability of the recommended method, it was applied for quantitation of PXM in real samples.
机译:背景吡罗昔康(PXM)属于非甾体抗炎药(NSAIDs)的一大类。 PXM已广泛应用于类风湿关节炎,淋病,骨关节炎,腰酸,神经痛、,痛的治疗。在提出的工作中,采用绿色和良性的样品预处理方法,称为温度控制离子液体分散液相微萃取(TCIL-DLPME),然后采用停流注射荧光法(SFIS)定量测定药物制剂和生物样品中的PXM。方法采用温度控制的离子液体分散液相微萃取(TCIL-DLPME)作为环境友好的样品富集方法,在定量前提取和分离PXM。六氟磷酸1-己基-3-甲基咪唑鎓([Hmim] [PF 6 ])离子液体(IL)在样品水溶液中的分散相对较高的温度。将PXM萃取到萃取器中,相分离后,通过停止流动注射荧光光谱法(SFIS)测定最终溶液中的PXM。结果与主要结论详细研究并优化了影响设计方法的不同因素,如IL量,稀释剂,pH和温度。该方法的线性动态范围为0.2-150μgl -1 ,检测极限(LOD)为0.046μgl -1 和3.1%的相对标准偏差(RSD)。此外,为了证明推荐方法的分析适用性,该方法被用于定量实际样品中的PXM。

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