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首页> 外文期刊>Advanced Pharmaceutical Bulletin >Analysis of Piroxicam in Pharmaceutical Formulation and Human Urine by Dispersive Liquid–Liquid Microextraction Combined with Spectrophotometry
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Analysis of Piroxicam in Pharmaceutical Formulation and Human Urine by Dispersive Liquid–Liquid Microextraction Combined with Spectrophotometry

机译:分散液-液微萃取-分光光度法分析药物配方和人尿中的吡罗昔康

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Purpose: Piroxicam,is non¨Csteroidal anti¨Cinflammatory and analgesic agent, which is widely used in the treatment of patients with rheumatologic disorders.A new analytical approach based on the dispersive liquid¨Cliquid microextraction (DLLME) has been developed for the extraction and determination of PX in pharmaceutical preparation and human urine.Methods: From the PX standard solution or solutions prepared from real samples, aliquot volumes were pipetted into centrifuge tubes and mixed with acetate buffer at pH 3.0 and NaCl solution. The contents were subjected to the DLLME, so 700 |ìL of methanol containing 70 |ìL of chloroform was injected rapidly into a sample solution. A cloudy solution was rapidly produced and the PX extracted into dispersedfine droplets. The mixture was centrifuged, thus thesefine droplets of chloroform were settled. The supernatant aqueous phase was readily decanted, then the remained organic phase was diluted with ethanol and the absorbance measured at 355?à3 nm against a reagent blank. Results: The main factors affecting the extraction efficiency such as pH, extraction and disperser solvent types and etc.were studied and optimizedsystematically. Under optimized conditions, the calibration graphs were linear over the range of 0.2 to 4.8 |ìg/mL.The limit of detection and relative standard deviation were found to be 0.058 |ìg/mL and 2.83%, respectively. Relative recoveries in the spiked samples ranged from 97 to 110%. Conclusion:Using the developed method PX can be analyzed in pharmaceutical formulation and human urine sample in a simpler, cheaper and more rapid manner
机译:目的:吡罗昔康(Piroxicam)是一种非甾体类抗炎镇痛药,被广泛用于风湿病患者的治疗。基于分散液-液体微萃取(DLLME)的新分析方法已被开发出来方法:从PX标准溶液或实际样品制备的溶液中,将等分试样的体积吸取到离心管中,并与pH 3.0的醋酸盐缓冲液和NaCl溶液混合。将内含物进行DLLME处理,因此将700μL含70μL氯仿的甲醇快速注入样品溶液中。快速产生浑浊的溶液,PX提取成分散的细小液滴。将混合物离心,从而使这些细小的氯仿液滴沉降。容易地倾析出上清液水相,然后将剩余的有机相用乙醇稀释,并针对试剂空白在355?3 nm处测量吸光度。结果:系统地研究和优化了影响萃取效率的主要因素,如pH,萃取和分散剂的溶剂类型等。在最佳条件下,校准曲线在0.2至4.8 g / mL范围内呈线性。检测限和相对标准偏差分别为0.058 g / mL和2.83%。加标样品的相对回收率在97%至110%之间。结论:使用开发的方法,PX可以以更简单,更便宜,更快速的方式在药物制剂和人尿液样品中进行分析

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