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首页> 外文期刊>Journal of Liquid Chromatography >RAPID DETERMINATION OF PRAZOSIN IN PERFUSION MEDIA BY HPLC WITH SOLID PHASE EXTRACTION
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RAPID DETERMINATION OF PRAZOSIN IN PERFUSION MEDIA BY HPLC WITH SOLID PHASE EXTRACTION

机译:固相萃取-HPLC快速测定灌流介质中的PRAZOSIN

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摘要

A method is described for the quantitation of prazosin in tissue culture medium used for in vitro perfusion of human placental lobules. Prazosin was extracted using solid phase cartridges and the samples analysed by high performance liquid chromatography. The analysis utilised a C-18 reversed-phase column maintained at 40 degrees C with quantitation by fluorescence detection. The assay was linear to 100 ng/mL, intra-assay coefficients of variation measured at concentrations of 5 and 50 ng/mL were 5.8 and 6.2% respectively and inter-assay coefficients of variation were 4.9 and 2.7% for the same concentrations. The mean recovery of prazosin was 90.9 and 85.2% from solutions with concentrations of 5 and 50 ng/mL respectively. The minimum detectable limit was 0.1 ng/mL and the internal standard for this assay was propranolol. Analysis of a range of endogenous and exogenous compounds likely to be present in pregnancy plasma revealed only minor interference from lignocaine.
机译:描述了一种在组织培养基中定量哌唑嗪的方法,该组织培养基用于人胎盘小叶的体外灌注。使用固相小柱萃取过唑啉,并通过高效液相色谱法分析样品。该分析利用通过荧光检测定量的保持在40℃的C-18反相柱。该测定法线性至100 ng / mL,在5和50 ng / mL的浓度下测得的测定内变异系数分别为5.8和6.2%,同一浓度下的测定间变异系数为4.9和2.7%。从浓度分别为5和50 ng / mL的溶液中,哌唑嗪的平均回收率分别为90.9%和85.2%。最小可检测限为0.1 ng / mL,该测定的内标为普萘洛尔。对妊娠血浆中可能存在的一系列内源性和外源性化合物进行分析后发现,利多卡因的干扰很小。

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