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首页> 外文期刊>Journal of separation science. >Capillary electrophoresis for the investigation of two novel aminoalkanol derivatives of 1,7-diethyl-8,9-diphenyl-4-azatricyclo[5.2.1.02,6] dec-8-ene-3,5,10-trione as potential anticancer drugs in water solution and serum
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Capillary electrophoresis for the investigation of two novel aminoalkanol derivatives of 1,7-diethyl-8,9-diphenyl-4-azatricyclo[5.2.1.02,6] dec-8-ene-3,5,10-trione as potential anticancer drugs in water solution and serum

机译:毛细管电泳,用于调查1,7-二乙基-8,9-二苯基-4-氮杂基-4-氮杂基-4-β-氮杂-3,5,10- Trione作为潜在抗癌药物的两种新氨基烷醇衍生物[5.2.1.02,6] 在水溶液和血清中

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摘要

A simple, rapid, capillary zone electrophoresis method was developed and validated for the analysis of two novel aminoalkanol derivatives (I) and (II) of 1,7-diethyl-8,9-diphenyl-4-azatricyclo[5.2.1.0(2,6)]dec-8-ene-3,5,10-trione, which were found in earlier studies as potential anticancer drugs. Samples were analyzed to demonstrate the specificity and stability indicating ability of the developed method. The samples were extracted using n-hexane-ethyl acetate mixture in the ratio of 90:10. Electrophoretic separation was performed on a eCAP fused silica capillary (37 cm length, 50 mu m inside diameter) with a 50 mM tetraborate buffer as a background electrolyte adjusted to pH = 2.5. The separation time of (I) and (II) was achieved within 7 min. In addition, analysis of the two compounds in the serum was conducted. Limits of detection of (I) and (II) by UV absorbance at 200 nm were achieved in the range of 87.4-92.1 ng/mL. The sufficient recovery was observed in the range of 90.3-99.8%. The quantification limits for the compounds (I) and (II) were in the range of 279.71-291.03 ng/mL, respectively. The method has been successfully applied to the analysis of compounds (I) and (II) in serum samples.
机译:开发并验证了一种简单,快速,毛细管区电泳方法,用于分析两种新型氨基烷醇衍生物(I)和(II)的1,7-二乙基-8,9-二苯基-4-氮杂基[5.2.1.0(2 6)] DEC-8-ENE-3,5,10-TRIONE,其在早期研究中被发现为潜在的抗癌药物。分析样品以证明所开发方法的特异性和稳定性表明能力。使用正己烷 - 乙酸乙酯混合物萃取样品,其比例为90:10。将电泳分离在与50mM四硼酸盐缓冲液中的ECAP熔融二氧化硅毛细管(37cm长,50μm,50μm,50μmm,50μmm,作为调节至pH = 2.5的背景电解质进行。 (I)和(II)的分离时间在7分钟内实现。此外,对血清中两种化合物的分析进行了分析。通过UV吸光度在200nm的范围内,在87.4-92.1ng / ml的范围内实现了(I)和(II)的检测限。在90.3-99.8%的范围内观察到充分的恢复。化合物(I)和(II)的定量限制分别为279.71-291.03ng / ml。该方法已成功应用于血清样品中化合物(I)和(II)的分析。

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