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Room-temperature phosphorimetry for the determination of trace contaminations of camptothecin in anticancer drugs

机译:室温荧光法测定抗癌药物中喜树碱的痕量污染

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Campthotecin derivatives, irinotecan (CPT-11) and topotecan (TPT), have been used for the treatment of cancer and camptothecin (CPT) is a potential contaminant in these anticancer medicines. In this work, room-temperature phosphorimetry was used to quantify either CPT as trace contaminants in anticancer drugs and CPT-11 as the main ingredient in anticancer medicines. Phosphorescence from CPT-11 was induced using Pb(NO_3)_2 in SDS treated cellulose substrate while CPT was selectively detected using TlNO_3 as a phosphorescence enhancer in either cellulose or nylon substrates. The limit of quantification for CPT and CPT-11 was in ng order. A detailed metrological study was made to calculate the combined uncertainty associated to the CPT phosphorescence measurement. Satisfactory analyte recoveries were obtained for CPT-11 as a main active ingredient of a pharmaceutical formulation. The selective determination of CPT in a matrix containing TPT was made using the higher order (2nd) derivative of the excitation spectra. The results demonstrated the applicability of the method due its simplicity, cost effectiveness and selectivity.
机译:喜树碱衍生物,伊立替康(CPT-11)和托泊替康(TPT)已用于治疗癌症,喜树碱(CPT)是这些抗癌药物中的潜在污染物。在这项工作中,使用室温磷光法对作为抗癌药物中痕量污染物的CPT和作为抗癌药物主要成分的CPT-11进行定量。在SDS处理过的纤维素底物中使用Pb(NO_3)_2诱导CPT-11发出磷光,而在纤维素或尼龙底物中使用TlNO_3作为磷光增强剂选择性地检测CPT。 CPT和CPT-11的定量限为ng顺序。进行了详细的计量研究,以计算与CPT磷光测量相关的组合不确定度。作为药物制剂的主要活性成分,CPT-11的分析物回收率令人满意。使用激发光谱的高阶(二阶)导数对包含TPT的基质中的CPT进行选择性测定。结果证明了该方法的简便性,成本效益和选择性,因此是适用的。

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