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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Determination of total and lactone form of a new camptothecin derivative gimatecan (ST1481) and its metabolite ST1698 in human plasma by high-performance liquid chromatography with fluorimetric detection.
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Determination of total and lactone form of a new camptothecin derivative gimatecan (ST1481) and its metabolite ST1698 in human plasma by high-performance liquid chromatography with fluorimetric detection.

机译:高效液相色谱-荧光检测法测定人血浆中新的喜树碱衍生物gimatecan(ST1481)及其代谢物ST1698的总内酯形式。

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摘要

A new sensitive high-performance liquid chromatographic (HPLC) method for the determination of gimatecan (ST1481), a new camptothecin derivative, and its metabolite (ST1698) in plasma sample has been developed. The method consisted of on-line column solid phase extraction of analytes from human plasma, chromatographic separation by isocratic elution, then fluorimetric detection. The limits of quantitation were 0.25 ng/mL for both the analytes. The recovery of the extraction procedure was in the range of 62.8-71.1% for all the compounds. Good linearity (R(2)>0.999) was observed within the calibration ranges studied: 0.25-25 ng/mL for both ST1481 and ST1698. Precision was in the range 1.2-4.3%, and accuracy was always lower than 4.7%. Surprisingly, after administration of ST1481 to humans, plasma concentrations found were higher than expected, while metabolite plasma concentrations were negligible. For this reason, a second calibration curve range was validated to quantify ST1481 in human plasma, ranging from 5 to 200 ng/mL. A good accuracy and precision were obtained, confirming the usefulness of the procedure. By using neutral analytical condition the intact lactone form was estimated in plasma samples from a patient. The lactone form amounted to 80-100% of the total ST1481.
机译:开发了一种用于测定血浆样品中的吉美替康(ST1481),新的喜树碱衍生物及其代谢产物(ST1698)的灵敏高效液相色谱(HPLC)新方法。该方法包括从人血浆中在线分析物在线柱固相萃取,通过等度洗脱进行色谱分离,然后进行荧光检测。两种分析物的定量限均为0.25 ng / mL。对于所有化合物,萃取过程的回收率在62.8-71.1%的范围内。在研究的校准范围内观察到良好的线性度(R(2)> 0.999):ST1481和ST1698均为0.25-25 ng / mL。精度在1.2-4.3%的范围内,精度始终低于4.7%。出人意料的是,将ST1481给予人后,发现血浆浓度高于预期,而代谢产物血浆浓度可忽略不计。因此,验证了第二个校准曲线范围以定量人类血浆中的ST1481,范围为5到200 ng / mL。获得了良好的精度和精确度,证实了该程序的有用性。通过使用中性分析条件,可以估算患者血浆样品中完整的内酯形式。内酯形式占全部ST1481的80-100%。

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