...
首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >A reversed-phase high performance liquid chromatography method for quantification of methotrexate in cancer patients serum
【24h】

A reversed-phase high performance liquid chromatography method for quantification of methotrexate in cancer patients serum

机译:反相高效液相色谱法测定癌症患者血清中甲氨蝶呤的含量

获取原文
获取原文并翻译 | 示例
           

摘要

A simple, rapid and sensitive reversed-phase high performance liquid chromatography (HPLC) method has been developed for the determination of methotrexate in human serum. After deproteinization of the serum with 40% silver nitrate solution, methotrexate and internal standard (IS) were separated on a reversed-phase column with a mobile phase consisting of 10 mM sodium phosphate buffer (pH6.40)-methanol (78:22%, v/v) and ultraviolet detection at 310 nm. The linearity is evaluated by a calibration curve in the concentration range of 0.05-10.0 mu g/mL and presented a correlation coefficient of 0.9995. The absolute recoveries were 97.52 +/- 13.9% and 96.87 +/- 3.7% for methotrexate and ferulic acid (internal standard), respectively. The intra- and inter-day precision were less 6.19 and 5.89%, respectively (n = 6). The limit of quantitation was 0.02 mu g/mL and the limit of detection was 0.006 mu g/mL. The complete analysis was achieved less than 10 min with no interference from endogenous components or 22 examined drugs. This method was validated by using serum samples from high-dose methotrexate treated patients with osteosarcoma, breast cancer, acute leukemia and lymphoma. The method was demonstrated to be a simple, rapid and reliable approach in quantification of methotrexate in serum samples from patients with high-dose methotrexate therapy. (C) 2015 Elsevier B.V. All rights reserved.
机译:开发了一种简单,快速,灵敏的反相高效液相色谱(HPLC)方法,用于测定人血清中的甲氨蝶呤。用40%硝酸银溶液对血清进行脱蛋白后,在反相柱上分离甲氨蝶呤和内标(IS),流动相由10 mM磷酸钠缓冲液(pH6.40)-甲醇(78:22% ,v / v)和310 nm的紫外线检测。在0.05-10.0μg / mL的浓度范围内,通过校准曲线评估线性,相关系数为0.9995。甲氨蝶呤和阿魏酸(内标)的绝对回收率分别为97.52 +/- 13.9%和96.87 +/- 3.7%。日内和日间精度分别低于6.19%和5.89%(n = 6)。定量限为0.02μg / mL,检出限为0.006μg / mL。不到10分钟即可完成完整分析,而不受内源性成分或22种检测药物的干扰。该方法通过使用高剂量甲氨蝶呤治疗的骨肉瘤,乳腺癌,急性白血病和淋巴瘤患者的血清样本进行了验证。该方法被证明是定量,高剂量甲氨蝶呤治疗患者血清样品中甲氨蝶呤的简单,快速和可靠的方法。 (C)2015 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号