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首页> 外文期刊>Journal of Chromatography, Biomedical Applications >Simultaneous determination of the lactone and carboxylate forms of the camptothecin derivative CPT-11 and its metabolite SN-38 in plasma by high-performance liquid chromatography
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Simultaneous determination of the lactone and carboxylate forms of the camptothecin derivative CPT-11 and its metabolite SN-38 in plasma by high-performance liquid chromatography

机译:高效液相色谱法同时测定血浆中喜树碱衍生物CPT-11及其代谢产物SN-38的内酯和羧酸盐形式

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摘要

CPT-11 (irinotecan) and mainly its metabolite SN-38 are potent antitumor derivatives of camptothecin. As the active lactone forms of both CPT-11 and SN-38 exist in ps-dependent equilibrium with their respective less potent open-ring hydroxy acid species, the simultaneous monitoring of both forms of both compounds is relevant. CPT-11 and SN-38 derivatives have quite different fluorescence responses. In order to avoid any compromise on the wavelength setting, we developed chromatographic conditions allowing simple automated wavelength setting changes which have been prevented using existing methods involving conventional C-18 columns. This was achieved by means of a Symmetry C-18 column combined to a gradient elution program using acetonitrile and 75 mM ammonium acetate plus 7.5 mM tetrabutylammonium bromide at pH 6.4. The developed conditions allowed an elution order suitable for a simple automated wavelength change in respect to reliable peak integration. CPT-11 and SN-38 derivatives were detected at lambda(ex) = 362 nm/lambda(em) = 425 nm and lambda(ex) = 375 nm/lambda(em) = 560 nn, respectively. The developed method allowed the detection of amounts less than 3 pg of each derivative injected on column. The method was successfully applied to pharmacokinetic and toxicokinetic studies in rat and dog. (C) 1998 Elsevier Science BN. All rights reserved. [References: 29]
机译:CPT-11(伊立替康)及其主要代谢产物SN-38是喜树碱的有效抗肿瘤衍生物。由于CPT-11和SN-38的活性内酯形式均以ps依赖的平衡状态存在,且它们各自的效力较低的开环羟基酸种类也很重要,因此同时监测这两种化合物的两种形式都很重要。 CPT-11和SN-38衍生物具有完全不同的荧光响应。为了避免对波长设置造成任何损害,我们开发了色谱条件,可进行简单的自动波长设置更改,而使用涉及传统C-18色谱柱的现有方法已避免了这种更改。这是通过将Symmetry C-18色谱柱与使用乙腈和75 mM乙酸铵加7.5 mM溴化四丁铵的pH 6.4的梯度洗脱程序组合在一起实现的。相对于可靠的峰积分,开发的条件使得洗脱顺序适合于简单的自动波长变化。 CPT-11和SN-38衍生物分别在λ= 362 nm /λ(em)= 425 nm和λ(ex)= 375 nm /λ(em)= 560 nn时检测到。开发的方法允许检测少于3 pg注入到色谱柱上的每种衍生物。该方法已成功应用于大鼠和狗的药代动力学和毒物动力学研究。 (C)1998 Elsevier Science BN。版权所有。 [参考:29]

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