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液相色谱分析人血清样品中抗癌生物碱洛托辛 A 及其一些新衍生物。

Liquid chromatographic analysis of the anticancer alkaloid luotonin A and some new derivatives in human serum samples.

机构信息

Sección Departamental Química Analítica, Facultad de Farmacia, Universidad Complutense de Madrid, Madrid, Spain.

出版信息

J Sep Sci. 2010 Jul;33(14):2086-93. doi: 10.1002/jssc.201000175.

Abstract

The quantitation of the natural cytotoxic and anti-inflammatory alkaloid luotonin A and five recently synthesized derivatives is described, constituting the first report of a HPLC method for the analysis of these compounds in human serum samples. The conditions for the chromatographic separation were optimized and the method was validated for the analysis of these compounds in biological samples according to international guidelines. An RP-HPLC method with fluorimetric detection and a C(18) stationary phase was applied. Different ACN/water mobile phases were assayed, including 0-4% of a mobile phase modifier such as tetrahydrofuran, dioxane or tert-butyl methyl ether. Isocratic and gradient elution conditions are compared. The influence of pH on the efficiency and resolution of the separation was also considered. The developed method was applied to the determination of luotonins in pooled human serum samples by gradient elution RP-HPLC using a simple cleanup procedure. The proposed chromatographic method exhibits satisfactory analytical figures of merit, with LOD from 1.0 x 10(-10) to 2.0 x 10(-10) M, intraday and interday precision below 6% except for the concentration level closest to LOD, and good agreement between experimental and theoretical concentrations. Therefore, the developed method is suitable, reliable, rapid, and simple.

摘要

描述了天然细胞毒性和抗炎生物碱洛图通 A 及其五种最近合成衍生物的定量分析方法,这是首次报道在人血清样品中分析这些化合物的 HPLC 方法。优化了色谱分离条件,并根据国际指南验证了该方法在生物样品中分析这些化合物的适用性。应用了带有荧光检测的反相高效液相色谱法和 C(18)固定相。考察了不同的乙腈/水流动相,包括 0-4%的流动相改性剂,如四氢呋喃、二恶烷或叔丁基甲基醚。比较了等度和梯度洗脱条件。还考虑了 pH 对分离效率和分辨率的影响。通过简单的净化程序,采用梯度洗脱反相高效液相色谱法,将开发的方法应用于混合人血清样品中洛图通的测定。所提出的色谱方法具有令人满意的分析性能,LOD 为 1.0×10(-10)至 2.0×10(-10)M,除了最接近 LOD 的浓度水平外,日内和日间精密度低于 6%,并且实验和理论浓度之间具有良好的一致性。因此,所开发的方法是合适的、可靠的、快速的和简单的。

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