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一种新型的柱前荧光衍生化高效液相色谱荧光检测法,用于草药中马兜铃酸的灵敏测定。

A novel pre-column fluorescent derivatization method for the sensitive determination of aristolochic acids in medicinal herbs by high-performance liquid chromatography with fluorescence detection.

机构信息

Department of Chemistry, Hong Kong Baptist University, Kowloon Tong, Kowloon, Hong Kong SAR, China.

出版信息

J Pharm Biomed Anal. 2010 Sep 21;53(1):37-42. doi: 10.1016/j.jpba.2010.03.014. Epub 2010 Mar 17.

Abstract

Aristolochic acids (AAs) are a family of structurally related nitrophenanthrene carboxylic acids existing in Aristolochia, Bragantia, and Asarum species. AAs have been proven to have nephrotoxic and carcinogenic toxicity. In this study, a novel pre-column fluorescence derivatization procedure followed by high-performance liquid chromatography-fluorescence detection (HPLC-FLD) is developed for the analysis of AAs in medicinal herbs. The nitro group in the phenanthrene ring of AAs was removed by NaBH(4) in water-THF (2:1, v/v), resulting in the corresponding aristolic acids. The analysis of AAs in medicinal herbs was based of the sensitive fluorescence detection of aristolic acids after the chemical derivatization. Because the produced aristolic acids are highly fluorescent the limit of detection (LOD) of AAI and AAII were lowered to 0.06 and 0.04 ng/mL, respectively, which is at least an order of magnitude lower than those in the reported HPLC and LC-MS methods. Good linearity with correlation coefficients higher than 0.997 were obtained for AAI and AII in the calibration ranges of 0.2-800 ng/mL. The derivatization conditions such as reaction temperature, time and the amount of NaBH(4) were optimized. The developed method provided satisfactory intra-day and inter-day precisions with RSDs less than 1.4% and 3.8%, respectively. The relative analytical error was less than 7% for the analysis of AAI and AAII in spiked matrix samples.

摘要

马兜铃酸(AAs)是一类结构相关的硝基菲羧酸,存在于马兜铃属、肿柄菊属和细辛属植物中。已证明 AAs 具有肾毒性和致癌毒性。在这项研究中,开发了一种新的柱前荧光衍生化方法,随后是高效液相色谱-荧光检测(HPLC-FLD),用于分析草药中的 AAs。AAs 中菲环上的硝基基团在水-THF(2:1,v/v)中被 NaBH(4)去除,生成相应的马兜铃酸。草药中 AAs 的分析基于化学衍生化后马兜铃酸的灵敏荧光检测。由于生成的马兜铃酸具有很强的荧光性,AAI 和 AAII 的检测限(LOD)分别降低到 0.06 和 0.04 ng/mL,比已报道的 HPLC 和 LC-MS 方法至少低一个数量级。AAI 和 AII 在 0.2-800 ng/mL 的校准范围内具有良好的线性关系,相关系数均高于 0.997。优化了衍生化条件,如反应温度、时间和 NaBH(4)的用量。该方法提供了令人满意的日内和日间精密度,RSD 分别小于 1.4%和 3.8%。在加标基质样品中分析 AAI 和 AAII 的相对分析误差小于 7%。

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