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固相萃取-液相色谱-串联质谱法提高马兜铃酸-DNA 加合物的制备和鉴定。

Improved preparation and identification of aristolochic acid-DNA adducts by solid-phase extraction with liquid chromatography-tandem mass spectrometry.

机构信息

State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.

出版信息

J Environ Sci (China). 2009;21(12):1769-76. doi: 10.1016/s1001-0742(08)62486-9.

Abstract

Aristolochic acid (AA) is a known nephrotoxin and potential carcinogen, which can form covalent DNA adducts after metabolic activation in vivo and in vitro. A simple method for preparation and characterization of aristolochic acid-DNA adducts was developed. Four AA-adducts were synthesized by a direct reaction of AAI/AAII with 2'-deoxynucleosides. The reaction mixture was first cleaned-up and pre-concentrated using solid phase extraction (SPE), and further purified by a reversed-phase high performance liquid chromatography (HPLC). By the application of developed SPE procedure, matrices and byproducts in reaction mixture could be greatly reduced and adducts of high purity (more than 94% as indicated by HPLC) were obtained. The purified AA-DNA adducts were identified and characterized with liquid-electrospray ionization-quadrupole-time of flight-mass spectrometry (LC-ESI-Q-TOF-MS/MS) and LC-Diode array detector-fluorescence (LC-DAD-FL) analysis. This work provides a robust tool for possible large-scale preparation of AA-DNA adduct standards, which can promote the further studies on carcinogenic and mutagenic mechanism of aristolochic acids.

摘要

马兜铃酸(AA)是一种已知的肾毒素和潜在的致癌物质,在体内和体外代谢激活后可以形成共价 DNA 加合物。本研究开发了一种简单的马兜铃酸-DNA 加合物的制备和表征方法。通过 AAI/AAII 与 2'-脱氧核苷的直接反应合成了 4 种 AA 加合物。反应混合物首先使用固相萃取(SPE)进行清洗和预浓缩,然后通过反相高效液相色谱(HPLC)进一步纯化。通过应用开发的 SPE 程序,可以大大减少反应混合物中的基质和副产物,并获得高纯度的加合物(HPLC 指示纯度超过 94%)。通过液相-电喷雾电离-四极杆-飞行时间质谱(LC-ESI-Q-TOF-MS/MS)和 LC-二极管阵列检测器-荧光(LC-DAD-FL)分析对纯化的 AA-DNA 加合物进行鉴定和表征。这项工作为可能的大规模制备 AA-DNA 加合物标准品提供了一种可靠的工具,这将有助于进一步研究马兜铃酸的致癌和致突变机制。

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