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

机译:液相色谱-串联质谱固相萃取改进马兜铃酸-DNA加合物的制备和鉴定

摘要

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.
机译:马兜铃酸(AA)是一种已知的肾毒素和潜在的致癌物,在体内和体外代谢激活后可形成共价DNA加合物。开发了一种简单的制备和表征马兜铃酸-DNA加合物的方法。通过AAI / AAII与2'-脱氧核苷的直接反应合成了4个AA加合物。首先将反应混合物净化并使用固相萃取(SPE)进行预浓缩,然后通过反相高效液相色谱(HPLC)进一步纯化。通过应用改进的SPE方法,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(如HPLC所示,纯度超过94%)。纯化的AA-DNA加合物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。这项工作为可能大规模制备AA-DNA加合物标准品提供了强大的工具,可以促进对马兜铃酸致癌和致突变机理的进一步研究。

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