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高效液相色谱法荧光检测法测定马兜铃酸。

Determination of aristolochic acids by high-performance liquid chromatography with fluorescence detection.

机构信息

Department of Chemistry, The Hong Kong University of Science and Technology , Clear Water Bay, Kowloon, Hong Kong.

出版信息

J Agric Food Chem. 2014 Jun 25;62(25):5859-64. doi: 10.1021/jf501609j. Epub 2014 Jun 17.

Abstract

Nephrotoxic and carcinogenic aristolochic acids (AAs) are naturally occurring nitrophenanthrene carboxylic acids in the herbal genus Aristolochia. The misuse of AA-containing herbs in preparing slimming drugs has caused hundred of cases of kidney disease in Belgium women in a slimming regime in the early 1990s. Accumulating evidence also suggested that prolong dietary intake of AA-contaminated food is one of the major causes to the Balkan endemic nephropathy that was first observed in the late 1950s. Therefore, analytical methods of high sensitivity are extremely important for safeguarding human exposure to AA-containing herbal medicines, herbal remedies, and food composites. In this paper, we describe the development of a new high-performance liquid chromatography coupled fluorescence detector (HPLC-FLD) method for the sensitive determination of AAs. The method makes use of a novel cysteine-induced denitration reaction that "turns on" the fluorescence of AAs for fluorometric detections. Our results showed that the combination of cysteine-induced denitration and HPLC-FLD analysis allows for sensitive quantification of AA-I and AA-II at detection limits of 27.1 and 25.4 ng/g, respectively. The method was validated and has been successfully applied in quantifying AAs in Chinese herbal medicines.

摘要

肾毒性和致癌性的马兜铃酸(AAs)是存在于草药马兜铃属中的天然硝基菲羧酸。20 世纪 90 年代初,在比利时妇女的减肥计划中,由于错误使用含 AAs 的草药来制备减肥药,导致了数百例肾脏疾病。越来越多的证据表明,长期食用受 AA 污染的食物是导致巴尔干地方性肾病(Balkan endemic nephropathy)的主要原因之一,这种疾病最早是在 20 世纪 50 年代末观察到的。因此,开发高灵敏度的分析方法对于保护人类接触含 AAs 的草药、草药制剂和食物混合物非常重要。在本文中,我们描述了一种新的高效液相色谱-荧光检测(HPLC-FLD)方法的开发,用于灵敏测定 AAs。该方法利用一种新型的半胱氨酸诱导的脱硝反应,使 AAs 的荧光“开启”,用于荧光检测。我们的结果表明,半胱氨酸诱导的脱硝与 HPLC-FLD 分析相结合,可以分别在检测限为 27.1 和 25.4ng/g 的情况下,对 AA-I 和 AA-II 进行灵敏定量。该方法经过验证,并已成功应用于中草药中 AAs 的定量分析。

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