Pena A, Seifrtová M, Lino C, Silveira I, Solich P
Group of Bromatology, Centre of Pharmaceutical Studies, Faculty of Pharmacy, University of Coimbra, Rua do Norte, 3000 Coimbra, Portugal.
Food Chem Toxicol. 2006 Sep;44(9):1449-54. doi: 10.1016/j.fct.2006.04.017. Epub 2006 May 11.
With increasing knowledge of the persistence of OTA in the food chain, exposure to this mycotoxin is a potential human health hazard to humans, and evaluating its presence in populations has become highly important. A sensitive and accurate analytical method for the determination of ochratoxin A in urine was validated, since is less invasive than blood monitoring. It involves extraction with 5% NaHCO3, immunoaffinity column (IAC) for clean-up and high performance liquid chromatography with fluorescence detection (HPLC-FD). The limit of quantification was 0.02 ng/mL of urine (1.3 ng/mL of the extract injected) and recovery of ochratoxin A from urine samples spiked at the three fortification levels, were higher than 90% with RSD lower than 9%. The identification of OTA was confirmed by methyl ester derivatization and then HPLC analysis. Based in ours first results we can assume that OTA conjugation with glucuronic acid in human urine occurs. In the present study, we follow up OTA levels in 60 urine samples of inhabitants from Coimbra city, Portugal, in order to evaluate population contamination, and the presence of OTA was found in 42 samples, at concentrations above the LOQ, ranged between 0.021 and 0.105 ng/mL.
随着对OTA在食物链中持久性的了解不断增加,接触这种霉菌毒素对人类健康构成潜在危害,评估其在人群中的存在情况变得极为重要。由于尿液检测比血液监测侵入性小,因此验证了一种灵敏且准确的尿液中赭曲霉毒素A的分析方法。该方法包括用5%的碳酸氢钠进行萃取、使用免疫亲和柱(IAC)进行净化以及采用荧光检测的高效液相色谱法(HPLC-FD)。定量限为尿液中0.02 ng/mL(进样提取物中1.3 ng/mL),在三个加标水平下从尿液样品中回收赭曲霉毒素A的回收率高于90%,相对标准偏差低于9%。通过甲酯衍生化然后进行HPLC分析来确认OTA的鉴定。基于我们的初步结果,可以假定人类尿液中OTA与葡萄糖醛酸发生了结合。在本研究中,我们跟踪了葡萄牙科英布拉市60名居民尿液样本中的OTA水平,以评估人群的污染情况,结果在42个样本中发现了OTA,其浓度高于定量限,范围在0.021至0.105 ng/mL之间。