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当瑞典哺乳期妇女受到的污染最小化时,其血清中未结合的双酚 A 水平低于 0.2ng/ml。

Serum levels of unconjugated bisphenol A are below 0.2ng/ml in Swedish nursing women when contamination is minimized.

机构信息

National Food Agency, P.O. Box 622, 751 26 Uppsala, Sweden.

National Food Agency, P.O. Box 622, 751 26 Uppsala, Sweden.

出版信息

Environ Int. 2014 Mar;64:56-60. doi: 10.1016/j.envint.2013.12.003. Epub 2013 Dec 22.

Abstract

In this study serum levels of bisphenol A (BPA) were investigated in primiparous women from Uppsala County, Sweden, sampled 3weeks after delivery 1996-2011, in both yearly pools of serum (n=39, temporal trend study) and in 208 individual samples also present in the pools. Possible contamination risks of BPA from blood sampling equipment and sample tubes, as well as from handling of the samples were evaluated. The unconjugated form of BPA was analyzed using a UPLC-MS/MS method with a limit of quantification (LOQ) of 0.2ng/ml. The results show that the levels of unconjugated BPA generally were <0.2ng/ml. The sampling equipment used when taking blood samples from the women and the tubes used for storage and processing of samples did not show any detectable BPA leakage. In the first analysis of the serum samples, unconjugated BPA levels ≥0.2ng/ml were found in 12% of the individual samples and in 21% of the trend samples. However, in reanalyses of individual serum samples from the same aliquot or from new aliquots, samples with BPA levels ≥0.2ng/ml in the first analysis did not have quantifiable BPA levels. Moreover, 11% of BPA spiked calibration samples (over 200) had higher levels than could be explained by the random error of the method. Thus BPA contamination of the biobanked samples probably occurred randomly during sample handling, pooling and processing. Equipment used for sampling of children and repeated blood sampling were leaking BPA. The results show the difficulties in analyzing compounds where samples are easily contaminated from exogenous sources. It also points out that it is questionable to use biobanked samples unless absence of BPA contamination from the sampling and storage materials, and during handling of the samples, can be proven.

摘要

在这项研究中,我们调查了瑞典乌普萨拉县的初产妇在分娩后 3 周(1996-2011 年)的血清双酚 A(BPA)水平,这些样本分别来自年度血清样本库(n=39,时间趋势研究)和 208 个也存在于样本库中的个体样本。我们评估了血液采样设备和样本管中 BPA 的潜在污染风险,以及样本处理过程中的风险。使用 UPLC-MS/MS 方法分析未结合的 BPA,定量下限(LOQ)为 0.2ng/ml。结果表明,未结合的 BPA 水平通常<0.2ng/ml。从女性身上采集血液样本时使用的采样设备和用于储存及处理样本的管都没有显示出任何可检测到的 BPA 泄漏。在对血清样本的第一次分析中,12%的个体样本和 21%的趋势样本中发现未结合的 BPA 水平≥0.2ng/ml。然而,在对同一等分或新等分的个体血清样本进行重新分析时,第一次分析中 BPA 水平≥0.2ng/ml 的样本没有可量化的 BPA 水平。此外,在 200 多个 BPA 加标校准样本中,有 11%的样本的水平高于方法随机误差所能解释的水平。因此,生物样本库中的样本在处理、混合和处理过程中可能随机受到 BPA 的污染。用于儿童采样和重复采血的设备存在 BPA 泄漏。这些结果表明,分析那些容易受到外源污染的化合物存在困难。这也表明,除非可以证明采样和储存材料中没有 BPA 污染,并且在处理样本过程中没有污染,否则使用生物样本库中的样本是值得怀疑的。

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