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首页> 外文期刊>Journal of Analytical Atomic Spectrometry >Trace element analysis of human urine collected after administration of Gd-based MRI contrast agents: characterizing spectral interferences using inorganic mass spectrometry
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Trace element analysis of human urine collected after administration of Gd-based MRI contrast agents: characterizing spectral interferences using inorganic mass spectrometry

机译:使用基于Gd的MRI造影剂后收集的人类尿液中的微量元素分析:使用无机质谱法表征光谱干扰

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摘要

Analysis of human urine is commonly used in biomonitoring studies to assess exposure to essential (e.g., Cu, Zn, Se) and non-essential (Pb, Cd, Pt) trace elements. These data are also used in epidemiological studies to evaluate potential associations between trace element exposure and various health outcomes within a population. Today most trace element analyses are typically performed using quadrupole-based inductively coupled plasma mass spectrometry (Q-ICP-MS). However, there is always the potential for spectral interferences with Q-ICP-MS instrumentation, especially when analyzing human specimens that may contain medications and other exogenous substances. Moreover, such xenobiotics may be unknown to the investigators. In a recent study focusing on environmental exposures and endometriosis: Endometriosis: Natural History, Diagnosis, and Outcomes (ENDO Study), urine specimens (n=619) were collected from participating women upon enrollment into the study or prior to surgery or pelvic magnetic resonance imaging (MRI), and analyzed for 21 trace elements by Q-ICP-MS. Here we report on some anomalous results observed for Se and Pt with elevated concentrations up to several orders of magnitude greater than what might be expected based on established reference intervals. Further investigations using Sector Field (SF-) ICP-MS instrumentation led to identification of doubly charged and polyatomic gadolinium (Gd) species traced to a Gd-based contrast agent that was administered to some subjects just prior to urine collection. Specifically, interferences from Gd~(2+) and several minor polyatomics were identified as interferences on all of the major isotopes of Se including ~(74)Se,~(76)Se,~(77)Se,~(78)Se,~(80)Se, and~(82)Se. While trace amounts of Pt were present in the urine, a number of Gd-containing polyatomic species were also evident as major interferences on all isotopes of Pt (~(190)Pt, ~(192)Pt,~(194)Pt,~(195)Pt,~(196)Pt, and~(198)Pt), including Gd-chlorides, Gd-argides, and Gd-oxides. These observations underscore the importance of considering potential isobaric interferences when interpreting unusual trace element results for clinical specimens.
机译:生物尿液分析通常用于生物监测研究中,以评估对必需微量元素(例如,铜,锌,硒)和非必需微量元素(Pb,Cd,Pt)的暴露。这些数据还用于流行病学研究,以评估微量元素暴露与人群中各种健康结果之间的潜在关联。如今,大多数痕量元素分析通常使用基于四极杆的电感耦合等离子体质谱仪(Q-ICP-MS)进行。但是,Q-ICP-MS仪器始终存在光谱干扰的可能性,尤其是在分析可能包含药物和其他外源性物质的人体标本时。此外,研究人员可能不知道这种异生素。在一项针对环境暴露和子宫内膜异位的最新研究中:子宫内膜异位:自然病史,诊断和结果(ENDO研究),在参加研究时或手术或盆腔磁共振之前从参与研究的妇女中收集了尿液标本(n = 619)。成像(MRI),并通过Q-ICP-MS分析21种微量元素。在这里,我们报告了一些观察到的有关硒和铂的异常结果,它们的浓度升高了几个数量级,比基于既定的参考间隔所预期的要大几个数量级。使用Sector Field(SF-)ICP-MS仪器进行的进一步研究导致鉴定出双电荷和多原子g(Gd)物种,这些物种可追溯到基于Gd的造影剂,该造影剂是在收集尿液之前施用于某些受试者的。具体来说,来自Gd〜(2+)和几个次要多原子的干扰被确定为对Se的所有主要同位素的干扰,包括〜(74)Se,〜(76)Se,〜(77)Se,〜(78)Se ,〜(80)Se和〜(82)Se。尽管尿液中存在痕量的Pt,但许多含Gd的多原子物质也被视为对Pt的所有同位素(〜(190)Pt,〜(192)Pt,〜(194)Pt,〜 (195)Pt,〜(196)Pt和〜(198)Pt),包括Gd氯化物,Gd固化物和Gd氧化物。这些观察结果强调了在解释临床标本的异常微量元素结果时考虑潜在的等压干扰的重要性。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2013年第6期|821-830|共10页
  • 作者单位

    Laboratory of Inorganic and Nuclear Chemistry, Wadsworth Center, New York State Department of Health, P.O. Box 509, Albany, NY, 12201-0509, USA,Department of Environmental Health Sciences, School of Public Health, The University at Albany, P.O. Box 509, Albany, NY, 12201-0509, USA;

    Laboratory of Inorganic and Nuclear Chemistry, Wadsworth Center, New York State Department of Health, P.O. Box 509, Albany, NY, 12201-0509, USA,Department of Environmental Health Sciences, School of Public Health, The University at Albany, P.O. Box 509, Albany, NY, 12201-0509, USA;

    Laboratory of Inorganic and Nuclear Chemistry, Wadsworth Center, New York State Department of Health, P.O. Box 509, Albany, NY, 12201-0509, USA,Department of Environmental Health Sciences, School of Public Health, The University at Albany, P.O. Box 509, Albany, NY, 12201-0509, USA;

    Division of Epidemiology, Statistics and Prevention Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, 6100 Executive Blvd Room 7B03, MSC 7510, Bethesda, MD, 20892-7510, USA;

    Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, The University of Utah School of Medicine, 30 N 1900 E, Rm 2B200, Salt Lake City, UT, 84132, USA,Department of Obstetrics and Gynecology, The University of Utah Nano Institute of Utah, 30 N1900 E, Rm 2B200, Salt Lake City, UT, 84132, USA;

    Division of Epidemiology, Statistics and Prevention Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, 6100 Executive Blvd Room 7B03, MSC 7510, Bethesda, MD, 20892-7510, USA;

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