首页> 外文期刊>Journal of trace elements in medicine and biology: Organ of the Society for Minerals and Trace Elements (GMS) >Validation of an optimized method for the determination of iodine in human breast milk by inductively coupled plasma mass spectrometry (ICPMS) after tetramethylammonium hydroxide extraction
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Validation of an optimized method for the determination of iodine in human breast milk by inductively coupled plasma mass spectrometry (ICPMS) after tetramethylammonium hydroxide extraction

机译:通过电感耦合等离子体质谱(ICPMS)在氢氧化氢氧化四甲基铵萃取后验证用电感耦合等离子体质谱法测定碘丙氨酸中的优化方法

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In this study a novel method to determine iodine concentrations in human breast milk was developed and validated. The iodine was analyzed by inductively coupled plasma mass spectrometry (ICPMS) following tetramethylammonium hydroxide (TMAH) extraction at 90 degrees C in disposable polypropylene tubes. While similar approaches have been used previously, this method adopted a shorter extraction time (1 h vs. 3 h) and used antimony (Sb) as the internal standard, which exhibited greater stability in breast milk and milk powder matrices compared to tellurium (Te). Method validation included: defining iodine linearity up to 200 mu g L-1; confirming recovery of iodine from NIST 1549 milk powder. A recovery of 94-98% was also achieved for the NIST 1549 milk powder and human breast milk samples spiked with sodium iodide and thyroxine (T4) solutions. The method quantitation limit (MQL) for human breast milk was 1.6 mu g L-1. The intra-assay and inter-assay coefficient of variation for the breast milk samples and NIST powder were <1% and <3.5%, respectively. NIST 1549 milk powder, human breast milk samples and calibration standards spiked with the internal standard were all stable for at least 2.5 months after extraction. The results of the validation process confirmed that this newly developed method provides greater accuracy and precision in the assessment of iodine concentrations in human breast milk than previous methods and therefore offers a more reliable approach for assessing iodine concentrations in human breast milk. (C) 2014 Elsevier GmbH. All rights reserved.
机译:在这项研究中,开发并验证了一种确定人母乳中碘浓度的新方法。在一次性聚丙烯管中以90℃氢氧化铵(TMAH)提取后,通过电感耦合等离子体质谱(ICPM)分析碘。虽然先前已经使用了类似的方法,但该方法采用较短的提取时间(1小时,3小时,3小时)和使用锑(Sb)作为内标,而与碲(TE相比,母乳和奶粉基质的稳定性表现出更大的稳定性(TE )。方法验证包括:定义高达200 mu g l-1的碘线性度;确认来自NIST 1549奶粉的碘回收。对于NIST 1549奶粉和用碘化钠和甲状腺素(T4)溶液掺入的人母乳样品,也达到了94-98%的回收率。人母乳的方法定量限(MQL)为1.6μgl-1。母乳样品和NIST粉末的测定内和测定间变异系数分别<1%和<3.5%。 NIST 1549奶粉,用内标掺入的人母乳样品和校准标准均稳定至少2.5个月后。验证过程的结果证实,这种新开发的方法在评估人母乳中的碘浓度方面提供了更高的准确性和精度,而不是先前的方法,为评估人母乳中碘浓度提供更可靠的方法。 (c)2014年Elsevier GmbH。版权所有。

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