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Microwave-assisted digestion using diluted acids for toxic element determination in medicinal plants by ICP-MS in compliance with United States pharmacopeia requirements

机译:ICP-MS使用稀释酸进行微波辅助消化测定药用植物中的有毒元素,符合美国药典的要求

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The United States Pharmacopeia (USP) has introduced new requirements for toxic element determination in medicinal plants. However, the digestion step is still challenging since sample preparation should provide digests fully compatible with the determination technique and suitable for application in routine analysis. The proposed method was developed for medicinal plant digestion using diluted nitric acid solutions for further determination of As, Cd, Hg and Pb by inductively coupled plasma mass spectrometry (ICP-MS) in compliance with USP chapter 2232 (Elemental Contaminants in Dietary Supplements) requirements. Sample masses up to 500 mg of Passiflora incamata L., Paulinia cupana, Maytenus ilicifolia and Peumus boldus were digested in closed vessels using HNO3 solutions (2 to 14.4 mol L-1) and also by the dry ashing method recommended in current pharmacopoeias for comparison of results. As, Cd and Pb were determined by ICP-MS and Hg by flow injection cold vapor generation (FI-CVG) coupled to ICP-MS. Accuracy was evaluated using spikes and certified reference materials (CRMs) of plants (peach leaves, NIST 1547 and olive leaves, BCR 062). Medicinal plant samples were digested efficiently using diluted HNO3 solutions (4 mol L-1) and agreement between 96 and 103% with CRM values was obtained for all analytes. The limits of detection (0.004 to 0.02 mu g g(-1)) were lower than those recommended by the USP (0.5 to 1.5 mu g g(-1)). Significant losses in dry ashing were observed for Pb, while Hg was completely lost during digestion. Using the proposed microwave-assisted digestion method, up to eight samples could be simultaneously digested using diluted HNO3 solution (4 mol L-1) that provides digests with a carbon content lower than 320 mg L-1. In this sense, reagent consumption and waste generation were minimized and these features are in agreement with the green chemistry recommendations.
机译:美国药典(USP)对药用植物中的有毒元素测定提出了新的要求。但是,消解步骤仍具有挑战性,因为样品制备应提供与测定技术完全兼容并适合常规分析的消解物。拟议的方法是根据美国药典第2232章(膳食补充剂中的元素污染物)要求开发的,用于使用稀硝酸溶液进行药用植物消化,以通过电感耦合等离子体质谱法(ICP-MS)进一步测定As,Cd,Hg和Pb。 。使用HNO3溶液(2至14.4 mol L-1)在封闭的容器中消化高达500 mg西番莲,波利尼亚杯,Maytenus ilicifolia和Peumus boldus的样品质量,并采用当前药典推荐的干灰化方法进行比较结果。 As,Cd和Pb通过ICP-MS测定,Hg通过与ICP-MS耦合的流动注射冷蒸气产生(FI-CVG)来确定。使用尖峰植物和认证的参考材料(CRM)(桃叶NIST 1547和橄榄叶BCR 062)评估准确性。使用稀释的HNO3溶液(4 mol L-1)有效地消化药用植物样品,所有分析物的CRM值在96%和103%之间。检测限(0.004至0.02μg g(-1))低于USP推荐的检测限(0.5至1.5μg g(-1))。铅在干灰中损失明显,而汞在消化过程中完全损失。使用建议的微波辅助消解方法,使用稀释的HNO3溶液(4 mol L-1)可同时消解多达8个样品,该溶液可提供碳含量低于320 mg L-1的消解物。从这个意义上讲,试剂的消耗和废物的产生被最小化,并且这些特征与绿色化学推荐相一致。

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