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浆液悬浮进样技术在电感耦合等离子体原子发射光谱法快速多元素分析多矿物质和多种维生素制剂中的应用

Use of slurry suspension sample introduction technique in fast multielement analysis of multimineral and multivitamin formulations by inductively coupled plasma atomic emission spectrometry.

作者信息

Zachariadis George A, Olympiou Agathi F

机构信息

Laboratory of Analytical Chemistry, Department of Chemistry, Aristotle University of Thessaloniki, GR-541 24 Thessaloniki, Greece.

出版信息

J Pharm Biomed Anal. 2008 Jul 15;47(3):541-6. doi: 10.1016/j.jpba.2008.02.010. Epub 2008 Feb 17.

DOI:10.1016/j.jpba.2008.02.010
PMID:18372140
Abstract

A slurry suspension sampling technique has been developed and optimized for rapid multielemental analysis of multivitamin/multimineral preparations using inductively coupled plasma atomic emission spectrometry (ICP-AES). The following macro-, micro- and trace-elements: Ca, Mg, Mn, Fe, Cr, Al, Ag, B, Ba, Bi, Cd, Co, Cu, Ga, In, Ni, Pb, Zn, As and Se were determined by the proposed method. The lower detection limits were obtained for Mn, Mg, Cu and Ca whereas the highest for Bi, Pb, As and Se. Consequently the method can be used as a fast screening method. A wet-acid mineralization method was applied as total recovery method for comparative purposes. Samples were prepared as slurries at a concentration of 5% (m/v) in aqueous acidic media (0.8 M HNO(3)). Various factors affecting the sensitivity of the method were optimized. The obtained results were subjected to two-way analysis of variance to examine any significant difference between the developed slurry procedure and the wet-acid complete decomposition. Finally, the slurry suspension technique was found to be applicable in routine quality control and contamination monitoring of multimineral preparations. For the analyzed commercial preparations, the found elemental concentrations are compared to those appearing in the label of the products.

摘要

已开发并优化了一种悬浮液进样技术,用于使用电感耦合等离子体原子发射光谱法(ICP-AES)对多种维生素/多种矿物质制剂进行快速多元素分析。通过该方法测定了以下常量、微量和痕量元素:钙(Ca)、镁(Mg)、锰(Mn)、铁(Fe)、铬(Cr)、铝(Al)、银(Ag)、硼(B)、钡(Ba)、铋(Bi)、镉(Cd)、钴(Co)、铜(Cu)、镓(Ga)、铟(In)、镍(Ni)、铅(Pb)、锌(Zn)、砷(As)和硒(Se)。锰、镁、铜和钙的检测限较低,而铋、铅、砷和硒的检测限最高。因此,该方法可用作快速筛选方法。为了进行比较,采用湿酸消解方法作为全回收方法。样品在酸性水介质(0.8 M HNO₃)中配制成浓度为5%(m/v)的悬浮液。优化了影响该方法灵敏度的各种因素。对所得结果进行双向方差分析,以检验所开发的悬浮液方法与湿酸完全分解方法之间是否存在显著差异。最后,发现悬浮液进样技术适用于多种矿物质制剂的常规质量控制和污染监测。对于所分析的市售制剂,将所发现的元素浓度与产品标签上显示的浓度进行比较。

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