Evaluation of extraction capabilities of protease, proteinase K, and TMAH for nanoparticle characterization in biological CRMs by spICP-MS.

IF 4.1 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS
Filip Gregar, Doaa Abouelenein, Katrin Loeschner, Zuzana Gajdosechova
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引用次数: 0

Abstract

Reliable method development and validation rely on certified reference materials (CRMs) that ideally provide accurate analyte values independent of sample preparation and analytical methodology. Although inorganic nanoparticles (NPs) are increasingly being investigated in biological systems, biological matrix CRMs certified for NP characterization are not yet available. In this study, five biological CRMs (DOLT-4, DOLT-5, DORM-4, DORM-5, and TORT-3) were extracted using three commonly employed protocols based on proteinase K, protease, and tetramethylammonium hydroxide (TMAH). The resulting extracts were analyzed by single-particle ICP-MS (spICP-MS) to determine particle number concentrations (PNCs) and particle size distributions (PSDs) of Ag-, Al-, Cu-, Cr-, Fe-, Hg-, Se-, Si-, Ti-, and Zn-containing nanoparticles. Both PNCs and PSDs varied substantially among the extraction protocols, demonstrating that sample preparation is a major source of variability in NP characterization. In addition to differences in extraction performance, elevated NP backgrounds were observed for several elements in the TMAH reagent, highlighting the importance of evaluating reagent-derived contamination when interpreting spICP-MS results. Investigation of Hg- and Se-containing NPs in DOLT-4, DORM-5, and TORT-3 further demonstrated that incomplete tissue digestion and residual matrix fragments complicate particle identification and interpretation. Overall, this work provides a systematic comparison of commonly used extraction strategies for the analysis of naturally occurring NPs in biological CRMs, identifies current limitations associated with sample preparation, and provides guidance for future method development and the design of biological CRMs for NP characterization.

用spICP-MS评价蛋白酶、蛋白酶K和TMAH在生物质粒纳米颗粒表征中的提取能力。
可靠的方法开发和验证依赖于经过认证的标准物质(crm),这些标准物质理想地提供独立于样品制备和分析方法的准确分析物值。尽管无机纳米颗粒(NPs)在生物系统中的研究越来越多,但用于NP表征的生物基质crm尚未获得认证。在本研究中,采用三种常用的基于蛋白酶K、蛋白酶和四甲基氢氧化铵(TMAH)的方案提取了5种生物基质(DOLT-4、DOLT-5、DORM-4、DORM-5和TORT-3)。采用单颗粒ICP-MS (spICP-MS)分析所得提取物,测定含Ag-、Al-、Cu-、Cr-、Fe-、Hg-、Se-、Si-、Ti-和zn纳米颗粒的颗粒数浓度(pnc)和粒径分布(psd)。在不同的提取方案中,pnc和psd都存在很大差异,这表明样品制备是NP表征变化的主要来源。除了提取性能的差异外,在TMAH试剂中观察到几种元素的NP背景升高,这突出了在解释spICP-MS结果时评估试剂衍生污染的重要性。对DOLT-4、DORM-5和TORT-3中含汞和含硒NPs的研究进一步表明,不完整的组织消化和残留的基质碎片使颗粒识别和解释复杂化。总的来说,这项工作为分析生物crm中天然存在的NPs提供了常用的提取策略的系统比较,确定了当前与样品制备相关的局限性,并为未来的方法开发和设计用于NP表征的生物crm提供了指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.00
自引率
4.70%
发文量
638
审稿时长
2.1 months
期刊介绍: Analytical and Bioanalytical Chemistry’s mission is the rapid publication of excellent and high-impact research articles on fundamental and applied topics of analytical and bioanalytical measurement science. Its scope is broad, and ranges from novel measurement platforms and their characterization to multidisciplinary approaches that effectively address important scientific problems. The Editors encourage submissions presenting innovative analytical research in concept, instrumentation, methods, and/or applications, including: mass spectrometry, spectroscopy, and electroanalysis; advanced separations; analytical strategies in “-omics” and imaging, bioanalysis, and sampling; miniaturized devices, medical diagnostics, sensors; analytical characterization of nano- and biomaterials; chemometrics and advanced data analysis.
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