Nano-zirconium-silicate solid-phase extraction method for the rapid quantification of pyrrolizidine alkaloids from plant extracts by UHPLC-QTOF-MS

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL Journal of pharmaceutical and biomedical analysis Pub Date : 2025-01-15 DOI:10.1016/j.jpba.2025.116675
Benedikt Schwarz , Shah Hussain , Christian W. Huck , Thomas Jakschitz , Moritz Rubner , Günther K. Bonn
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Abstract

The aim of this work was to develop and validate a rapid dispersive-solid-phase extraction method for the quantification of pyrrolizidine alkaloids (PA) from plant extracts. The method was focused on the significant removal of the intricate matrix to ensure good sensitivity for the subsequent instrumental analysis of PA. This was achieved by employing nano-zirconium silicate (NZS) as a dispersive-SPE sorbent. The specific affinity of NZS for PAs allowed for the effective removal of a substantial portion of the complex matrix, thereby significantly improving the sensitivity of the method, compared to the common methods, were no specific enrichment of the PAs on the SPE sorbent is achieved. Ultra-high-performance liquid chromatography coupled to high resolution time-of-flight mass spectrometry (UHPLC/TOF MS) was used for the qualitative and quantitative analysis of PA. The procedure demonstrated high recoveries for the standard compounds spiked into a blank verbena extract at different concentrations. Recovery rates of 72–95 % for PA, and 30–70 % for their respective N-oxides (PANO) could be obtained. The method was compared to the most commonly used C18 SPE sorbent, and demonstrated a significant lower limit of quantification (LOQ) of 0.64–4.5 ng mL−1 as compared to 4.98–25.7 ng mL−1. The method was validated in accordance with ICH guidelines. PA standards had a linear response between 5 and 150 ng mL −1 and demonstrated a co-efficient of variance below ± 3 % with a % relative error below ± 15. The presented analytical approach was also tested for the determination of PA from contaminated Verbenae herba extract with success. The presented scheme improves the clean-up efficacy of the already used stationary phases for PA analysis and provides a great alternative analytical tool for the isolation of PAs from plant extracts.
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纳米硅酸锆固相萃取- UHPLC-QTOF-MS快速定量测定植物提取物中吡咯利西啶类生物碱。
本研究的目的是建立并验证一种快速分离-固相萃取法定量测定植物提取物中吡咯利西啶类生物碱的方法。该方法的重点是去除复杂的矩阵,以确保后续PA仪器分析的良好灵敏度。这是通过采用纳米硅酸锆(NZS)作为分散- spe吸附剂来实现的。NZS对PAs的特异性亲和力允许有效去除大部分复合基质,从而显着提高了该方法的灵敏度,与常规方法相比,SPE吸附剂上没有实现PAs的特异性富集。采用超高效液相色谱-高分辨率飞行时间质谱(UHPLC/TOF MS)对PA进行定性和定量分析。在不同浓度的空白马鞭草提取物中加入标准化合物,回收率高。PA的回收率为72 ~ 95 %,n -氧化物(PANO)的回收率为30 ~ 70 %。该方法与最常用的C18固相萃取吸附剂进行了比较,定量下限为0.64-4.5 ng mL-1,而下限为4.98-25.7 ng mL-1。该方法按照ICH指南进行验证。PA标准品在5 ~ 150 ng mL -1之间具有线性响应,方差系数低于± 3 %,相对误差低于± 15 %。用该方法对污染马鞭草提取物中PA的测定也取得了成功。该方案提高了固定相对PA分析的清洁效率,为从植物提取物中分离PA提供了一个很好的替代分析工具。
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
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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