Qualitative and quantitative analysis of major components in Abelmoschus manihot flowers treated with different drying methods using UHPLC Q-exactive MS and HPLC-PDA

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
Shaoqing Zhu , Wei Wang , Xiang Liu , Chengxue Yi , Li Li , Zhenhua Zhu , Sheng Guo , Jin-ao Duan
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引用次数: 0

Abstract

The flowers of Abelmoschus manihot (L.) Medic are commonly used in clinical practice in China to cure forms of chronic kidney disease. Despite a long history of traditional use, the flowers obtained by different drying technologies have never been fully chemically characterized, and the ranges of constituents between different drying methods have not been comprehensively reported. To establish a quality control and chemical characterization method, a total of 14 batches of samples corresponding to 14 postharvest treatments were studied. Seven flavonoids were quantified using a HPLC-PDA method. The method was validated in terms of linearity (r > 0.999), precision (intra- and inter-day: 0.7–1.4 %), accuracy (99.90–100.7 %), detection limit (0.34–0.46 µg/mL) and quantification limit (1.15–1.52 µg/mL). The contents of total flavonoids in manihot flowers were as follows in descending order: Infrared Drying (50.96 mg/g) > Microwave Drying (41.84 mg/g) ≈ Hot-air Drying (39.58 mg/g) ≈ Fresh (39.35 mg/g) ≈ Primary Drying (38.95 mg/g). Principal component analysis showed that samples processed with Fresh, Primary Drying, and the investigated three modern drying methods were well classified into three domains, indicating an important difference between drying methods. For the purpose of saving the flavonoids contents, infrared drying under 80–100 °C would be most acceptable. Furthermore, using UHPLC Q-Exactive Orbitrap MS data with targeted and non-targeted approaches, 28 compounds were identified in Abelmoschus manihot samples. Flavonoids were the main group of compounds found in Abelmoschus manihot flowers. The study could provide the scientific evidence for the selection and optimization of appropriate drying method for manihot flowers, and also provide the reference for the formation of generic primary drying processing technology for medicinal flowers containing flavonoids.
利用超高效液相色谱 Q-exactive MS 和高效液相色谱-PDA 对采用不同干燥方法处理的马齿苋花中的主要成分进行定性和定量分析。
在中国的临床实践中,Abelmoschus manihot (L.) Medic 的花通常用于治疗各种慢性肾病。尽管传统使用历史悠久,但通过不同干燥技术获得的花朵从未进行过全面的化学表征,不同干燥方法之间的成分范围也未见全面报道。为了建立一种质量控制和化学特征描述方法,我们对 14 种采后处理方法的 14 批样品进行了研究。采用 HPLC-PDA 方法对七种黄酮类化合物进行了定量分析。该方法的线性(r > 0.999)、精密度(日内和日间:0.7-1.4 %)、准确度(99.90-100.7 %)、检出限(0.34-0.46 µg/mL)和定量限(1.15-1.52 µg/mL)均得到了验证。马尼芦花中总黄酮的含量由高到低依次为红外烘干(50.96 mg/g)>微波烘干(41.84 mg/g)≈热风烘干(39.58 mg/g)≈新鲜(39.35 mg/g)≈一次烘干(38.95 mg/g)。主成分分析表明,用新鲜、初级干燥和所研究的三种现代干燥方法处理的样品被很好地分为三个域,表明不同干燥方法之间存在重要差异。为了保留黄酮类化合物的含量,80-100 °C下的红外干燥是最可接受的。此外,利用超高效液相色谱 Q-Exactive Orbitrap MS 数据,采用靶向和非靶向方法,在马齿苋样品中鉴定出 28 种化合物。黄酮类化合物是在马齿苋花中发现的主要化合物。该研究可为选择和优化适宜的芒果花干燥方法提供科学依据,也可为形成含黄酮类化合物药用花卉的通用初级干燥加工技术提供参考。
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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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