用经验证的仪器薄层色谱法同时测定Desmodium oojeinensis树皮和根中的羽扇豆醇、豆甾醇和白桦脂素

IF 1.1 4区 化学 Q4 CHEMISTRY, ANALYTICAL Jpc-journal of Planar Chromatography-modern Tlc Pub Date : 2024-04-30 DOI:10.1007/s00764-024-00297-w
Shital Ingole, Balu Ghule, Kundan Patil, Nikita Takale
{"title":"用经验证的仪器薄层色谱法同时测定Desmodium oojeinensis树皮和根中的羽扇豆醇、豆甾醇和白桦脂素","authors":"Shital Ingole, Balu Ghule, Kundan Patil, Nikita Takale","doi":"10.1007/s00764-024-00297-w","DOIUrl":null,"url":null,"abstract":"<p><i>Desmodium oojeinensis</i> (Roxb.) H. Ohashi (DO) plant has been traditionally known to possess astringent, anti-inflammatory, hepatoprotective, wound healing, antimicrobial, rejuvenating, etc., activities. Since standardization of medicinal plants is essential to assess their quality by determining the active chemical constituents, the present work was aimed to estimate lupeol, stigmasterol, and betulin in DO bark and roots by a validated thin-layer chromatography (TLC) method. The proposed instrumental TLC method was validated in terms of linearity and range, limit of detection (LOD) and limit of quantification (LOQ), accuracy, precision, robustness and specificity. The mobile phase containing hexane‒ethyl acetate (8.5:1.5, <i>V/V</i>) and TLC aluminum plate, precoated with silica gel 60 F<sub>254</sub> as stationary phase were used. Anisaldehyde‒H<sub>2</sub>SO<sub>4</sub> reagent was used for post-chromatographic derivatization. Data for the calibration plots of lupeol, stigmasterol and betulin showed linearity with <i>y</i> = 20.097<i>x</i> + 5124.9 (<i>r</i><sup>2</sup> = 0.9906), <i>y</i> = 12.466<i>x</i> + 1518.5 (<i>r</i><sup>2</sup> = 0.99472), and <i>y</i> = 10.902<i>x</i> + 545.3 (<i>r</i><sup>2</sup> = 0.9944) regression equations, respectively, in 100–500 ng band<sup>−1</sup> concentrations. Lupeol, stigmasterol, and betulin were eluted at <i>R</i><sub>F</sub> [± standard deviation (SD)] 0.42 ± 0.01, 0.27 ± 0.01, and 0.19 ± 0.01, respectively. The LOD and LOQ for lupeol, stigmasterol, and betulin were found to be 12.75 and 38.64 ng band<sup>−1</sup>, 18.02 and 54.59 ng band<sup>−1</sup>, and 13.35 and 40.46 ng band<sup>−1</sup>, respectively. Stability study revealed that lupeol, stigmasterol, and betulin were stable in chloroform at 25 ± 2 °C for 24 h with <i>%RSD</i> value of 0.69, 1.07, and 1.64, respectively. The proposed work showed good precision, robustness and specificity of the method. Average percentage recoveries of lupeol, stigmasterol, and betulin from the chloroform extracts of DO bark and roots were 97.43 ± 0.47, 97.69 ± 0.59; 97.02 ± 1.04, 97.89 ± 0.65, 98.18 ± 0.73, and 97.68 ± 1.09, respectively. The contents (% <i>w/w</i>; <i>n</i> = 3) of lupeol, stigmasterol, and betulin in the chloroform extracts of bark and roots of DO were found to be 2.15 ± 0.03 and 0.45 ± 0.06, 0.43 ± 0.03 and 0.40 ± 0.05, and 2.65 ± 0.04 and 2.13 ± 0.05, respectively, on dry weight basis of the extracts.</p>","PeriodicalId":17616,"journal":{"name":"Jpc-journal of Planar Chromatography-modern Tlc","volume":null,"pages":null},"PeriodicalIF":1.1000,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Simultaneous estimation of lupeol, stigmasterol and betulin in Desmodium oojeinensis bark and roots by a validated instrumental thin-layer chromatography method\",\"authors\":\"Shital Ingole, Balu Ghule, Kundan Patil, Nikita Takale\",\"doi\":\"10.1007/s00764-024-00297-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><i>Desmodium oojeinensis</i> (Roxb.) H. Ohashi (DO) plant has been traditionally known to possess astringent, anti-inflammatory, hepatoprotective, wound healing, antimicrobial, rejuvenating, etc., activities. Since standardization of medicinal plants is essential to assess their quality by determining the active chemical constituents, the present work was aimed to estimate lupeol, stigmasterol, and betulin in DO bark and roots by a validated thin-layer chromatography (TLC) method. The proposed instrumental TLC method was validated in terms of linearity and range, limit of detection (LOD) and limit of quantification (LOQ), accuracy, precision, robustness and specificity. The mobile phase containing hexane‒ethyl acetate (8.5:1.5, <i>V/V</i>) and TLC aluminum plate, precoated with silica gel 60 F<sub>254</sub> as stationary phase were used. Anisaldehyde‒H<sub>2</sub>SO<sub>4</sub> reagent was used for post-chromatographic derivatization. Data for the calibration plots of lupeol, stigmasterol and betulin showed linearity with <i>y</i> = 20.097<i>x</i> + 5124.9 (<i>r</i><sup>2</sup> = 0.9906), <i>y</i> = 12.466<i>x</i> + 1518.5 (<i>r</i><sup>2</sup> = 0.99472), and <i>y</i> = 10.902<i>x</i> + 545.3 (<i>r</i><sup>2</sup> = 0.9944) regression equations, respectively, in 100–500 ng band<sup>−1</sup> concentrations. Lupeol, stigmasterol, and betulin were eluted at <i>R</i><sub>F</sub> [± standard deviation (SD)] 0.42 ± 0.01, 0.27 ± 0.01, and 0.19 ± 0.01, respectively. The LOD and LOQ for lupeol, stigmasterol, and betulin were found to be 12.75 and 38.64 ng band<sup>−1</sup>, 18.02 and 54.59 ng band<sup>−1</sup>, and 13.35 and 40.46 ng band<sup>−1</sup>, respectively. Stability study revealed that lupeol, stigmasterol, and betulin were stable in chloroform at 25 ± 2 °C for 24 h with <i>%RSD</i> value of 0.69, 1.07, and 1.64, respectively. The proposed work showed good precision, robustness and specificity of the method. Average percentage recoveries of lupeol, stigmasterol, and betulin from the chloroform extracts of DO bark and roots were 97.43 ± 0.47, 97.69 ± 0.59; 97.02 ± 1.04, 97.89 ± 0.65, 98.18 ± 0.73, and 97.68 ± 1.09, respectively. The contents (% <i>w/w</i>; <i>n</i> = 3) of lupeol, stigmasterol, and betulin in the chloroform extracts of bark and roots of DO were found to be 2.15 ± 0.03 and 0.45 ± 0.06, 0.43 ± 0.03 and 0.40 ± 0.05, and 2.65 ± 0.04 and 2.13 ± 0.05, respectively, on dry weight basis of the extracts.</p>\",\"PeriodicalId\":17616,\"journal\":{\"name\":\"Jpc-journal of Planar Chromatography-modern Tlc\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2024-04-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Jpc-journal of Planar Chromatography-modern Tlc\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1007/s00764-024-00297-w\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jpc-journal of Planar Chromatography-modern Tlc","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s00764-024-00297-w","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

摘要

Desmodium oojeinensis (Roxb.) H. Ohashi(DO)植物具有收敛、消炎、保肝、伤口愈合、抗菌、恢复活力等传统功效。由于药用植物的标准化对于通过测定其活性化学成分来评估其质量至关重要,因此本研究旨在通过有效的薄层色谱(TLC)方法来评估 DO 树皮和根中的羽扇豆醇、豆甾醇和白桦脂素含量。该方法的线性范围、检出限(LOD)和定量限(LOQ)、准确度、精密度、稳健性和特异性均得到了验证。流动相为正己烷-乙酸乙酯(8.5:1.5, V/V),固定相为预涂硅胶 60 F254 的 TLC 铝板。苯甲醛-H2SO4 试剂用于色谱后衍生。羽扇豆醇、豆甾醇和桦木醇的校准图数据显示,在 100-500 ng band-1 浓度范围内,其线性回归方程分别为 y = 20.097x + 5124.9 (r2 = 0.9906)、y = 12.466x + 1518.5 (r2 = 0.99472) 和 y = 10.902x + 545.3 (r2 = 0.9944)。羽扇豆醇、豆甾醇和白桦脂的洗脱率[± 标准偏差 (SD)]分别为 0.42 ± 0.01、0.27 ± 0.01 和 0.19 ± 0.01。羽扇豆醇、豆甾醇和白桦脂的最低检出限和最低定量限分别为 12.75 和 38.64 ng band-1、18.02 和 54.59 ng band-1 以及 13.35 和 40.46 ng band-1。稳定性研究表明,羽扇豆醇、豆甾醇和白桦脂在氯仿中于 25 ± 2 °C、24 h 内稳定,其 %RSD 值分别为 0.69、1.07 和 1.64。该方法具有良好的精密度、稳健性和特异性。DO树皮和根的氯仿提取物中羽扇豆醇、豆甾醇和白桦脂素的平均回收率分别为97.43 ± 0.47、97.69 ± 0.59、97.02 ± 1.04、97.89 ± 0.65、98.18 ± 0.73和97.68 ± 1.09。按提取物干重计算,DO 树皮和根的氯仿提取物中羽扇豆醇、豆甾醇和白桦脂素的含量(% w/w;n = 3)分别为 2.15 ± 0.03 和 0.45 ± 0.06,0.43 ± 0.03 和 0.40 ± 0.05,以及 2.65 ± 0.04 和 2.13 ± 0.05。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Simultaneous estimation of lupeol, stigmasterol and betulin in Desmodium oojeinensis bark and roots by a validated instrumental thin-layer chromatography method

Desmodium oojeinensis (Roxb.) H. Ohashi (DO) plant has been traditionally known to possess astringent, anti-inflammatory, hepatoprotective, wound healing, antimicrobial, rejuvenating, etc., activities. Since standardization of medicinal plants is essential to assess their quality by determining the active chemical constituents, the present work was aimed to estimate lupeol, stigmasterol, and betulin in DO bark and roots by a validated thin-layer chromatography (TLC) method. The proposed instrumental TLC method was validated in terms of linearity and range, limit of detection (LOD) and limit of quantification (LOQ), accuracy, precision, robustness and specificity. The mobile phase containing hexane‒ethyl acetate (8.5:1.5, V/V) and TLC aluminum plate, precoated with silica gel 60 F254 as stationary phase were used. Anisaldehyde‒H2SO4 reagent was used for post-chromatographic derivatization. Data for the calibration plots of lupeol, stigmasterol and betulin showed linearity with y = 20.097x + 5124.9 (r2 = 0.9906), y = 12.466x + 1518.5 (r2 = 0.99472), and y = 10.902x + 545.3 (r2 = 0.9944) regression equations, respectively, in 100–500 ng band−1 concentrations. Lupeol, stigmasterol, and betulin were eluted at RF [± standard deviation (SD)] 0.42 ± 0.01, 0.27 ± 0.01, and 0.19 ± 0.01, respectively. The LOD and LOQ for lupeol, stigmasterol, and betulin were found to be 12.75 and 38.64 ng band−1, 18.02 and 54.59 ng band−1, and 13.35 and 40.46 ng band−1, respectively. Stability study revealed that lupeol, stigmasterol, and betulin were stable in chloroform at 25 ± 2 °C for 24 h with %RSD value of 0.69, 1.07, and 1.64, respectively. The proposed work showed good precision, robustness and specificity of the method. Average percentage recoveries of lupeol, stigmasterol, and betulin from the chloroform extracts of DO bark and roots were 97.43 ± 0.47, 97.69 ± 0.59; 97.02 ± 1.04, 97.89 ± 0.65, 98.18 ± 0.73, and 97.68 ± 1.09, respectively. The contents (% w/w; n = 3) of lupeol, stigmasterol, and betulin in the chloroform extracts of bark and roots of DO were found to be 2.15 ± 0.03 and 0.45 ± 0.06, 0.43 ± 0.03 and 0.40 ± 0.05, and 2.65 ± 0.04 and 2.13 ± 0.05, respectively, on dry weight basis of the extracts.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
2.20
自引率
18.80%
发文量
66
审稿时长
>12 weeks
期刊介绍: JPC - Journal of Planar Chromatography - Modern TLC is an international journal devoted exclusively to the publication of research papers on analytical and preparative planar chromatography. The journal covers all fields of planar chromatography, on all kinds of stationary phase (paper, layer, gel) and with various modes of migration of the mobile phase (capillary action or forced flow).
期刊最新文献
A novel validated instrumental thin-layer chromatographic method and marker-based standardization of liquid herbal formulation using atropine, rutin and vanillin as biomarkers Evaluation of greenness, blueness, and whiteness with analytical quality by design assisted instrumental reversed-phase thin-layer chromatography‒densitometric approach to estimate monosodium glutamate in commercial food samples using green-ultrasound-assisted extraction technique Thin-layer chromatography image analysis with leave-1-out method and cross-sectional study for quality assessment of a polyherbal preparation ‘Phikud Navakot’ A validated phytochemical marker based HPTLC method for the segregation of Bauhinia vahlii Wight and Arn. from geologically different samples of Indian zones Rapid authentication of five medicinal seeds from Cruciferae family based on high-performance thin-layer chromatography
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1