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}
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.
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).