{"title":"建立高效薄层色谱法同时测定网麻和马蹄莲中α - Amyrin、桦木素和β -谷甾醇的方法并进行验证","authors":"Sahaya Mercy Jaquline Robert, Vidhu Aeri","doi":"10.1002/sscp.202300092","DOIUrl":null,"url":null,"abstract":"Abstract High‐performance thin‐layer chromatography (HPTLC), a top‐notch technique in the field of analysis, is quite irreplaceable when it comes to identifying and standardizing medicinal plants . Marsdenia tenacissima and Leptadenia reticulata have claimed traditional uses like anti‐cancer, anti‐inflammatory, anti‐depressant, hepatoprotection, etc., with few similar phytoconstituents. In this study, a precise and validated HPTLC densitometric method was developed for the identification of α‐amyrin, β‐sitosterol, and betulin in the above‐mentioned plants by static maceration with ethanol and aqueous‐ethanol extracts. The developed method was evaluated by linearity, range, accuracy, precision, limit of detection, limit of quantification, robustness, and specificity. The markers were subjected to ascending development with toluene: ethyl acetate: glacial acetic acid at a ratio of 8:1.5:0.5 v/v/v, air‐dried, and derivatized with anisaldehyde‐sulfuric acid. The retardation factor values of the markers were found to be 0.63 (α‐amyrin), 0.52 (β‐sitosterol), and 0.64 (betulin) for L. reticulata , and 0.55 (α‐amyrin), 0.45 (β‐sitosterol), and 0.57 (betulin) for M. tenacissima . The chromatographic results suggest that the developed method suits all three markers and can be simultaneously identified in both plants.","PeriodicalId":21639,"journal":{"name":"SEPARATION SCIENCE PLUS","volume":"124 16","pages":"0"},"PeriodicalIF":1.3000,"publicationDate":"2023-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Development and validation of high‐performance thin‐layer chromatography method for simultaneous estimation of α‐Amyrin, Betulin, and β‐Sitosterol in <i>Leptadenia reticulata</i> and <i>Marsdenia tenacissima</i>\",\"authors\":\"Sahaya Mercy Jaquline Robert, Vidhu Aeri\",\"doi\":\"10.1002/sscp.202300092\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract High‐performance thin‐layer chromatography (HPTLC), a top‐notch technique in the field of analysis, is quite irreplaceable when it comes to identifying and standardizing medicinal plants . Marsdenia tenacissima and Leptadenia reticulata have claimed traditional uses like anti‐cancer, anti‐inflammatory, anti‐depressant, hepatoprotection, etc., with few similar phytoconstituents. In this study, a precise and validated HPTLC densitometric method was developed for the identification of α‐amyrin, β‐sitosterol, and betulin in the above‐mentioned plants by static maceration with ethanol and aqueous‐ethanol extracts. The developed method was evaluated by linearity, range, accuracy, precision, limit of detection, limit of quantification, robustness, and specificity. The markers were subjected to ascending development with toluene: ethyl acetate: glacial acetic acid at a ratio of 8:1.5:0.5 v/v/v, air‐dried, and derivatized with anisaldehyde‐sulfuric acid. The retardation factor values of the markers were found to be 0.63 (α‐amyrin), 0.52 (β‐sitosterol), and 0.64 (betulin) for L. reticulata , and 0.55 (α‐amyrin), 0.45 (β‐sitosterol), and 0.57 (betulin) for M. tenacissima . The chromatographic results suggest that the developed method suits all three markers and can be simultaneously identified in both plants.\",\"PeriodicalId\":21639,\"journal\":{\"name\":\"SEPARATION SCIENCE PLUS\",\"volume\":\"124 16\",\"pages\":\"0\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2023-11-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"SEPARATION SCIENCE PLUS\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/sscp.202300092\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"SEPARATION SCIENCE PLUS","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/sscp.202300092","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Development and validation of high‐performance thin‐layer chromatography method for simultaneous estimation of α‐Amyrin, Betulin, and β‐Sitosterol in Leptadenia reticulata and Marsdenia tenacissima
Abstract High‐performance thin‐layer chromatography (HPTLC), a top‐notch technique in the field of analysis, is quite irreplaceable when it comes to identifying and standardizing medicinal plants . Marsdenia tenacissima and Leptadenia reticulata have claimed traditional uses like anti‐cancer, anti‐inflammatory, anti‐depressant, hepatoprotection, etc., with few similar phytoconstituents. In this study, a precise and validated HPTLC densitometric method was developed for the identification of α‐amyrin, β‐sitosterol, and betulin in the above‐mentioned plants by static maceration with ethanol and aqueous‐ethanol extracts. The developed method was evaluated by linearity, range, accuracy, precision, limit of detection, limit of quantification, robustness, and specificity. The markers were subjected to ascending development with toluene: ethyl acetate: glacial acetic acid at a ratio of 8:1.5:0.5 v/v/v, air‐dried, and derivatized with anisaldehyde‐sulfuric acid. The retardation factor values of the markers were found to be 0.63 (α‐amyrin), 0.52 (β‐sitosterol), and 0.64 (betulin) for L. reticulata , and 0.55 (α‐amyrin), 0.45 (β‐sitosterol), and 0.57 (betulin) for M. tenacissima . The chromatographic results suggest that the developed method suits all three markers and can be simultaneously identified in both plants.