Sharmin Sultana, Md Lokman Hossain, Tom Sostaric, Lee Yong Lim, Kevin J Foster, Cornelia Locher
{"title":"使用氯化铝作为衍生试剂,通过 HPTLC 分析法研究黄酮类化合物","authors":"Sharmin Sultana, Md Lokman Hossain, Tom Sostaric, Lee Yong Lim, Kevin J Foster, Cornelia Locher","doi":"10.3390/molecules29215161","DOIUrl":null,"url":null,"abstract":"<p><p>This is the first study to report on high performance thin layer chromatography (HPTLC) generated spectrophotometric data to systematically capture flavonoid compounds using optimized derivatization with either AlCl<sub>3</sub> or NaNO<sub>2</sub>-AlCl<sub>3</sub>-NaOH as visualisation reagents. While the traditional AlCl<sub>3</sub> colorimetric method using UV-Vis analysis provides valuable insights into the presence of flavonoids and allows derivation of the total flavonoid content (TFC) of a sample, HPTLC fingerprints obtained after spraying with AlCl<sub>3</sub> or NaNO<sub>2</sub>-AlCl<sub>3</sub>-NaOH enable the visualization of the various flavonoids present in a sample based on their respective absorption shifts, thus complementing the traditional TFC assay. In this study, 40 different flavonoids representing different classes (flavonols, flavanolols, flavan-3-ol, flavones, flavanones, and isoflavonoids) were analysed. Upon derivatization with AlCl<sub>3</sub> most of the investigated flavonoids recorded bathochromic shifts, yielding characteristic λ<sub>max</sub> values between 370 and 420 nm, while spraying with NaNO<sub>2</sub>-AlCl<sub>3</sub>-NaOH triggered hyperchromic shifts, and thus an increase in absorbance intensity in flavonoids with particular substitution patterns. A few non-flavonoid components with structural similarities to flavonoids (e.g., rosmarinic acid, gallic acid, aspirin, salicylic acid) served as the negative control in this study to determine whether the derivatization reagents allowed exclusive detection of flavonoids. The method was then applied to the analysis of flavonoid containing supplements as well as red clover honey to demonstrate the method's application in the analysis of natural products.</p>","PeriodicalId":19041,"journal":{"name":"Molecules","volume":"29 21","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11547264/pdf/","citationCount":"0","resultStr":"{\"title\":\"Investigating Flavonoids by HPTLC Analysis Using Aluminium Chloride as Derivatization Reagent.\",\"authors\":\"Sharmin Sultana, Md Lokman Hossain, Tom Sostaric, Lee Yong Lim, Kevin J Foster, Cornelia Locher\",\"doi\":\"10.3390/molecules29215161\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>This is the first study to report on high performance thin layer chromatography (HPTLC) generated spectrophotometric data to systematically capture flavonoid compounds using optimized derivatization with either AlCl<sub>3</sub> or NaNO<sub>2</sub>-AlCl<sub>3</sub>-NaOH as visualisation reagents. While the traditional AlCl<sub>3</sub> colorimetric method using UV-Vis analysis provides valuable insights into the presence of flavonoids and allows derivation of the total flavonoid content (TFC) of a sample, HPTLC fingerprints obtained after spraying with AlCl<sub>3</sub> or NaNO<sub>2</sub>-AlCl<sub>3</sub>-NaOH enable the visualization of the various flavonoids present in a sample based on their respective absorption shifts, thus complementing the traditional TFC assay. In this study, 40 different flavonoids representing different classes (flavonols, flavanolols, flavan-3-ol, flavones, flavanones, and isoflavonoids) were analysed. Upon derivatization with AlCl<sub>3</sub> most of the investigated flavonoids recorded bathochromic shifts, yielding characteristic λ<sub>max</sub> values between 370 and 420 nm, while spraying with NaNO<sub>2</sub>-AlCl<sub>3</sub>-NaOH triggered hyperchromic shifts, and thus an increase in absorbance intensity in flavonoids with particular substitution patterns. A few non-flavonoid components with structural similarities to flavonoids (e.g., rosmarinic acid, gallic acid, aspirin, salicylic acid) served as the negative control in this study to determine whether the derivatization reagents allowed exclusive detection of flavonoids. 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Investigating Flavonoids by HPTLC Analysis Using Aluminium Chloride as Derivatization Reagent.
This is the first study to report on high performance thin layer chromatography (HPTLC) generated spectrophotometric data to systematically capture flavonoid compounds using optimized derivatization with either AlCl3 or NaNO2-AlCl3-NaOH as visualisation reagents. While the traditional AlCl3 colorimetric method using UV-Vis analysis provides valuable insights into the presence of flavonoids and allows derivation of the total flavonoid content (TFC) of a sample, HPTLC fingerprints obtained after spraying with AlCl3 or NaNO2-AlCl3-NaOH enable the visualization of the various flavonoids present in a sample based on their respective absorption shifts, thus complementing the traditional TFC assay. In this study, 40 different flavonoids representing different classes (flavonols, flavanolols, flavan-3-ol, flavones, flavanones, and isoflavonoids) were analysed. Upon derivatization with AlCl3 most of the investigated flavonoids recorded bathochromic shifts, yielding characteristic λmax values between 370 and 420 nm, while spraying with NaNO2-AlCl3-NaOH triggered hyperchromic shifts, and thus an increase in absorbance intensity in flavonoids with particular substitution patterns. A few non-flavonoid components with structural similarities to flavonoids (e.g., rosmarinic acid, gallic acid, aspirin, salicylic acid) served as the negative control in this study to determine whether the derivatization reagents allowed exclusive detection of flavonoids. The method was then applied to the analysis of flavonoid containing supplements as well as red clover honey to demonstrate the method's application in the analysis of natural products.
期刊介绍:
Molecules (ISSN 1420-3049, CODEN: MOLEFW) is an open access journal of synthetic organic chemistry and natural product chemistry. All articles are peer-reviewed and published continously upon acceptance. Molecules is published by MDPI, Basel, Switzerland. Our aim is to encourage chemists to publish as much as possible their experimental detail, particularly synthetic procedures and characterization information. There is no restriction on the length of the experimental section. In addition, availability of compound samples is published and considered as important information. Authors are encouraged to register or deposit their chemical samples through the non-profit international organization Molecular Diversity Preservation International (MDPI). Molecules has been launched in 1996 to preserve and exploit molecular diversity of both, chemical information and chemical substances.