HPLC Method for Simultaneous Quantitative Detection of Quercetin and Curcuminoids in Traditional Chinese Medicines

Objectives: Quercetin and curcuminoids are important bioactive compounds found in many herbs. Previously reported high performance liquid chromatography ultraviolet (HPLC-UV) methods for the detection of quercetin and curcuminoids have several disadvantages, including unsatisfactory separation...

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Main Authors: Lee Fung Ang, Mun Fei Yam, Yvonne Tan Tze Fung, Peh Kok Kiang, Yusrida Darwin
Format: Article
Language:English
Published: Korean Pharmacopuncture Institute 2014-12-01
Series:Journal of Pharmacopuncture
Subjects:
Online Access:http://dx.doi.org/10.3831/KPI.2014.17.035
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spelling doaj-c011cca11a0b4cd3bf41c4ca7a3017662020-11-24T21:22:39ZengKorean Pharmacopuncture InstituteJournal of Pharmacopuncture2093-69662234-68562014-12-01174364910.3831/KPI.2014.17.035HPLC Method for Simultaneous Quantitative Detection of Quercetin and Curcuminoids in Traditional Chinese MedicinesLee Fung Ang0Mun Fei Yam1Yvonne Tan Tze Fung2Peh Kok Kiang3Yusrida Darwin4School of Pharmaceutical Sciences, Universiti Sains Malaysia, 11800, Penang, MalaysiaSchool of Pharmaceutical Sciences, Universiti Sains Malaysia, 11800, Penang, MalaysiaSchool of Pharmaceutical Sciences, Universiti Sains Malaysia, 11800, Penang, MalaysiaSchool of Pharmaceutical Sciences, Universiti Sains Malaysia, 11800, Penang, MalaysiaSchool of Pharmaceutical Sciences, Universiti Sains Malaysia, 11800, Penang, MalaysiaObjectives: Quercetin and curcuminoids are important bioactive compounds found in many herbs. Previously reported high performance liquid chromatography ultraviolet (HPLC-UV) methods for the detection of quercetin and curcuminoids have several disadvantages, including unsatisfactory separation times and lack of validation according the standard guidelines of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use. Methods: A rapid, specific, reversed phase, HPLC-UV method with an isocratic elution of acetonitrile and 2% v/v acetic acid (40% : 60% v/v) (pH 2.6) at a flow rate of 1.3 mL/minutes, a column temperature of 35°C, and ultraviolet (UV) detection at 370 nm was developed. The method was validated and applied to the quantification of different types of market available Chinese medicine extracts, pills and tablets. Results: The method allowed simultaneous determination of quercetin, bisdemethoxycurcumin, demethoxycurcumin and curcumin in the concentration ranges of 0.00488 ─ 200 μg/mL, 0.625 ─ 320 μg/mL, 0.07813 ─ 320 μg/mL and 0.03906 ─ 320 μg/mL, respectively. The limits of detection and quantification, respectively, were 0.00488 and 0.03906 μg/mL for quercetin, 0.62500 and 2.50000 μg/mL for bisdemethoxycurcumin, 0.07813 and 0.31250 μg/mL for demethoxycurcumin, and 0.03906 and 0.07813 μg/mL for curcumin. The percent relative intra day standard deviation (% RSD) values were 0.432 ─ 0.806 μg/mL, 0.576 ─ 0.723 μg/ mL, 0.635 ─ 0.752 μg/mL and 0.655 ─ 0.732 μg/mL for quercetin, bisdemethoxycurcumin, demethoxycurcumin and curcumin, respectively, and those for intra day precision were 0.323 ─ 0.968 μg/mL, 0.805 ─ 0.854 μg/mL, 0.078 ─ 0.844 μg/mL and 0.275 ─ 0.829 μg/mL, respectively. The intra day accuracies were 99.589% ─ 100.821%, 98.588% ─ 101.084%, 9.289% ─ 100.88%, and 98.292% ─ 101.022% for quercetin, bisdemethoxycurcumin, demethoxycurcumin and curcumin, respectively, and the inter day accuracy were 99.665% ─ 103.06%, 97.669% ─ 103.513%, 99.569% ─ 103.617%, and 97.929% ─ 103.606%, respectively. Conclusion: The method was found to be simple, accurate and precise and is recommended for routine quality control analysis of commercial Chinese medicine products containing the flour flavonoids as their principle components in the extracts.http://dx.doi.org/10.3831/KPI.2014.17.035curcuminoidhigh-performance liquid chromatography (HPLC)international conference harmonisation (ICH)quercetin
collection DOAJ
language English
format Article
sources DOAJ
author Lee Fung Ang
Mun Fei Yam
Yvonne Tan Tze Fung
Peh Kok Kiang
Yusrida Darwin
spellingShingle Lee Fung Ang
Mun Fei Yam
Yvonne Tan Tze Fung
Peh Kok Kiang
Yusrida Darwin
HPLC Method for Simultaneous Quantitative Detection of Quercetin and Curcuminoids in Traditional Chinese Medicines
Journal of Pharmacopuncture
curcuminoid
high-performance liquid chromatography (HPLC)
international conference harmonisation (ICH)
quercetin
author_facet Lee Fung Ang
Mun Fei Yam
Yvonne Tan Tze Fung
Peh Kok Kiang
Yusrida Darwin
author_sort Lee Fung Ang
title HPLC Method for Simultaneous Quantitative Detection of Quercetin and Curcuminoids in Traditional Chinese Medicines
title_short HPLC Method for Simultaneous Quantitative Detection of Quercetin and Curcuminoids in Traditional Chinese Medicines
title_full HPLC Method for Simultaneous Quantitative Detection of Quercetin and Curcuminoids in Traditional Chinese Medicines
title_fullStr HPLC Method for Simultaneous Quantitative Detection of Quercetin and Curcuminoids in Traditional Chinese Medicines
title_full_unstemmed HPLC Method for Simultaneous Quantitative Detection of Quercetin and Curcuminoids in Traditional Chinese Medicines
title_sort hplc method for simultaneous quantitative detection of quercetin and curcuminoids in traditional chinese medicines
publisher Korean Pharmacopuncture Institute
series Journal of Pharmacopuncture
issn 2093-6966
2234-6856
publishDate 2014-12-01
description Objectives: Quercetin and curcuminoids are important bioactive compounds found in many herbs. Previously reported high performance liquid chromatography ultraviolet (HPLC-UV) methods for the detection of quercetin and curcuminoids have several disadvantages, including unsatisfactory separation times and lack of validation according the standard guidelines of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use. Methods: A rapid, specific, reversed phase, HPLC-UV method with an isocratic elution of acetonitrile and 2% v/v acetic acid (40% : 60% v/v) (pH 2.6) at a flow rate of 1.3 mL/minutes, a column temperature of 35°C, and ultraviolet (UV) detection at 370 nm was developed. The method was validated and applied to the quantification of different types of market available Chinese medicine extracts, pills and tablets. Results: The method allowed simultaneous determination of quercetin, bisdemethoxycurcumin, demethoxycurcumin and curcumin in the concentration ranges of 0.00488 ─ 200 μg/mL, 0.625 ─ 320 μg/mL, 0.07813 ─ 320 μg/mL and 0.03906 ─ 320 μg/mL, respectively. The limits of detection and quantification, respectively, were 0.00488 and 0.03906 μg/mL for quercetin, 0.62500 and 2.50000 μg/mL for bisdemethoxycurcumin, 0.07813 and 0.31250 μg/mL for demethoxycurcumin, and 0.03906 and 0.07813 μg/mL for curcumin. The percent relative intra day standard deviation (% RSD) values were 0.432 ─ 0.806 μg/mL, 0.576 ─ 0.723 μg/ mL, 0.635 ─ 0.752 μg/mL and 0.655 ─ 0.732 μg/mL for quercetin, bisdemethoxycurcumin, demethoxycurcumin and curcumin, respectively, and those for intra day precision were 0.323 ─ 0.968 μg/mL, 0.805 ─ 0.854 μg/mL, 0.078 ─ 0.844 μg/mL and 0.275 ─ 0.829 μg/mL, respectively. The intra day accuracies were 99.589% ─ 100.821%, 98.588% ─ 101.084%, 9.289% ─ 100.88%, and 98.292% ─ 101.022% for quercetin, bisdemethoxycurcumin, demethoxycurcumin and curcumin, respectively, and the inter day accuracy were 99.665% ─ 103.06%, 97.669% ─ 103.513%, 99.569% ─ 103.617%, and 97.929% ─ 103.606%, respectively. Conclusion: The method was found to be simple, accurate and precise and is recommended for routine quality control analysis of commercial Chinese medicine products containing the flour flavonoids as their principle components in the extracts.
topic curcuminoid
high-performance liquid chromatography (HPLC)
international conference harmonisation (ICH)
quercetin
url http://dx.doi.org/10.3831/KPI.2014.17.035
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