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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Korean Pharmacopuncture Institute
2014-12-01
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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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