A stability-indicating HPLC method for determination of chemical markers in Boesenbergia rotunda extract capsules
69
Issued Date
2025-01-01
Resource Type
ISSN
25868195
eISSN
25868470
Scopus ID
2-s2.0-85214300449
Journal Title
Pharmaceutical Sciences Asia
Volume
52
Issue
1
Start Page
55
End Page
64
Rights Holder(s)
SCOPUS
Bibliographic Citation
Pharmaceutical Sciences Asia Vol.52 No.1 (2025) , 55-64
Suggested Citation
Suphakijudomkarn P., Suwanvecho C., Sithisarn P., Khemawoot P., Rojsanga P. A stability-indicating HPLC method for determination of chemical markers in Boesenbergia rotunda extract capsules. Pharmaceutical Sciences Asia Vol.52 No.1 (2025) , 55-64. 64. doi:10.29090/psa.2025.01.24.AB0626 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/102914
Title
A stability-indicating HPLC method for determination of chemical markers in Boesenbergia rotunda extract capsules
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Corresponding Author(s)
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Abstract
Boesenbergia rotunda, or krachai in Thai, is a medicinal plant with the potential for medicinal and nutraceutical development because of its pharmacological properties. Therefore, a well-developed and accurate analytical method is crucial to ensure the appropriate quality control of B. rotunda products. This study aimed to develop a simple stability-indicating HPLC-UV method for the quantitative determination of pinocembrin, pinostrobin, and panduratin A contents in B. rotunda extract capsules. HPLC chromatographic conditions were optimized using a C18 column. The mobile phase comprised of 0.1% formic acid in water and methanol in acetonitrile using a gradient system at a flow rate of 1 mL/min. The detection wavelength was 300 nm. The method was validated according to the guidelines of the International Conference on Harmonization (ICH Q2) for linearity, accuracy, precision, and specificity. Forced degradation studies under acid, base, oxidation, and sun photolytic conditions were also performed. The forced degradation of B. rotunda extract capsule showed that all selected chemical constituents were stable in acid and oxidative conditions, but they were highly labile under basic and photolytic conditions. There was no interference from impurities, degradation products, or excipients in the HPLC chromatogram at the retention times of those standards indicating the specificity of the analytical method. The developed HPLC method promoted linear correlations in the range of 10–200 µg/mL for pinocembrin, 50–1000 µg/mL for pinostrobin, and 5–100 µg/mL for panduratin A, with correlation coefficients (r) > 0.99. The recoveries were acceptable for all markers. Relative standard deviations (RSDs) of repeatability and intermediate precision were less than 2.0%. HPLC method has been successfully developed and validated for quantitative analysis of chemical markers in B. rotunda extract capsules. This study provides a promising chemical analysis approach for quality control and standardization of herbal medicines, especially B. rotunda products in the future.