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Validated Quantitative (1)H NMR Method for Simultaneous Quantification of Indole Alkaloids in Uncaria rhynchophylla

[Image: see text] Uncariae Ramulus Cum Uncis, known as “Gou-Teng” in Chinese, is derived mainly from the dried hook-bearing stems of Uncaria rhynchophylla. Quantitative determination of monoterpenoid indole alkaloids is critical for controlling its quality. In the present study, a rapid, accurate, a...

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Autores principales: Yin, Tianpeng, Lu, Jingguang, Liu, Qinghua, Zhu, Guoyuan, Zhang, Wei, Jiang, Zhihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8638010/
https://www.ncbi.nlm.nih.gov/pubmed/34870003
http://dx.doi.org/10.1021/acsomega.1c04464
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author Yin, Tianpeng
Lu, Jingguang
Liu, Qinghua
Zhu, Guoyuan
Zhang, Wei
Jiang, Zhihong
author_facet Yin, Tianpeng
Lu, Jingguang
Liu, Qinghua
Zhu, Guoyuan
Zhang, Wei
Jiang, Zhihong
author_sort Yin, Tianpeng
collection PubMed
description [Image: see text] Uncariae Ramulus Cum Uncis, known as “Gou-Teng” in Chinese, is derived mainly from the dried hook-bearing stems of Uncaria rhynchophylla. Quantitative determination of monoterpenoid indole alkaloids is critical for controlling its quality. In the present study, a rapid, accurate, and precise method was developed for the simultaneous quantitation of four characteristic components, namely, rhynchophylline (1), isorhynchophylline (2), corynoxeine (3), and isocorynoxeine (4), through (1)H NMR spectrometry techniques. This method was performed on a 600 MHz NMR spectrometer with optimized acquisition parameters for performing quantitative experiments within 14 min. The highly deshielded signal of NH was at δ(H) 10–11 in the aprotic solvent DMSO-d(6), which enables satisfactory separation of the signals to be integrated. Validation of the quantitative method was also performed in terms of specificity, linearity, sensitivity, accuracy, and precision. The method is linear in the concentration range of 25–400 μg/mL. The lower limit of quantification is 25 μg/mL. The intra- and interday relative standard deviation across three validation runs over the entire concentration range is less than 2.51%. The accuracy determined at three concentrations was within ±4.4% in terms of relative error. The proposed qNMR method was demonstrated to be a powerful tool for quantifying the alkaloids in traditional Chinese medicines (TCMs) due to its unique advantages of high precision, rapid analysis, and nonrequirement of standard compounds for calibration curve preparation. Moreover, qNMR represents a feasible alternative to high-performance liquid chromatography-based methods for the quality control of TCMs.
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spelling pubmed-86380102021-12-03 Validated Quantitative (1)H NMR Method for Simultaneous Quantification of Indole Alkaloids in Uncaria rhynchophylla Yin, Tianpeng Lu, Jingguang Liu, Qinghua Zhu, Guoyuan Zhang, Wei Jiang, Zhihong ACS Omega [Image: see text] Uncariae Ramulus Cum Uncis, known as “Gou-Teng” in Chinese, is derived mainly from the dried hook-bearing stems of Uncaria rhynchophylla. Quantitative determination of monoterpenoid indole alkaloids is critical for controlling its quality. In the present study, a rapid, accurate, and precise method was developed for the simultaneous quantitation of four characteristic components, namely, rhynchophylline (1), isorhynchophylline (2), corynoxeine (3), and isocorynoxeine (4), through (1)H NMR spectrometry techniques. This method was performed on a 600 MHz NMR spectrometer with optimized acquisition parameters for performing quantitative experiments within 14 min. The highly deshielded signal of NH was at δ(H) 10–11 in the aprotic solvent DMSO-d(6), which enables satisfactory separation of the signals to be integrated. Validation of the quantitative method was also performed in terms of specificity, linearity, sensitivity, accuracy, and precision. The method is linear in the concentration range of 25–400 μg/mL. The lower limit of quantification is 25 μg/mL. The intra- and interday relative standard deviation across three validation runs over the entire concentration range is less than 2.51%. The accuracy determined at three concentrations was within ±4.4% in terms of relative error. The proposed qNMR method was demonstrated to be a powerful tool for quantifying the alkaloids in traditional Chinese medicines (TCMs) due to its unique advantages of high precision, rapid analysis, and nonrequirement of standard compounds for calibration curve preparation. Moreover, qNMR represents a feasible alternative to high-performance liquid chromatography-based methods for the quality control of TCMs. American Chemical Society 2021-11-16 /pmc/articles/PMC8638010/ /pubmed/34870003 http://dx.doi.org/10.1021/acsomega.1c04464 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Yin, Tianpeng
Lu, Jingguang
Liu, Qinghua
Zhu, Guoyuan
Zhang, Wei
Jiang, Zhihong
Validated Quantitative (1)H NMR Method for Simultaneous Quantification of Indole Alkaloids in Uncaria rhynchophylla
title Validated Quantitative (1)H NMR Method for Simultaneous Quantification of Indole Alkaloids in Uncaria rhynchophylla
title_full Validated Quantitative (1)H NMR Method for Simultaneous Quantification of Indole Alkaloids in Uncaria rhynchophylla
title_fullStr Validated Quantitative (1)H NMR Method for Simultaneous Quantification of Indole Alkaloids in Uncaria rhynchophylla
title_full_unstemmed Validated Quantitative (1)H NMR Method for Simultaneous Quantification of Indole Alkaloids in Uncaria rhynchophylla
title_short Validated Quantitative (1)H NMR Method for Simultaneous Quantification of Indole Alkaloids in Uncaria rhynchophylla
title_sort validated quantitative (1)h nmr method for simultaneous quantification of indole alkaloids in uncaria rhynchophylla
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8638010/
https://www.ncbi.nlm.nih.gov/pubmed/34870003
http://dx.doi.org/10.1021/acsomega.1c04464
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