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Quality evaluation of Huaijiao pill by chromatographic fingerprint and simultaneous determination of its major bioactive components()
For quality control purpose, an approach of combining chromatographic fingerprint of Huaijiao pill (HP) and simultaneous determination of its major bioactive components was developed using high performance liquid chromatography coupled with diode array detector (HPLC--DAD). For fingerprint analysis,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Xi'an Jiaotong University
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762603/ https://www.ncbi.nlm.nih.gov/pubmed/29403990 http://dx.doi.org/10.1016/j.jpha.2016.03.001 |
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author | Wang, Shuangqin Zhang, Jingjing Liu, Juan Qian, Guangsheng Fu, Chunmei |
author_facet | Wang, Shuangqin Zhang, Jingjing Liu, Juan Qian, Guangsheng Fu, Chunmei |
author_sort | Wang, Shuangqin |
collection | PubMed |
description | For quality control purpose, an approach of combining chromatographic fingerprint of Huaijiao pill (HP) and simultaneous determination of its major bioactive components was developed using high performance liquid chromatography coupled with diode array detector (HPLC--DAD). For fingerprint analysis, 16 peaks were selected as the characteristic peaks to evaluate the similarities of different samples collected from different batches of three manufacturers. The similarities of 17 Huaijiao pill samples were beyond 0.966, indicating that samples from different batches and manufacturers were, to some extent, consistent. Additionally, simultaneous quantification of seven bioactive markers, namely sophoricoside, baicalin, naringin, genistein, rutin, quercetin and 5-O-methylvisammioside, in HP was performed to interpret the quality consistency. The validation of the proposed approach was acceptable, with the accuracy of 90.2%–106.9% in recovery test. The intra-day and inter-day precisions of the method were evaluated and the RSD values were less than 2.81%. The results from the quantitative data showed that the contents of six marker compounds (except for 5-O-methylvisammioside) were quite consistent between batches produced by one manufacturer and significantly distinctive among different manufacturers. The proposed approach was expected to be developed as a powerful tool for the quality control of HP. |
format | Online Article Text |
id | pubmed-5762603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Xi'an Jiaotong University |
record_format | MEDLINE/PubMed |
spelling | pubmed-57626032018-02-05 Quality evaluation of Huaijiao pill by chromatographic fingerprint and simultaneous determination of its major bioactive components() Wang, Shuangqin Zhang, Jingjing Liu, Juan Qian, Guangsheng Fu, Chunmei J Pharm Anal Original Article For quality control purpose, an approach of combining chromatographic fingerprint of Huaijiao pill (HP) and simultaneous determination of its major bioactive components was developed using high performance liquid chromatography coupled with diode array detector (HPLC--DAD). For fingerprint analysis, 16 peaks were selected as the characteristic peaks to evaluate the similarities of different samples collected from different batches of three manufacturers. The similarities of 17 Huaijiao pill samples were beyond 0.966, indicating that samples from different batches and manufacturers were, to some extent, consistent. Additionally, simultaneous quantification of seven bioactive markers, namely sophoricoside, baicalin, naringin, genistein, rutin, quercetin and 5-O-methylvisammioside, in HP was performed to interpret the quality consistency. The validation of the proposed approach was acceptable, with the accuracy of 90.2%–106.9% in recovery test. The intra-day and inter-day precisions of the method were evaluated and the RSD values were less than 2.81%. The results from the quantitative data showed that the contents of six marker compounds (except for 5-O-methylvisammioside) were quite consistent between batches produced by one manufacturer and significantly distinctive among different manufacturers. The proposed approach was expected to be developed as a powerful tool for the quality control of HP. Xi'an Jiaotong University 2016-08 2016-03-15 /pmc/articles/PMC5762603/ /pubmed/29403990 http://dx.doi.org/10.1016/j.jpha.2016.03.001 Text en © 2016 Xi'an Jiaotong University. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Wang, Shuangqin Zhang, Jingjing Liu, Juan Qian, Guangsheng Fu, Chunmei Quality evaluation of Huaijiao pill by chromatographic fingerprint and simultaneous determination of its major bioactive components() |
title | Quality evaluation of Huaijiao pill by chromatographic fingerprint and simultaneous determination of its major bioactive components() |
title_full | Quality evaluation of Huaijiao pill by chromatographic fingerprint and simultaneous determination of its major bioactive components() |
title_fullStr | Quality evaluation of Huaijiao pill by chromatographic fingerprint and simultaneous determination of its major bioactive components() |
title_full_unstemmed | Quality evaluation of Huaijiao pill by chromatographic fingerprint and simultaneous determination of its major bioactive components() |
title_short | Quality evaluation of Huaijiao pill by chromatographic fingerprint and simultaneous determination of its major bioactive components() |
title_sort | quality evaluation of huaijiao pill by chromatographic fingerprint and simultaneous determination of its major bioactive components() |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762603/ https://www.ncbi.nlm.nih.gov/pubmed/29403990 http://dx.doi.org/10.1016/j.jpha.2016.03.001 |
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