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The development of an herbal material quality control strategy considering the effects of manufacturing processes
BACKGROUND: Quality by design (QbD) is an advanced drug quality control concept that has been gradually implemented in the optimization of manufacturing processes of Chinese medicines. However, the variation of Chinese medicinal material quality has rarely been considered in published works. Because...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6760055/ https://www.ncbi.nlm.nih.gov/pubmed/31572490 http://dx.doi.org/10.1186/s13020-019-0262-9 |
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author | Pan, Jingjing He, Siyuan Zheng, Jiayao Shao, Jingyuan Li, Ning Gong, Yunqi Gong, Xingchu |
author_facet | Pan, Jingjing He, Siyuan Zheng, Jiayao Shao, Jingyuan Li, Ning Gong, Yunqi Gong, Xingchu |
author_sort | Pan, Jingjing |
collection | PubMed |
description | BACKGROUND: Quality by design (QbD) is an advanced drug quality control concept that has been gradually implemented in the optimization of manufacturing processes of Chinese medicines. However, the variation of Chinese medicinal material quality has rarely been considered in published works. Because manufacturing processes may lower the variation introduced through different batches of materials, a material quality control strategy should be developed considering the influences of manufacturing processes. METHODS: In this work, the processes of extraction, concentration, water precipitation, and chromatography for notoginseng total saponin (NTS) production were investigated while considering Panax notoginseng quality variation as a sample. Ten process parameters were studied simultaneously using a definitive screening design. After the process critical quality attributes (CQAs) were determined, critical process parameters (CPPs) and critical material attributes (CMAs) were identified simultaneously. Then, models utilizing the CMAs, CPPs, and process CQAs were developed. The design space was then calculated using a Monte Carlo simulation method with an acceptable probability of 0.90. A material quality control strategy considering the influences of manufacturing processes was proposed. RESULTS: The ginsenoside Rd purity and total saponin purity in the eluate were identified as process CQAs. The ethanol solution concentration used for extraction, the ethanol solution concentration used for elution, and elution time were identified as CPPs. The extractable dry matter content of Panax notoginseng was one of the CMAs. The extractable contents of notoginsenoside R(1), ginsenoside Rg(1), ginsenoside Rb(1), and ginsenoside Rd were the other CMAs. The inequalities implemented to discriminate the high quality and low quality of Panax notoginseng were developed according to the NTS standard of the Xuesaitong injection. Low quality Panax notoginseng should not be released for NTS production. High quality Panax notoginseng can be treated with feasible manufacturing processing parameters. Verification experiments were carried out successfully for 2 batches of high quality Panax notoginseng. CONCLUSIONS: In this work, a quality control strategy for herbal materials was developed considering the matching of process characteristics and material quality attributes. This strategy is promising for application to other Chinese medicines. |
format | Online Article Text |
id | pubmed-6760055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67600552019-09-30 The development of an herbal material quality control strategy considering the effects of manufacturing processes Pan, Jingjing He, Siyuan Zheng, Jiayao Shao, Jingyuan Li, Ning Gong, Yunqi Gong, Xingchu Chin Med Research BACKGROUND: Quality by design (QbD) is an advanced drug quality control concept that has been gradually implemented in the optimization of manufacturing processes of Chinese medicines. However, the variation of Chinese medicinal material quality has rarely been considered in published works. Because manufacturing processes may lower the variation introduced through different batches of materials, a material quality control strategy should be developed considering the influences of manufacturing processes. METHODS: In this work, the processes of extraction, concentration, water precipitation, and chromatography for notoginseng total saponin (NTS) production were investigated while considering Panax notoginseng quality variation as a sample. Ten process parameters were studied simultaneously using a definitive screening design. After the process critical quality attributes (CQAs) were determined, critical process parameters (CPPs) and critical material attributes (CMAs) were identified simultaneously. Then, models utilizing the CMAs, CPPs, and process CQAs were developed. The design space was then calculated using a Monte Carlo simulation method with an acceptable probability of 0.90. A material quality control strategy considering the influences of manufacturing processes was proposed. RESULTS: The ginsenoside Rd purity and total saponin purity in the eluate were identified as process CQAs. The ethanol solution concentration used for extraction, the ethanol solution concentration used for elution, and elution time were identified as CPPs. The extractable dry matter content of Panax notoginseng was one of the CMAs. The extractable contents of notoginsenoside R(1), ginsenoside Rg(1), ginsenoside Rb(1), and ginsenoside Rd were the other CMAs. The inequalities implemented to discriminate the high quality and low quality of Panax notoginseng were developed according to the NTS standard of the Xuesaitong injection. Low quality Panax notoginseng should not be released for NTS production. High quality Panax notoginseng can be treated with feasible manufacturing processing parameters. Verification experiments were carried out successfully for 2 batches of high quality Panax notoginseng. CONCLUSIONS: In this work, a quality control strategy for herbal materials was developed considering the matching of process characteristics and material quality attributes. This strategy is promising for application to other Chinese medicines. BioMed Central 2019-09-24 /pmc/articles/PMC6760055/ /pubmed/31572490 http://dx.doi.org/10.1186/s13020-019-0262-9 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Pan, Jingjing He, Siyuan Zheng, Jiayao Shao, Jingyuan Li, Ning Gong, Yunqi Gong, Xingchu The development of an herbal material quality control strategy considering the effects of manufacturing processes |
title | The development of an herbal material quality control strategy considering the effects of manufacturing processes |
title_full | The development of an herbal material quality control strategy considering the effects of manufacturing processes |
title_fullStr | The development of an herbal material quality control strategy considering the effects of manufacturing processes |
title_full_unstemmed | The development of an herbal material quality control strategy considering the effects of manufacturing processes |
title_short | The development of an herbal material quality control strategy considering the effects of manufacturing processes |
title_sort | development of an herbal material quality control strategy considering the effects of manufacturing processes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6760055/ https://www.ncbi.nlm.nih.gov/pubmed/31572490 http://dx.doi.org/10.1186/s13020-019-0262-9 |
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