Development of a comprehensive method combining UHPLC-CAD fingerprint, multi-components quantitative analysis for quality evaluation of Zishen Yutai Pills: A step towards quality control of Chinese patent medicine
•A comprehensive quality evaluation strategy was developed for Zishen Yutai Pills.•Charged aerosol detector could provide more peaks and greater sensitivity than that of UV.•281 compounds were identified or tentatively identified based on accurate mass and fragments.•Positive-negative conversion MRM...
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| Veröffentlicht in: | Journal of pharmaceutical and biomedical analysis 2020-11, Vol.191, p.113570-113570, Article 113570 |
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| container_title | Journal of pharmaceutical and biomedical analysis |
| container_volume | 191 |
| creator | Cao, Jiliang Lei, Ting Wu, Sijia Li, Hongyi Deng, Yun Lin, Ruizhen Ning, Na Geng, Chunxian Wang, Shengpeng Wu, Xu Li, Peng Wang, Yitao |
| description | •A comprehensive quality evaluation strategy was developed for Zishen Yutai Pills.•Charged aerosol detector could provide more peaks and greater sensitivity than that of UV.•281 compounds were identified or tentatively identified based on accurate mass and fragments.•Positive-negative conversion MRM technique was used to get best quantitative sensitivity.
Zishen Yutai Pills (ZYP) is a well-known Chinese patent medicine which has been used to prevent recurrent miscarriage and treat threatened abortion in China. In this study, a comprehensive strategy combining ultrahigh performance liquid chromatography coupled with charged aerosol detector (UHPLC-CAD) fingerprint and multi-components quantitative analysis was developed and validated for quality evaluation of ZYP. For fingerprint analysis, a total of 52 characteristic peaks were selected to evaluate the similarities of 16 batches of ZYP. In addition, combining the chemical fingerprint profile with an advanced hybrid LTQ-Orbitrap mass spectrometer, 281 compounds were identified or tentatively identified in ZYP based on chemical standards, accurate mass and fragmentation information. Moreover, 18 chemical markers were simultaneously determined within 13 min by ultra-performance liquid chromatography couple to tandem mass spectrometry (UPLC-MS/MS) with positive-negative conversion multiple reaction monitor (+/-MRM) technique. This method has been validated and exhibited satisfactory sensitivity, precision, reproducibility and accuracy. The validated quantitative method was successfully applied to the analysis of 16 batches of ZYP samples. The combination of UHPLC-CAD fingerprint and multi-components quantification has been proved to be an efficient and reliable strategy for quality control of ZYP and could be considered as a reference for quality evaluation of Chinese patent medicine. |
| doi_str_mv | 10.1016/j.jpba.2020.113570 |
| format | Article |
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Zishen Yutai Pills (ZYP) is a well-known Chinese patent medicine which has been used to prevent recurrent miscarriage and treat threatened abortion in China. In this study, a comprehensive strategy combining ultrahigh performance liquid chromatography coupled with charged aerosol detector (UHPLC-CAD) fingerprint and multi-components quantitative analysis was developed and validated for quality evaluation of ZYP. For fingerprint analysis, a total of 52 characteristic peaks were selected to evaluate the similarities of 16 batches of ZYP. In addition, combining the chemical fingerprint profile with an advanced hybrid LTQ-Orbitrap mass spectrometer, 281 compounds were identified or tentatively identified in ZYP based on chemical standards, accurate mass and fragmentation information. Moreover, 18 chemical markers were simultaneously determined within 13 min by ultra-performance liquid chromatography couple to tandem mass spectrometry (UPLC-MS/MS) with positive-negative conversion multiple reaction monitor (+/-MRM) technique. This method has been validated and exhibited satisfactory sensitivity, precision, reproducibility and accuracy. The validated quantitative method was successfully applied to the analysis of 16 batches of ZYP samples. The combination of UHPLC-CAD fingerprint and multi-components quantification has been proved to be an efficient and reliable strategy for quality control of ZYP and could be considered as a reference for quality evaluation of Chinese patent medicine.</description><identifier>ISSN: 0731-7085</identifier><identifier>EISSN: 1873-264X</identifier><identifier>DOI: 10.1016/j.jpba.2020.113570</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Chemical characterization ; Chemical fingerprint ; Multi-components quantitative analysis ; Quality evaluation ; Zishen Yutai Pills</subject><ispartof>Journal of pharmaceutical and biomedical analysis, 2020-11, Vol.191, p.113570-113570, Article 113570</ispartof><rights>2020 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c333t-698ac19cc32590fababee90c5cc9cfebae31518a42ff8c22d30bcf84fdac71cc3</citedby><cites>FETCH-LOGICAL-c333t-698ac19cc32590fababee90c5cc9cfebae31518a42ff8c22d30bcf84fdac71cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0731708520314564$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids></links><search><creatorcontrib>Cao, Jiliang</creatorcontrib><creatorcontrib>Lei, Ting</creatorcontrib><creatorcontrib>Wu, Sijia</creatorcontrib><creatorcontrib>Li, Hongyi</creatorcontrib><creatorcontrib>Deng, Yun</creatorcontrib><creatorcontrib>Lin, Ruizhen</creatorcontrib><creatorcontrib>Ning, Na</creatorcontrib><creatorcontrib>Geng, Chunxian</creatorcontrib><creatorcontrib>Wang, Shengpeng</creatorcontrib><creatorcontrib>Wu, Xu</creatorcontrib><creatorcontrib>Li, Peng</creatorcontrib><creatorcontrib>Wang, Yitao</creatorcontrib><title>Development of a comprehensive method combining UHPLC-CAD fingerprint, multi-components quantitative analysis for quality evaluation of Zishen Yutai Pills: A step towards quality control of Chinese patent medicine</title><title>Journal of pharmaceutical and biomedical analysis</title><description>•A comprehensive quality evaluation strategy was developed for Zishen Yutai Pills.•Charged aerosol detector could provide more peaks and greater sensitivity than that of UV.•281 compounds were identified or tentatively identified based on accurate mass and fragments.•Positive-negative conversion MRM technique was used to get best quantitative sensitivity.
Zishen Yutai Pills (ZYP) is a well-known Chinese patent medicine which has been used to prevent recurrent miscarriage and treat threatened abortion in China. In this study, a comprehensive strategy combining ultrahigh performance liquid chromatography coupled with charged aerosol detector (UHPLC-CAD) fingerprint and multi-components quantitative analysis was developed and validated for quality evaluation of ZYP. For fingerprint analysis, a total of 52 characteristic peaks were selected to evaluate the similarities of 16 batches of ZYP. In addition, combining the chemical fingerprint profile with an advanced hybrid LTQ-Orbitrap mass spectrometer, 281 compounds were identified or tentatively identified in ZYP based on chemical standards, accurate mass and fragmentation information. Moreover, 18 chemical markers were simultaneously determined within 13 min by ultra-performance liquid chromatography couple to tandem mass spectrometry (UPLC-MS/MS) with positive-negative conversion multiple reaction monitor (+/-MRM) technique. This method has been validated and exhibited satisfactory sensitivity, precision, reproducibility and accuracy. The validated quantitative method was successfully applied to the analysis of 16 batches of ZYP samples. The combination of UHPLC-CAD fingerprint and multi-components quantification has been proved to be an efficient and reliable strategy for quality control of ZYP and could be considered as a reference for quality evaluation of Chinese patent medicine.</description><subject>Chemical characterization</subject><subject>Chemical fingerprint</subject><subject>Multi-components quantitative analysis</subject><subject>Quality evaluation</subject><subject>Zishen Yutai Pills</subject><issn>0731-7085</issn><issn>1873-264X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kc9u1DAQxiNEJZaWF-DkIweytfNnkyAuq7S0SCvRQysBF8uZjFmvHDu1na32QXkfbC3iyMnyzPy-0Tdflr1ndM0o21wf1od5EOuCFrHAyrqhr7IVa5syLzbV99fZijYlyxva1m-yt94fKKU166pV9vsGj6jtPKEJxEoiCNhpdrhH49URyYRhb8dUHJRR5hd5un_Y9Xm_vSEyftHNTpnwkUyLDipPrDVRypPnRZiggghJRRihT155Iq1LHa3CieBR6CX2rUmLfyofd5IfSxCKPCit_SeyJT7gTIJ9EW70_0CwJjirE9XvlUGPZBYhGZhwVBArV9mFFNrju7_vZfb05faxv8933-6-9ttdDmVZhnzTtQJYB1AWdUelGMSA2FGoATqQOAgsWc1aURVStlAUY0kHkG0lRwENi9hl9uGsOzv7vKAPfFIeUGth0C6eF1XFNpRVdRVHi_MoOOu9Q8nj5SbhTpxRnjLkB54y5ClDfs4wQp_PEEYTR4WOe1BoINp0CIGPVv0P_wMA2qyw</recordid><startdate>20201130</startdate><enddate>20201130</enddate><creator>Cao, Jiliang</creator><creator>Lei, Ting</creator><creator>Wu, Sijia</creator><creator>Li, Hongyi</creator><creator>Deng, Yun</creator><creator>Lin, Ruizhen</creator><creator>Ning, Na</creator><creator>Geng, Chunxian</creator><creator>Wang, Shengpeng</creator><creator>Wu, Xu</creator><creator>Li, Peng</creator><creator>Wang, Yitao</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20201130</creationdate><title>Development of a comprehensive method combining UHPLC-CAD fingerprint, multi-components quantitative analysis for quality evaluation of Zishen Yutai Pills: A step towards quality control of Chinese patent medicine</title><author>Cao, Jiliang ; Lei, Ting ; Wu, Sijia ; Li, Hongyi ; Deng, Yun ; Lin, Ruizhen ; Ning, Na ; Geng, Chunxian ; Wang, Shengpeng ; Wu, Xu ; Li, Peng ; Wang, Yitao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c333t-698ac19cc32590fababee90c5cc9cfebae31518a42ff8c22d30bcf84fdac71cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Chemical characterization</topic><topic>Chemical fingerprint</topic><topic>Multi-components quantitative analysis</topic><topic>Quality evaluation</topic><topic>Zishen Yutai Pills</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cao, Jiliang</creatorcontrib><creatorcontrib>Lei, Ting</creatorcontrib><creatorcontrib>Wu, Sijia</creatorcontrib><creatorcontrib>Li, Hongyi</creatorcontrib><creatorcontrib>Deng, Yun</creatorcontrib><creatorcontrib>Lin, Ruizhen</creatorcontrib><creatorcontrib>Ning, Na</creatorcontrib><creatorcontrib>Geng, Chunxian</creatorcontrib><creatorcontrib>Wang, Shengpeng</creatorcontrib><creatorcontrib>Wu, Xu</creatorcontrib><creatorcontrib>Li, Peng</creatorcontrib><creatorcontrib>Wang, Yitao</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cao, Jiliang</au><au>Lei, Ting</au><au>Wu, Sijia</au><au>Li, Hongyi</au><au>Deng, Yun</au><au>Lin, Ruizhen</au><au>Ning, Na</au><au>Geng, Chunxian</au><au>Wang, Shengpeng</au><au>Wu, Xu</au><au>Li, Peng</au><au>Wang, Yitao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a comprehensive method combining UHPLC-CAD fingerprint, multi-components quantitative analysis for quality evaluation of Zishen Yutai Pills: A step towards quality control of Chinese patent medicine</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><date>2020-11-30</date><risdate>2020</risdate><volume>191</volume><spage>113570</spage><epage>113570</epage><pages>113570-113570</pages><artnum>113570</artnum><issn>0731-7085</issn><eissn>1873-264X</eissn><abstract>•A comprehensive quality evaluation strategy was developed for Zishen Yutai Pills.•Charged aerosol detector could provide more peaks and greater sensitivity than that of UV.•281 compounds were identified or tentatively identified based on accurate mass and fragments.•Positive-negative conversion MRM technique was used to get best quantitative sensitivity.
Zishen Yutai Pills (ZYP) is a well-known Chinese patent medicine which has been used to prevent recurrent miscarriage and treat threatened abortion in China. In this study, a comprehensive strategy combining ultrahigh performance liquid chromatography coupled with charged aerosol detector (UHPLC-CAD) fingerprint and multi-components quantitative analysis was developed and validated for quality evaluation of ZYP. For fingerprint analysis, a total of 52 characteristic peaks were selected to evaluate the similarities of 16 batches of ZYP. In addition, combining the chemical fingerprint profile with an advanced hybrid LTQ-Orbitrap mass spectrometer, 281 compounds were identified or tentatively identified in ZYP based on chemical standards, accurate mass and fragmentation information. Moreover, 18 chemical markers were simultaneously determined within 13 min by ultra-performance liquid chromatography couple to tandem mass spectrometry (UPLC-MS/MS) with positive-negative conversion multiple reaction monitor (+/-MRM) technique. This method has been validated and exhibited satisfactory sensitivity, precision, reproducibility and accuracy. The validated quantitative method was successfully applied to the analysis of 16 batches of ZYP samples. The combination of UHPLC-CAD fingerprint and multi-components quantification has been proved to be an efficient and reliable strategy for quality control of ZYP and could be considered as a reference for quality evaluation of Chinese patent medicine.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.jpba.2020.113570</doi><tpages>1</tpages></addata></record> |
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| subjects | Chemical characterization Chemical fingerprint Multi-components quantitative analysis Quality evaluation Zishen Yutai Pills |
| title | Development of a comprehensive method combining UHPLC-CAD fingerprint, multi-components quantitative analysis for quality evaluation of Zishen Yutai Pills: A step towards quality control of Chinese patent medicine |
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