Article(id=1319291482666807422, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291312826863771, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2026.08.044, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1792473200718, onlineDateStr=2026-10-20, pubDate=1786291200000, pubDateStr=2026-08-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1792473200718, onlineIssueDateStr=2026-10-20, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1792473200718, creator=13701087609, updateTime=1792473200718, updator=13701087609, issue=Issue{id=1319291312826863771, tenantId=1146029695717560320, journalId=1255847919539208197, year='2026', volume='44', issue='8', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1786291200000', pubDateStr='2026-08-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1792473160225, creator='13701087609', updateTime=1792473382588, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1319292245547799195, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291312826863771, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1319292245652656796, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291312826863771, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=215, endPage=218, ext={EN=ArticleExt(id=1319291482918465663, articleId=1319291482666807422, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Study on Determination of Seven Active Ingredients in Pudilan Anti-Inflammatory Tablets (蒲地蓝消炎片) by UPLC-MS Method, columnId=1256183365644968140, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Platform of Provincial Project, runingTitle=null, highlight=null, articleAbstract=
Objective To investigate the determination of seven active ingredients in Pudilan Anti-Inflammatory Tablets (蒲地蓝消炎片) by ultra-high performance liquid chromatography-mass spectrometry (UPLC-MS) method.
Method UPLC-MS was used to quantitatively analyze the seven main active ingredients in Pudilan Anti-Inflammatory Tablets. The differences in the contents of these active ingredients in the samples of Pudilan Anti-Inflammatory Tablets from different manufacturers were compared, aiming to provide scientific basis for the quality evaluation of Pudilan Anti-Inflammatory Tablets.
Result A certain amount of standard solution stock solution for each active ingredient was accurately measured and transferred to a 5 mL volumetric flask. According to the established chromatographic analysis conditions, the measurement results were obtained in the form of peak area. The peak area data was applied to the corresponding standard curve equations for calculation and recording. The results indicated that within the studied concentration range, there was a good linear correlation between the peak area of each active ingredient and its mass concentration. The relative standard deviation (RSD) values of precision in different active ingredients (chlorogenic acid, caffeic acid, chicory acid, purple violet spirit, baicalin, luteolin and baicalin in the same order of stability, reproducibility and recovery rate) were 0.99%, 0.31%, 1.20%, 1.47%, 1.31%, 1.29% and 0.33%, respectively. The RSD values of chromatographic peak area were all less than 1.46%, indicating that the instrument had good precision. After recording peak areas at 0, 3, 6, 12, 24, 48 h to evaluate stability, the RSD values of different active ingredients in Pudilan Anti-Inflammatory Tablets were 1.14%, 0.10%, 0.84%, 0.53%, 0.46%, 0.66% and 0.84%, respectively, indicating that the stability of the test solution was better within 24 hours. The peak area was measured to evaluate the repeatability, and the RSD values of different active ingredients in Pudilan Anti-Inflammatory Tablets were 1.28%, 1.75%, 1.43%, 1.04%, 2.39%, 0.93% and 2.61%, respectively, indicating that UPLC-MS/MS technology had good repeatability. The average RSD recovery rates of the active ingredients were 99.53% (RSD 2.38%), 100.63% (RSD 2.27%), 98.95% (RSD 2.29%), 101.58% (RSD 1.38%), 100.95% (RSD 2.25%), 97.26% (RSD 0.91%) and 98.56% (RSD 1.92%), respectively. There were significant differences in various effective ingredients in samples of Pudilan Anti-Inflammatory Tablets from different manufacturers.
Conclusion UPLC-MS technology, with its excellent precision, stability and repeatability, can comprehensively reveal the quality status of Pudilan Anti-Inflammatory Tablets from different batches and manufacturers. This method has important positive effects on objectively evaluating drug quality, ensuring the drug quality and improving the clinical efficacy.
, authors=Xiaojun DING
1, Yunbo NI
1, Yajun TANG
2, Tao YAN
1, authorsList=Xiaojun DING, Yunbo NI, Yajun TANG, Tao YAN, authorCompany=null, correspAuthors=Tao YAN, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1319291483245621376, articleId=1319291482666807422, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=UPLC-MS法测定蒲地蓝消炎片中7种有效成分含量的研究, columnId=1256183369033965799, journalTitle=中华中医药学刊, columnName=省级项目平台, runingTitle=null, highlight=null, articleAbstract=
目的 探究超高效液相色谱-质谱联用技术(Ultra-high performance liquid chromatography-mass spectrometry,HPLC-MS)法测定蒲地蓝消炎片中7种有效成分含量。
方法 通过UPLC-MS,对蒲地蓝消炎片中的7种主要活性成分进行定量分析,比较不同生产厂家的蒲地蓝消炎片样品中这些活性成分的含量差异,旨在为蒲地蓝消炎片的质量评估提供科学依据。
结果 精确量取一定量每种有效成分的标准溶液储备液,并将其转移到5 mL的量瓶中。依据既定的色谱分析条件进行测定,测定结果以峰面积的形式获得。将这些峰面积数据应用到相应的标准曲线方程中进行计算和记录。结果表明,在所研究的质量浓度范围内,每种有效成分的峰面积与其质量浓度间呈现出良好的线性相关性。不同有效成分(绿原酸、咖啡酸、菊苣酸、紫堇灵、黄芩苷、木犀草素、汉黄芩苷,以下稳定性、重现性、加样回收率顺序与这一顺序一致)中精密度的RSD分别为0.99%、0.31%、1.20%、1.47%、1.31%、1.29%、0.33%,色谱峰面积的相对标准偏差(Relative standard deviation of chromatographic peak area,RSD)值均小于1.46%,提示该仪器有较好精密度。经0、3、6、12、24、48 h记录峰面积评估稳定性,不同蒲地蓝消炎片有效成分RSD分别为1.14%、0.10%、0.84%、0.53%、0.46%、0.66%、0.84%,提示供试品溶液24 h内稳定性较优。测定峰面积评估重复性,不同蒲地蓝消炎片有效成分RSD分别为1.28%、1.75%、1.43%、1.04%、2.39%、0.93%、2.61%,提示UPLC-MS/MS技术具有较好的重复性。有效成分RSD平均回收率分别为99.53%(RSD为2.38%)、100.63%(RSD为2.27%)、98.95%(RSD为2.29%)、101.58%(RSD为1.38%)、100.95%(RSD为2.25%)、97.26%(RSD为0.91%)、98.56%(RSD为1.92%)。不同厂家蒲地蓝消炎片样品中各种有效成分均存在显著差异。
结论 UPLC-MS技术以其卓越的精密度、稳定性和重复性,能全面地揭示不同批次和不同生产厂家的蒲地蓝消炎片的质量状况,该方法对于客观评估药品质量、确保药品的质量和提升临床疗效都具有重要的积极影响。
, authors=丁小军
1, 倪云波
1, 唐亚军
2, 闫涛
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丁小军(1980-),男,浙江宁波人,主管中药师,学士,研究方向:中药学。
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