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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Comparative analysis of multiple representative components in the herb pair Astragali Radix-Curcumae Rhizoma and its single herbs by UPLC-QQQ-MS
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Comparative analysis of multiple representative components in the herb pair Astragali Radix-Curcumae Rhizoma and its single herbs by UPLC-QQQ-MS

机译:UPLC-QQQ-MS对Herb对Astragali radix-Curcumae Rhizoma和唯一草药多种代表性组分的比较分析

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摘要

Highlights ? An UPLC-QQQ-MS method for determination of representative components in Astragali Radix-Curcumae Rhizoma was developed. ? Developed and optimized method showed good validation results. ? Method was successfully applied to comparative analysis of Astragali Radix-Curcumae Rhizoma and its single herbs. ? This is the first report for simultaneous analysis of 17 compounds in Astragali Radix-Curcumae Rhizomaby UPLC-QQQ-MS. Abstract The herb-pair, Astragali Radix (AR) and Curcumae Rhizoma (CR), often occurs in traditional herbal prescriptions used for cancer treatment in Asian areas. In clinical application, the AR-CR herb pair was often produced by different preparation methods or with raw materials from different sources, which raised a challenge for quality control of the herb-pair medicines. In this paper, ultra high performance liquid chromatography coupled to triple quadrupole tandem mass spectrometry method (UPLC-QQQ-MS) was applied for the first time to simultaneously determine 17 main bioactive components for quality control of AR-CR herb pair. The chromatographic separation was studied on an ACQUITY UPLC BEH C 18 column (100mm×2.1mm, 1.7μm) with a mobile phase composed of 0.1% aqueous formic acid and acetonitrile using a gradient elution in 12min. The proposed method was optimized and validated by good linearity (r 2 >0.9970), limit of detection (0.33–10.78ng/mL), limit of quantification (0.81–2.54ng/mL), intra- and inter-day precisions (RSD≤3.64%, RSD≤5.68%), stability (RSD≤4.29%), repeatability (RSD≤5.98%), recovery (90.20–107.60%). The established method was successfully applied to comparative analysis of main bioactive components in AR-CR herb pair and its single herbs, and quality evaluation of different batches of clinical dispensing granules. Compared to the single herb, the content of most liposoluble constituents such as curcumenol, curdione, isocurcumenol, furanodienone, curcumol, and germacrone were remarkable increased in their herb pair, suggesting mixed preparation produced synergistic effects on promoting the extraction of bioactive ingredients. This study is the first time to report the rapid and simultaneous analysis of 17 compounds in AR-CR herb pair by UPLC-QQQ-MS, and provides a feasible method for holistic quality control of preparations containing AR-CR herb-pair.
机译:强调 ?开发了用于测定阿斯塔格利植物莪术莪术中的代表性组分的ULLC-QQQ-MS方法。还是开发和优化的方法显示出良好的验证结果。还是方法已成功应用于黄芪植物莪术莪术的比较分析及其单一草药。还是这是第一个同时分析17种化合物在黄芪中17种化合物的报告 - 莪术Rhizomaby UPLC-QQQ-MS。摘要草本对,黄芪黄芪(Ar)和莪术 - Rhizoma(Cr)通常发生在亚洲地区的传统草药处方。在临床应用中,AR-CR草本对通常由不同的制备方法或来自不同来源的原料生产,这提出了草药对药物质量控制的挑战。本文首次施加与三重四极杆串联质谱法(UPLC-QQQ-MS)偶联的超高效液相色谱法,同时测定AR-CR草本对的质量控制的17个主要生物活性组分。在诸如甲酸水溶液和12mIN中使用梯度洗脱的梯度洗脱,研究了色谱分离在诸如UPLC BEH C 18柱(100mm×2.1mm,1.7μm)上的流动相,使用梯度洗脱组成0.1%甲酸和乙腈。通过良好的线性度(R 2> 0.9970),检测极限(0.33-10.78ng / ml),定量限制(0.81-2.54ng / ml),内部和日内诊断限制(RSD ≤3.64%,rsd≤5.68%),稳定性(RSD≤4.29%),重复性(RSD≤5.98%),恢复(90.20-107.60%)。成熟的方法已成功应用于Ar-Cr Herb对的主要生物活性组分及其单一草药的比较分析,以及不同批次的临床分配颗粒的质量评价。与单个草本植物相比,其莪术成分如莪术成分,呋喃二烯酮,莪术和Germacoron的含量显着增加,其在其草药对中显着增加,表明混合制剂对促进生物活性成分的提取产生了协同作用。本研究是第一次通过UPLC-QQQ-MS报告AR-CR HERB对中的17个化合物的快速和同时分析,为含AR-CR草本对的制剂的整体质量控制提供了可行的方法。

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