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基于定量指纹图谱技术的经典名方清骨散对照提取物质量传递分析

[Analysis on quality value transmitting of Qinggusan reference sample of classical prescription based on quantitative fingerprint technology].

作者信息

Xu Xin, Wei Tong, Xue Qianqian, Ai Jiahao, Li Guixin, Liu Zhongguo, Li Dan, Hou Jincai, Jin Hongli, Liu Yanfang, Liang Xinmiao

机构信息

1. Ganjiang Chinese Medicine Innovation Center,Nanchang 330000,China;2. Jiangxi Provincial Key Laboratory for Pharmacodynamic Material Basis of Traditional Chinese Medicine,Nanchang 330000,China.

3. Dalian Institute of Chemical Physics,Chinese Academy of Sciences,Dalian 116023,China.

出版信息

Se Pu. 2023 Feb;41(2):142-151. doi: 10.3724/SP.J.1123.2022.09024.

Abstract

Qinggusan is the 69th prescription in the first batch of "Catalogue of Ancient Chinese Classic Formulas". In modern clinical practice, Qinggusan is mainly used to treat noninfectious fever. However, because few studies on Qinggusan reference samples and their quality value transfer are available, the development and promotion of its compound preparations are restricted. Therefore, establishing an accurate and comprehensive quality control method to clarify the critical quality attributes of Qinggusan reference samples is of great importance. In this study, 15 batches of Qinggusan reference samples were processed to determine the range of their dry extract ratios. Quantitative high-performance liquid chromatography (HPLC) fingerprint analysis was performed using a Waters Symmetry Shield RP18 column (250 mm×4.6 mm, 5 μm) with acetonitrile-0.1% (v/v) formic acid aqueous solution as the mobile phase in gradient elution mode. The flow rate was 1.0 mL/min, the column temperature was 30 ℃, and the detection wavelength was 254 nm. The HPLC fingerprints of the Qinggusan reference samples were established under these conditions to evaluate their similarity. The established method was systematically validated and found to demonstrate good precision, repeatability, and sample stability. Subsequently, characteristic peaks were identified and attributed by HPLC-quadrupole-time-of-flight-mass spectrometry (HPLC-Q-TOF-MS) analysis. MS was performed in electrospray ionization mode, the data were collected in both positive- and negative-ion modes, and the detection range was 50-2000. The contents and transfer rate ranges of the index components, namely, gentiopicrin, mangiferin, picroside Ⅱ, picroside Ⅰ, and glycyrrhizic acid, were determined to analyze the quality value transfer of the samples. The results demonstrated that the dry extract rate of the 15 batches of Qinggusan reference samples ranged from 24.10% to 26.88% and that their fingerprint similarities were generally greater than 0.95. Twelve common peaks were identified by reference identification, literature comparison, and high-resolution MS analysis. Twelve compounds, including six iridoid glycosides, two flavonoids, one alkaloid, one triterpenoid saponin, and two others. Among them, L-picein, androsin, picroside Ⅳ, picroside Ⅱ and picroside Ⅰ were from Picrorhizae Rhizoma, loganin acid, swertiamarin and gentiopicrin were from Gentianae Macrophyllae Radix, neomangiferin and mangiferin were from Anemarrhenae Rhizoma, dichotomine B was from Stellariae Radix, and glycyrrhizic acid was from Glycyrrhizae Radix et Rhizoma. The five key components presented good linear relationships in their respective linear ranges, and all correlation coefficients were higher than 0.999. The relative standard deviations (RSDs) of precision, stability, and repeatability were less than 1.3%. The average recoveries varied between 95.92% and 102.5%, with RSDs less than 3.9%; these values meet the requirements defined in the 2020 edition of the Chinese Pharmacopoeia. The contents of gentiopicrin, mangiferin, picroside Ⅱ, picroside Ⅰ, and glycyrrhizic acid in the 15 batches of reference samples were in the range of 17.92-27.55, 1.83-4.42, 23.08-36.44, 8.43-15.04, and 0.94-2.39 mg/g, respectively, and their transfer rates from the decoction pieces to the reference samples were 47.91%-63.95%, 22.96%-59.39%, 60.82%-77.82%, 64.25%-99.53%, and 15.30%-39.30%, respectively. In this study, the chemical components of Qinggusan reference samples were comprehensively identified and their quality value transfer was studied through the combination of HPLC fingerprinting and MS. Clarification of the critical quality attributes of Qinggusan reference samples could provide a basis for the quality control of Qinggusan compound preparations.

摘要

清骨散是首批《古代经典名方目录》中的第69号方剂。在现代临床实践中,清骨散主要用于治疗非感染性发热。然而,由于关于清骨散对照品及其质量值传递的研究较少,其复方制剂的开发和推广受到限制。因此,建立准确、全面的质量控制方法以阐明清骨散对照品的关键质量属性具有重要意义。本研究对15批次清骨散对照品进行处理,测定其干膏率范围。采用Waters Symmetry Shield RP18柱(250 mm×4.6 mm,5 μm),以乙腈-0.1%(v/v)甲酸水溶液为流动相,采用梯度洗脱模式进行定量高效液相色谱(HPLC)指纹图谱分析。流速为1.0 mL/min,柱温为30℃,检测波长为254 nm。在这些条件下建立清骨散对照品的HPLC指纹图谱以评价其相似度。所建立的方法经过系统验证,结果表明具有良好的精密度、重复性和样品稳定性。随后,通过HPLC-四极杆-飞行时间质谱(HPLC-Q-TOF-MS)分析对特征峰进行鉴定和归属。质谱采用电喷雾电离模式,数据在正离子和负离子模式下采集,检测范围为50 - 2000。测定指标成分龙胆苦苷、芒果苷、胡黄连苷Ⅱ、胡黄连苷Ⅰ和甘草酸的含量及转移率范围,以分析样品的质量值传递。结果表明,15批次清骨散对照品的干膏率范围为24.10%至26.88%,其指纹图谱相似度一般大于0.95。通过对照品鉴定、文献比较和高分辨质谱分析鉴定出12个共有峰。确定了12种化合物,包括6种环烯醚萜苷、2种黄酮类、1种生物碱、1种三萜皂苷及其他2种。其中,L-松脂素、安格洛辛、胡黄连苷Ⅳ、胡黄连苷Ⅱ和胡黄连苷Ⅰ来源于胡黄连,马钱子酸、獐牙菜苦苷和龙胆苦苷来源于秦艽,新芒果苷和芒果苷来源于知母,双分法明B来源于银柴胡,甘草酸来源于甘草。5种关键成分在各自线性范围内呈现良好的线性关系,所有相关系数均高于0.999。精密度、稳定性和重复性的相对标准偏差(RSD)均小于1.3%。平均回收率在95.92%至102.5%之间,RSD小于3.9%;这些值符合《中国药典》2020年版规定的要求。15批次对照品中龙胆苦苷、芒果苷、胡黄连苷Ⅱ、胡黄连苷Ⅰ和甘草酸的含量分别为17.92 - 27.55、1.83 - 4.42、23.08 - 36.44、8.43 - 15.04和0.94 - 2.39 mg/g,其从饮片到对照品的转移率分别为47.91% - 63.95%、22.96% - 59.39%、60.82% - 77.82%、64.25% - 99.53%和15.30% - 39.30%。本研究通过HPLC指纹图谱和质谱联用技术对清骨散对照品的化学成分进行了全面鉴定,并研究了其质量值传递。阐明清骨散对照品的关键质量属性可为清骨散复方制剂的质量控制提供依据。

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