[基于定量指纹技术的青骨散经典方参样质量值传递分析]。

IF 1.2 4区 化学 Q4 CHEMISTRY, ANALYTICAL
Xin Xu, Tong Wei, Qianqian Xue, Jiahao Ai, Guixin Li, Zhongguo Liu, Dan Li, Jincai Hou, Hongli Jin, Yanfang Liu, Xinmiao Liang
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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 <i>m/z</i> 50-2000. 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引用次数: 0

摘要

青骨散是第一批《中国古代经典方剂目录》中的第69个方剂。在现代临床实践中,青骨散主要用于治疗非传染性发热。但由于对青骨散参比样品及其质量值转移的研究较少,制约了其复方制剂的开发和推广。因此,建立准确、全面的质量控制方法,明确青谷山参比样品的关键质量属性具有重要意义。本研究对15批青骨散参比样品进行处理,确定其干提物比的范围。采用Waters Symmetry Shield RP18色谱柱(250 mm×4.6 mm, 5 μm),以乙腈-0.1% (v/v)甲酸水溶液为流动相,梯度洗脱,进行高效液相色谱(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。在此条件下建立青谷山参比样品的HPLC指纹图谱,评价其相似度。系统验证了所建立的方法,发现其具有良好的精密度、重复性和样品稳定性。随后,通过HPLC-Q-TOF-MS(四极杆飞行时间质谱)分析鉴定和归属特征峰。质谱采用电喷雾电离方式,数据采集采用正离子和负离子两种模式,检测范围为m/z 50-2000。测定龙胆苦苷、芒果苷、苦苷Ⅱ、苦苷Ⅰ、甘草酸等指标成分的含量及转移率范围,分析样品的质量值转移。结果表明,15批青骨散参比样品的干提取率在24.10% ~ 26.88%之间,指纹相似度均大于0.95。通过参考文献鉴定、文献比对和高分辨率质谱分析鉴定出12个共有峰。十二种化合物,包括六种环烯醚萜苷、两种黄酮类化合物、一种生物碱、一种三萜皂苷和其他两种化合物。其中,l -花青素、雄雄素、微苦苷Ⅳ、微苦苷Ⅱ和微苦苷Ⅰ来源于苦甘草,马鞭草酸、獐牙苦苷和龙胆苦苷来源于龙胆,新甘菊素和芒果苷来源于苦参,二氯胺B来源于星参,甘草酸来源于甘草酸。5个关键成分在各自的线性范围内呈良好的线性关系,相关系数均大于0.999。精密度、稳定性、重复性的相对标准偏差(rsd)均小于1.3%。平均加样回收率在95.92% ~ 102.5%之间,rsd < 3.9%,符合2020年版《中国药典》要求。15批参比样品中龙胆苦苷、芒果苷、苦苷Ⅱ、苦苷Ⅰ、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、0.94 ~ 2.39 mg/g,从饮片到参比样品的传递率分别为47.91% ~ 63.95%、22.96% ~ 59.39%、60.82% ~ 77.82%、64.25% ~ 99.53%、15.30% ~ 39.30%。本研究通过HPLC指纹图谱和质谱相结合的方法,对青骨散参比样品的化学成分进行综合鉴定,并对其质量值传递进行研究,明确青骨散参比样品的关键质量属性,为青骨散复方制剂的质量控制提供依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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

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 m/z 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.

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来源期刊
色谱
色谱 CHEMISTRY, ANALYTICAL-
CiteScore
1.30
自引率
42.90%
发文量
7198
期刊介绍: "Chinese Journal of Chromatography" mainly reports the basic research results of chromatography, important application results of chromatography and its interdisciplinary subjects and their progress, including the application of new methods, new technologies, and new instruments in various fields, the research and development of chromatography instruments and components, instrument analysis teaching research, etc. It is suitable for researchers engaged in chromatography basic and application technology research in scientific research institutes, master and doctoral students in chromatography and related disciplines, grassroots researchers in the field of analysis and testing, and relevant personnel in chromatography instrument development and operation units. The journal has columns such as special planning, focus, perspective, research express, research paper, monograph and review, micro review, technology and application, and teaching research.
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