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采用 HPLC-DAD-MS/MS 的新策略对 银黄制剂进行质量控制和定性分析。

A new strategy for quality control and qualitative analysis of Yinhuang preparations by HPLC-DAD-MS/MS.

机构信息

Key Laboratory of New Drug & Clinical Application, Xuzhou Medical College, Xuzhou, Jiangsu, China.

出版信息

Anal Bioanal Chem. 2012 Oct;404(6-7):1851-65. doi: 10.1007/s00216-012-6281-3. Epub 2012 Aug 12.

Abstract

A combinative method using fingerprint analysis (FA) and multi-ingredients quantification (MIQ) was developed and validated for the quality control of Yinhuang (YH) preparations including granule, capsule, and lozenge by high-performance liquid chromatography coupled with diode array detection (HPLC-DAD). Common peaks with or without standard references in FA were confirmed or identified by electrospray ionization tandem mass spectrometry (ESI-MS/MS). The chromatographic separations were achieved on a Sepax GP-C(18) column (250 mm × 4.6 mm i.d., 5 μm) with a gradient elution using a mixture of 0.1 % formic acid methanol solution and 0.1 % formic acid water solution. In quantitative analysis, nine bioactive constituents (chlorogenic acid, caffeic acid, luteoloside, baicalin, luteolin, wogonoside, baicalein, wogonin, and oroxylin A) were simultaneously determined. The detection wavelength was set at 275 nm, 320 nm, and 350 nm according to the absorption properties of the nine quantified compounds. The linearity, recovery, intraday and interday precision, accuracy, limit of detection (LOD) and quantification (LOQ), repeatability and stability were all tested and good results were obtained. In the FA, 320 nm was selected. The correlation coefficients of similarity were determined on the basis of the relative retention time (RRT) and relative peak area (RPA) of 20 common peaks in chromatographic fingerprints. Results indicated that both the RRT and RPA of 20 common peaks shared a close similarity. From the 20 common peaks, 18 compounds, including the nine quantified compounds, were identified or tentatively characterized by comparing their retention times, UV spectra, and MS spectra with those of standard compounds or literature data. The study not only presents a powerful and reliable analytical tool for the quality control of YH preparations, but also provides the chemical evidence for revealing the material basis of their therapeutic effects.

摘要

建立并验证了一种结合指纹分析(FA)和多成分定量(MIQ)的方法,用于高效液相色谱-二极管阵列检测(HPLC-DAD)结合控制包括颗粒剂、胶囊剂和口含片在内的茵黄(YH)制剂的质量。FA 中使用电喷雾电离串联质谱(ESI-MS/MS)对具有或不具有标准参考物的共有峰进行确认或鉴定。色谱分离在 Sepax GP-C(18)柱(250 mm×4.6 mm id,5 μm)上进行,采用 0.1%甲酸甲醇溶液和 0.1%甲酸水溶液的混合物进行梯度洗脱。在定量分析中,同时测定了 9 种生物活性成分(绿原酸、咖啡酸、芦丁、黄芩苷、木樨草苷、汉黄芩苷、黄芩素、汉黄芩素和木蝴蝶苷 A)。检测波长根据 9 种定量化合物的吸收特性分别设置为 275nm、320nm 和 350nm。线性、回收率、日内和日间精密度、准确度、检测限(LOD)和定量限(LOQ)、重复性和稳定性均经过测试,结果良好。在 FA 中,选择 320nm。根据 20 个共有峰的相对保留时间(RRT)和相对峰面积(RPA),确定相似度相关系数。结果表明,20 个共有峰的 RRT 和 RPA 具有密切的相似性。从 20 个共有峰中,通过比较保留时间、紫外光谱和质谱与标准化合物或文献数据,鉴定或初步鉴定了 18 种化合物,包括 9 种定量化合物。该研究不仅为 YH 制剂的质量控制提供了一种强大可靠的分析工具,而且为揭示其治疗作用的物质基础提供了化学依据。

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