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Characterization and quantification of major constituents of Xue Fu Zhu Yu by UPLC-DAD-MS/MS.

机译:用UPLC-DAD-MS / MS对血府逐瘀的主要成分进行表征和定量。

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摘要

Xue Fu Zhu Yu (XFZY), a classic recipe in traditional Chinese medicine (TCM), has been demonstrated to show protective effects on cardiovascular system. For quality control of XFZY products, qualitative analysis using ultra high performance liquid chromatography with diode-array detector-tandem mass spectrometry (UPLC-DAD-MS) was undertaken. Twenty-eight compounds from XFZY were simultaneously detected; among them, seventeen compounds were unequivocally identified, and another eight compounds were tentatively characterized. According to qualitative results, a new method for quantitative analysis of XFZY has been established by ultra high performance liquid chromatography coupled with diode array detector (UPLC-DAD). Twelve representative compounds unequivocally identified were used as chemical markers in quantitative analysis, including 5-hydroxymethyl-2-furaldehyde (5-HMF), hydroxysafflor yellow A (HSYA), amygdalin, albiflorin, paeoniflorin, liquiritin, ferulic acid (FA), naringin, hesperidin, neohesperidin (NH), isoliquiritigenin (IL) and glycyrrhizic acid (GA), which were derived from nine of eleven herbs of XFZY except Platycodon grandiflorum (Jacq.) A. DC. (Jiegeng) and Bupleurum chinense DC. (Chaihu). This UPLC method was validated in terms of linearity, LOD and LOQ, precision, repeatability, stability, and recovery tests. Quality control of XFZY products in total fourteen samples by four dosage forms was examined by this method, and results confirmed its feasibility and reliability in practice.
机译:血府逐瘀(XFZY)是传统中药(TCM)的经典配方,已被证明对心血管系统具有保护作用。为了对XFZY产品进行质量控制,进行了使用超高效液相色谱与二极管阵列检测器串联质谱(UPLC-DAD-MS)的定性分析。同时检测到XFZY中的28种化合物。其中,明确鉴定出17种化合物,并初步鉴定了另外8种化合物。根据定性结果,建立了超高效液相色谱-二极管阵列检测器(UPLC-DAD)结合定量分析XFZY的新方法。明确鉴定的十二种代表性化合物被用作定量分析中的化学标记物,包括5-羟甲基-2-糠醛(5-HMF),羟红花黄A(HSYA),苦杏仁苷,白花素,pa药花青素,液体白蛋白,阿魏酸(FA),柚皮苷,橙皮苷,新橙皮苷(NH),异黄体生成素(IL)和甘草酸(GA),它们来自XFZY的11种草药中的9种,除了桔梗(Jacq。)A. DC。 (J)和柴胡DC。 (柴胡)此UPLC方法已通过线性,LOD和LOQ,精度,可重复性,稳定性和恢复测试方面的验证。该方法检测了十四种样品中四种剂型对XFZY产品的质量控制,结果证实了其可行性和可靠性。

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