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Qualitative analysis and quality control of Traditional Chinese Medicine preparation Tanreqing injection by LC-TOF/MS and HPLC-DAD-ELSD

机译:LC-TOF / MS和HPLC-DAD-ELSD对坦热清中药制剂的定性分析与质量控制

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摘要

Tanreqing injection, a classical Traditional Chinese Medicine formulation, consists of Radix Scutellariae baicalensis, Fel selenarcti, Cornu naemorhedi, Flos lonicerae and Forsythiae fructus, having a marked curative effect on the diseases of the upper respiratory tract. In order to clarify its chemical profile, a method based on liquid chromatography coupled with time-of-flight mass spectrometry was proposed, and 53 compounds were identified on a formula database of 515 known compounds with the aid of accurate mass measurement for molecular ions and characteristic fragment ions. Using the chemical fingerprints for the purpose of quality control, a high performance liquid chromatography coupled with photodiode array detection and evaporative light scattering detection (HPLC-DAD-ELSD) was developed in this study. The chromatographic fingerprints were evaluated by the dual similarities (S and Sa€2) of an ultra-violet chromatogram, in combination with SE of an ELSD chromatogram, reflecting the complexity of Tanreqing injection with the consideration of both large and small peaks. In addition, the established HPLC-DAD-ELSD method was successfully applied to the quantitative analysis of the five ingredients (chlorogenic acid, caffeic acid, baicalin, ursodeoxycholic acid and chenodeoxycholic acid) and fingerprint analysis in 11 batches of Tanreqing injections. The results obtained in this research will provide the basis for quality control of Tanreqing injections.
机译:坦热清注射液是一种经典的传统中药配方,由黄S 、,藤,山茱Corn,金银花和连翘组成,对上呼吸道疾病有明显的治疗作用。为了阐明其化学特征,提出了一种基于液相色谱-飞行时间质谱联用的方法,并借助精确的分子离子和质谱质量测量,在515种已知化合物的分子式数据库中鉴定出53种化合物。特征碎片离子。使用化学指纹进行质量控制的目的,本研究开发了一种结合了光电二极管阵列检测和蒸发光散射检测(HPLC-DAD-ELSD)的高效液相色谱仪。通过紫外色谱图的双重相似性(S和Sa€2)结合ELSD色谱图的SE对色谱指纹图谱进行了评估,反映了Tanreqing进样的复杂性,同时考虑了大峰和小峰。此外,已建立的HPLC-DAD-ELSD方法已成功地用于11批痰热清注射液中五种成分(绿原酸,咖啡酸,黄ical苷,熊去氧胆酸和鹅去氧胆酸)的定量分析和指纹图谱分析。本研究获得的结果将为坦热清注射液的质量控制提供基础。

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