Identification and Quantitation of Cardiac Hypertrophy Inhibitory Components in Trichosanthis Pericarpium Injection Based on UHPLC‐QE‐MS and Spectrum–Effect Relationships

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Authors: Ziyan Bian, Xing Wang, He Li, Jinguo Ding, Ying Dong, Cao Xiaoxia, Fengjie Zhou, Siqi Du, Nan Li, Miaomiao Jiang, Yuhong Li, Han Zhang
+1 more Peng Zhang
Cited by: 0
References: 20

Abstract

Trichosanthis Pericarpium injection (TPI) is a Chinese patent medicine for coronary heart disease and stable angina pectoris. This study aimed to integrate UHPLC-QE-MS with fingerprint-effect relationships, chemometrics, and spectrum-effect relationship analyses to accurately screen active components and quantify quality markers in TPI. First, the impact of TPI on Ang II-induced cardiomyocyte hypertrophy was assessed in vitro, confirming its inhibitory effects on cardiac hypertrophy for the first time. Next, 57 compounds were identified using UHPLC-QE-MS. Twelve batches of TPI were characterized by UPLC-UV, and these fingerprint spectra were correlated with their inhibitory effects on cardiac hypertrophy using Pearson correlation analysis and PLSR methods. Five key compounds were identified: trigonelline, adenine, adenosine, guanosine, and vanillic acid. Among them, except for adenosine, the four compounds showed significant anti-hypertrophy activity. Finally, a rapid UHPLC-QQQ-MS/MS quantification method revealed that trigonelline and guanosine had high content, minimal variation, and significant inhibitory effects, establishing them as suitable quality control indicators for TPI. This study provides valuable support for the pharmacodynamic material basis and quality control of Trichosanthis Pericarpium and TPI and for the quality evaluation of complex chemical ingredient products.

Fields of Study & Subjects

Traditional Chinese Medicine Analysis Phytochemistry and Biological Activities Analytical Methods in Pharmaceuticals

Publication details

Journal / source
Biomedical Chromatography
Volume
40
Issue
4
Pages
e70397–e70397
Publication date
6 March 2026
Language
EN