Characterization of chemical components of Periplocae Cortex and their metabolites in rats using ultra‐performance liquid chromatography coupled with quadrupole time‐of‐flight mass spectrometry

• Published in: Biomedical chromatography 2020-04, Vol.34 (4), p.e4807-n/a
• Main Authors: Li, Zi‐ting, Zhang, Feng‐xiang, Chen, Wei‐wu, Chen, Ming‐hao, Tang, Xi‐yang, Ye, Meng‐nan, Yao, Zhi‐hong, Yao, Xin‐sheng, Dai, Yi
• Format: Article
• Language: English
• Subjects: Administration, Oral; Aldehydes - analysis; Aldehydes - chemistry; Animals; C21 steroidal glycosides; Chromatography, High Pressure Liquid - methods; Drugs, Chinese Herbal - administration & dosage; Drugs, Chinese Herbal - analysis; Drugs, Chinese Herbal - chemistry; Drugs, Chinese Herbal - metabolism; Glycosides - analysis; Glycosides - chemistry; Male; Mass Spectrometry - methods; metabolite profiling; Periploca - chemistry; Periplocae Cortex; Plant Bark - chemistry; Plant Roots - chemistry; Rats; Rats, Sprague-Dawley; traditional Chinese medicine; Triterpenes - analysis; Triterpenes - chemistry
• ISSN: 0269-3879; 1099-0801
• DOI: 10.1002/bmc.4807

Periplocae Cortex, named Xiang‐Jia‐Pi in China, has been widely used to treat autoimmune diseases, especially rheumatoid arthritis. However, the in vivo substances of Periplocae Cortex remain unknown yet. In this study, an ultra‐performance liquid chromatography coupled with quadrupole time‐of‐flight mass spectrometry was used for profiling the chemical components and related metabolites of Periplocae Cortex. A total of 98 constituents were identified or tentatively characterized in Periplocae Cortex: 42 C21 steroidal glycosides, 10 cardiac glycosides, 23 organic acids, 4 aldehydes, 7 triterpenes, and 12 other types. Among them, 18 components were unambiguously identified by comparison with reference standards. In addition, 176 related xenobiotics (34 prototypes and 142 metabolites) were screened out and characterized in rats’ biosamples (plasma, urine, bile, and feces) after the oral administration of Periplocae Cortex. Moreover, the metabolic fate of periplocoside S‐4a, a C21 steroidal glycoside, was proposed for the first time. In summary, phase II reactions (methylation, glucuronidation, and sulfation), phase I reactions (hydrolysis reactions, oxygenation, and reduction), and their combinations were the predominant metabolic reactions of Periplocae Cortex in rat. It is the first report to reveal the in vivo substances and metabolism feature of Periplocae Cortex. This study also provided meaningful information for further pharmacodynamics study of Periplocae Cortex, as well as its quality control research.