Exploration of the Dynamic Variations of the Characteristic Constituents and the Degradation Products of Catalpol during the Process of Radix Rehmanniae

• Published in: Molecules (Basel, Switzerland) Vol. 29; no. 3; p. 705
• Main Authors: Yang, Jingjing, Zhang, Lihua, Zhang, Mengyue, Yang, Mingxuan, Zou, Lin, Cui, Ying, Yang, Jing, Chai, Xin, Wang, Yuefei
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.02.2024
• Subjects: Acetates; Amino acids; Backup software; catalpol; Chromatography; degradation products; Liquid chromatography; Medicine, Chinese; NMR; Nuclear magnetic resonance; processing; Product introduction; Radix Rehmanniae; Spectrum analysis; UPLC-PDA; China; catalpol; processing; degradation products; UPLC-PDA; Radix Rehmanniae
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules29030705

Radix Rehmanniae (RR), a famous traditional Chinese medicine (TCM) widely employed in nourishing and invigorating the kidney, has three common processing forms in clinical practice, including fresh Radix Rehmanniae (FRR), raw Radix Rehmanniae (RRR), and processed Radix Rehmanniae (PRR). However, until now, there has been less exploration of the dynamic variations in the characteristic constituents and degradation products of catalpol as a representative iridoid glycoside with the highest content in RR during the process from FRR to PRR. In this study, an ultra-performance liquid chromatography coupled with photodiode array detector (UPLC-PDA) method was successfully established for the simultaneous determination of ten characteristic components to explore their dynamic variations in different processed products of RR. Among them, iridoid glycosides, especially catalpol, exhibited a sharp decrease from RRR to PRR. Then, three degradation products of catalpol were detected under simulated processing conditions (100 °C, pH 4.8 acetate buffer solution), which were isolated and identified as jiofuraldehyde, cataldehyde, and norviburtinal, respectively. Cataldehyde was first reported as a new compound. Moreover, the specificity of norviburtinal in self-made PRR samples was discovered and validated, which was further confirmed by testing in commercially available PRR samples. In conclusion, our study revealed the decrease in iridoid glycosides and the production of new degradation substances during the process from FRR to PRR, which is critical for unveiling the processing mechanism of RR.