Jun Ren , Jin Zhuo , Xuejing Sun , Huijie Zhang , Haisheng Zeng , Lei Wang , Wei Wang , Yijun Chen
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引用次数: 0
Abstract
Bufadienolides, the primary active constituents of the traditional Chinese medicine Venenum bufonis, exhibit significant pharmacological activity. However, the potential pharmacokinetic effects of drug-drug interactions among these compounds under combination treatment have not yet been investigated. Thus, this study focused on three representative bufadienolides (resibufogenin, bufalin, and arenobufagin) as the research subjects and assessed the pharmacokinetic interactions among them under co-administration conditions. Firstly, we developed a validated UPLC-QqQ-MS/MS analytical method using digoxigenin as the internal standard (IS) and performed accurate quantification of these compounds in all samples under multiple reaction monitoring (MRM) mode. This analytical method delivered high levels of specificity, recovery, accuracy, precision, and preserved sample stability. Subsequently, pharmacokinetic data for the three compounds under both single-agent and combination treatment conditions were analyzed using non-compartmental modeling. The results demonstrated significant pharmacokinetic variability among different bufadienolide compounds, reflecting distinct structure-pharmacokinetic relationships. Under combination treatment, the pharmacokinetic parameters were significantly altered due to mutual interactions among the bufadienolide compounds. In conclusion, this study has established a drug-drug interaction network for bufadienolides, providing a scientific foundation for the rational clinical application of Venenum Bufonis-based formulations. These findings may facilitate the optimized development of multi-component therapies with cardiotonic pharmacological activity, particularly in the treatment of cardiovascular diseases.
期刊介绍:
This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome.
Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.