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Journal of Chinese Pharmaceutical Sciences ›› 2025, Vol. 34 ›› Issue (7): 633-643.DOI: 10.5246/jcps.2025.07.047

• Original articles • Previous Articles     Next Articles

Pharmacokinetic study of 3-(4-chlorophenyl)-7-[2-(piperazin-1-yl)ethoxy]-4H-chromen-4-one, a derivative of soybean isoflavone by LC-MS/MS in normal rats

Junrong Hao1,2, Mengqiang Lian3, Shuang Li4,5, Hongyan Yin1,2, Chunyan Guo1,2,*()   

  1. 1 Department of Pharmacy, Hebei North University, Zhangjiakou 075000, Hebei, China
    2 Hebei Key Laboratory of Neuropharmacology, Zhangjiakou 075000, Hebei, China
    3 Youji (Tianjin) Medicine Technology Co., Ltd., Tianjin 300450, China
    4 Jianyuan Precision Medicines (Zhangjiakou) Co., Ltd., Zhangjiakou 075000, Hebei, China
    5 Hebei Anti-Tumor Molecular Target Technology Innovation Center, College of Life Science, Hebei Normal University, Shijiazhuang 050024, Hebei, China
  • Received:2025-03-27 Revised:2025-04-16 Accepted:2025-04-23 Online:2025-07-31 Published:2025-07-31
  • Contact: Chunyan Guo
  • Supported by:
    Scientific Research Projects of Hebei North University (Grant No. XJ2024022).

Abstract:

3-(4-Chlorophenyl)-7-[2-(piperazin-1-yl)ethoxy]-4H-chromen-4-one (CPEO-43) is a derivative of soybean isoflavone (SI), synthesized by introducing a chlorine atom and a piperazine group into the structure of natural SI. In vitro experiments have demonstrated that CPEO-43 exhibits a notable inhibitory effect on both A549 cells and HCT116 cells. For the further development and utilization of CPEO-43, this study aims to establish and validate a liquid chromatography-tandem mass spectrometry (LC-MS/MS) quantitative analysis method for the pharmacokinetic study of CPEO-43. Normal rats were intragastrically administered different doses (2, 6, and 20 mg/kg) of CPEO-43, and blood was taken from the ocular venous plexus at different time points. The blood concentration of CPEO-43 at different time points was determined using LC-MS/MS technology, and the pharmacokinetic parameters of the compound were calculated using the pharmacokinetic software DAS. The results indicated that the established LC-MS/MS method complies with the standards for bioanalytical method validation in the Chinese Pharmacopoeia (CHP) and can be applied to the pharmacokinetic study of CPEO-43. The pharmacokinetic software DAS non-compartmental model was successfully used to calculate the Cmax, Tmax, t1/2, AUC0–∞, MRTs, CL, and Vd pharmacokinetic parameters of the compound at different doses. The results were as follows: 62.0 ± 10.5, 222.0 ± 28.7, and 1384.5 ± 376.4 ng/mL; 8.5 ± 1.2, 6.0 ± 0.0, and 11.0 ± 6.2 h; 15.6, 15.0, and 18.5 h; 1517.8 ± 317.0, 5328.7 ± 864.4, and 45556.3 ± 22735.6 ng·h/mL; 17.8 ± 1.2, 17.7 ± 0.8, and 20.0 ± 3.2 h; 1370.3 ± 305.9, 1153.5 ± 205.6, and 505.3 ± 179.8 mL/kg/h; 30843.0 ± 7458.0, 24344.0 ± 5237.0, and 13950.3 ± 5996.9 mL/kg. These characteristics are of great significance for understanding the in vivo process of the drug, formulating dosing regimens, and evaluating the safety and efficacy of the drug.

Key words: 3-(4-Chlorophenyl)-7-[2-(piperazin-l-yl)ethoxy]-4H-chromen-4-one, Soybean isoflavone, LC-MS/MS, Pharmacokinetics

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