Effect of particle design on pharmacokinetics of Shenling Baizhu Pulvis in rats
10.7501/j.issn.0253-2670.2020.19.011
- VernacularTitle: 粒子设计对参苓白术散在大鼠体内药动学过程的影响
- Author:
Xiao ZHOU
1
Author Information
1. School of Pharmacy, Shaanxi University of Chinese Medicine
- Publication Type:Journal Article
- Keywords:
Atractylenolide I;
Atractylenolide II;
Bioavailability;
Ginsenoside Rb1;
Ginsenoside Re;
Ginsenoside Rg1;
LC-MS;
Modification;
Pachymic acid;
Particle design;
Pharmacokinetics;
Shenling Baizhu Pulvis
- From:
Chinese Traditional and Herbal Drugs
2020;51(19):4925-4933
- CountryChina
- Language:Chinese
-
Abstract:
Objective: Using LC-MS to explore the pharmacokinetic process in rats of Shenling Baizhu Pulvis (SBP), which was modified by particle design technology. Methods: Particle design powder of SBP was prepared by particle design technology. A scientific and feasible LC-MS analysis method was established to determine the blood concentration of index compounds such as ginsenoside Re (GI-Re), ginsenoside Rb1 (GI-Rb1), ginsenoside Rg1 (GI-Rg1), atractylenolide I (AT-I), atractylenolide II (AT-II) and pachymic acid (PA) in rats at different time points after administration. DAS 3.2.8 pharmacokinetic software was adopted to analyze the data, which related to blood concentration of index compounds, and the pharmacokinetics parameters were calculated by the non-compartmental model. Results: LC-MS analysis method was established, which has a good linear relationship and specificity for the index compounds in rats, and the RSD of precision, accuracy, extraction recovery and stability were all less than 5% or 10%. Compared with ordinary powder, the particle design powder displayed increased Cmax and AUC0-∞ after administration, and the AUC0-∞ of GI-Re, GI-Rb1, GI-Rg1, AT-I, AT-II and PA were increased to 1.52, 2.02, 1.22, 1.41, 1.13 and 1.43 times, respectively. Conclusion: The LC-MS analysis method meet the requirements of biological sample analysis in Pharmacopoeia of the People's Republic of China. After particle design and modification, the absorption speed of SBP in vivo become faster and the bioavailability is improved significantly.
