PAN Ying. Comparison of Pharmacokinetics of Ferulic Acid after Oral Administration of Rhizoma Ligustici Chuanxiong and Tongmai Formulations in Rats[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(4): 193-196.
PAN Ying. Comparison of Pharmacokinetics of Ferulic Acid after Oral Administration of Rhizoma Ligustici Chuanxiong and Tongmai Formulations in Rats[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(4): 193-196. DOI: 10.13422/j.cnki.syfjx.2011.04.064.
Objective:To Compare the pharmacokinetics of ferulic acid after oral administration of the ex-tracts from Rhizoma Ligustici Chuanxiong and Tongmai formulations in rats.Method:The blood samples were col-lected at different time points after oral administration of the extracts from Rhizoma Ligustici Chuanxiong and Tong-mai formulations(equivalent to 9.0 mg.kg-1 ferulic acid) to wistar rats respectively.The plasma concentration of ferulic acid was measured by HPLC after extracted with ethyl acetate
and then pharmacokinetic parameters were cal-culated from the plasma concentration-time data with the 3P97 software.Result:The mean plasma concentration-time curves of ferulic acid after oral administration of the extracts from Rhizoma Ligustici Chuanxiong and Tongmai formu-lations were fitted to one compartment open model.The(Ke) s of the extracts from Rhizoma Ligustici Chuanxiong and Tongmai formulations were(0.015 ± 0.002)
(0.008 ± 0.001) min
t1/2(Ke) were(46.850 ± 5.414)
(87.033 ± 11.025)min respectively.Significant differences were found between the two groups(P < 0.01).There existed significant differences(P < 0.05)in AUC and CL /F(s)between the extracts from Rhizoma Ligustici Chua-nxiong and Tongmai formulations.(AUC)s were(328.440 ± 115.461)
(625.718 ± 139.798)μg.min-1.mL-1
CL / F(s)were(0.032 ± 0.013)
(0.015 ± 0.004)L.kg-1.min-1 respectively.Conclusion:The work proved that the com-patibility of Radix Salviae Miltiorrhiza and Radix Puerahae with Rhizoma Ligustici Chuanxiong could reduce the elimi-nation rate
prolong the action time of ferulic acid in vivo and enhance the ferulic acid biological exploitability.