OBJECTIVE To compare the pharmacokinetic parameters of Xuesaitong dispersible tablets and common tablets in Beagle dogs.METHODS Using double cycle crossover trial, six Beagle dogs were treated with single oral dose of 100 mg of Xuesai- tong dispersible tablets and conventional tablets and determining the pharmacokinetic parameters of ginsenoside Rbl and Rgl in Xuesai-tong dispersible tablets and conventional tablets in Beagle dog plasma.RESULTS The ginsenoside Rbl and Rgl peak concentration of Xuesetong dispersible tablets in Beagle dog plasma was significantly higher than that of Xuesaitong tablets, the ginsenoside Rgl peak tittle of Xuesaitong dispersible tablets in Beagle dog plasma was significantly earlier than that of Xuesaitong tablets.Addnl., the ginsenoside Rbl peak time exhibited ahead of the trend, which is in line with the characteristics of rapid disintegration and absorption of preparation in vivo.CONCLUSION The plasma exposure in two preparation of ginsenoside Rbl and Rgl in Beagle dog holds fairly basic and no significant difference.But the Pmax of the main ingredients of Panax ginseng saponins Rbl and Rgl in Xuesaitong dispersed tablets, is significantly higher than that of the film coated tablets, and peak time is significantly shortened, which could promote the drug absorption.