《Table 2Stability of salidroside at distinct conditions (n=5) .》

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《Salidroside shows a particular pharmacokinetic property in model rats of myocardial ischemia》

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The sensitive method we developed was successfully used for the determination of the pharmacokinetic properties of SD rats treated with salidroside.After orally administration of salidroside（20，50，and 100 mg/kg）in normal rats，salidroside was rapidly absorbed because of a mean Tmaxwas about 40 min and Cmaxvalues was about（4.5±1.48），（11.18±2.52） ，and（13.59±4.65）μg/m L，which are listed in Table 3.The mean drug concentration–time curves of salidroside，linearity of AUC0～∞–dosage are shown in Fig.5，and the regression equation is:y=0.3319 x+1981.5.