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Metabolic Pharmacokinetics in Rats: Differences between Pure Amygdalin and Amygdalin in a Decoction of Peach Seeds

机译:大鼠的代谢药代动力学:桃籽汤中纯苦杏仁苷和苦杏仁苷的差异

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The pharmacokinetics of prunasin after oral administration of amygdalin or a decoction of peach seeds was determined and compared in rats. A C18 column was used for separation at a column temperature of 25 oC. The mobile phase consisted of 20% aqueous acetonitrile, and the flow rate was 0.5 mL/min. After oral administration of a decoction of peach seeds, prunasin was absorbed rapidly, reaching a maximum plasma concentration (Cmax) of 62.1 mg/L within 45 min. After oral administration of amygdalin, the absorption of prunasin was delayed. The Cmax of prunasin was 42.9 mg/L and was reached at 60 min. Values for the pharmacokinetic parameters of prunasin, including Tmax, Cmax, AUC, T1/2, CL/F, and V1/F, were significantly different for the oral administration of amygdalin compared with that of a decoction of peach seeds.
机译:测定并比较了大鼠口服苦杏仁苷或桃子汤后的李宁的药代动力学。使用C18色谱柱在25 oC的色谱柱温度下进行分离。流动相由20%乙腈水溶液组成,流速为0.5 mL / min。口服桃子汤后,维生素A迅速吸收,在45分钟内血浆最高浓度(Cmax)达到62.1 mg / L。口服苦杏仁苷后,梅毒的吸收被延迟。梅花run的Cmax为42.9 mg / L,在60分钟时达到。苦杏仁苷的口服给药与桃子汤的口服相比,包括Tmax,Cmax,AUC,T1 / 2,CL / F和V1 / F在内的梅毒的药代动力学参数值明显不同。

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