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首页> 外文期刊>Analytical methods >Pharmacokinetic properties of ephedrine, amygdalin and glycyrrhizic acid after oral gavage of San-Ao-decoction in beagle dogs using a UPLC-MS method
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Pharmacokinetic properties of ephedrine, amygdalin and glycyrrhizic acid after oral gavage of San-Ao-decoction in beagle dogs using a UPLC-MS method

机译:使用UPLC-MS方法对圣比耳汤灌胃后的麻黄碱,苦杏仁苷和甘草酸的药代动力学特性

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An ultra performance liquid chromatography-mass spectrometric (UPLC-MS) method was developed to investigate the pharmacokinetic properties of ephedrine, amygdalin and glycyrrhizic acid after oral gavage of San-Ao-decoction (SA) in beagle dogs. Beagle dogs plasma samples were pretreated using liquid-liquid extraction, and chromatographic separation was performed on a C_(18) column using a linear gradient of water and formic acid (0.1%). The pharmacokinetic parameters of ephedrine, amygdalin and glycyrrhizic acid from SA in beagle dogs were quantitatively determined by UPLC with photodiode array detection (PDA). The qualitative detection of the three compounds was accomplished by selected ion monitoring in negative/positive ion modes ESI-MS. Detection was based on the multiple reaction monitoring with the precursor-to-product ion transitions m/z 166.096-116.983 (ephedrine) and m/z 456.351-323.074 (amygdalin) and m/z 821.606-351.062 (glycyrrhizic acid). The selectivity, sensitivity, linearity, accuracy, precision, extraction recovery, ion suppression and stability were within the acceptable ranges. The method described above was successfully applied to reveal the pharmacokinetic properties of ephedrine, amygdalin and glycyrrhizic acid after oral gavage of SA in beagle dogs.
机译:建立了一种超高效液相色谱-质谱(UPLC-MS)方法,研究了在圣比奥汤(SA)口服灌胃对小猎犬狗中麻黄碱,苦杏仁苷和甘草酸的药代动力学特性。使用液-液萃取预处理比格犬血浆样品,并使用水和甲酸(0.1%)的线性梯度在C_(18)色谱柱上进行色谱分离。通过UPLC和光电二极管阵列检测(PDA)定量测定比格犬中SA中的麻黄碱,苦杏仁苷和甘草酸的药代动力学参数。三种化合物的定性检测是通过在负离子/正离子模式ESI-MS中选择离子监测来完成的。检测基于多反应监测,前体-产物离子跃迁为m / z 166.096-116.983(麻黄碱)和m / z 456.351-323.074(阿米达林)和m / z 821.606-351.062(甘草酸)。选择性,灵敏度,线性,准确度,精密度,提取回收率,离子抑制和稳定性均在可接受的范围内。成功地应用上述方法揭示了在比格犬中口服SA后麻黄碱,苦杏仁苷和甘草酸的药代动力学特性。

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