首页> 外文期刊>The Journal of automatic chemistry >Development of an Ultra-High Performance Liquid Chromatography Method for Simultaneous Determination of Six Active Compounds in Fructus aurantii and Rat Plasma and Its Application to a Comparative Pharmacokinetic Study in Rats Administered with Different Doses
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Development of an Ultra-High Performance Liquid Chromatography Method for Simultaneous Determination of Six Active Compounds in Fructus aurantii and Rat Plasma and Its Application to a Comparative Pharmacokinetic Study in Rats Administered with Different Doses

机译:同时测定a实和大鼠血浆中六种活性成分的超高效液相色谱方法的建立及其在不同剂量大鼠的比较药代动力学研究中的应用

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A rapid, accurate, and sensitive ultra-high performance liquid chromatography (UHPLC) method was established for simultaneously detecting naringin, hesperidin, neohesperidin, meranzin hydrate, naringenin, and hesperetin in Fructus aurantii (FA) decoction. Analysis was performed on Waters BEH (R) C18 (50?mm?×?2.1?mm, 1.7?m) at a flow rate of 0.2?mL/min by using (A) acetonitrile and (B) 0.5% acetic acid-water as the mobile phase. The method was well validated on linearity, precision, recoveries, and stability. Then, we used the same UHPLC conditions for quantitative analysis of meranzin hydrate, naringenin, and hesperetin in rat plasma. The method proved to be linear within the concentration ranges of 3.3–3300?ng/mL for meranzin hydrate, 6.95–3555?ng/mL for naringenin, and 1.8–236?ng/mL for hesperetin. The RSD of precision ranged from 1.22% to 9.08%, and the average extraction recovery ranged from 96.49?±?1.42% to 102.01?±?3.16%. Besides, we performed a comparative pharmacokinetic study after oral administration of FA decoction at a low dose of 15?g/kg and high dose of 30?g/kg body weight for seven days to rats. The AUC(0–t) and Cmax of meranzin hydrate, naringenin, and hesperetin were multiplied significantly with the increase of FA dosage, and the t1/2 of meranzin hydrate was faster than naringenin and hesperetin in the two groups.
机译:建立了一种快速,准确,灵敏的超高效液相色谱(UHPLC)方法,用于同时检测黄ru(FA)汤中的柚皮苷,橙皮苷,新橙皮苷,水合黑素,橙皮苷和橙皮素。使用(A)乙腈和(B)0.5%乙酸,以0.2?mL / min的流速在Waters BEH(R)C18(50?mm?×?2.1?mm,1.7?m)上进行分析。以水为流动相。该方法在线性,精密度,回收率和稳定性方面得到了很好的验证。然后,我们使用相同的UHPLC条件对大鼠血浆中的melanzin水合物,naringenin和hesperetin进行定量分析。事实证明,该方法在水合美兰津的浓度范围为3.3–3300?ng / mL,柚皮苷为6.95–3555ngng / mL,橙皮素为1.8–236?ng / mL的范围内是线性的。精密度的RSD范围为1.22%至9.08%,平均提取回收率范围为96.49%±1.42%至102.01%±3.16%。此外,我们以低剂量15?g / kg体重和30?g / kg体重的高剂量口服FA汤对大鼠7天后进行了比较药代动力学研究。随着FA剂量的增加,水合物黑素,柚皮素和橙皮素的AUC(0–t)和Cmax显着增加,两组中水合物黑素素的t1 / 2快于柚皮素和橙皮素。

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