首页> 外文期刊>Scientific reports. >Pharmacokinetic comparison between quercetin and quercetin 3-O-β-glucuronide in rats by UHPLC-MS/MS
【24h】

Pharmacokinetic comparison between quercetin and quercetin 3-O-β-glucuronide in rats by UHPLC-MS/MS

机译:槲皮素与槲皮素3-O-β-葡萄糖醛酸苷在大鼠体内的药代动力学比较

获取原文
           

摘要

Quercetin is a natural flavonoid widely distributed in human diet and functional foods. Quercetin 3-O-β-glucuronide (Q3G) is present in wine and some medicinal plants. Quercetin and Q3G may be metabolized from each other in vivo. While quercetin has been the subject of many studies, the pharmacokinetic profiles of quercetin and Q3G (in animals) have not yet been compared. Herein, we prepared a column-based method for rapid isolation of Q3G from Nelumbo nucifera. Then, we developed an UHPLC-MS/MS method to compare the pharmacokinetics of quercetin and Q3G. Our results showed that the plasma concentration-time curves of quercetin and Q3G show two maxima (Tmax1?≈?0.75?h, Tmax2?≈?5?h). After oral administration of 100?mg/kg quercetin or 100?mg/kg Q3G in rats, predominantly Q3G was detected in plasma with AUC at 39529.2?±?6108.2?mg·h·L(-1) or 24625.1?±?1563.8?mg·h·L(-1), 18-fold higher than quercetin with AUC at 1583.9?±?583.3?mg·h·L(-1) or 1394.6?±?868.1?mg·h·L(-1), respectively. After intravenous injection of 10?mg/kg in rats, Q3G showed extensive tissue uptake in kidney (409.2?±?118.4?ng/g), liver (166.1?±?52.9?ng/g), heart (97.7?±?22.6?ng/g), and brain (5.8?±?1.2?ng/g). In conclusion, we have shown that Q3G is a major active component in plasma and tissue for oral administration of quercetin or Q3G.
机译:槲皮素是一种广泛存在于人类饮食和功能性食品中的天然类黄酮。葡萄酒和一些药用植物中存在槲皮素3-O-β-葡糖醛酸(Q3G)。槲皮素和Q3G可能在体内彼此代谢。槲皮素已成为许多研究的主题,但槲皮素和Q3G(在动物中)的药代动力学图谱尚未进行比较。在这里,我们准备了一种基于柱的方法,用于从莲子中快速分离Q3G。然后,我们开发了一种UHPLC-MS / MS方法来比较槲皮素和Q3G的药代动力学。我们的结果表明,槲皮素和Q3G的血浆浓度-时间曲线显示出两个最大值(Tmax1?≈?0.75?h,Tmax2?≈?5?h)。在大鼠中口服100?mg / kg槲皮素或100?mg / kg Q3G后,血浆中AUC的Q3G含量最高,为39529.2?±?6108.2?mg·h·L(-1)或24625.1?±?1563.8 ?mg·h·L(-1)为1583.9?±?583.3?mg·h·L(-1)或1394.6?±?868.1?mg·h·L(-1)的槲皮素和AUC的18倍), 分别。在大鼠静脉注射10?mg / kg后,Q3G显示肾脏(409.2?±?118.4?ng / g),肝脏(166.1?±?52.9?ng / g),心脏(97.7?±?)的大量组织摄取。 22.6?ng / g)和大脑(5.8?±?1.2?ng / g)。总之,我们已经证明Q3G是血浆和组织中口服槲皮素或Q3G的主要活性成分。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号