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Pharmacokinetics and Tissue Distribution Study of Pinosylvin in Rats by Ultra-High-Performance Liquid Chromatography Coupled with Linear Trap Quadrupole Orbitrap Mass Spectrometry

机译:高效液相色谱-线性捕集四极杆Orbitrap质谱联用研究品尼松在大鼠体内的药代动力学和组织分布

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摘要

Pinosylvin is a potential anti-inflammatory and antioxidant compound and the major effective medicinal ingredient in the root of Lindera reflexa Hemsl. However, few investigations have been conducted regarding the pharmacokinetics, excretion, characteristics of tissue distribution, and major metabolites of pinosylvin in rats after oral administration. To better understand the behavior and mechanisms of action underlying the activity of pinosylvin in vivo, we established a simple, sensitive, and reliable ultra-high-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method for quantifying pinosylvin in rat plasma, urine, feces, and various tissues (including heart, liver, spleen, lung, kidneys, large intestine, small intestine, and stomach). Noncompartmental pharmacokinetic parameters indicated that pinosylvin is rapidly distributed and taken up by tissues. The time to peak (maximum) concentration (Tmax) was 0.137 h, and the apparent elimination half-life (t1/2) was 1.347±0.01 h. The results of the tissue distribution study suggest that pinosylvin is widely distributed to various tissues; the highest concentration was observed after 10 min in the stomach, followed by the heart, lung, spleen, and kidneys. Results of the excretion study suggest that a small amount of pinosylvin is excreted from the urine and feces in the parent form; the 73 h accumulative excretion ratios of urine and feces were 0.82% and 0.11%, respectively. It is likely that pinosylvin is mostly metabolized in vivo. Nine metabolites were found, and the main metabolic pathways of pinosylvin in rats included glucuronidation, hydroxylation, and methylation. Four metabolites had higher concentrations in the stomach, suggesting that the stomach is a potential target organ of pinosylvin. In conclusion, the present study may provide a material basis for studying the pharmacological action of pinosylvin and provides meaningful information for the clinical treatment of chronic gastritis and gastric ulcers using Radix Linderae Reflexae.
机译:Pinosylvin是潜在的抗炎和抗氧化化合物,是反射性Lindera Hemsl根中的主要有效药用成分。但是,关于口服给药后大鼠体内的药代动力学,排泄,组织分布特征以及松果酚的主要代谢物的研究很少。为了更好地了解体内的松果酚活性的行为和作用机理,我们建立了一种简单,灵敏且可靠的超高效液相色谱串联质谱法(UPLC-MS / MS),用于定量大鼠血浆中的松果酚。 ,尿液,粪便和各种组织(包括心脏,肝脏,脾脏,肺,肾脏,大肠,小肠和胃)。非房室药代动力学参数表明松果酚迅速分布并被组织吸收。达到峰值(最大)浓度(Tmax)的时间为0.137 h,表观消除半衰期(t1 / 2)为1.347±0.01 h。组织分布研究的结果表明,松果酚广泛分布于各种组织中。在胃中10分钟后观察到最高浓度,其次是心脏,肺,脾脏和肾脏。排泄研究的结果表明,少量的松果酚以母体形式从尿液和粪便中排出。尿和粪便的73 h累积排泄率分别为0.82%和0.11%。 Pinosylvin可能大部分在体内代谢。发现了九种代谢物,并且大鼠体内的松果油的主要代谢途径包括葡萄糖醛酸化,羟基化和甲基化。四种代谢物在胃中的浓度较高,表明胃是松果酚的潜在靶器官。综上所述,本研究可为研究松果酚的药理作用提供物质基础,并为使用灵芝反射片治疗慢性胃炎和胃溃疡提供有意义的信息。

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