首页> 外文期刊>European journal of drug metabolism and pharmacokinetics >Improved Oral Absorption of Quercetin from Quercetin Phytosome (R), a New Delivery System Based on Food Grade Lecithin
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Improved Oral Absorption of Quercetin from Quercetin Phytosome (R), a New Delivery System Based on Food Grade Lecithin

机译:从槲皮素植物体(R)的改善口服吸收槲皮素,基于食物级卵磷脂的新型递送系统

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Background and ObjectivesThe importance of quercetin and flavonoids in the diet and as food supplements is well known, and literature studies support their potential use to treat several human diseases. Many beneficial properties have been described for quercetin, so much effort has been directed into overcoming the major drawbacks of this natural compoundits poor solubility and low oral absorption. The aims of this study were to compare a new food-gradelecithin-based formulation of quercetin, Quercetin Phytosome((R)), to unformulated quercetin in terms of solubility in simulated gastrointestinal fluids and oral absorption in a randomized crossover pharmacokinetic study of healthy volunteers.MethodsThe solubility of the new formulation was determined by in vitro incubation in simulated gastrointestinal fluids, and quercetin was detected by ultra performance liquid chromatography. A single-dose, randomized, six-sequence/three-period crossover clinical trial (3x3x3 crossover design) with a balanced carryover effect was conducted in healthy volunteers under fasting conditions. Twelve healthy volunteers of both sexes with an age range of 18-50years were recruited; one dose of quercetin and two different doses of Quercetin Phytosome were administered orally as film-coated tablets. Pharmacokinetic samples were collected at twelve time points (from 0h to 24h) after administration, and quercetin levels were measured by HPLC/MS/MS. Data were analyzed using the Phoenix WinNonlin (v.6.4) software package, and the most significant pharmacokinetic parameters were calculated. Statistical analysis involved performing a two-way ANOVA with repeated measures followed by post hoc analysis (Tukey's test).ResultsSignificant improvements in both in vitro solubility and oral absorption (in terms of both exposure and maximum concentration achieved) by healthy volunteers in a human clinical study were obtained with the Quercetin Phytosome formulation as compared to unformulatedquercetin.ConclusionsA more soluble formulation of quercetin based on lecithin, Quercetin Phytosome, has recently been developed, and was found to facilitate the attainment of very high plasma levels of quercetinup to 20 times more than usually obtained following a dose of quercetinwhen the novel formulation was administered orally in human volunteers, and it did not have any notable side effects. These results suggest that Quercetin Phytosome allows the oral administration of quercetin in a safe and bioavailable manner, thus facilitating the effective utilization of this natural compound to treat various human diseases.
机译:背景和客观槲皮素和黄酮类化合物在饮食中的重要性和食品补充剂是众所周知的,文献研究支持他们潜在的用来治疗几种人类疾病。已经针对槲皮素描述了许多有益的特性,因此越来越大的努力克服了这种天然复合性差的溶解度和低口腔吸收的主要缺点。本研究的目的是将槲皮素,槲皮素((r))的槲皮素,槲皮素((r))的溶解度的溶解度和健康志愿者的随机交叉药代动力学研究中的口腔吸收的溶解度进行比较槲皮素的新食物 - 植物体((r))。 。通过在模拟胃肠流体中的体外孵育来确定新配方的溶解度,通过超级性能液相色谱检测槲皮素。在禁食条件下的健康志愿者中,在健康的志愿者中进行单剂量,随机,六序/三周期交叉临床试验(3x3x3交叉设计)。招募了十二岁的性别志愿者,招聘了18-50岁的年龄范围;一种剂量的槲皮素和两种不同剂量的植物植物组,作为膜涂层片剂给予口服。在给药后,在12个时间点(0H至24h)收集药代动力学样品,通过HPLC / MS / MS测量槲皮素水平。使用Phoenix Winnonlin(V.6.4)软件包进行分析数据,并计算最重要的药代动力学参数。统计分析涉及具有重复措施的双向ANOVA,然后进行HOC分析(Tukey的测试)。在体外溶解度和口服吸收(在患有人类临床中的健康志愿者而言,在体外溶解度和口腔吸收(在均匀浓度方面取得最大浓度)的改善与植酸素植物体配制相比,获得了槲皮素的纯细胞体制素。结合基于卵磷脂的槲皮素更可溶的植物素,植物植物体最近已经开发出来,并发现促进了槲皮素的非常高的血浆水平超过20倍。通常在剂量的槲皮素后获得新型制剂的槲皮素,在人类志愿者口服给药,它没有任何显着的副作用。这些结果表明,槲皮素植物体允许以安全和生物可利用的方式口服槲皮素施用,从而有效利用这种天然化合物治疗各种人类疾病。

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