首页> 外文期刊>Planta medica: Natural products and medicinal plant research >Comparison of Pharmacokinetics and Biodistribution of 10-Deacetylbaccatin III after Oral Administration as Pure Compound or in Taxus chinensis Extract: A Pilot Study
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Comparison of Pharmacokinetics and Biodistribution of 10-Deacetylbaccatin III after Oral Administration as Pure Compound or in Taxus chinensis Extract: A Pilot Study

机译:口服给予纯化合物或在红豆杉提取物中的10-去乙酰基浆果赤霉素III的药代动力学和生物分布比较:一项初步研究

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摘要

Taxanes are a class of bioactive compounds isolated from the Taxus species. 10-Deacetylbaccatin III is one of the popular taxane compounds with antitumor activity, but the pharmacokinetic profile of this compound remains elusive. Previously, we prepared the taxane fractions from the twigs and leaves of Taxus chinensis var. mairei containing 20.4% 10-deacetylbaccatin III. This study aimed to investigate the pharmacokinetics of 10deacetylbaccatin III and biodistribution, and explore the potential changes when it was administered in the form of taxane extracts. A simple, sensitive, and reliable liquid chromatographytandem mass spectrometry method was developed and validated for the quantitative determination of 10-deacetylbaccatin III in biosamples. The results showed that 10-deacetylbaccatin III, after oral dosing, displayed a quick absorption into the blood and distribution into major organs. Oral administration of 10-deacetylbaccatin III in the form of taxane mixtures led to a 16-fold in-crease in the systemic exposure of pure 10-deacetylbaccatin III, with the AUC0-U in the plasma increasing from 25.75 +/- 11.34 to 231.36 +/- 70.12 mu g h/L ( p < 0.0001). Moreover, the concentrations of 10-deacetylbaccatin III in major tissues were significantly enhanced when given in taxane extracts. These findings revealed pharmacokinetic interactions in the taxane components from T. chinensis var. mairei, which contributed to an enhanced systemic exposure of pharmacologically active taxanes.
机译:紫杉烷是从紫杉属物种中分离出来的一类生物活性化合物。 10-脱乙酰浆果赤霉素III是具有抗肿瘤活性的流行紫杉烷化合物之一,但该化合物的药代动力学特征仍然难以捉摸。以前,我们是从红豆杉的嫩枝和叶片中制备紫杉烷馏分的。含有20.4%的10-去乙酰基浆果赤霉素III的玛莱。这项研究旨在调查10脱乙酰基浆果赤霉素III的药代动力学和生物分布,并探索以紫杉烷提取物形式给药时的潜在变化。建立了一种简单,灵敏,可靠的液相色谱串联质谱分析方法,并验证了该方法可用于定量测定生物样品中的10-脱乙酰浆果赤霉素III。结果显示,口服给药后的10-脱乙酰浆果赤霉素III表现出快速吸收到血液中和分布到主要器官中的作用。紫杉烷混合物形式的10-去乙酰基浆果赤霉素III的口服导致全身10-去乙酰基浆果赤霉素III的全身暴露增加了16倍,血浆中的AUC0-U从25.75 +/- 11.34增加到231.36。 +/- 70.12 mu gh / L(p <0.0001)。此外,当从紫杉烷提取物中给予时,主要组织中10-脱乙酰浆果赤霉素III的浓度显着增加。这些发现揭示了来自中华三叶草的紫杉烷组分中的药代动力学相互作用。 mairei,这有助于增加药理活性紫杉烷的全身暴露。

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