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In-Vitro Sorbent-Mediated Removal of Edoxaban from Human Plasma and Albumin Solution

机译:体外吸附剂介导从人血浆和白蛋白溶液中去除Edoxaban

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Background and ObjectiveBased on previous experience of sorbent-mediated ticagrelor, dabigatran, and radiocontrast agent removal, we set out in this study to test the effect of two sorbents on the removal of edoxaban, a factor Xa antagonist direct oral anticoagulant.MethodsWe circulated 100?mL of edoxaban solution during six first-pass cycles through 40-mL sorbent columns (containing either CytoSorb in three passes or Porapak Q 50–80 mesh in the remaining three passes) during experiments using human plasma and 4% bovine serum albumin solution as drug vehicles. Drug concentration was measured by liquid chromatography-tandem mass spectrometry.ResultsEdoxaban concentration in two experiments performed with human plasma dropped from 276.8 to 2.7?ng/mL and undetectable concentrations, respectively, with CytoSorb or Porapak Q 50–80 mesh ( p =?0.0031). The average edoxaban concentration decreased from 407?ng/mL?±?216?ng/mL to 3.3?ng/mL?±?7?ng/mL ( p =?0.017), for a removal rate of 99% across all six samples of human plasma (two samples) and bovine serum albumin solution (four samples). In four out of the six adsorbed samples, the drug concentrations were undetectable.ConclusionSorbent-mediated technology may represent a viable pathway for edoxaban removal from human plasma or albumin solution.
机译:背景和基础上以前的吸附剂介导的TiCagreloLor,Dabigatran和radiocontraster去除的经验,我们在本研究中阐述了两种吸附剂对去除Edoxaban的效果,是一种因子Xa拮抗剂直接口服抗凝血剂。近奇的Xa拮抗剂直接抗凝血剂。在使用人血浆和4%牛血清白蛋白溶液作为药物的实验期间,在六个首次循环中通过40ml吸附剂柱(含有三次通过的胞嘧啶Q 50-80含量)的六种先进的循环溶液(在其余三次通过中的杂散β。车辆。通过液相色谱 - 串联质谱法测量药物浓度。分别用人血浆进行的两种实验中的两种实验中的浓度分别从276.8〜2.7?Ng / mL和未检测的浓度进行,患有胞流或Porapak Q 50-80网格(P = 0.0031 )。 Edoxaban浓度的平均浓度从407〜Ng / mlαα±216℃下降到3.3?Ng / mlααα7?7?Ng / ml(p = 0.017),除以全部六个99%的去除率人血浆(两个样品)和牛血清白蛋白溶液(四个样品)样品。在六个吸附样品中的四个中,未检测到的药物浓度。结合介导的技术可以代表从人血浆或白蛋白溶液中去除的埃希南巴的活性途径。

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