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Pharmacokinetics of BMEDA after Intravenous Administration in Beagle Dogs

机译:比格犬静脉给药后BMEDA的药代动力学

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摘要

The pharmacokinetics of N,N-bis(2-mercapatoethly)-N',N'-diethylenediamine (BMEDA), a molecule that can form a chelate with rhenium-188 (188Re) to produce the 188Re-BMEDA-liposomes, was studied. In this work, beagles received a single injection of BMEDA, at doses of 1, 2, or 5 mg/kg; the concentration of BMEDA in the beagles’ plasma was then analyzed and determined by liquid chromatography-mass spectrometry/mass spectrometry. Based on the pharmacokinetic parameters of BMEDA, we found that male and female animals shared similar patterns indicating that the pharmacokinetics of BMEDA is independent of gender differences. In addition, the pharmacokinetics of BMEDA was seen to be non-linear because the increase of mean AUC0–t and AUC0–∞ values tend to be greater than dose proportional while the mean Vss and CL values of BMEDA appeared to be dose dependent. The information on the pharmacokinetics of BMEDA generated from this study will serve as a basis to design appropriate pharmacology and toxicology studies for future human use.
机译:N,N-双(2-巯基乙基)-N',N'-二亚乙基二胺(BMEDA)的药代动力学,该分子可与rh 188( 188 Re)形成螯合物研究了 188 Re-BMEDA-脂质体。在这项工作中,小猎犬接受了1、2或5 mg / kg的BMEDA单次注射;然后通过液相色谱-质谱/质谱法分析和测定比格犬血浆中BMEDA的浓度。基于BMEDA的药代动力学参数,我们发现雄性和雌性动物具有相似的模式,这表明BMEDA的药代动力学与性别差异无关。此外,由于平均AUC0–t和AUC0–∞值的增加往往大于剂量比例,而BMEDA的平均Vss和CL值似乎与剂量有关,因此BMEDA的药代动力学是非线性的。这项研究产生的有关BMEDA药代动力学的信息将为设计适当的药理学和毒理学研究提供基础,以供将来人类使用。

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