[Allapinin pharmacokinetics after its single intravenous administration].

A G Khakimov, O V Semeikin, I N Merkulova, E P Frolova, A V Mazaev
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引用次数: 0

Abstract

Allapinin after i.v. bolus infusion in a dose of 30 mg is relatively quickly eliminated from blood (in patients without congestive heart failure half-elimination period is 2.4 +/- 0.5 h and clearance is 79.0 +/- 8.9 l/h) which makes a good reason for its intravenous infusion according to the scheme "load dose + drop infusion". Marked heart failure in patients with acute myocardial infarction compared to patients without heart failure results in reduced elimination rate, decreased clearance, significantly increased plasma allapinin concentration which should be taken in account when choosing the regime of drug infusion. The elimination of allapinin is mainly metabolic and not renal (only about 17% of the drug is excreted with urine).

【单次静脉给药后Allapinin药代动力学】。
Allapinin静脉滴注30mg后从血液中清除相对较快(无充血性心力衰竭患者半消除期为2.4 +/- 0.5 h,清除率为79.0 +/- 8.9 l/h),因此按“负荷剂量+滴注”方案静脉滴注Allapinin是有充分理由的。与无心衰患者相比,急性心肌梗死患者明显心衰导致清除率降低,清除率降低,血浆allapinin浓度明显升高,在选择药物输注方案时应考虑到这一点。allapinin的消除主要是代谢而不是肾脏(只有约17%的药物随尿液排出)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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