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丙吡胺对利多卡因与人血浆蛋白的置换作用。

Displacement of lidocaine from human plasma proteins by disopyramide.

作者信息

Bonde J, Jensen N M, Burgaard P, Angelo H R, Graudal N, Kampmann J P, Pedersen L E

出版信息

Pharmacol Toxicol. 1987 Feb;60(2):151-5. doi: 10.1111/j.1600-0773.1987.tb01515.x.

Abstract

Displacement from human plasma proteins of lidocaine by disopyramide was investigated in serum from nine patients receiving lidocaine treatment because of severe ventricular arrhythmias. From each patient disopyramide in concentrations of 5.9 and 14.7 mumol/l was added to three different serum concentrations of lidocaine and the displacement was examined. At a serum concentration of disopyramide of 14.7 mumol/l the percentage of unbound lidocaine increased from 30.4 +/- 0.2 to 36.3 +/- 0.2% (mean +/- S.E.M., P less than 0.001) at an average total serum concentration of lidocaine of 22.7 mumol/l. The study implies a stronger binding affinity of disopyramide than lidocaine to alpha-1-acid glycoprotein. We recommend caution when using disopyramide immediately after an infusion of lidocaine. With the dosage regimen used serum concentrations considerably above the suggested therapeutic level were achieved in the majority of patients.

摘要

在9名因严重室性心律失常接受利多卡因治疗的患者的血清中,研究了丙吡胺对利多卡因从人血浆蛋白中的置换作用。向来自每位患者的三种不同血清浓度的利多卡因中加入浓度为5.9和14.7μmol/l的丙吡胺,并检测置换情况。在丙吡胺血清浓度为14.7μmol/l时,利多卡因平均总血清浓度为22.7μmol/l,未结合的利多卡因百分比从30.4±0.2%增加到36.3±0.2%(平均值±标准误,P<0.001)。该研究表明丙吡胺对α-1-酸性糖蛋白的结合亲和力比利多卡因更强。我们建议在输注利多卡因后立即使用丙吡胺时要谨慎。在所使用的给药方案下,大多数患者的血清浓度大大高于建议的治疗水平。

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