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舌下给药后采血部位对犬药代动力学参数的影响。

The impact of the site of blood sampling on pharmacokinetic parameters following sublingual dosing to dogs.

作者信息

Sohlberg E, Halldin M M, Annas A, Königsson K, Jansson B, Pehrson R, Borg N

机构信息

Innovative Medicines CNS&Pain, DMPK, AstraZeneca R&D, SE-151 85 Södertälje, Sweden.

出版信息

J Pharmacol Toxicol Methods. 2013 Jan-Feb;67(1):1-4. doi: 10.1016/j.vascn.2012.10.004. Epub 2012 Nov 5.

Abstract

INTRODUCTION

Drugs are most commonly administered orally, but some potential drug candidates are not suited for oral administration due to poor absorption, high first pass metabolism or gastrointestinal side effects. The interest for transmucosal dosing for systemic drug delivery is increasing, e.g. buccal, sublingual and nasal routes. The evaluation of the systemic plasma concentration and the derivation of the pharmacokinetic parameters of candidate compounds in preclinical studies are essential for drug development. The effect of site of blood sampling on the measured drug concentration, in both animals and humans, is to some extent known but it is not always taken into consideration in the design of pharmacological and toxicological studies.

METHODS

Blood samples were collected both from leg and jugular veins from beagle dogs following a single sublingual dosing of Compound A in order to determine the impact of different sites of blood sampling on plasma pharmacokinetics. Plasma was prepared by centrifugation and plasma concentrations of Compound A were determined by protein precipitation and liquid chromatography followed by mass spectrometric detection. The pharmacokinetic parameters were calculated by non-compartment methods.

RESULTS

Sampling from the jugular vein resulted in higher and more variable exposure during the absorption phase compared to sampling from a leg vein. The plasma exposure in the jugular vein, in terms of C(max), was 4-fold compared to that in the leg vein and an approximately 2-fold bioavailability was observed.

DISCUSSION

The aim of this investigation was to determine the impact of the different sites of blood sampling on assessing systemic plasma exposure and pharmacokinetic parameters for Compound A following sublingual dosing to dogs. The results demonstrate the significant impact that the site of blood sampling has on PK parameters, and raise concerns of using the jugular vein as a site of sampling after sublingual and other transmucosal routes of dosing in the head region.

摘要

引言

药物最常通过口服给药,但由于吸收不良、首过代谢高或胃肠道副作用,一些潜在的候选药物不适合口服给药。全身给药的经粘膜给药方式,如颊部、舌下和鼻腔给药途径,越来越受到关注。在临床前研究中评估候选化合物的全身血浆浓度和药代动力学参数的推导对于药物开发至关重要。在动物和人类中,采血部位对所测药物浓度的影响在一定程度上是已知的,但在药理和毒理学研究设计中并不总是予以考虑。

方法

对比格犬单次舌下给予化合物A后,从腿部静脉和颈静脉采集血样,以确定不同采血部位对血浆药代动力学的影响。通过离心制备血浆,采用蛋白沉淀和液相色谱-质谱检测法测定化合物A的血浆浓度。采用非房室方法计算药代动力学参数。

结果

与从腿部静脉采血相比,在吸收阶段从颈静脉采血导致更高且更具变异性的暴露量。颈静脉的血浆暴露量,以C(max)计,是腿部静脉的4倍,观察到的生物利用度约为2倍。

讨论

本研究的目的是确定不同采血部位对评估犬舌下给药后化合物A的全身血浆暴露量和药代动力学参数的影响。结果表明采血部位对药代动力学参数有显著影响,并引发了在头部区域进行舌下和其他经粘膜给药途径后将颈静脉作为采血部位的担忧。

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