Population Pharmacokinetics of Sildenafil in Dogs With Naturally Occurring Pulmonary Hypertension.

IF 1.4 4区 农林科学 Q3 PHARMACOLOGY & PHARMACY
Mariko Yata, Teresa C DeFrancesco, John D Bonagura, Mark G Papich
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引用次数: 0

Abstract

The pharmacokinetics of sildenafil are ill-defined in dogs with naturally occurring pulmonary hypertension (PH). Because the plasma concentrations of sildenafil have not been reported for dogs with this disease, this study aimed to describe the population pharmacokinetics of sildenafil in a sample of dogs with PH. Twenty client-owned dogs with spontaneous PH associated with diverse comorbidities and receiving orally administered sildenafil were enrolled in a prospective, open-label, steady-state population pharmacokinetic study. Dogs underwent a sparse-sampling blood collection protocol after the morning dose of sildenafil. Plasma sildenafil concentrations were determined using high-pressure liquid chromatography and mass spectrometry. Population pharmacokinetic analysis with nonlinear mixed effects modeling was performed, and selected covariates were evaluated in the model. Sildenafil was rapidly absorbed (absorption half-life 1.1 h) but variable (CV 94%) and reached maximal plasma concentrations at 2.51 h. The estimated elimination half-life was 2.9 h. However, substantial individual variability in pharmacokinetics of sildenafil was evident, unexplained by the covariates examined, and attributed primarily to the high variability in absorption. This finding supports the need for a large-scale study to identify the source of this variability to better guide therapy in poor responders to initial therapy with this drug.

西地那非在自然发生肺动脉高压犬体内的群体药代动力学。
西地那非在患有自然发生的肺动脉高压(PH)的狗体内的药代动力学不明确。由于西地那非的血浆浓度尚未被报道,因此本研究旨在描述西地那非在PH狗样本中的群体药代动力学。20只客户拥有的自发性PH伴有多种合并症并接受口服西地那非的狗被纳入了一项前瞻性、开放标签、稳态群体药代动力学研究。狗在早晨给药西地那非后进行了少量血样采集。采用高压液相色谱和质谱法测定血浆西地那非浓度。采用非线性混合效应模型进行群体药代动力学分析,并对模型中选定的协变量进行评价。西地那非吸收迅速(吸收半衰期1.1 h),但变化较大(CV 94%),在2.51 h时达到最大血药浓度。估计消除半衰期为2.9 h。然而,西地那非的药代动力学存在明显的个体差异,这无法通过所检查的协变量来解释,主要归因于吸收的高度变异性。这一发现支持了大规模研究的必要性,以确定这种变异的来源,以便更好地指导对该药物初始治疗反应较差的治疗。
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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来源期刊
CiteScore
3.10
自引率
15.40%
发文量
69
审稿时长
8-16 weeks
期刊介绍: The Journal of Veterinary Pharmacology and Therapeutics (JVPT) is an international journal devoted to the publication of scientific papers in the basic and clinical aspects of veterinary pharmacology and toxicology, whether the study is in vitro, in vivo, ex vivo or in silico. The Journal is a forum for recent scientific information and developments in the discipline of veterinary pharmacology, including toxicology and therapeutics. Studies that are entirely in vitro will not be considered within the scope of JVPT unless the study has direct relevance to the use of the drug (including toxicants and feed additives) in veterinary species, or that it can be clearly demonstrated that a similar outcome would be expected in vivo. These studies should consider approved or widely used veterinary drugs and/or drugs with broad applicability to veterinary species.
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