优化小分子和生物制剂经心脏灌注用于啮齿动物脑渗透和生物分布研究

IF 1.7 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Keumhan Noh, Xingrong Liu, Cong Wei
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引用次数: 1

摘要

有效地从脑血管系统中清除血液对于准确评估候选药物的脑渗透和生物分布至关重要,特别是对于生物制剂,因为它们的血液浓度大大高于脑浓度。经心肌灌注已被广泛用于清除脑内残留血液;然而,文献中报道的灌注条件(如灌注速率和时间)各不相同,这些方法在血液去除中的性能尚未得到深入的研究。在本研究中,通过测量脑血红蛋白水平来评估灌注条件的有效性。对亚硝酸钠(NaNO2)作为灌注液添加剂在不同浓度下的性能进行了评价。在不破坏血脑屏障(BBB)完整性的情况下,2% NaNO2灌注20分钟可显著改善小鼠血液清除。在小鼠中,优化的灌注方法显著降低了单克隆抗体的测量脑血浆比(Kp,brain),这是由于去除了血液污染和具有中至高血脑屏障通透性的小分子,以及可能由于灌注过程中流出脑的通量而具有高脑不结合分数(fu,brain)。添加或不添加NaNO2均能明显去除大鼠脑内残余血,但在添加或不添加2% NaNO2的各组间,脑内Kp值无显著差异。总之,我们首次成功地建立了一种评估小分子和生物制剂在啮齿动物脑内渗透的灌注方法。经心包灌注2% NaNO2可有效清除脑内残留血液,显著提高生物制剂脑穿透性评估。然而,对于小分子,可能不进行经心肌灌注,因为小分子化合物可以通过灌注过程从大脑中冲走。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Optimizing transcardial perfusion of small molecules and biologics for brain penetration and biodistribution studies in rodents

Optimizing transcardial perfusion of small molecules and biologics for brain penetration and biodistribution studies in rodents

Efficiently removing blood from the brain vasculature is critical to evaluate accurately the brain penetration and biodistribution of drug candidates, especially for biologics as their blood concentrations are substantially higher than the brain concentrations. Transcardial perfusion has been used widely to remove residual blood in the brain; however, the perfusion conditions (such as the perfusion rate and time) reported in the literature are quite varied, and the performance of these methods on blood removal has not been investigated thoroughly. In this study, the effectiveness of the perfusion conditions was assessed by measuring brain hemoglobin levels. Sodium nitrite (NaNO2) as an additive in the perfusate was evaluated at different concentrations. Blood removal was significantly improved with 2% NaNO2 over a 20 min perfusion in mouse without disrupting the integrity of the blood-brain barrier (BBB). In mice, the optimized perfusion method significantly lowered the measured brain-to-plasma ratio (Kp,brain) for monoclonal antibodies due to the removal of blood contamination and small molecules with a moderate-to-high BBB permeability and with a high brain-unbound-fraction (fu,brain) presumably due to flux out of the brain during perfusion. Perfusion with or without NaNO2 clearly removed the residual blood in rat brain but with no difference observed in Kp,brain between the perfusion groups with or without 2% NaNO2. In conclusion, a perfusion method was successfully developed to evaluate the brain penetration of small molecules and biologics in rodents for the first time. The transcardial perfusion with 2% NaNO2 effectively removed the residual blood in the brain and significantly improved the assessment of brain penetration of biologics. For small molecules, however, transcardial perfusion may not be performed, as small molecule compounds could be washed away from the brain by the perfusion procedure.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
35
审稿时长
6-12 weeks
期刊介绍: Biopharmaceutics & Drug Dispositionpublishes original review articles, short communications, and reports in biopharmaceutics, drug disposition, pharmacokinetics and pharmacodynamics, especially those that have a direct relation to the drug discovery/development and the therapeutic use of drugs. These includes: - animal and human pharmacological studies that focus on therapeutic response. pharmacodynamics, and toxicity related to plasma and tissue concentrations of drugs and their metabolites, - in vitro and in vivo drug absorption, distribution, metabolism, transport, and excretion studies that facilitate investigations related to the use of drugs in man - studies on membrane transport and enzymes, including their regulation and the impact of pharmacogenomics on drug absorption and disposition, - simulation and modeling in drug discovery and development - theoretical treatises - includes themed issues and reviews and exclude manuscripts on - bioavailability studies reporting only on simple PK parameters such as Cmax, tmax and t1/2 without mechanistic interpretation - analytical methods
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