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抗新冠病毒药物奈玛特韦可穿过血脑屏障,并与制剂表现出草药-药物药代动力学相互作用。

The anti-COVID-19 drug nirmatrelvir crosses the blood‒brain barrier and exhibits herb-drug pharmacokinetic interactions with formulations.

作者信息

Lee Wan-Hsin, Kung Yen-Ying, Sun Chung-Kai, Chang Chun-Hao, Peng Wen-Ya, Lin Lie-Chwen, Hsu Chung-Hua, Yang Muh-Hwa, Tsai Tung-Hu

机构信息

Institute of Traditional Medicine, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.

Center for Traditional Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.

出版信息

Heliyon. 2024 Jul 20;10(15):e34820. doi: 10.1016/j.heliyon.2024.e34820. eCollection 2024 Aug 15.

Abstract

AIM OF THE STUDY

Our hypothesis is that nirmatrelvir can penetrate the blood‒brain barrier and reach effective concentrations in the brain. Furthermore, herbal formulations can help maintain nirmatrelvir levels in the body, suggesting potential interactions between these medications.

MATERIALS AND METHODS

To investigate this hypothesis, an animal model combining multisite microdialysis, ultrahigh-performance liquid chromatography and tandem mass spectrometry (UHPLC-MS/MS) methods was developed to monitor nirmatrelvir levels in the blood and brain of rats.

RESULTS

The pharmacokinetic results showed that the area under the curve (AUC) of nirmatrelvir in the blood and brain was 798.3 ± 58.56 and 187.2 ± 23.46 min μg/mL, respectively, after the administration of nirmatrelvir alone (15 mg/kg, iv). When the formulations were administered for five consecutive days prior to drug administration, the AUC of nirmatrelvir in the blood increased.

CONCLUSIONS

These results provide constructive preclinical information that the concentrations of nirmatrelvir in the blood and brain were greater than the effective concentration (EC) for more than 6 h, and the formulations had synergistic pharmacokinetic effects by increasing the concentration of nirmatrelvir in the blood.

摘要

研究目的

我们的假设是,奈玛特韦能够穿透血脑屏障并在大脑中达到有效浓度。此外,草药配方有助于维持奈玛特韦在体内的水平,这表明这些药物之间可能存在相互作用。

材料与方法

为了验证这一假设,我们建立了一种结合多部位微透析、超高效液相色谱和串联质谱(UHPLC-MS/MS)方法的动物模型,以监测大鼠血液和大脑中的奈玛特韦水平。

结果

药代动力学结果显示,单独静脉注射奈玛特韦(15mg/kg)后,血液和大脑中奈玛特韦的曲线下面积(AUC)分别为798.3±58.56和187.2±23.46min·μg/mL。在给药前连续五天给予草药配方后,血液中奈玛特韦的AUC增加。

结论

这些结果提供了有建设性的临床前信息,即血液和大脑中奈玛特韦的浓度在6小时以上均高于有效浓度(EC),且草药配方通过提高血液中奈玛特韦的浓度产生协同药代动力学效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93c4/11336326/6e90e0d3313c/ga1.jpg

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