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在结核病预防性治疗小鼠模型中,使用利福喷汀和利福布汀的动态口服给药来模拟长效制剂的暴露情况。

Using dynamic oral dosing of rifapentine and rifabutin to simulate exposure profiles of long-acting formulations in a mouse model of tuberculosis preventive therapy.

作者信息

Chang Yong S, Li Si-Yang, Pertinez Henry, Betoudji Fabrice, Lee Jin, Rannard Steven P, Owen Andrew, Nuermberger Eric L, Ammerman Nicole C

机构信息

Center for Tuberculosis Research, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Touro College of Osteopathic Medicine-Middletown, Middletown, New York, USA (current address).

出版信息

bioRxiv. 2023 Apr 12:2023.04.12.536604. doi: 10.1101/2023.04.12.536604.

Abstract

Administration of tuberculosis preventive therapy (TPT) to individuals with latent tuberculosis infection is an important facet of global tuberculosis control. The use of long-acting injectable (LAI) drug formulations may simplify and shorten regimens for this indication. Rifapentine and rifabutin have anti-tuberculosis activity and physiochemical properties suitable for LAI formulation, but there are limited data available for determining the target exposure profiles required for efficacy in TPT regimens. The objective of this study was to determine exposure-activity profiles of rifapentine and rifabutin to inform development of LAI formulations for TPT. We utilized a validated paucibacillary mouse model of TPT in combination with dynamic oral dosing of both drugs to simulate and understand exposure-activity relationships to inform posology for future LAI formulations. This work identified several LAI-like exposure profiles of rifapentine and rifabutin that, if achieved by LAI formulations, could be efficacious as TPT regimens and thus can serve as experimentally-determined targets for novel LAI formulations of these drugs. We present novel methodology to understand the exposure-response relationship and inform the value proposition for investment in development of LAI formulations that has utility beyond latent tuberculosis infection.

摘要

对潜伏性结核感染个体进行结核预防治疗(TPT)是全球结核病控制的一个重要方面。使用长效注射(LAI)药物制剂可能会简化并缩短针对该适应症的治疗方案。利福喷汀和利福布汀具有抗结核活性和适合制成LAI制剂的理化性质,但用于确定TPT治疗方案疗效所需的目标暴露特征的数据有限。本研究的目的是确定利福喷汀和利福布汀的暴露-活性特征,以为TPT的LAI制剂开发提供信息。我们利用经过验证的TPT少菌型小鼠模型,并结合两种药物的动态口服给药,来模拟和理解暴露-活性关系,以为未来LAI制剂的用药剂量提供依据。这项工作确定了利福喷汀和利福布汀的几种类似LAI的暴露特征,如果通过LAI制剂实现这些特征,作为TPT治疗方案可能有效,因此可作为这些药物新型LAI制剂的实验确定目标。我们提出了新颖的方法来理解暴露-反应关系,并为投资开发LAI制剂的价值主张提供信息,该方法的效用超出了潜伏性结核感染的范畴。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5897/10120629/d3624a9bc4c3/nihpp-2023.04.12.536604v1-f0001.jpg

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