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Br-贝达喹啉在小鼠结核病模型中的放射性合成及正电子发射断层显像(PET)生物成像

Radiosynthesis and PET Bioimaging of Br-Bedaquiline in a Murine Model of Tuberculosis.

作者信息

Ordonez Alvaro A, Carroll Laurence S, Abhishek Sudhanshu, Mota Filipa, Ruiz-Bedoya Camilo A, Klunk Mariah H, Singh Alok K, Freundlich Joel S, Mease Ronnie C, Jain Sanjay K

机构信息

Russell H. Morgan Department of Radiology and Radiological Science , Johns Hopkins University School of Medicine , Baltimore , Maryland 21287 , United States.

Department of Pharmacology, Physiology, and Neuroscience , Rutgers University-New Jersey Medical School , Newark , New Jersey 07101 , United States.

出版信息

ACS Infect Dis. 2019 Dec 13;5(12):1996-2002. doi: 10.1021/acsinfecdis.9b00207. Epub 2019 Jul 29.

Abstract

Bedaquiline is a promising drug against tuberculosis (TB), but limited data are available on its intralesional pharmacokinetics. Moreover, current techniques rely on invasive tissue resection, which is difficult in humans and generally limited even in animals. In this study, we developed a novel radiosynthesis for Br-bedaquiline and performed noninvasive, longitudinal whole-body positron emission tomography (PET) in live, -infected mice over 48 h. After the intravenous injection, Br-bedaquiline distributed to all organs and selectively localized to adipose tissue and liver, with excellent penetration into infected lung lesions (86%) and measurable penetration into the brain parenchyma (15%). Ex vivo high resolution, two-dimensional autoradiography, and same section hematoxylin/eosin and immunofluorescence provided detailed intralesional drug biodistribution. PET bioimaging and high-resolution autoradiography are novel techniques that can provide detailed, multicompartment, and intralesional pharmacokinetics of new and existing TB drugs. These technologies can significantly advance efforts to optimize drug dosing.

摘要

贝达喹啉是一种很有前景的抗结核药物,但关于其病灶内药代动力学的数据有限。此外,目前的技术依赖于侵入性组织切除,这在人体中很难实施,即使在动物中通常也受到限制。在本研究中,我们开发了一种新型的¹¹Br-贝达喹啉放射性合成方法,并在感染结核的活体小鼠身上进行了48小时的无创、纵向全身正电子发射断层扫描(PET)。静脉注射后,¹¹Br-贝达喹啉分布到所有器官,并选择性地定位于脂肪组织和肝脏,能很好地渗透到感染的肺部病变中(86%),并可测量到其渗透到脑实质中(15%)。离体高分辨率二维放射自显影以及同一切片的苏木精/伊红染色和免疫荧光提供了详细的病灶内药物生物分布情况。PET生物成像和高分辨率放射自显影是新技术,可提供新型和现有抗结核药物详细的多室及病灶内药代动力学信息。这些技术可显著推动优化给药剂量的研究工作。

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