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用于细菌感染成像的镓标记去铁胺衍生物:功能化铁载体复合物的制备与筛选

Ga-labeled deferoxamine derivatives for imaging bacterial infection: Preparation and screening of functionalized siderophore complexes.

作者信息

Ioppolo Joseph A, Caldwell Deanna, Beiraghi Omid, Llano Lisset, Blacker Megan, Valliant John F, Berti Paul J

机构信息

Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4M1, Canada.

Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4M1, Canada.

出版信息

Nucl Med Biol. 2017 Sep;52:32-41. doi: 10.1016/j.nucmedbio.2017.05.010. Epub 2017 Jun 1.

Abstract

INTRODUCTION

Deferoxamine (DFO) is a siderophore that bacteria use to scavenge iron and could serve as a targeting vector to image bacterial infection where current techniques have critical limitations. [Ga]-DFO, which is a mimetic of the corresponding iron complex, is taken up by bacteria in culture, however in vivo it clears too rapidly to allow for imaging of infection. In response, we developed several new DFO derivatives to identify those that accumulate in bacteria, and at sites of infection, and that could potentially have improved pharmacokinetics.

METHODS

A library of DFO derivatives was synthesized by functionalizing the terminal amine group of DFO using three different carbamate-forming reactions. Uptake of [Ga]-DFO and the Ga-labeled derivatives by bacteria and the biodistribution of lead compounds were studied.

RESULTS

Ga-labeled DFO derivatives were prepared and isolated in >90% radiochemical yield and >95% radiochemical purity. The derivatives had significant but slower uptake rates in Staphylococcus aureus than [Ga]-DFO (6% to 60% of the control rate), with no uptake for the most lipophilic derivatives. Biodistribution studies in mice with a S. aureus infection in one thigh revealed that the ethyl carbamate derivative had an excellent infected-to-non-infected ratio (11:1), but high non-specific localization in the gall bladder, liver and small intestine.

CONCLUSIONS

The work reported shows that it is possible to functionalize DFO-type siderophores and retain active uptake of the Ga-labeled complexes by bacteria. Novel Ga-labeled DFO derivatives were specifically taken up by S. aureus and selected derivatives demonstrated in vivo localization at sites of infection. ADVANCES IN KNOWLEDGE AND IMPLICATIONS FOR PATIENT CARE: Ga-labeled DFO derivatives were actively transported by bacteria using the iron-siderophore pathway, suggesting that it is possible to develop siderophore-based radiopharmaceuticals for imaging bacterial infection.

摘要

引言

去铁胺(DFO)是一种铁载体,细菌利用它来获取铁,并且在当前技术存在关键局限性的情况下,它可以作为一种靶向载体用于细菌感染成像。[镓]-DFO是相应铁络合物的模拟物,可被培养中的细菌摄取,然而在体内它清除过快,无法对感染进行成像。作为回应,我们开发了几种新的DFO衍生物,以确定那些在细菌以及感染部位积累且可能具有改善药代动力学的衍生物。

方法

通过使用三种不同的形成氨基甲酸酯的反应对DFO的末端胺基进行功能化,合成了一个DFO衍生物库。研究了[镓]-DFO和镓标记的衍生物被细菌摄取的情况以及先导化合物的生物分布。

结果

制备并分离出了镓标记的DFO衍生物,其放射化学产率>90%,放射化学纯度>95%。这些衍生物在金黄色葡萄球菌中的摄取率显著但比[镓]-DFO慢(为对照率的6%至60%),最具亲脂性的衍生物没有摄取。在一只大腿患有金黄色葡萄球菌感染的小鼠身上进行的生物分布研究表明,氨基甲酸乙酯衍生物具有出色的感染与未感染比率(11:1),但在胆囊、肝脏和小肠中有较高的非特异性定位。

结论

所报道的工作表明,对DFO型铁载体进行功能化并保留细菌对镓标记络合物的主动摄取是可能的。新型镓标记的DFO衍生物被金黄色葡萄球菌特异性摄取,并且选定的衍生物在体内感染部位有定位显示。知识进展及对患者护理的意义:镓标记的DFO衍生物通过铁载体途径被细菌主动转运,这表明有可能开发基于铁载体的放射性药物用于细菌感染成像。

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