A novel nitroreductase-enhanced MRI contrast agent and its potential application in bacterial imaging

硝基还原酶 化学 磁共振成像 背景(考古学) 荧光 体外 荧光寿命成像显微镜 烟酰胺腺嘌呤二核苷酸 生物物理学 生物化学 医学 NAD+激酶 生物 放射科 古生物学 物理 量子力学
作者
Yun Liu,Leilei Zhang,Marc Nazaré,Qingqiang Yao,Hai‐Yu Hu
出处
期刊:Acta Pharmaceutica Sinica B [Elsevier BV]
卷期号:8 (3): 401-408 被引量:35
标识
DOI:10.1016/j.apsb.2017.11.001
摘要

Nitroreductases (NTRs) are known to be able to metabolize nitro-substituted compounds in the presence of reduced nicotinamide adenine dinucleotide (NADH) as an electron donor. NTRs are present in a wide range of bacterial genera and, to a lesser extent, in eukaryotes hypoxic tumour cells and tumorous tissues, which makes it an appropriate biomarker for an imaging target to detect the hypoxic status of cancer cells and potential bacterial infections. To evaluate the specific activation level of NTR, great efforts have been devoted to the development of fluorescent probes to detect NTR activities using fluorogenic methods to probe its behaviour in a cellular context; however, NTR-responsive MRI contrast agents are still by far underexplored. In this study, para-nitrobenzyl substituted T1-weighted magnetic resonance imaging (MRI) contrast agent Gd-DOTA-PNB (probe 1) has been designed and explored for the possible detection of NTR. Our experimental results show that probe 1 could serve as an MRI-enhanced contrast agent for monitoring NTR activity. The in vitro response and mechanism of the NTR catalysed reduction of probe 1 have been investigated through LC-MS and MRI. Para-nitrobenzyl substituted probe 1 was catalytically reduced by NTR to the intermediate para-aminobenzyl substituted probe which then underwent a rearrangement elimination reaction to Gd-DOTA, generating the enhanced T1-weighted MR imaging. Further, LC-MS and MRI studies of living Escherichia coli have confirmed the NTR activity detection ability of probe 1 at a cellular level. This method may potentially be used for the diagnosis of bacterial infections.
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