Imaging the Bacterial Cell Wall Using N-Acetyl Muramic Acid-Derived Positron Emission Tomography Radiotracers

被引:4
|
作者
Lee, Sang Hee [1 ]
Kim, Jung Min [1 ]
Lopez-Alvarez, Marina [1 ]
Wang, Chao [1 ]
Sorlin, Alexandre M. [1 ]
Bobba, Kondapa Naidu [1 ]
Pichardo-Gonzalez, Priamo A. [1 ]
Blecha, Joseph [1 ]
Seo, Youngho [1 ]
Flavell, Robert R. [1 ,2 ,3 ]
Engel, Joanne [4 ,5 ]
Ohliger, Michael A. [1 ,6 ]
Wilson, David M. [1 ]
机构
[1] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, UCSF Helen Diller Family Comprehens Canc Ctr, Dept Radiol & Biomed Imaging, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94158 USA
[4] Univ Calif San Francisco, Dept Med, San Francisco, CA 94158 USA
[5] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94158 USA
[6] Zuckerberg San Francisco Gen Hosp, Dept Radiol, San Francisco, CA 94110 USA
基金
美国国家卫生研究院;
关键词
infection imaging; peptidoglycan; N-acetyl muramic acid; positron emission tomography; fluorine-18; RADIOSYNTHESIS; EFFICIENT;
D O I
10.1021/acssensors.3c01477
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Imaging infections in patients is challenging using conventional methods, motivating the development of positron emission tomography (PET) radiotracers targeting bacteria-specific metabolic pathways. Numerous techniques have focused on the bacterial cell wall, although peptidoglycan-targeted PET tracers have been generally limited to the short-lived carbon-11 radioisotope (t(1/2) = 20.4 min). In this article, we developed and tested new tools for infection imaging using an amino sugar component of peptidoglycan, namely, derivatives of N-acetyl muramic acid (NAM) labeled with the longer-lived fluorine-18 (t(1/2) = 109.6 min) radioisotope. Muramic acid was reacted directly with 4-nitrophenyl 2-[F-18]fluoropropionate ([F-18]NFP) to afford the enantiomeric NAM derivatives (S)-[F-18]FMA and (R)-[F-18]FMA. Both diastereomers were easily isolated and showed robust accumulation by human pathogens in vitro and in vivo, including Staphylococcus aureus. These results form the basis for future clinical studies using fluorine-18-labeled NAM-derived PET radiotracers.
引用
收藏
页码:4554 / 4565
页数:12
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