Oligoethyleneoxy-Modified 99mTc-Labeled β-Amyloid Imaging Probes with Improved Brain Pharmacokinetics for Single-Photon Emission Computed Tomography.
Xiaoyang ZhangYaqin HouCheng PengChu WangXiang WangZhigang LiangJing LuBaian ChenJiapei DaiBoli LiuMeng-Chao CuiPublished in: Journal of medicinal chemistry (2018)
An oligoethyleneoxy linker was introduced for conjugation between 99mTc/Re-bis(aminoethanethiol) (BAT) and β-amyloid (Aβ) binding scaffolds. Rhenium complexes exhibited high to moderate binding affinity to Aβ1-42 aggregates and efficient fluorescent staining to Aβ plaques in brain tissue. After radiolabeling, the 99mTc-labeled probes revealed improved brain pharmacokinetics in normal ICR mice. Probe [99mTc]15 with potent binding affinity (Ki = 13.4 nM) and the highest initial brain uptake (2.10% ID/g at 2 min) in normal ICR mice was evaluated further. In vitro autoradiography showed specific labeling of Aβ plaques by [99mTc]15 in transgenic (Tg) mouse brain tissue. Ex vivo autoradiography further demonstrated its efficient labeling of Aβ plaques in a living Tg mouse. In vivo single photon emission computed tomography (SPECT)/CT imaging in six rhesus monkeys revealed remarkably improved brain uptakes (1.94-2.63% ID within 20 min) of [99mTc]15, making it highly potential to be used in humans for Aβ plaques imaging in the brain.
Keyphrases
- computed tomography
- resting state
- white matter
- functional connectivity
- cerebral ischemia
- living cells
- magnetic resonance imaging
- positron emission tomography
- quantum dots
- multiple sclerosis
- fluorescence imaging
- metabolic syndrome
- neoadjuvant chemotherapy
- adipose tissue
- high intensity
- skeletal muscle
- mass spectrometry
- anti inflammatory
- blood brain barrier
- climate change
- transcription factor
- wild type