Easily automated radiosynthesis of [(18)F]P10A-1910 and its clinical translation to quantify phosphodiesterase 10A in human brain.

Easily automated radiosynthesis of [(18)F]P10A-1910 and its clinical translation to quantify phosphodiesterase 10A in human brain.
复制标题

[18F]P10A-1910 的轻松自动化放射合成及其临床转化以量化人脑中的磷酸二酯酶 10A

DOI:
10.3389/fbioe.2022.983488
复制
发表时间:
2022
影响因子:
5.7
通讯作者:
Wang, Lu
Wang, Lu
中科院分区:
工程技术2区
文献类型:
--
作者:
Wei, Huiyi;Wei, Junjie;Zhang, Shaojuan;Dong, Shiliang;Li, Guocong;Ran, Wenqing;Dong, Chenchen;Zhang, Weibin;Che, Chao;Luo, Wenzhao;Xu, Hao;Dong, Zhiyong;Wang, Jinghao;Wang, Lu

文献摘要

参考文献

相似文献

Our previous work showed that [18F]P10A-1910 was a potential radioligand for use in imaging phosphodiesterase 10A (PDE10A). Specifically, it had high brain penetration and specific binding that was demonstrated in both rodents and non-human primates. Here, we present the first automatic cGMP-level production of [18F]P10A-1910 and translational PET/MRI study in living human brains. Successful one-step radiolabeling of [18F]P10A-1910 on a GE TRACERlab FX2N synthesis module was realized via two different methods. First, formulated [18F]P10A-1910 was derived from heating spirocyclic iodonium ylide in a tetra-n-butyl ammonium methanesulfonate solution. At the end of synthesis, it was obtained in non-decay corrected radiochemical yields (n.d.c. RCYs) of 12.4 ± 1.3%, with molar activities (MAs) of 90.3 ± 12.6 μmol (n = 7) (Method I). The boronic pinacol ester combined with copper and oxygen also delivered the radioligand with 16.8 ± 1.0% n. d.c. RCYs and 77.3 ± 20.7 GBq/μmol (n = 7) MAs after formulation (Method II). The radiochemical purity, radionuclidic purity, solvent residue, sterility, endotoxin content and other parameters were all validated for human use. Consistent with the distribution of PDE10A in the brain, escalating uptake of [18F]P10A-1910 was observed in the order of cerebellum (reference region), substantial nigra, caudate and putamen. The non-displaceable binding potential (BP ND) was estimated by simplified reference-tissue model (SRTM); linear regressions demonstrated that BP ND was well correlated with the most widely used semiquantitative parameter SUV. The strongest correlation was observed with SUV(50–60 min) (R 2 = 0.966, p < 0.01). Collectively, these results indicated that a static scan protocol could be easily performed for PET imaging of PDE10A. Most importantly, that [18F]P10A-1910 is a promising radioligand to clinically quantify PDE10A.
DOI: 10.1016/j.biocel.2004.09.009
发表时间: 2005-05-01
影响因子: 4
作者:
Chinta, SJ;Andersen, JK
通讯作者: Andersen, JK
DOI: 10.1369/jhc.6a6930.2006
发表时间: 2006-11-01
影响因子: 3.2
作者:
Coskran, Timothy M.;Morton, Daniel;Stephenson, Diane T.
通讯作者: Stephenson, Diane T.
DOI: 10.1038/nrdp.2017.13
发表时间: 2017-03-23
影响因子: 81.5
作者:
Poewe, Werner;Seppi, Klaus;Lang, Anthony E.
通讯作者: Lang, Anthony E.
DOI: 10.1016/s0378-1119(99)00171-7
发表时间: 1999-06-24
期刊: GENE
影响因子: 3.5
作者:
Loughney, K;Snyder, PB;Florio, VA
通讯作者: Florio, VA
DOI: 10.1073/pnas.87.1.288
发表时间: 1990-01-01
影响因子: 11.1
作者:
CHARBONNEAU, H;PRUSTI, RK;BEAVO, JA
通讯作者: BEAVO, JA