𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and evaluation of two fluorine-18 labelled phenylbenzothiazoles as potential in vivo tracers for amyloid plaque imaging

✍ Scribed by K. Serdons; D. Vanderghinste; M. Van Eeckhoudt; P. Borghgraef; H. Kung; F. Van Leuven; T. de Groot; G. Bormans; A. Verbruggen


Publisher
John Wiley and Sons
Year
2009
Tongue
French
Weight
368 KB
Volume
52
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Uncharged derivatives of thioflavin‐T have known in vitro and in vivo affinity for amyloid β. We synthesized and evaluated two derivatives with a fluorine‐18 labelled fluoropropoxy substituent either at the 6‐position or at the 2′‐position of the 2‐(4′‐aminophenyl)‐1,3‐benzothiazole core with the aim to get suitable radiotracers to perform amyloid plaque imaging. The fluorine‐18 labelled compounds were obtained by nucleophilic substitution of the corresponding tosyl precursors with [^18^F]fluoride with a radiochemical yield of 50%, yielding 6‐(3′′‐[^18^F]fluoropropoxy)‐2‐(4′‐aminophenyl)‐1,3‐benzothiazole ([^18^F]2) and 2‐[2′‐(3′′‐[^18^F]fluoropropoxy)‐4′‐aminophenyl]‐1,3‐benzothiazole ([^18^F]3) with a specific activity between 33 and 51 GBq/µmol. The identity of the radiolabelled compounds was confirmed using radio‐LC‐MS and by comparing retention times on RP‐HPLC. Biodistribution studies in healthy mice showed for both compounds a relatively high initial brain uptake, which was significantly higher for [^18^F]2 than for [^18^F]3 (4.5% ID/g versus 3.0% ID/g, p<0.05). Wash‐out from control brain was faster for [^18^F]3. In vitro binding affinity tests using human AD brain homogenates revealed that only compound 2 has affinity for fibrillar amyloid β (K~i~=14.5 nM). This was confirmed by the incubation of transgenic APP mouse brain sections with the cold compounds, where 3 did not stain any structure whereas 2 stained amyloid plaques present in APP mouse brain. These data suggest that [^18^F]2 may be a useful tracer for in vivo visualization of fibrillar amyloid β. Copyright © 2009 John Wiley & Sons, Ltd.


📜 SIMILAR VOLUMES


Synthesis and evaluation of two uncharge
✍ K. Serdons; D. Vanderghinste; M. Van Eeckhoudt; J. Cleynhens; T. de Groot; G. Bo 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 French ⚖ 264 KB

## Abstract Thioflavin‐T is a fluorescent dye for __in vitro__ detection of fibrillar amyloid β, a protein found in the brain of patients suffering from Alzheimer's disease. We synthesized and biologically evaluated two uncharged ^99m^Tc‐labeled derivatives of thioflavin‐T. The precursors for label

Synthesis, radiosynthesis and in vivo ev
✍ S. De Bruyne; T. L. Boos; L. wyffels; J. L. Goeman; K. C. Rice; F. De Vos 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 French ⚖ 223 KB 👁 1 views

## Abstract Dopamine transporter (DAT) neuroimaging is a useful tool in Parkinson's disease diagnosis, staging and follow‐up providing information on the integrity of the dopaminergic neurotransmitter system __in vivo__. 4‐(2‐(Bis(4‐fluorophenyl)methoxy)ethyl)‐1‐(4‐iodobenzyl)piperidine (7) has nan

Synthesis and in vivo evaluation in mice
✍ P. Blanckaert; I. Burvenich; F. Devos; G. Slegers 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 French ⚖ 119 KB 👁 1 views

## Abstract This work reports the synthesis, radiolabelling and __in vivo__ evaluation in NMRI mice of [^123^I]‐(4‐fluorophenyl)[1‐(3‐iodophenethyl)piperidin‐4‐yl]methanone ([^123^I]‐3‐I‐CO) as a potential SPECT tracer for the 5‐HT~2A~ receptor. The tributylstannylprecursor was synthesized with a 1