Radiosynthesis of novel pitavastatin derivative ([ 18 F]PTV-F1) as a tracer for hepatic OATP using a one-pot synthetic procedure

J Labelled Comp Radiopharm. 2016 Nov;59(13):565-575. doi: 10.1002/jlcr.3464. Epub 2016 Oct 2.

Abstract

Pitavastatin is an antihyperlipidemic agent, a potent inhibitor of 3-hydroxymethyl-glutaryl-CoA reductase, which is selectively taken up into the liver mainly via hepatic organic anion transporting polypeptide 1B1 (OATP1B1). OATP1B1 can accept a variety of organic anions, and previous reports indicated that it is responsible for the hepatic clearance of several clinically used anionic drugs. Therefore, the pharmacokinetics and the hepatic distribution of pitavastatin provide an insight into the function of OATP1B1 in humans. For the development of the in vivo evaluation of OATP1B1 function by positron emission tomography imaging, we designed a novel [18 F]pitavastatin derivative ([18 F]PTV-F1), in which a [18 F]fluoroethoxy group is substituted for the [18 F]fluoro group of [18 F]pitavastatin, with the aim of convenient radiolabeling protocol and high radiochemical yield. In vitro studies suggested that transport activities of PTV-F1 mediated by OATP1B1 and OATP1B3 were very similar to those of pitavastatin and PTV-F1 was metabolically stable in human liver microsomes. In the radiosynthesis of [18 F]PTV-F1 from the tosylate precursor, nucleophilic fluorination and subsequent deprotection were performed using a one-pot procedure. [18 F]PTV-F1 was obtained with a radiochemical yield of 45% ± 3% (n = 3), and the operating time for the radiosynthesis of [18 F]PTV-F1 is very short (30 minutes) compared with [18 F]pitavastatin.

Keywords: fluorine-18; one-pot radiosynthesis; pitavastatin derivatives; positron emission tomography.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Transport
  • Chemistry Techniques, Synthetic / methods*
  • Fluorine Radioisotopes / chemistry*
  • Liver / metabolism*
  • Organic Anion Transporters / metabolism*
  • Quinolines / chemical synthesis*
  • Quinolines / chemistry
  • Quinolines / metabolism*
  • Radiochemistry / methods*

Substances

  • Fluorine Radioisotopes
  • Organic Anion Transporters
  • Quinolines
  • pitavastatin