Quantification of 11C-laniquidar kinetics in the brain

FE Froklage, R Boellaard, E Bakker… - Journal of Nuclear …, 2015 - Soc Nuclear Med
Overexpression of the multidrug efflux transport P-glycoprotein may play an important role in
pharmacoresistance. 11C-laniquidar is a newly developed tracer of P-glycoprotein …

Radiation dose of the P-glycoprotein tracer 11C-laniquidar

A Postnov, FE Froklage, A van Lingen… - Journal of Nuclear …, 2013 - Soc Nuclear Med
Resistance to current drug therapy is an important issue in the treatment of epilepsy.
Inadequate access of central nervous system drugs to their targets in the brain may be …

Tariquidar-induced P-glycoprotein inhibition at the rat blood–brain barrier studied with (R)-11C-verapamil and PET

JP Bankstahl, C Kuntner, A Abrahim… - Journal of Nuclear …, 2008 - Soc Nuclear Med
The multidrug efflux transporter P-glycoprotein (P-gp) is expressed in high concentrations at
the blood–brain barrier (BBB) and is believed to be implicated in resistance to central …

The influence of mass of [11C]-laniquidar and [11C]-N-desmethyl-loperamide on P-glycoprotein blockage at the blood–brain barrier

L Moerman, C Dumolyn, P Boon, F De Vos - Nuclear medicine and biology, 2012 - Elsevier
INTRODUCTION: An earlier report suggested that mass amount of PET tracers could be an
important factor in brain uptake mediated by P-glycoprotein. Thereby, this study investigated …

P-glycoprotein function at the blood–brain barrier in humans can be quantified with the substrate radiotracer 11C-N-desmethyl-loperamide

WC Kreisl, JS Liow, N Kimura, N Seneca… - Journal of Nuclear …, 2010 - Soc Nuclear Med
Permeability-glycoprotein (P-gp), an efflux transporter in several organs, acts at the blood–
brain barrier to protect the brain from exogenous toxins. P-gp almost completely blocks brain …

Synthesis and evaluation of [11C]XR9576 to assess the function of drug efflux transporters using PET

K Kawamura, F Konno, J Yui, T Yamasaki… - Annals of nuclear …, 2010 - Springer
Objective XR9576 (tariquidar) is an anthranilic acid derivative and potent P-glycoprotein (P-
gp) inhibitor. XR9576 has undergone phase I and II studies as combined chemotherapy …

[HTML][HTML] [11C] glyburide PET imaging for quantitative determination of the importance of Organic Anion-Transporting Polypeptide transporter function in the human …

S Marie, L Breuil, Z Chalampalakis… - Biomedicine & …, 2022 - Elsevier
Abstract Organic Anion-Transporting Polypeptides (OATPs) are known to control the liver
uptake of many drugs. Non-hepatic expression of OATPs has been reported although …

Evaluation of [11C] laniquidar as a tracer of P-glycoprotein: radiosynthesis and biodistribution in rats

G Luurtsema, RC Schuit, RP Klok, J Verbeek… - Nuclear medicine and …, 2009 - Elsevier
At present, P-glycoprotein (P-gp) function can be studied using positron emission
tomography (PET) together with a labelled P-gp substrate such as (R)-[11C] verapamil. Such …

Interaction of 11C-tariquidar and 11C-elacridar with P-glycoprotein and breast cancer resistance protein at the human blood–brain barrier

M Bauer, R Karch, M Zeitlinger, J Stanek… - Journal of Nuclear …, 2013 - Soc Nuclear Med
The adenosine triphosphate-binding cassette transporters P-glycoprotein (Pgp) and breast
cancer resistance protein (BCRP) are 2 major gatekeepers at the blood–brain barrier (BBB) …

Increased permeability-glycoprotein inhibition at the human blood–brain barrier can be safely achieved by performing PET during peak plasma concentrations of …

WC Kreisl, R Bhatia, CL Morse, AE Woock… - Journal of Nuclear …, 2015 - Soc Nuclear Med
The permeability-glycoprotein (P-gp) efflux transporter is densely expressed at the blood–
brain barrier, and its resultant spare capacity requires substantial blockade to increase the …