Abstract
Introduction: P-glycoprotein (P-gp), an efflux transporter, is a significant barrier to drug entry into the brain and the fetus. The positron emission tomography (PET) ligand, [11C]-verapamil, has been used to measure in vivo P-gp activity at various tissue-blood barriers of humans and animals. Since verapamil is extensively metabolized in vivo, it is important to quantify the extent of verapamil metabolism in order to interpret such P-gp activity. Therefore, we developed a rapid solid-phase extraction (SPE) method to separate, and then quantify, verapamil and its radiolabeled metabolites in plasma. Methods: Using high-performance liquid chromatography (HPLC), we established that the major identifiable circulating radioactive metabolite of [11C]-verapamil in plasma of humans and the nonhuman primate, Macaca nemestrina, was [11C]-D-617/717. Using sequential and differential pH elution on C8 SPE cartridges, we developed a rapid method to separate [11C]-verapamil and [11C]-D-617/717. Recovery was measured by spiking the samples with the corresponding nonradioactive compounds and assaying these compounds by HPLC. Results: Verapamil and D-617/717 recovery with the SPE method was >85%. When the method was applied to PET studies in humans and nonhuman primates, significant plasma concentration of D-617/717 and unknown polar metabolite(s) were observed. The SPE and the HPLC methods were not significantly different in the quantification of verapamil and D-617/717. Conclusions: The SPE method simultaneously processes multiple samples in less than 5 min. Given the short half-life of [11C], this method provides a valuable tool to rapidly determine the concentration of [11C]-verapamil and its [11C]-metabolites in human and nonhuman primate plasma.
Original language | English (US) |
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Pages (from-to) | 911-917 |
Number of pages | 7 |
Journal | Nuclear Medicine and Biology |
Volume | 35 |
Issue number | 8 |
DOIs | |
State | Published - Nov 2008 |
Externally published | Yes |
Keywords
- Human
- M. nemestrina
- Macaque
- Metabolites
- P-Glycoprotein
- PET
- SPE
- [C]-Verapamil
ASJC Scopus subject areas
- Molecular Medicine
- Radiology Nuclear Medicine and imaging
- Cancer Research