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Bioanalytical method development and pharmacokinetics of MCI-92, a sigma-1 receptor ligand.

Abstract
Sigma-1 receptors are found throughout the nervous system and play a role in regulating nociception. They are highly expressed in nerve injury, making them a potential target for the treatment of neuropathic pain. Although sigma-1 receptor antagonists have been shown to have anti-nociceptive and anti-allodynic effects, improved selectivity of these ligands is needed to further investigate their potential to treat neuropathic pain. MCI-92 is a novel, selective sigma-1 receptor ligand developed to address this need. A sensitive and rapid ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method was developed and validated for the quantification of MCI-92 in mouse plasma and brain homogenate. A structural analog of the analyte, MCI-147, was used as the internal standard (IS). The chromatographic separation was achieved on an Acquity UPLC BEH C18 column using a mobile phase consisting of water acidified with 0.1 % v/v formic acid and acetonitrile with gradient elution over 3.2 min. The method was linear over a concentration range of 1-200 ng/mL. Multiple reaction monitoring in the positive ionization mode was used for the mass spectrometric quantitation using m/z transitions 369.2 > 126.0 for MCI-92 and 448.9 > 350.1 for the IS. The method was successfully applied to the analysis of plasma and brain samples obtained in the course of oral and intravenous pharmacokinetic studies in CD-1 mice. MCI-92 showed a high volume of distribution (11.3 ± 0.6 L/kg) and rapid clearance (6.1 ± 0.8 L/h/kg) from systemic circulation. The concentration of the MCI-92 was higher in the brain than in plasma throughout all terminal time points, indicating high blood-to-brain partitioning and slow brain clearance.
AuthorsRaluca Popa, Shyam H Kamble, Raju S Kanumuri, Tamara I King, Erin C Berthold, Sebastiano Intagliata, Abhisheak Sharma, Christopher R McCurdy
JournalJournal of pharmaceutical and biomedical analysis (J Pharm Biomed Anal) Vol. 191 Pg. 113610 (Nov 30 2020) ISSN: 1873-264X [Electronic] England
PMID32971495 (Publication Type: Journal Article)
CopyrightCopyright © 2020 Elsevier B.V. All rights reserved.
Chemical References
  • Ligands
  • Receptors, sigma
  • sigma-1 receptor
Topics
  • Animals
  • Chromatography, High Pressure Liquid
  • Chromatography, Liquid
  • Ligands
  • Mice
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, sigma
  • Reproducibility of Results
  • Tandem Mass Spectrometry

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