An HPLC-UV validated bioanalytical method for measurement of in vitro phase 1 kinetics of α-synuclein binding bifunctional compounds. (3rd August 2022)

• Record Type: Journal Article
• Authors: Aigbogun, Omozojie P.; Nwabufo, Chukwunonso K.; Owens, Madeline N.; Allen, Kevin J. H.; Lee, Jeremy S.; Phenix, Christopher P.; Krol, Ed S.
• Is Part Of: Xenobiotica. Volume 52:Number 8(2022)
• Page Start: 916
• Page End: 927
• Publication Date: 2022-08-03
• Subjects: Microsomal metabolism -- method validation -- positron emission tomography -- imaging probe design -- α-synuclein -- Parkinson's disease -- enzyme kinetics; Metabolism -- Periodicals; Drugs -- Physiological effect -- Periodicals; Food additives -- Periodicals; Chemicals -- Physiological effect -- Periodicals; Biochemistry -- Periodicals; Pharmaceutical Preparations -- metabolism -- Periodicals; Metabolism -- Periodicals; 574.133
• DOI: 10.1080/00498254.2022.2140315
• Languages: English
• ISSNs: 0049-8254

Abstract

Abstract: Aggregates of the protein α-synuclein are associated with pathophysiology of Parkinson's disease and are present in Lewy Bodies found in the brains of Parkinson's patients. We previously demonstrated that bifunctional compounds composed of caffeine linked via a six carbon chain to either 1-aminoindan (C8 -6-I) or nicotine (C8 -6-N) bind α-synuclein and protect yeast cells from α-synuclein mediated toxicity. A critical step in development of positron emission tomography (PET) probes for neurodegenerative diseases is evaluation of their metabolic stability. We determined that C8 -6-I, and C8 -6-N both undergo phase 1 P450 metabolism in mouse, rat, and human liver microsomes. We utilised this metabolic information to guide the design of fluorinated analogues for use as PET probes and determined that the fluorine in 19 F-C8 -6-I and 19 F-C8 -6-N is stable to P450 enzymes. We have developed and validated an analytical HPLC-UV method following FDA and EMA guidelines to measure in vitro phase 1 kinetics of these compounds and determine their Vmax, KM and CLint, u in mouse liver microsomes. We found that C8 -6-I and 19 F-C8 -6-I have a two- to fourfold lower CLint, u than C8 -6-N, and 19 F-C8 -6-N. Our approach shows a simple, specific, and effective system to design and develop compounds as PET probes.