Kinetics of the Absorption, Distribution, Metabolism, and Excretion of Lobeglitazone, a Novel Activator of Peroxisome Proliferator-Activated Receptor Gamma in Rats.

Article Details

Citation

Lee JH, Noh CK, Yim CS, Jeong YS, Ahn SH, Lee W, Kim DD, Chung SJ

Kinetics of the Absorption, Distribution, Metabolism, and Excretion of Lobeglitazone, a Novel Activator of Peroxisome Proliferator-Activated Receptor Gamma in Rats.

J Pharm Sci. 2015 Sep;104(9):3049-59. doi: 10.1002/jps.24378. Epub 2015 Feb 3.

PubMed ID
25648999 [ View in PubMed
]
Abstract

This study was performed to determine biopharmaceutical properties of lobeglitazone (LB), a novel thiazolidinedione-based activator of peroxisome proliferator-activated receptor gamma, in rats. In parallel artificial membrane permeability assay and Madin-Darby canine kidney (MDCK) cell permeability assays of LB, the activator was found to interact with multidrug-resistance protein 1 (MDR1) and OATP1B1. The concentration resulting in 50% inhibition value for LB in MDR1 expressing MDCK cells was approximately 12.5 +/- 3.61 muM. LB had adequate stability (i.e., 56% remaining at 0.5 h) in rat liver microsomes. A cytochrome P450 (CYP) inhibitory potency study indicated that LB is primarily interacted with CYP1A2, 2C9, and 2C19. In rats, LB appeared to be readily absorbed after an oral administration (an absolute bioavailability of approximately 95%). Following intravenous administration, LB exhibited linear pharmacokinetics in the dose range of 0.5-2 mg/kg. The primary distribution site was the liver but it was also distributed to heart, lungs, and fat tissue. The excretion of LB to the urine, bile, feces, and intestine was insignificant (i.e., <10% of the dose) in rats. These observations suggest that, despite the fact that it interacts with some drug transporters and metabolizing enzymes, the pharmacokinetics of LB were linear with a high oral bioavailability.

DrugBank Data that Cites this Article

Drugs
Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
LobeglitazonePeroxisome proliferator-activated receptor gammaProteinHumans
Yes
Activator
Details
Drug Enzymes
DrugEnzymeKindOrganismPharmacological ActionActions
LobeglitazoneCytochrome P450 1A2ProteinHumans
No
Inhibitor
Details
LobeglitazoneCytochrome P450 2C19ProteinHumans
No
Inhibitor
Details
LobeglitazoneCytochrome P450 2C9ProteinHumans
No
Inhibitor
Details
Drug Transporters
DrugTransporterKindOrganismPharmacological ActionActions
LobeglitazoneP-glycoprotein 1ProteinHumans
No
Not AvailableDetails
LobeglitazoneSolute carrier organic anion transporter family member 1B1ProteinHumans
No
Inhibitor
Details
LobeglitazoneSolute carrier organic anion transporter family member 3A1ProteinHumans
No
Inhibitor
Details