Initial Pharmacokinetics and Bioavailability of PSC 833, a P-Glycoprotein Antagonist

• Published in: Journal of clinical pharmacology 1997-02, Vol.37 (2), p.123-128
• Main Authors: Lush, Richard M., Meadows, Beverly, Fojo, Antonio T., Kalafsky, Gaetana, Smith, Harold T., Bates, Susan, Figg, William D.
• Format: Article
• Language: English
• Subjects: Administration, Oral; Adult; Antineoplastic agents; Antineoplastic Agents, Phytogenic - administration & dosage; Antineoplastic Combined Chemotherapy Protocols - therapeutic use; ATP Binding Cassette Transporter, Subfamily B, Member 1 - antagonists & inhibitors; Biological and medical sciences; Biological Availability; Chemotherapy; Cyclosporins - administration & dosage; Cyclosporins - pharmacokinetics; Drug Resistance, Multiple; Female; Half-Life; Humans; Infusions, Intravenous; Male; Medical sciences; Metabolic Clearance Rate; Middle Aged; Neoplasms - drug therapy; Neoplasms - metabolism; Pharmacology. Drug treatments; Vinblastine - administration & dosage
• ISSN: 0091-2700; 1552-4604
• DOI: 10.1002/j.1552-4604.1997.tb04770.x

Resistant cancer cells have been shown to overexpress a 170‐kd membrane glycoprotein called P‐glycoprotein. P‐glycoprotein, a product of the multidrug resistance 1 gene, functions as an energy‐dependent efflux pump that decreases intracellular drug concentrations. A variety of nonchemotherapeutic agents have been shown to inhibit P‐glycoprotein—dependent drug efflux including cyclosporin. PSC 833 is a nonimmunosuppressive derivative of cyclosporin D with the ability to reverse multidrug resistance because of P‐glycoprotein overexpression in vitro. As part of early clinical development of PSC 833, the authors investigated the bioavailability of an oral formulation of PCS 833. PSC 833 (3 mg/kg) was administered as a 2‐hour intravenous infusion on day 1 of the treatment cycle. Serial blood samples for the determination of PSC 833 whole blood concentrations were obtained after both the intravenous and oral doses. On day 5 of the study, patients received a single oral dose (9 mg/kg) of PSC 833. A total of 14 patients were treated. The intravenous data were best described by a two‐compartment open model. The oral data also were described using a two‐compartment model, with oral absorption incorporating a lag time to account for possible delays in absorption. There was large intra‐ and interpatient variability in the pharmacokinetics of PSC 833 in these patients. The absolute bioavailability of PSC 833 was 34% but ranged from 3% to 58% of the administered dose. The clearance (Cl) of PSC 833, in general, was consistent between the two dose forms administered. The pharmacokinetic behavior of PSC 833 appears to be similar to that of cyclosporine.