The role of unbound drug in pharmacokinetics/pharmacodynamics and in therapy.

Abstract

The evolution of research on drug protein binding is discussed with the unbound concentration (Cu) and the unbound fraction (fu) as protagonists. Particular attention is paid to the mechanisms via which alterations in binding affect the pharmacokinetics (PK) and the effect, or independently the pharmacodynamics (PD). Apart from albumin, the important alpha-acid glycoprotein (AGP), as well as specific drug classes and applications in the clinic and development (routine monitoring, cancer and HIV therapy, allometry) are addressed. The flaws with the classical method of indirectly calculating the Cu or the unbound PK/PD parameters, based on the fu in vitro, are related to the intrinsic complexity and variability in the outcomes. Increased focus is urged on directly estimating the unbound PK/PD and also on using population statistical methods.

• Authors: Rosario Calvo, John C Lukas, Monica Rodriguez, Nerea Leal, Elena Suarez
• Journal: Current pharmaceutical design (Curr Pharm Des) Vol. 12 Issue 8 Pg. 977-87 ( 2006) ISSN: 1381-6128 [Print] United Arab Emirates
• PMID: 16533165 (Publication Type: Journal Article)

Chemical References

• Anti-Retroviral Agents
• Antineoplastic Agents
• Blood Proteins
• Orosomucoid
• Serum Albumin

Topics

• Animals
• Anti-Retroviral Agents (pharmacokinetics, pharmacology, therapeutic use)
• Antineoplastic Agents (pharmacokinetics, pharmacology, therapeutic use)
• Blood Proteins (metabolism)
• Drug Monitoring (methods)
• HIV Infections (drug therapy, metabolism)
• Humans
• Models, Animal
• Models, Biological
• Neoplasms (drug therapy, metabolism)
• Orosomucoid (metabolism)
• Protein Binding
• Serum Albumin (metabolism)
• Species Specificity