Volume 30, Issue 2 pp. 118-121

Pharmacokinetics of Liposomal Amphotericin B During Extracorporeal Albumin Dialysis

Helene Vogelsinger

Helene Vogelsinger

Clinical Pharmacokinetics Unit and

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Michael Joannidis

Michael Joannidis

Medical Intensive Care Research Unit, Laboratory of Inflammation Research;

Medical Intensive Care Unit and

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Jordan Kountchev

Jordan Kountchev

Medical Intensive Care Research Unit, Laboratory of Inflammation Research;

Medical Intensive Care Unit and

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Rosa Bellmann-Weiler

Rosa Bellmann-Weiler

Infectious Diseases Unit, Division of General Internal Medicine, Department of Internal Medicine, Innsbruck Medical School, Innsbruck, Austria

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Christian J. Wiedermann

Christian J. Wiedermann

Clinical Pharmacokinetics Unit and

Present address: Department of Internal Medicine, General Hospital of Bolzano, Bolzano, Italy.

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Romuald Bellmann

Corresponding Author

Romuald Bellmann

Clinical Pharmacokinetics Unit and

Medical Intensive Care Unit and

Dr. Romuald Bellmann, Division of General Internal Medicine, Department of Internal Medicine, Innsbruck Medical School, Anichstrasse 35, A-6020 Innsbruck, Austria. E-mail: [email protected]Search for more papers by this author
First published: 20 January 2006
Citations: 9

Abstract

Abstract: Extracorporeal blood purification techniques such as hemofiltration or albumin dialysis can exert a significant, but not easily predictable influence on plasma pharmacokinetics of antimicrobial agents. The effect of albumin dialysis on the pharmacokinetics of liposomal amphotericin B (AMB) and other lipid-formulated drugs has not been investigated so far. Therefore, plasma concentrations of liberated and liposomal AMB were measured in a patient, who obtained liposomal AMB for suspected invasive mycosis and required albumin dialysis because of cholestatic liver failure caused by graft versus host disease after bone marrow transplantation. Liberated and liposomal AMB were separated by solid phase extraction and measured by high performance liquid chromatography. No excessive AMB elimination took place during albumin dialysis. Plasma levels of liposomal AMB exceeded those of liberated AMB. Pharmacokinetic data were comparable to those obtained previously in patients on hemofiltration and in critically ill patients without extracorporeal blood purification.

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