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PMID: 12934165 Published · ppublish English Journal Article Review

Pharmacokinetics of peginterferons.

Seminars in liver disease ·Vol. 23 Suppl 1 ·2003-00-00 ·Pages 23-8

Zeuzem S, Welsch C, Herrmann E

Abstract

Two polyethylene glycol (PEG)-modified interferons are approved for the treatment of chronic hepatitis C. The pharmocokinetic properties of the branched 40 kDa pegylated interferon alfa-2a differ from the linear 12 kDa pegylated interferon alfa-2b. The absorption half-life of standard interferon alfa is 2.3 hours, while absorption half-lives for peginterferon alfa-2a and alfa-2b are 50 hours and 4.6 hours, respectively. The volume of distribution for peginterferon alfa-2a is considerably restricted, while the volume of distribution for peginterferon alfa-2b is only approximately 30% lower than that for conventional interferon. Because of its large size, the 40 kD peginterferon alfa-2a has a more than 100-fold reduction in renal clearance compared with conventional interferon alfa. Clearance of peginterferon alfa-2b is about one-tenth that of unmodified interferon alfa. Although data are limited, both drugs appear to show differences in the initial viral decay pattern in patients with chronic hepatitis C. However, it remains unknown whether these differences in the initial viral decline predict differences in the primary clinical endpoint, sustained virological response.

MeSH Terms
Antiviral Agents/administration & dosage,pharmacokinetics Dose-Response Relationship, Drug Drug Carriers Drug Therapy, Combination Hepatitis C, Chronic/drug therapy Humans Interferon alpha-2 Interferon-alpha/administration & dosage,pharmacokinetics Polyethylene Glycols/administration & dosage,pharmacokinetics Recombinant Proteins Ribavirin/administration & dosage Serum Albumin/administration & dosage,pharmacokinetics Serum Albumin, Human
Chemicals
Antiviral Agents Drug Carriers Interferon alpha-2 Interferon-alpha Recombinant Proteins Serum Albumin albuferon Polyethylene Glycols Ribavirin peginterferon alfa-2b peginterferon alfa-2a Serum Albumin, Human
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Zeuzem Stefan
Department of Medicine, Division of Gastroenterology, Hepatology, and Endocrinology, Saarland University Hospital, Homburg/Saar, Germany. Zeuzem@uniklinik-saarland.de
Welsch Christoph
Herrmann Eva
Article Info
Journal
Seminars in liver disease
Abbr.
Semin Liver Dis
ISSN
0272-8087
Published
2003-00-00
Pages
23-8
Language
English
Region
United States
NLM ID
8110297
Subset
IM
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