Etanercept clearance during an in vitro model of continuous venovenous hemofiltration
Document Type
Article
Publication Title
Blood Purification
Abstract
Background/Aims: Etanercept is a tumor necrosis factor-α antagonist used in inflammation-mediated conditions. Continuous venovenous hemofiltration (CVVH) has also been used in patients with inflammatory conditions. This study evaluated etanercept clearance using an in vitro CVVH model. Methods: Etanercept clearance was assessed in vitro in bovine blood at 1-3 mg/l final serum concentration, and urea control at 750 mg/l. CVVH was performed using polyacrylonitrile, polysulfone, and polymethylmethacrylate filters at 3 l/h ultrafiltrate and 200 ml/min blood flow rates. Transmembrane clearance was estimated using sieving coefficient calculations, and adsorptive removal rate was approximated using a mass balance calculation. Results: Urea sieving coefficient remained constant (1.04 ± 0.01). Ultrafiltrate etanercept concentrations were undetectable (sieving coefficient < 0.02) and transmembrane and adsorptive clearances were negligible. Conclusion: Etanercept is not cleared appreciably by transmembrane or adsorptive mechanisms in CVVH using polyacrylonitrile, polysulfone, or polymethylmethacrylate hemofilters. Copyright © 2009 S. Karger AG, Basel.
First Page
348
Last Page
353
DOI
10.1159/000232936
Publication Date
12-1-2009
Recommended Citation
Fleming, Geoffrey M.; Salama, Noha N.; Eid, Saada K.; Cooke, Kenneth R.; and Mueller, Bruce A., "Etanercept clearance during an in vitro model of continuous venovenous hemofiltration" (2009). Pharmaceutical and Administrative Sciences Faculty Publications. 247.
https://doi.org/10.1159/000232936
https://collections.uhsp.edu/pharm-admin-sciences_pubs/247