Local Release of Fibrinolytic Agents for Adhesion Prevention

TitleLocal Release of Fibrinolytic Agents for Adhesion Prevention
Publication TypeJournal Article
Year of Publication1995
AuthorsWest, JL, Dunn, RC, Hubbell, JA
JournalJournal of Surgical Research
Volume59
Issue6
Pagination759 - 763
Date Published12/1995
ISSN00224804
Keywordsadhesion prevention; Drug delivery vehicle; hydrogels; streptokinase; tissue plasminogen activator; urokinase plasminogen activator
Abstract

Tissue plasminogen activator (tPA), urokinase plasminogen activator (uPA), and streptokinase were evaluated for their ability to reduce postsurgical adhesion formation in a rat uterine horn devascularization and serosal injury model in a blinded, randomized study. Small doses of tPA, uPA, or streptokinase were delivered over approximately a 4-day period either from a biodegradable hydrogel matrix or as four daily intraperitoneal injections. The hydrogel was formed upon the uterine horns by photopolymerization of an aqueous precursor solution containing dissolved drug. A control group that received no treatment had an average extent of adhesion formation of 72 ± 15% (mean ± SEM, percentage of the length of the uterine horns involved in adhesions). Application of this formulation of the hydrogel alone reduced the extent of adhesion formation to 22 ± 10% by functioning as a mechanical barrier. When tPA was released from the hydrogel, adhesion formation was reduced to 4 ± 3%, while when tPA was given by intraperitoneal injection, adhesion formation was only reduced to 49 ± 8%. Local delivery of urokinase reduced adhesion formation to 6 ± 6%, but intraperitoneal injection of urokinase did not reduce adhesion formation. Streptokinase did not reduce adhesion formation when administered by intraperitoneal injection and increased adhesion formation to 45 ± 9% when locally released relative to the hydrogel alone. These results suggest that both tPA and uPA may be used to prevent adhesion formation when delivered locally.

DOI10.1006/jsre.1995.1236
Short TitleJ Surg Res
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