Effects of Intraperitoneal Mitomycin C Adsorbed on Activated Carbon on Adhesion Formation and Mesothelial Cells In Vitro

Objective: To investigate the incidence of adhesions after intraperitoneal instillation of mitomycin C adsorbed on activated carbon (MMC-CH). Design: Animal and laboratory studies. Setting: University hospital, Germany. Animals: 90 Sprague-Dawley rats. Interventions: Laparotomy, small bowel anastomo...

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Veröffentlicht in:The European journal of surgery 2000, Vol.166 (7), p.572-576
Hauptverfasser: Jansen, Marc, Fass, Jürgen, Langejürgen, Elke, Forsch, Sabine, Tietze, Lothar, Schumpelick, Volker
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Sprache:eng
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Zusammenfassung:Objective: To investigate the incidence of adhesions after intraperitoneal instillation of mitomycin C adsorbed on activated carbon (MMC-CH). Design: Animal and laboratory studies. Setting: University hospital, Germany. Animals: 90 Sprague-Dawley rats. Interventions: Laparotomy, small bowel anastomosis, and intraperitoneal instillation of saline (controls, n = 27), activated carbon alone (n = 24) or MMC-CH (n = 26). Cultures of monolayers of human mesothelial cells. Main outcome measures: Measurements of adhesions by planimetry. Toxicity of mitomycin C alone and charcoal alone in mesothelial cell monolayers as reflected by cell proliferation and measurement of lactate dehydrogenase activity. Concentrations of plasminogen activator (tPA) and plasminogen activator inhibitor 1 (PAI-1) as measures of the fibrinolytic activity of mesothelial cells. Results: Both activated carbon and MMC-CH caused a significant increase of adhesion formation in rats. Activated carbon also reduced the fibrinolytic activity of mesothelial cells, and mitomycin C caused concentration-dependent cytotoxicity in vitro. Conclusions: Activated carbon combined with high concentrations of mitomycin C may cause intraperitoneal infective complications by increasing the rate of adhesion formation and reducing the fibrinolytic activity of mesothelial cells. We recommend a new absorbable carrier for intraperitoneal chemotherapy.
ISSN:1102-4151
1741-9271
DOI:10.3109/110241500750008664