부산대학교 도서관

Reactive oxygen species synthesized by endothelial cells may be responsible for cell damage and altered physiologic function. After endotoxin stimulation, free radicals including H2O2 are produced. We have developed a method of intracellular drug delivery using albumin microcapsules. Catalase would be an excellent compound to alter H2O2 production. However, the large molecular size of catalase limits cellular penetration. Endothelial cells have been previously shown to readily phagocytoze albumin microcapsules. Methods: Catalase was added to an albumin solution to form a 10% solution of catalase. Microspheres from 2 to 7 μm in size were formed using a Bucchi spray dryer. Human endothelial cells were incubated with varying concentrations of microencapsulated catalase. The cells were then exposed to Escherichia coli endotoxin to determine if increased intracellular penetration of catalase would inhibit H2O2, nitrate, and cytokine synthesis. Results: There was a 7.2-fold increase in endothelial intracellular catalase after 48 h incubation. H2O2 was inhibited by 72%, nitrate 96%, TNF 90%, IL1 21%, IL6 42%. Conclusions: These results demonstrate that inhibition of H2O2 as a result of increased intracellular delivery of catalase inhibits proinflammatory cytokine synthesis after endotoxin exposure. [ABSTRACT FROM AUTHOR]