Journal of Antimicrobial Chemotherapy, Vol 41, 297-300, Copyright © 1998 by The British Society for Antimicrobial Chemotherapy
B Robibaro, H Vorbach, G Weigel, A Weihs, M Hlousek, E Presterl, A Georgopoulos, A Griesmacher and W Graninger
The use of human venous endothelial cells for testing antibiotic solutions
for intravenous compatibility provides a valuable alternative to animal
models. In order to evaluate the effect of vancomycin and teicoplanin on
the viability of human umbilical venous endothelial cells, intracellular
ATP levels were measured by a luciferin-luciferase assay. Prostacyclin
(PGI2) and thromboxane A2 (TXA2) were determined by direct
radioimmunoassay. Vancomycin at concentrations of 5 and 10 mg/mL reduced
the intracellular ATP content by 18.7% and 69.9%, respectively, within 60
min. In contrast, cellular energy charge remained significantly higher
after incubation with teicoplanin at 5 and 10 mg/mL (reduction 8.7% and
15.5%, respectively). Neither vancomycin nor teicoplanin at a concentration
of 2 mg/mL led to significant ATP decline. However, endothelial cells
incubated with vancomycin resulted in significantly lower release of PGI2
and TXA2 compared with teicoplanin. These results show that teicoplanin is
more compatible with endothelial cells than vancomycin, and that both
antibiotics are well tolerated if diluted to a final concentration of 2
mg/mL.
ORIGINAL ARTICLES
Endothelial cell compatibility of glycopeptide antibiotics for intravenous use
Department of Infectious Diseases, University Hospital of Vienna, Austria.
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