Authors: Tolga Guler Zubeyde Akin Polat Eyup Yayci Tijen Atacag Ali Cetin
Publish Date: 2012/09/18
Volume: 287, Issue: 2, Pages: 217-222
Abstract
Cultivation of HUVEC was performed in an incubator having 5 CO2 at 37 °C and with predefined supplemented medium until cell monolayers attained confluence which occurred after 7 days The assays were performed in the exponential growth phase of the cells The cell viability was assessed using the cleavage of tetrazolium salts added to the culture medium Heparin sodium enoxaparin sodium bemiparin sodium and nadroparin calcium with concentrations of 100 10 and 1 IU/100 μL were used for the proliferation assay in which cells were incubated for 24 48 and 72 h with these drugs The experiments were conducted in four replicatesAmong the study drugs with maximal concentration used in the experiments 100 IU/100 μL heparin was found to be associated with the lowest viability score in 24 and 48 h while bemiparin showed the lowest at 72 h Bemiparin 100 IU/100 μL was significantly associated with lower viability score than that of bemiparin 10 IU/100 μL and bemiparin 1 IU/100 μL at every time interval Among gradual concentrations of enoxaparin however concentration of 1 IU/100 μL was associated with the lowest viability scores at every time point Heparin 1 IU/100 μL nadroparin 100 IU/100 μL and enoxaparin 100 IU/100 μL groups had the highest viability score after 72 h of incubationAmong low molecular weight heparins LMWHs 100 IU/100 μL concentration of bemiparin was associated with a more pronounced effect on reducing viability of HUVEC after 72 h of incubation while nadroparin 100 IU/100 μL and enoxaparin 100 IU/100 μL showed the least effects LMWHs differ both from each other and heparin with respect to their effects on cellular viability of HUVEC in dose and timedependent manner
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