Antiinflammatory activity in mouse assessed as reduction of zymosan-induced number of neutrophils recovered from peritoneal exudates at 10 ng, iv administered 5 mins before zymosan challenge measured after 4 hrs by light microscopy/flow cytometry
Antiinflammatory activity in mouse assessed as reduction of zymosan-induced neutrophil recruitment during peritonitis at 10 ng, iv administered 5 mins before zymosan challenge measured after 4 hrs by light microscopy/flow cytometry
Pro-resolving activity in human macrophages assessed as increase of phagocytosis of fluorescence-labeled yeast cell wall particles at 100 nM to 10 pM preincubated for 15 mins measured after 60 mins
Pro-resolving activity in human macrophages assessed as increase of phagocytosis of bisbenzimide-labeled apoptotic neutrophils at 100 nM to 10 pM preincubated for 15 mins measured after 60 mins
Anti-inflammatory activity in FVB mouse with zymosan-induced sterile peritonitis assessed as reduction in PMN infiltration in peritoneal inflammatory exudates at 10 ng, ip measured at 4 hrs dosed 10 mins before zymosan challenge by light microscopy and flow cytometry
Anti-inflammatory activity in FVB mouse with zymosan-induced sterile peritonitis assessed as reduction in PGD2 in peritoneal inflammatory exudates at 10 ng, ip dosed 10 mins before zymosan challenge by LC-MS/MS based targeted lipid mediator metabololipidomics
Anti-inflammatory activity in FVB mouse with zymosan-induced sterile peritonitis assessed as reduction in PGF2alpha in peritoneal inflammatory exudates at 10 ng, ip dosed 10 mins before zymosan challenge by LC-MS/MS based targeted lipid mediator metabololipidomics
Anti-inflammatory activity in FVB mouse with zymosan-induced sterile peritonitis assessed as reduction in TXB2 in peritoneal inflammatory exudates at 10 ng, ip dosed 10 mins before zymosan challenge by LC-MS/MS based targeted lipid mediator metabololipidomics
Inhibition of LTB4-induced cell adhesion to fibronectin in human primary PMN at 0.1 to 10 nM pre-incubated for 10 mins followed by LTB4 stimulation by flow cytometry
Drug metabolism in human HepG2 cells assessed as (5Z,8R,9E,11E,13Z,15S,17Z)-8,15-Dihydroxyicosa-5,9,11,13,17-pentaenoic Acid formation at 13 uM incubated for 4 hrs by RP-HPLC/MS analysis
Drug metabolism in human HepG2 cells assessed as 3Z,6R,7E,9E,11Z,13S,15Z)-6,13-Dihydroxyoctadeca-3,7,9,11,15-pentaenoic Acid formation at 13 uM incubated for 4 hrs by RP-HPLC/MS analysis
Drug metabolism in human HepG2 cells assessed as (5Z,8R,9E,11E,13Z,15S,17Z)-8,15-Dihydroxyicosa-5,9,11,13,17-pentaenoic Acid formation at 13 uM incubated for 4 hrs by tandem mass spectrometric analysis
Drug metabolism in human HepG2 cells assessed as 3Z,6R,7E,9E,11Z,13S,15Z)-6,13-Dihydroxyoctadeca-3,7,9,11,15-pentaenoic Acid formation at 13 uM incubated for 4 hrs by tandem mass spectrometric analysis
Drug metabolism in human HepG2 cells treated with 13 uM Protectin-D1 assessed as compound formation incubated for 4 hrs by by tandem mass spectrometric analysis
Drug metabolism in human HepG2 cells assessed as (5Z,8R,9E,11E,13Z,15S,17Z)-8,15-Dihydroxyicosa-5,9,11,13,17-pentaenoic Acid formation at 13 uM after 30 mins by LC-MS/MS analysis
Drug metabolism in human HepG2 cells assessed as 3Z,6R,7E,9E,11Z,13S,15Z)-6,13-Dihydroxyoctadeca-3,7,9,11,15-pentaenoic Acid formation at 13 uM after 30 mins by LC-MS/MS analysis