“…In the same paper, the half-life of radiolabeled adenosine was about 1.5 s and this fast kinetics has made stopping solution a popular choice when adenosine release needs to be instantly captured to prevent elimination. However, there are three limitations to studying kinetic changes of adenosine: (1) researchers have used variety of cocktails [3,[30][31][32] to inhibit either red blood cell uptake or deaminase degradation of adenosine so that the results are difficult to compare; (2) the ultrafast kinetic change of adenosine makes sampling and timing extremely challenging [30][31][32]; (3) the presence of a short adenosine spike after ischemia condition might not be pharmacologically meaningful. In contrast, determination of the sustained elevation or depression of adenosine basal level by sensitive LC-MS/MS methods may provide consistent results and meaningful insights regarding adenosine steady state, regulation and sustained action on heart.…”