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This propensity of infected erythrocytes to expose PS could be used to target antimalarials specifically to infected cells using peptides that accumulate predominantly in PS-exposing cells (Lawrence et al., 2018) or with liposomes conjugated to PS binding peptides (Tagami et al., 2015)

Tesamorelin's longer half-life and ipamorelin's roughly two-hour window are reflected in how those compounds were scheduled in research, whereas sermorelin's very short half-life shaped its own study designs