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The reason for these findings would be that oral administration of apo A-I mimetics is more effective due to the intestine being the main site of action (Hogarth et al., 2003)

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To improve the selectivity, in this work, we design and synthesize a malononitrile-functionalized TPE derivative, TPE-DCV, which can undergo addition reaction with thiol group to the alkene bond, leading to the change in its fluorescence in the system (Figure 1)

S., Graciliano, N