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enhanced programmed cell death-1 expression on macrophage membranes and coated them onto rapamycin (RAPA)-loaded PLGA core to fabricate a novel nano-platform (PD-1-MM@PLGA/RAPA) (Fig

Biodistribution of Mb@ 177 Lu/Gd-NTs at 672 h post-injection showed that, except for obvious uptake in tumors, Mb@ 177 Lu/Gd-NTs accumulated in the liver and spleen, showing the in vivo behavior characteristics of nanoparticles (Fig

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