These results are highly significant, as they indicate for the first time that it may be possible to “tune” liposomes to change their distribution in vivo , as we have shown fairly substantial changes by just adjusting the depth and coverage of the PEG shielding and matching this to the length of PEG spacers between the component lipids and the functional groups attached to them.
← all excerpts
Incorporation of paramagnetic, fluorescent and PET/SPECT contrast agents into liposomes for multimodal imaging.
1
—
—