This study was mainly focused on the development of a dual-
ligand liposomal delivery system for targeting the delivery of
paclitaxel (PTX) to
lung cancer. The specific
ligand peptide HAIYPRH (T7) and the cationic
cell-penetrating peptide TAT were connected with
phospholipid via a
polyethylene glycol (PEG) spacer to prepare the dual-
ligand liposomes (T7/TAT-LP-PTX). Physicochemical characterizations of T7/TAT-LP-PTX, such as particle size, ΞΆ potential, morphology, encapsulation efficiency, and in vitro PTX release, were also evaluated. In the cellular uptake study, the T7/TAT-LP endocytosed by the A549 cells was 2.26-, 3.48- and 8.56-fold higher than TAT-LP, T7-LP and LP, respectively. The IC50 values of TAT-LP-PTX, T7-LP-PTX and LP-PTX were much higher than those of T7/TAT-LP-PTX, respectively. The homing specificity of T7/TAT-LP was evaluated on the
tumor spheroids, which revealed that T7/TAT-LP was more efficaciously internalized in
tumor cells than TAT-LP, T7-LP and LP, respectively. Compared to LP, TAT-LP and T7-LP, T7/TAT-LP showed the strongest cell uptake property, and the highest accumulation ability in
tumor spheroids in vitro. In the in vivo study, the T7/TAT-LP-PTX exhibited the best inhibitory effect of
tumor growth for A549-bearing mice. Collectively, these results suggested that T7/TAT-LP-PTX is a promising drug delivery system for the treatment of
lung cancer.