Non-small cell lung cancer (NSCLC) is one of the frequently-occurring disease in the world, and the treatment effects are usually unsatisfactory.
Vinblastine is an anti-microtubule drug in clinic. In this study, a nanostructured
liposome was designed and prepared for treating NSCLC. In the
liposomes,
peanut agglutinin (PNA) was modified on the liposomal surface, 3-(N-(N',N'-dimethylaminoethane)carbamoyl)
cholesterol was used as cationic materials, and
vinblastine was encapsulated in the aqueous core of
liposomes, respectively. The PNA modified
vinblastine cationic
liposomes were approximately 100 nm in size with a positive potential. In vitro results showed that the targeting
liposomes could significantly enhance cellular uptake, selectively accumulate in LLT cells, and dramatically initiate apoptosis via activating
pro-apoptotic proteins and apoptotic
enzymes, thus leading to the strongest antitumor efficacy to LLT cells. In vivo results demonstrated that the targeting
liposomes could display a prolonged circulation time in the blood, accumulate more drug in
tumor location, and induce most of
tumor cells apoptosis. As a result, a robust overall antitumor efficacy in
tumor-bearing mice was observed subsequently. In conclusion, the
chemotherapy using the PNA modified
vinblastine cationic
liposomes could provide a potential strategy for treating
non-small cell lung cancer.