Encapsulating anticancer drugs in
liposomes improves their therapeutic window by enhancing antitumor efficacy and reducing side effects. To devise more effective liposomal formulations for antitumor
therapy, many research groups have tried to develop
tumor-targeting
liposomes with enhanced drug release. Previously, we developed
doxorubicin (Dox)-encapsulated AG73
peptide-modified
liposomes (AG73-Dox), which targeted
cancer and endothelial cells, and ultrasound (US) imaging gas-entrapping
liposomes, called "Bubble
liposomes" (BLs). In this study, to enhance the antitumor effect of AG73-Dox, we combined AG73-Dox with BLs and US. First, to determine whether the addition of BLs and application of US could enhance the cytotoxicity of AG73-Dox, we evaluated the cytotoxicity of the combination of AG73-Dox with BLs and US. BLs and US enhanced cytotoxicity of AG73-Dox more than they enhanced nontargeted Dox-encapsulated
liposomes. Next, we examined the intracellular behavior of Dox
after treatment with BLs and US. The combination of AG73-Dox with BLs and US did not enhance cellular uptake of Dox, but it did promote drug release in the cytoplasm. To further elucidate the release of Dox in the cytoplasm, we blocked cellular uptake via endosomes at a low temperature. As a result, BLs and US did not have an enhanced drug-release effect until AG73-Dox was taken up into cells. Thus, the combination of AG73-Dox with BLs and US may be useful for
cancer therapy as a dual-function drug delivery system with targeted and controlled release.