Co-delivery of d-(KLAKLAK)2 peptide and doxorubicin using a pH-sensitive nanocarrier for synergistic anticancer treatment

Abstract

Currently, one of the most important challenges in the development of nanotechnology-based anticancer treatments is the failure of nanoparticles to escape from the endo-lysosomal compartment and the resulting elimination of endocytosed nanoparticles via the exocytosis pathway without drug release. A pH-sensitive nanoparticle composed of poly(ethylene glycol)–poly(L-lysine)(-grafted 2,3 dimethyl maleic anhydride)–poly(lactic acid) triblock copolymer (PEG–PLL(-g-DMA)–PLA) with a pro-apoptotic peptide (D-(KLAKLAK)₂) and an anticancer drug doxorubicin (Dox) (DTM(Pep, Dox)) was prepared and evaluated for its antiproliferative activity against tumor cells. Due to the membrane-lytic ability of the peptide and the “proton sponge” effect of the pH-sensitive nanocarrier, DTM(Pep, Dox) accelerated the disruption of the endo-lysosomal membrane and displayed enhanced anticancer activities, arising from strong synergism, under in vitro and in vivo conditions. The prepared formulations are anticipated to be of potential use in nanotechnology-based combination therapy and it is believed that this novel formulation will have new applications in advanced tumor therapy.