Abstract

Paclitaxel (PTX) loaded multilayered liposomes were prepared using layer-by-layer assembly in an effort to improve the stabilization of the liposomal compositions for PTX delivery. Stearyl amine was used to provide positive charge to the PTX-liposomes, and subsequently coated with anionic polyacrylic acid (PAA) followed by cationic chitosan. Various process variables were optimized and the optimum formulation was found to have particle size of 215±17nm, zeta potential of +27.9±3.4mV and encapsulation efficiency of 70.93±2.39%. The lyophilized chitosan–PAA–PTX–liposomes formulation was stable in simulated gastrointestinal fluids and at different environmental conditions (4°C and 25°C). In vitro drug release experiments demonstrated that chitosan–PAA–PTX-liposomes formulation exhibited obvious sustained release behaviors compared to PTX-liposomes. Furthermore, chitosan–PAA–PTX-liposomes formulation revealed enhanced PTX induced cytotoxicity in human cervical cancer cell culture experiments compared to PTX-liposomes. In conclusion, the approach presented herein will provide a promising solution for PTX delivery.

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