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Poly(lactic-co-glycolic acid) (PLGA) nanoparticles are widely used in tumor targeted drug delivery system owing to its non immunogenicity and biodegradable characteristics.However, the naked PLGA nanoparticles not only have low drug loading but also can be rapidly removed from blood circulation by the immune system.Therefore, the aim of this study was to focus on the preparation of both active and passive tumor targeting lipid hybrid PLGA nanoparticles (LNPs) to enhance drug loading and drug delivery efficiency.