Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1424335 | Journal of Controlled Release | 2012 | 9 Pages |
Effective targeting drug delivery for cancer therapy still remains a formidable challenge due to the complication and heterogeneity of malignant tumors. Herein, a multifunctional targeting strategy was proposed, in which a novel pH-sensitive polymethacrylates (PMA)-grafted poly(amidoamine) (PAMAM) nano delivery system was designed to be responsive to the acidic tumor microenvironment, and thereby trigger drug release in the intra-tumoral space. In addition, folate-PEGylation was applied to modify the surface of PMA-PAMAM nanoparticles in order to enhance tumor selectivity via both active and passive targeting mechanisms: folate receptor targeting, long circulation and EPR effect. The utility and efficacy of such system was demonstrated both in vitro and in vivo. Tumor drug accumulation was significantly enhanced by folate-PEGylated PMA-PAMAM nanoparticles, and such observation corresponded to their strong inhibition of tumor growth in tumor-bearing mice, demonstrating the success of the multifunctional targeting delivery. This multifunctional targeting strategy provides a promising solution to improve targeting drug delivery for combating the complex cancer diseases.
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