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  • Polymer-based nanoparticles...
    Chen, Yan; Li, NingXi; Xu, Bei; Wu, Min; Yan, XiaoYan; Zhong, LiJun; Cai, Hong; Wang, Ting; Wang, QiuJu; Long, FangYi; Jiang, Gang; Xiao, HongTao

    Biomedicine & pharmacotherapy, October 2019, 2019-Oct, 2019-10-00, 20191001, 2019-10-01, Volume: 118
    Journal Article

    A newly developed based on PEG-PLGA co-delivery nanoparticles for chemo-gene combined therapy to suppress colorectal carcinoma Display omitted •The design for a combination therapy for sorafenib and PEDF in a nano-formulation aimed to increase anti-tumor effect on CRC was the first time.•Sora@PEDF-NPs showed better inhibition effect on CRC compared with single loaded nanoparticles in vitro and in vivo.•Sora@PEDF-NPs could decrease the acute toxicity comparing with free Sora on Bal b/c mice.•The PEDF would not increase the toxicity of Sora@PEDF-NPs verified by acute toxicity analysis. Combination treatment through simultaneous delivery of anticancer drugs and gene with nano-formulation has been demonstrated to be an elegant and efficient approach for colorectal cancer therapy. Recently, sorafenib being studied in combination therapy in colorectal cancer (CRC) attracted attention of researchers. On the basis of our previous study, pigment epithelium-derived factor (PEDF) loaded nanoparticles showed good effect on CRC in vitro and in vivo. Herein, we designed a combination therapy for sorafenib (Sora), a multi-kinase inhibitor and PEDF, a powerful antiangiogenic gene, in a nano-formulation aimed to increase anti-tumor effect on CRC for the first time. Sora and PEDF were simultaneously encapsulated in PEG-PLGA based nanoparticles by a modified double-emulsion solvent evaporation method. The obtained co-encapsulated nanoparticles (Sora@PEDF-NPs) showed high entrapment efficiency of both Sora and PEDF — and exhibited a uniform spherical morphology. The release profiles of Sora and PEDF were in a sustained manner. The most effective tumor growth inhibition in the C26 cells and C26-bearing mice was observed in the Sora@PEDF-NPs in comparison with none-drug nanoparticles, free Sora, mono-drug nanoparticles (Sora-NPs and PEDF-NPs) and the mixture of Sora-NPs and equivalent PEDF-NPs (Mix-NPs). More importantly, Sora@PEDF-NPs showed lower toxicity than free Sora in mice according to the acute toxicity test. The serologic biochemical analysis and mice body weight during therapeutic period revealed that Sora@PEDF-NPs had no obvious toxicity. All the data demonstrated that the simultaneously loaded nanoparticles with multi-kinase inhibitor and anti-angiogenic gene might be one of the most potential formulations in the treatment of colorectal carcinoma in clinic and worthy of further investigation.