A Versatile Platform Based on Black Phosphorus Nanosheets with Enhanced Stability for Cancer Synergistic Therapy.

Cancer can be effectively treated by photothermal therapy in combination with chemotherapy. Black phosphorus (BP) nanosheets (NSs) have been considered as a promising nanocarrier for synergistic chemo/photothermal therapy. However, the intrinsic instability of bare BP is a great challenge for drug delivery applications. Herein, we coated the BP NSs with polydopamine (PDA), and prepared a novel nanocapsule BP@PDA-PEG-FA that was modified with targeting polymer mercapto group-poly(ethylene glycol)-folic acid (HS-PEG-FA). The nanocapsule was loaded with doxorubicin (DOX) as a model drug for cervical cancer therapy. This BP-based drug delivery system exhibited enhanced stability, significantly high photothermal efficiency, and targeting ability for cancer cells. Furthermore, DOX was released from the DOX-loaded BP NSs in a tumor microenvironment at low pH under near-infrared (NIR) laser irradiation, demonstrating the effects of synergistic therapy. Both in vitro and in vivo experiments proved that the synergistic therapy combining chemotherapy with photothermal therapy had high biocompatibility, outstanding antitumor efficacy and potential clinical application.

A multifunctional nanoplatform for cancer chemo-photothermal synergistic therapy and overcoming multidrug resistance.

The integration of various therapy strategies into a single nanoplatform for synergistic cancer treatment has presented a great prospect. Herein, docetaxel (DTX)-loaded poly lactic-co-glycolic acid (PLGA)-coated polydopamine modified with d-α-tocopherol polyethylene glycol 1000 succinate (TPGS) was synthesized for chemo-photothermal synergistic therapy against cancer. Firstly, the DTX-loaded PLGA NPs were prepared by a facile and robust nanoprecipitation method. Then, they were coated with dopamine to achieve the photothermal effects and to be further modified with TPGS, which can inhibit the P-glycoprotein-mediated multidrug resistance (MDR). The near-infrared (NIR) laser irradiation triggered DTX release from DTX-loaded PLGA NPs@PDA-TPGS, and then the chemo-photothermal therapy effect could be enhanced. The in vitro experimental results illustrated that DTX-loaded PLGA NPs@PDA-TPGS exhibits excellent photothermal conservation properties and remarkable cell-killing efficiency. In vivo antitumor studies further confirmed that DTX-loaded PLGA NPs@PDA-TPGS could present an outstanding synergistic antitumor efficacy compared with any monotherapy. This work exhibits a novel nanoplatform, which could not only load chemotherapy drugs efficiently, but could also improve the therapeutic effect of chemotherapy drugs by overcoming MDR and light-mediated photothermal cancer therapy.