期刊
JOURNAL OF MATERIALS CHEMISTRY B
卷 10, 期 12, 页码 2047-2056出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1tb02522h
关键词
-
资金
- Natural Science Foundation of Jiangsu province [BK20201419]
Nano drug delivery systems using molybdenum disulfide (MoS2) nanosheets camouflaged with red blood cell membrane (RBC membrane) have been developed for tumor therapy. The MoS2-RBC nanocomposites exhibit good stability, biocompatibility, and immune evasion ability. The system shows pH-dependent drug release behavior and the combination of chemotherapy and photothermal therapy is more effective than single therapy. In vivo experiments confirm the accumulation of the carrier materials at the tumor site and the complete inhibition of tumor growth with minimal side effects.
Nano drug delivery systems are a research hotspot in the field of tumor therapy. In this work, molybdenum disulfide (MoS2) nanosheets were selected as the base material and a natural red blood cell membrane (RBC membrane) was camouflaged on the nanosheets to enhance their dispersibility and tumor targeting profile. The camouflaged molybdenum disulfide nanocomposites (MoS2-RBC) were successfully prepared by incubation. This nanomaterial has good stability and biocompatibility with a good immune evasion ability. MoS2 has a large specific surface area and unique layered structure, which provides favorable conditions for the loading of anticancer drugs. Adriamycin hydrochloride (DOX) was used as the model drug and the drug loading capacity was 98.98%. In the tumor microenvironment, the red cell membrane modified MoS2 drug delivery system (MoS2-RBC-DOX) showed obvious pH-dependent release behavior. In addition, the excellent photothermal properties of MoS2 are conducive to the release of drugs, thus improving the efficacy. According to the cell tests, MoS2-RBC had no cytotoxicity toward tumor cells, while DOX loading induced dose-dependent cytotoxicity. Furthermore, MoS2-RBC has a favorable photothermal effect, and chemotherapy combined with photothermal therapy is more effective than any single therapy. In vivo fluorescence imaging and in vivo photothermal imaging experiments confirmed the promoted accumulation of carrier materials at the tumor site after RBC membrane modification. Finally, in vivo antitumor studies showed that photothermal/chemotherapy combined with MoS2-RBC could completely inhibit tumor growth, and the body weights of mice fluctuated within the normal range without significant decrease. In summary, this MoS2-RBC drug delivery system provides a safe, rapid and effective option for future treatment of breast cancer.
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