Li Minghui, Cui Xinyu, Wei Feng, Li Chao, Han Xiaojun
State Key Laboratory of Urban Water Resource and Environment, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150001, China.
Department of Pharmaceutics, Daqing Campus of Harbin Medical University, Daqing 163319, China.
Nanomaterials (Basel). 2022 Apr 26;12(9):1464. doi: 10.3390/nano12091464.
Cell-derived drug carriers have increasingly gained the interest of the scientific community due to their ability to imitate various natural properties of their source cells. We developed theranostics nanoplatforms composed of mesoporous silica nanoparticles (MSNs), indocyanine green (ICG) molecules, microRNAs-137 (miR-137), red-blood-cell membranes (RM), and tumor-targeting cyclo Arg-Gly-Asp-d-Phe-Cys peptides (cRGD(fC)), which were abbreviated as MSNs/ICG/miR/RM/RGD particles. These particles possessed photothermal and gene therapy properties due to ICG and miR-137, respectively. The photothermal conversion efficiency was ~18.7%. Upon 808 nm light irradiation, the tumor inhibition rate reached 94.9% with dosage of 10 mg/kg. The developed nanoplatform possessed unique properties, such as exceptional biocompatibility, immune escaping, and specific recognition, which was also used for near-infrared fluorescence, photoacoustic (PA) bimodal imaging-guided tumor recognition.
细胞衍生的药物载体因其能够模仿其来源细胞的各种天然特性而越来越受到科学界的关注。我们开发了由介孔二氧化硅纳米颗粒(MSNs)、吲哚菁绿(ICG)分子、微小RNA-137(miR-137)、红细胞膜(RM)和肿瘤靶向环精氨酸-甘氨酸-天冬氨酸-苯丙氨酸-半胱氨酸肽(cRGD(fC))组成的诊疗纳米平台,简称为MSNs/ICG/miR/RM/RGD颗粒。这些颗粒分别由于ICG和miR-137而具有光热和基因治疗特性。光热转换效率约为18.7%。在808 nm光照射下,剂量为10 mg/kg时肿瘤抑制率达到94.9%。所开发的纳米平台具有独特的特性,如优异的生物相容性、免疫逃逸和特异性识别,还用于近红外荧光、光声(PA)双模态成像引导的肿瘤识别。