Preparation and evaluation in vitro of doxorubicin loaded mimetic exosomes-based delivery system

被引:2
作者
He, Suna [1 ]
Pan, Haofeng [1 ]
Qian, Xingyue [1 ]
Zhang, Junyang [2 ]
Zhang, Runfang [1 ]
机构
[1] Henan Univ Sci & Technol, Coll Basic Med & Forens Med, Dept Pharm, Luoyang, Peoples R China
[2] Henan Univ Sci & Technol, Coll Anim Sci & Technol, Luoyang, Peoples R China
关键词
Mimetic exosomes; drug delivery system; in vitro release; cytotoxicity; CANCER; NANOVESICLES; CYTOTOXICITY; RESISTANCE; THERAPY; GROWTH; BREAST; TUMORS;
D O I
10.36721/PJPS.2023.36.3.REG.895-900.1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Exosomes are focused as natural drug delivery vehicles with the advantages of biocompatible, biodegradable and non-immunogenic. However, the low yield of exosomes is one of the challenges that constrain its application. Mimetic exosomes (m-Exo) are the novel cell-derived nano-carriers with similar properties to exosomes and the substantially greater yield is attractive. Herein, in order to evaluate the feasibility of m-Exo as drug delivery vehicles, M-Exo derived from red blood cells were prepared via ultrasonic method, characterized and loaded with doxorubicin (DOX-m-Exo). The preparation methods of DOX-m-Exo were optimized, drug loading as the evaluated index. The drug release and cytotoxicity in vitro were studied by dialysis method and MTT method, respectively. The results demonstrated that m-Exo successfully prepared showed spherical morphology and the particle size and Zeta potential were 161nm with a narrow PDI 0.238 and -25.7mV, respectively, the mixed solution of 0.085% NaCl and 0.47% glucose as the dilution medium. The drug loading of DOX-m-Exo prepared by electroporation was up to 57 mu g/ml. What's more, DOX-m-Exo displayed sustained release behavior and similar cytotoxicity against MCF-7 cells to DOX solution. In conclusion, the studies laid a certain foundation for m-Exo serving as novel and promising drug delivery vehicles.
引用
收藏
页码:895 / 900
页数:6
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