共 50 条
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
相关论文