siRNA delivery system based on magnetic nanovectors: Characterization and stability evaluation

被引:13
作者
Abdelrahman, Mohammed [1 ,2 ]
Eyrolles, Laurence Douziech [1 ]
Alkarib, Suad Y. [3 ]
Herve-Aubert, Katel [1 ]
Ben Djemaa, Sanaa [1 ]
Marchais, Herve [1 ]
Chourpa, Igor [1 ]
David, Stephanie [1 ]
机构
[1] Univ Francois Rabelais Tours, EA Nanomedicaments & Nanosondes 6295, 31 Ave Monge, F-37200 Tours, France
[2] Univ Gezira, Dept Pharmaceut, Fac Pharm, POB 20, Wad Madani, Sudan
[3] Karary Univ, Dept Pharmaceut, Coll Pharm, Khartoum, Sudan
关键词
Small interfering RNA; Magnetic siRNA nanovectors (MSN); Superparamagnetic iron oxide nanoparticles (SPION); Capillary electrophoresis (CE); Purification; CAPILLARY-ELECTROPHORESIS; DNA FRAGMENTS; NANOPARTICLES; PURIFICATION; OLIGONUCLEOTIDES; MECHANISMS; ANTISENSE; CHITOSAN;
D O I
10.1016/j.ejps.2017.05.062
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Gene therapy and particularly small interfering RNA (siRNA) is a promising therapeutic method for treatment of various human diseases, especially cancer. However the lack of an ideal delivery system limits its clinical applications. Effective anticancer drug development represents the key for translation of research advances into medicines. Previously we reported, the optimization of magnetic siRNA nanovectors (MSN) formulation based on superparamagnetic iron oxide nanoparticles (SPION) and chitosan for systemic administration. This work aimed at using rational design to further optimize and develop MSN. Therefore, formulated MSN were first purified, then their physical and chemical properties were studied mainly through capillary electrophoresis. 95% of siRNA was found enclosed within the purified MSN (pMSN). pMSN showed colloidal stability at pH 7.4, effective protection of siRNA against ribonuclease degradation up to 24 hours and few siRNA release (less than 10%) at pH 7.4. These findings push toward further evaluation studies in vitro and/or in vivo, indicating the appropriateness of pMSN for cancer theranostics.
引用
收藏
页码:287 / 293
页数:7
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