Polymeric nanoparticles for siRNA delivery: Production and applications

被引:86
|
作者
Cavallaro, Gennara [1 ]
Sardo, Carla [1 ]
Craparo, Emanuela Fabiola [1 ]
Porsio, Barbara [1 ]
Giammona, Gaetano [1 ]
机构
[1] Univ Palermo, Lab Biocompatible Polymers, Dept Sci & Tecnol Biol Chim & Farmaceut STEBICEF, Via Archirafi 32, I-90129 Palermo, Italy
关键词
siRNA delivery; Polymeric non viral vectors; Polyaspartamide; Polyethylenimine; Chitosan; Inulin; SMALL INTERFERING RNA; CHITOSAN-GRAFT-POLYETHYLENIMINE; ACCELERATED BLOOD CLEARANCE; TARGETING GENE DELIVERY; MOLECULAR-WEIGHT; IN-VITRO; POLYASPARTAMIDE COPOLYMERS; CELLULAR INTERNALIZATION; CATIONIC POLYASPARTAMIDE; COLLOIDAL STABILITY;
D O I
10.1016/j.ijpharm.2017.04.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Gene therapy through the use of siRNA and a polymeric carrier are becoming an efficient therapeutic option to conventional pharmaceutical formulations for the treatment of deadly diseases, such as cancer, pulmonary, ocular and neurodegenerative diseases. However, several considerations regarding the stability, formulation, and efficacy have to be faced up until these systems could be considered to be a marketable pharmaceutical products for to extend siRNA application to clinical practice. This review is focused on the key challenges of siRNA therapeutics, with special attention on the faced obstacles and on the formulation-related difficulties, providing a list of requirements needed for obtaining an ideal carrier for siRNA. Moreover, the current non-viral polymers investigated for the realization of efficient carriers for siRNA are described, with a special attention on synthetic polyamines such as polyethylenimine (PEI), polysaccharides such as chitosan and inulin (INU), and polyaminoacids such as alpha,beta-poly(N-2hydroxyethyl)-d,l-aspartamide (PHEA) and poly-L-lysine (PLL). (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:313 / 333
页数:21
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