| Literature DB >> 32568525 |
Raut Bholakant1, Hongliang Qian1, Junmei Zhang1, Xin Huang1, Dechun Huang1, Jan Feijen2, Yinan Zhong1, Wei Chen1.
Abstract
Small interfering RNAs (siRNAs) have recently emerged as a new class of biopharmaceuticals for the treatment of various diseases, including genetic diseases, viral infections, heritable disorders, and most prominently, cancer. However, clinical applications of siRNA-based therapeutics through intravenous administration have been limited due to their rapid degradation and renal clearance, poor cellular uptake, low cytoplasmic release by escaping endocytic uptake, and off-target effects. The success of siRNA-based therapeutics depends upon the design and creation of efficient delivery vectors that should be able to protect siRNA from in vivo degradation and specifically deliver siRNA to cytosol of target cells. Over the past decade, myriad types of carrier systems composed of cationic polymers have been designed for delivery of siRNA to tumor cells. In this review, we overview recent advances in siRNA delivery by using these promising nonviral carrier systems in diverse approaches to overcome the delivery hindrances and provide valuable understanding to direct the future design of siRNA delivery carriers.Entities:
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Year: 2020 PMID: 32568525 DOI: 10.1021/acs.biomac.0c00438
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.988