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Efficient siRNA Delivery with Non-viral Polymeric Vehicles

期刊

PHARMACEUTICAL RESEARCH
卷 26, 期 3, 页码 657-666

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11095-008-9774-1

关键词

cationic polymer; gene therapy; polymeric carrier; small interfering RNA

资金

  1. Korea Healthcare technology RD Project
  2. Ministry of Health and Welfare, Republic of Korea [A080919]
  3. Nano-Biotechnology Project (Regenomics)
  4. Ministry of Science and Technology, Republic of Korea [850-20080090]
  5. National Institute of Health, USA (NIH) [CA 107070]
  6. NATIONAL CANCER INSTITUTE [R01CA107070] Funding Source: NIH RePORTER

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Sequence-specific gene silencing using small interfering RNA (siRNA) provides a potent and specific method for gene expression, thus is now being evaluated in clinical trials as a novel therapeutic strategy. As a results, there has been a significant surge of interest in the application of siRNA in therapeutics as a means of silencing the specific gene function. However, for siRNA technology to be valuable and effective, the development of efficient siRNA delivery strategy is essential for improving biological activities such as stability, cellular uptake, sequence-specificity, devoid of nonspecific knockdown and toxic side effects. Accordingly, a number of delivery systems, both viral and nonviral, have been reported and some of them successfully used for the introduction of siRNA into cells both in vitro and in vivo. Here, we discuss the current understanding of synthetic siRNA delivery mechanism and strategies of siRNA delivery by non-viral polymeric vehicles which are currently used in vitro and in vivo.

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