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Review
. 2014:88:13-36.
doi: 10.1016/B978-0-12-800148-6.00002-X.

Lipid nanoparticles for gene delivery

Affiliations
Review

Lipid nanoparticles for gene delivery

Yi Zhao et al. Adv Genet. 2014.

Abstract

Nonviral vectors which offer a safer and versatile alternative to viral vectors have been developed to overcome problems caused by viral carriers. However, their transfection efficacy or level of expression is substantially lower than viral vectors. Among various nonviral gene vectors, lipid nanoparticles are an ideal platform for the incorporation of safety and efficacy into a single delivery system. In this chapter, we highlight current lipidic vectors that have been developed for gene therapy of tumors and other diseases. The pharmacokinetic, toxic behaviors and clinic trials of some successful lipids particles are also presented.

Keywords: Gene delivery; Lipid nanoparticles.

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Figures

Figure 2.1
Figure 2.1
Scheme of a lipid nanoparticle (LNP) formed by lipids (yellow), helper lipids (brown), and polyethylene glycol (PEG). Lipids condense and stabilize nucleic acids, which promote the stabilization of LNP. (See the color plate.)
Figure 2.2
Figure 2.2
A sampling of lipids as nonviral vectors for gene delivery.

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