DNA Amplification in Neutral Liposomes for Safe and Efficient Gene Delivery

Authors
Lee, SangminKoo, HeebeomNa, Jin HeeLee, Kyung EunJeong, Seo YoungChoi, KuiwonKim, Sun HwaKwon, Ick ChanKim, Kwangmeyung
Issue Date
2014-05
Publisher
AMER CHEMICAL SOC
Citation
ACS NANO, v.8, no.5, pp.4257 - 4267
Abstract
In general, traditional gene carriers contain strong cationic charges to efficiently load anionic genes, but this cationic character also leads to destabilization of plasma membranes and causes severe cytotoxicity. Here, we developed a PCR-based nanofactory as a safe gene delivery system. A few template plasmid DNA can be amplified by PCR inside liposomes about 200 nm in diameter, and the quantity of loaded genes highly Increased by more than 8.8-fold. The liposome membrane was composed of neutral lipids free from cationic charges. Consequently, this system is nontoxic, unlike other traditional cationic gene carriers. Intense red fluorescent protein (REP) expression in CHO-K1 cells showed that the amplified genes could be successfully transfected to cells. Animal experiments with the luciferase gene also showed in vivo gene expression by our system without toxicity. We think that this PCR-based nanofactory system can overcome the toxicity problem that is the critical limitation of current gene delivery to clinical application.
Keywords
TARGETED DELIVERY; IN-VIVO; PROTEIN; NANOPARTICLES; THERAPY; TARGETED DELIVERY; IN-VIVO; PROTEIN; NANOPARTICLES; THERAPY; polymerase chain reaction; neutral liposomes; gene delivery; nanofactory
ISSN
1936-0851
URI
https://pubs.kist.re.kr/handle/201004/126814
DOI
10.1021/nn501106a
Appears in Collections:
KIST Article > 2014
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