Formulation of a Peptide Nucleic Acid Based Nucleic Acid Delivery Construct

被引:20
作者
Millili, Peter G. [1 ,4 ]
Yin, Daniel H. [5 ]
Fan, Hailiong [5 ]
Naik, Ulhas P. [1 ,2 ,3 ,4 ]
Sullivan, Millicent O. [1 ,4 ]
机构
[1] Univ Delaware, Dept Chem Engn, Newark, DE 19716 USA
[2] Univ Delaware, Dept Biol Sci, Newark, DE 19716 USA
[3] Univ Delaware, Dept Chem & Biochem, Newark, DE 19716 USA
[4] Univ Delaware, Delaware Biotechnol Inst, Newark, DE 19716 USA
[5] Merck Res Labs, Dept Pharmaceut Res, West Point, PA 19486 USA
关键词
POLY-L-LYSINE; HUMAN TUMOR XENOGRAFT; IN-VIVO; MOLECULAR-WEIGHT; GENE DELIVERY; VASCULAR-PERMEABILITY; CELLULAR UPTAKE; PLASMID DNA; BIOLOGICAL CHARACTERIZATION; POLYELECTROLYTE COMPLEXES;
D O I
10.1021/bc900328j
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Gene delivery biomaterials need to lie designed to efficiently achieve nuclaer delivery of plasmid DNA. Polyeations have been used to pacakge DNA and other nucleic acids within submicrometer-sized particles, offering protection from shear-induced or enzymatic degradation. However, cytotoxicity issues coupled with limited in vivo transfection efficiencies minimize the effectiveness of this approach. In an effort to improve upon existing technologies aimed at delivering nucleic acids, an alternative approach to DNA packaging was explored. Peptide nucleic acids (PNAs) were used to directly functionalize DNA with poly(ethylene glycol) (PEG) chains that provide a steric layer and inhibit multimolecualr aggregation during complexation. DNA prePEGylation by this strategy was predicted to enable the formation of more homogeneous and efficiently packaged polyplexes. In this work, DNA-PNA-peptide-PEG (DP3) conjugates were synthesized and self-assembled with 25 kDa poly(ethylenimine) (PEI). Complexes with small standard deviations and average diameters ranging 30-50 nm were created, with mininial dependence of complex size oil N/P ratio (PEI amines to DNA phosphates). Furthermore, PEI-DNA interactions were altered by the derivatization strategy resulting in tighter compaction of the PEI-DP3 complexes in comparison to PEI-DNA complexes. Transfection experiments in Chinese hamster ovary (CHO) cells revealed comparable transfection efficiencies but reduced cytotoxicities of the PEI-DP3 complexes relative to PEI-DNA complexes. The enhanced Cellular activities of the PEI-DP3 complexes were maintained following the removal of free PEI from the PFI-DP3 formulations, whereas the cellular activity of the conventional PEI-DNA formulations Was reduced by free PEI removal. These findings suggest that DNA prePEGylation by the PNA-based strategy might provide a way to circumvent cytotoxicity and formulation issues related to the use of PEI for in vivo gene delivery.
引用
收藏
页码:445 / 455
页数:11
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