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논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2015.1
- 수록면
- 55 - 69 (15page)
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Objective: A major limitation in gene delivery applications employing nanocarriers is the inflammatory response elicited when administered in vivo. The mode of complexation of the oligonucleotide with the carrier can alter its interactions with biomolecules, a fact that has not been explored for lipoplexes hitherto. Materials: Liposomes prepared by thin film hydration were used to form lipoplexes of si-RNA and DNA, which exhibited a smaller size and a shift toward negative zeta potential when compared with blank liposomes. Results: The oligonucleotides wrap over the liposome surface and the surface coverage depends on the number of base pairs. The colloidal stability, protein resistance and cell uptake of lipoplexes were found to be dependent on surface charge and PEG. The lipoplexes with si-RNA did not induce cytokine production in BALB/c mice. Conclusion: The results highlight the importance of PEGylation for achieving good protein resistance without compromising cell uptake and therapeutic efficiency.
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