Remaut K, Lucas B, Raemdonck K, Braeckmans K, Demeester J, De Smedt S C
Laboratory of General Biochemistry and Physical Pharmacy, Ghent University, Harelbekestraat 72, 9000 Ghent, Belgium.
Biomacromolecules. 2007 Apr;8(4):1333-40. doi: 10.1021/bm0611578. Epub 2007 Mar 15.
Among the cationic polymers, polyethyleneimine (PEI) is a promising candidate for delivery of oligodeoxynucleotides (ODNs). In this study, we wondered whether pegylation of PEI influences the complexation with ODNs. We especially aimed to investigate whether ODNs are differently protected against enzymatic degradation in PEI and polyethylene glycol-polyethyleneimine (PEG-PEI) polyplexes. Using fluorescence resonance energy transfer combined with fluorescence correlation spectroscopy, we found that PEI/ODN polyplexes remain to protect the ODNs they carry over a prolonged period of time while in PEG-PEI/ODN polyplexes the degradation of the ODNs slowly proceeds. We attribute this to the fact that PEI seems to compact the ODNs more firmly in the polyplexes' core than PEG-PEI, which apparently also results in a better protection against enzymatic degradation. These observations may also influence the efficiency of PEI-based ODN delivery in vivo, where pegylation is an attractive strategy to enhance the stability of the polyplexes in the blood stream.
在阳离子聚合物中,聚乙烯亚胺(PEI)是递送寡脱氧核苷酸(ODN)的一个有前景的候选者。在本研究中,我们想知道PEI的聚乙二醇化是否会影响其与ODN的复合。我们特别旨在研究ODN在PEI和聚乙二醇 - 聚乙烯亚胺(PEG - PEI)多聚体中对酶促降解的保护作用是否不同。结合荧光共振能量转移与荧光相关光谱法,我们发现PEI/ODN多聚体在较长时间内仍能保护其所携带的ODN,而在PEG - PEI/ODN多聚体中ODN的降解则缓慢进行。我们将此归因于这样一个事实,即PEI似乎比PEG - PEI更牢固地在多聚体核心中压缩ODN,这显然也导致了对酶促降解的更好保护。这些观察结果可能也会影响基于PEI的ODN体内递送效率,在体内聚乙二醇化是增强多聚体在血流中稳定性的一种有吸引力的策略。