Wakebayashi Daisuke, Nishiyama Nobuhiro, Itaka Keiji, Miyata Kanjiro, Yamasaki Yuichi, Harada Atsushi, Koyama Hiroyuki, Nagasaki Yukio, Kataoka Kazunori
Department of Materials Science and Engineering, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
Biomacromolecules. 2004 Nov-Dec;5(6):2128-36. doi: 10.1021/bm040009j.
An acetal-poly(ethylene glycol)-poly(2-(dimethylamino)ethyl methacrylate) (acetal-PEG-PAMA) block copolymer spontaneously associated with plasmid DNA (pDNA) to form water-soluble complexes (polyion complex micelle: PIC micelle) in aqueous solution. Physicochemical characteristics and transfection efficiency of the PIC micelles thus prepared were studied here, focusing on the residual molar mixing ratio (N/P ratio) of AMA units in acetal-PEG-PAMA to the phosphate units in pDNA. With the N/P ratio increasing to unity, acetal-PEG-PAMA cooperatively formed complex micelles with pDNA through electrostatic interaction, allowing pDNA to condense effectively. Dynamic light scattering measurements revealed that the PIC micelle at N/P > or = 3 had a constant size of approximately 90-100 nm. Eventually, acetal-PEG-PAMA/pDNA micelles underwent no precipitation even after long-term storage for more than 1 month at all N/P ratios. The PIC micelles were stable even in the presence of excess polyanions, poly(vinyl sulfate), in contrast to polyplexes based on the PAMA homopolymer, yet this stabilization effect was highly dependent on the N/P ratio to reach a plateau at N/P = 3-4. This character may be attributed to the increased hydrophobicity in the vicinity of the complexed pDNA. Furthermore, the pDNA in the micelle was adequately protected from DNase I attack. The transfection ability of the PIC micelles toward 293 cells was remarkably enhanced with an increasing N/P ratio as high as 25. The zeta-potential of the micelles with a high N/P ratio was an appreciably large positive value, suggesting a noncooperative micelle formation. This deviated micellar composition with an excess cationic nature as well as the presence of free acetal-PEG-PAMA may play a substantial role in the enhanced transfection efficiency of the PIC micelle system in the high N/P ratio (approximately 25) region.
一种缩醛 - 聚乙二醇 - 聚(甲基丙烯酸2 - (二甲氨基)乙酯)(缩醛 - PEG - PAMA)嵌段共聚物在水溶液中与质粒DNA(pDNA)自发缔合形成水溶性复合物(聚离子复合胶束:PIC胶束)。本文研究了如此制备的PIC胶束的物理化学特性和转染效率,重点关注缩醛 - PEG - PAMA中AMA单元与pDNA中磷酸单元的残余摩尔混合比(N/P比)。随着N/P比增加到1,缩醛 - PEG - PAMA通过静电相互作用与pDNA协同形成复合胶束,使pDNA有效凝聚。动态光散射测量表明,N/P≥3时的PIC胶束具有约90 - 100 nm的恒定尺寸。最终,缩醛 - PEG - PAMA/pDNA胶束在所有N/P比下即使长期储存超过1个月也不会沉淀。与基于PAMA均聚物的多聚体相比,PIC胶束即使在存在过量聚阴离子聚(乙烯基硫酸盐)的情况下也很稳定,然而这种稳定作用高度依赖于N/P比,在N/P = 3 - 4时达到平稳状态。这种特性可能归因于复合pDNA附近疏水性的增加。此外,胶束中的pDNA受到充分保护,免受DNase I攻击。随着N/P比增加高达25,PIC胶束对293细胞的转染能力显著增强。高N/P比胶束的zeta电位是相当大的正值,表明形成了非协同胶束。这种具有过量阳离子性质的偏离胶束组成以及游离缩醛 - PEG - PAMA的存在可能在高N/P比(约25)区域PIC胶束系统增强的转染效率中起重要作用。