Department of Bioengineering, The University of Utah, 20 S. 2030 E., Rm. 108, Salt Lake City, UT 84112, USA.
Biomaterials. 2011 May;32(15):3845-54. doi: 10.1016/j.biomaterials.2011.01.077. Epub 2011 Feb 26.
This study investigated the potential of creating a charged polymeric micelle-based nucleic acid delivery system that could easily be reconstituted by the addition of water. (PLGA(36kDa))(2)-b-bPEI(25kDa) (PLGA MW 36 kDa, bPEI M(w) 25 kDa, PLGA:bPEI block ratio = 2) was synthesized and used to prepare cationic micelles. The copolymer retained proton-buffering capability from the bPEI block within the endosomal pH range. Micelle/pDNA complexes retained their particle size (100-150 nm) and surface charge (30-40 mV) following reconstitution. It was found that adding a small amount of low molecular weight bPEI (1.8 kDa) completely shielded pDNA in the micelle/pDNA complexes and enhanced transfection efficiency 50-100 fold for both fresh and reconstituted complexes without affecting complex size. Transfection efficiency for "reconstituted" micelle/pDNA/bPEI(1.8kDa) (WR 1) complexes was 16-fold higher than its "fresh" counterpart. Although transfection levels achieved using "reconstituted" micelle/pDNA/bPEI(1.8kDa) complexes were 3.6-fold lower than control "fresh" bPEI(25kDa)/pDNA (N/P 5) complexes, transfection levels were 39-fold higher than "reconstituted" bPEI(25kDa)/pDNA (N/P 5) complexes. The micelle/pDNA/bPEI(1.8kDa) system showed very low cytotoxicity in MCF7 cells even with pDNA doses up to 20 μg, and transfection levels increased linearly with increasing pDNA dose. These results indicate that this PLGA-b-bPEI polymeric micelle-based system is well suited as a reconstitutable gene delivery system, and has high potential for use as a delivery system for gene therapy applications.
这项研究旨在开发一种带电荷的聚合物胶束核酸递送系统,该系统可通过加水轻易重构。(PLGA(36kDa))(2)-b-bPEI(25kDa)(PLGA MW 36 kDa,bPEI M(w)25 kDa,PLGA:bPEI 嵌段比=2)被合成并用于制备阳离子胶束。共聚物在内涵体 pH 范围内保留了 bPEI 嵌段的质子缓冲能力。胶束/ pDNA 复合物在重构后保持其粒径(100-150nm)和表面电荷(30-40mV)。结果发现,添加少量低分子量 bPEI(1.8kDa)可完全屏蔽胶束/ pDNA 复合物中的 pDNA,并将新鲜和重构复合物的转染效率提高 50-100 倍,而不影响复合物的大小。“重构”的胶束/ pDNA/bPEI(1.8kDa)(WR1)复合物的转染效率比其“新鲜”对应物高 16 倍。尽管使用“重构”胶束/ pDNA/bPEI(1.8kDa)复合物实现的转染水平比对照“新鲜”bPEI(25kDa)/ pDNA(N/P 5)复合物低 3.6 倍,但比“重构”bPEI(25kDa)/ pDNA(N/P 5)复合物高 39 倍。该胶束/ pDNA/bPEI(1.8kDa)系统在 MCF7 细胞中甚至在高达 20μg 的 pDNA 剂量下表现出非常低的细胞毒性,并且转染水平随 pDNA 剂量的增加呈线性增加。这些结果表明,这种基于 PLGA-b-bPEI 聚合物胶束的系统非常适合作为可重构基因递送系统,并且具有作为基因治疗应用的递送系统的高潜力。