Chen Dan, He Bin-Bin, Zhao Dan-Jun, Jiang Qi-Ying, Wang Zhong-Ren, Zhou Jun, Yu Hai, Wang Qing-Qing, Tang Gu-Ping
Institute of Chemical Biology and Pharmaceutical Chemistry, Zhejiang University, Hangzhou 310028, China.
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2009 Jan;38(1):31-8. doi: 10.3785/j.issn.1008-9292.2009.01.005.
To develop a novel gene delivery vector with poly-aspartamide-glutamic acid and polyethylenimine as the backbone.
alpha, beta-poly-(N-2-hydroxypropyl)-D, L-aspartamide-glutamic acid (PHPAG) was synthesized and low molecular weight polyethylenimine (PEI 1.8 kDa) was grafted to form PHPAG-PEI 1800. Chemical and biological characterization of the polymer was identified.
The polymer was confirmed by (1)H-NMR, and the molecular weight was about 1.2 x 10(4). The ability of DNA binding was showed by gel retardation assay at N/P ratio of 3. 5. MTT assay showed that the polymer was non toxic in COS-7 and A293 cell lines. In vitro test demonstrated that it had high transfection efficiency in B16 and Hela cell lines.
PHPAG-PEI 1800 was successfully synthesized,which might be a potential vector for gene delivery.
以聚天冬酰胺-谷氨酸和聚乙烯亚胺为骨架开发一种新型基因递送载体。
合成α,β-聚(N-2-羟丙基)-D,L-天冬酰胺-谷氨酸(PHPAG),并接枝低分子量聚乙烯亚胺(PEI 1.8 kDa)以形成PHPAG-PEI 1800。对该聚合物进行化学和生物学表征。
通过(1)H-NMR确认该聚合物,分子量约为1.2×10(4)。凝胶阻滞试验显示在N/P比为3.5时具有DNA结合能力。MTT试验表明该聚合物在COS-7和A293细胞系中无毒。体外试验表明它在B16和Hela细胞系中具有高转染效率。
成功合成了PHPAG-PEI 1800,其可能是一种潜在的基因递送载体。