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A biodegradable gene transfer vector, poly(ethylenimine)-grafted-poly[(aspartic acid)-co-lysine] has been developed by thermal polycondensation of aspartic acid and lysine, and branch poly(ethylenimine) (Mw less than 600) was grafted to the backbone. The polymer was characterized by 1H NMR. It appeared lower cytotoxity compared to poly(ethylenimine) (25KDa), which was quantified by MTT assay. Electrophoresis indicated that the polymer could retardate DNA at N/P ratio 1.2-1.8 (w/w). Transfection efficiency of the complexes was studied in NT2 cell lines. It was 1.5 fold higher than molecular weight PEI (Mw = 25KDa).
A biodegradable gene transfer vector, poly (ethylenimine) -grafted-poly [(aspartic acid) -co-lysine] has been developed by thermal polycondensation of aspartic acid and lysine, and branch poly (ethylenimine) (Mw less than 600) It was lower than cytotoxity compared to poly (ethylenimine) (25 KDa), which was quantified by MTT assay. Electrophoresis indicated that the polymer could retard DNA at N / P ratio 1.2-1.8 ( w / w). Transfection efficiency of the complexes was studied in NT2 cell lines. It was 1.5 fold higher than molecular weight PEI (Mw = 25 kDa).