TY - JOUR
T1 - Dextran-graft-linear poly(ethylene imine)s for gene delivery
T2 - Importance of the linking strategy
AU - Ochrimenko, Sofia
AU - Vollrath, Antje
AU - Tauhardt, Lutz
AU - Kempe, Kristian
AU - Schubert, Stephanie
AU - Schubert, Ulrich S.
AU - Fischer, Dagmar
PY - 2014/11/26
Y1 - 2014/11/26
N2 - Low molar mass linear poly(ethylene imine)s (lPEI) were grafted onto dextran via different synthesis routes aiming at the elucidation of structure-property relationships of dextran-graft-linear poly(ethylene imine) (dex-g-lPEI) conjugates for gene delivery applications. Beside the molar mass of well-defined lPEIs and the linker unit, also the amount of lPEI in the polymeric vectors was varied. The synthesized dextran modifications were characterized regarding their chemical structure and showed enhanced complexation and stabilization of DNA against enzymatic degradation. The transfection efficiency of dex-g-lPEIs was increased compared to unmodified lPEI and revealed a dependency of the used linking strategy. All complexes of DNA and dex-g-lPEIs were found to be nontoxic, but the synthesis route showed a strong influence on the aggregation of red blood cells. In conclusion, the linking strategy of lPEI to dextran has a significant impact on the physicochemical characteristics of DNA/polymer complexes, the biocompatibility as well as the transfection efficiency.
AB - Low molar mass linear poly(ethylene imine)s (lPEI) were grafted onto dextran via different synthesis routes aiming at the elucidation of structure-property relationships of dextran-graft-linear poly(ethylene imine) (dex-g-lPEI) conjugates for gene delivery applications. Beside the molar mass of well-defined lPEIs and the linker unit, also the amount of lPEI in the polymeric vectors was varied. The synthesized dextran modifications were characterized regarding their chemical structure and showed enhanced complexation and stabilization of DNA against enzymatic degradation. The transfection efficiency of dex-g-lPEIs was increased compared to unmodified lPEI and revealed a dependency of the used linking strategy. All complexes of DNA and dex-g-lPEIs were found to be nontoxic, but the synthesis route showed a strong influence on the aggregation of red blood cells. In conclusion, the linking strategy of lPEI to dextran has a significant impact on the physicochemical characteristics of DNA/polymer complexes, the biocompatibility as well as the transfection efficiency.
KW - Biocompatibility
KW - Cationized dextran
KW - Gene delivery
KW - Poly(ethylene imine)
KW - Structure-property relationship
UR - http://www.scopus.com/inward/record.url?scp=84907333541&partnerID=8YFLogxK
U2 - 10.1016/j.carbpol.2014.07.048
DO - 10.1016/j.carbpol.2014.07.048
M3 - Article
C2 - 25256523
AN - SCOPUS:84907333541
SN - 0144-8617
VL - 113
SP - 597
EP - 606
JO - Carbohydrate Polymers
JF - Carbohydrate Polymers
ER -