TY - JOUR
T1 - Parallel high-throughput screening of polymer vectors for nonviral gene delivery
T2 - Evaluation of structure-property relationships of transfection
AU - Rinkenauer, Alexandra C.
AU - Vollrath, Antje
AU - Schallon, Anja
AU - Tauhardt, Lutz
AU - Kempe, Kristian
AU - Schubert, Stephanie
AU - Fischer, Dagmar
AU - Schubert, Ulrich S.
PY - 2013/9/9
Y1 - 2013/9/9
N2 - In recent years, "high-throughput" (HT) has turned into a keyword in polymer research. In this study, we present a novel HT workflow for the investigation of cationic polymers for gene delivery applications. For this purpose, various poly(ethylene imine)s (PEI) were used as representative vectors and investigated via HT-assays in a 96-well plate format, starting from polyplex preparation up to the examination of the transfection process. In detail, automated polyplex preparation, complex size determination, DNA binding affinity, polyplex stability, cytotoxicity, and transfection efficiency were performed in the well plate format. With standard techniques, investigation of the biological properties of polymers is quite time-consuming, so only a limited number of materials and conditions (such as pH, buffer composition, and concentration) can be examined. The approach described here allows many different polymers and parameters to be tested for transfection properties and cytotoxicity, giving faster insights into structure-activity relationships for biological activity.
AB - In recent years, "high-throughput" (HT) has turned into a keyword in polymer research. In this study, we present a novel HT workflow for the investigation of cationic polymers for gene delivery applications. For this purpose, various poly(ethylene imine)s (PEI) were used as representative vectors and investigated via HT-assays in a 96-well plate format, starting from polyplex preparation up to the examination of the transfection process. In detail, automated polyplex preparation, complex size determination, DNA binding affinity, polyplex stability, cytotoxicity, and transfection efficiency were performed in the well plate format. With standard techniques, investigation of the biological properties of polymers is quite time-consuming, so only a limited number of materials and conditions (such as pH, buffer composition, and concentration) can be examined. The approach described here allows many different polymers and parameters to be tested for transfection properties and cytotoxicity, giving faster insights into structure-activity relationships for biological activity.
KW - combinatorial workflow
KW - heparin
KW - high-throughput screening
KW - nonviral gene delivery
KW - poly(ethylene imine)
KW - polyplex stability
KW - transfection
UR - http://www.scopus.com/inward/record.url?scp=84883810449&partnerID=8YFLogxK
U2 - 10.1021/co400025u
DO - 10.1021/co400025u
M3 - Article
C2 - 23886244
AN - SCOPUS:84883810449
SN - 2156-8952
VL - 15
SP - 475
EP - 482
JO - ACS Combinatorial Science
JF - ACS Combinatorial Science
IS - 9
ER -