TY - JOUR
T1 - Ex Vivo and In Vitro Studies on the Cytotoxicity and Immunomodulative Properties of Poly(2-isopropenyl-2-oxazoline) as a New Type of Biomedical Polymer
AU - Kroneková, Zuzana
AU - Mikulec, Marcel
AU - Petrenčíková, Nadežda
AU - Paulovičová, Ema
AU - Paulovičová, Lucia
AU - Jančinová, Viera
AU - Nosál', Radomír
AU - Reddy, Palem S.
AU - Shimoga, Ganesh D.
AU - Chorvát, Dušan
AU - Kronek, Juraj
N1 - Publisher Copyright:
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2016/8/1
Y1 - 2016/8/1
N2 - Poly(2-alkenyl-2-oxazoline)s are promising functional polymers for a variety of biomedical applications, such as drug delivery systems, peptide conjugates, or gene delivery. In this study, poly(2-isopropenyl-2-oxazoline) (PIPOx) is prepared through free-radical polymerization initiated with azobisisobutyronitrile. Reactive 2-oxazoline units in the side chain support an addition reaction with different compounds containing a carboxylic group, which facilitates the preparation of polymers labeled with two different fluorescent dyes. The cytotoxicities of 2-oxazoline monomers, PIPOx, and fluorescently labeled PIPOx are evaluated in vitro using an 3-(4,5-Dimethyldiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay and ex vivo using a cell proliferation assay with adenosine triphosphate bioluminescence. The cell uptake of labeled PIPOx is used to determine the colocalization of PIPOx with cell organelles that are part of the endocytic pathway. For the first time, it is shown that poly(2-isopropenyl-2-oxazoline) is a biocompatible material and is suitable for biomedical applications; further, its immunomodulative properties are evaluated. (Figure presented.).
AB - Poly(2-alkenyl-2-oxazoline)s are promising functional polymers for a variety of biomedical applications, such as drug delivery systems, peptide conjugates, or gene delivery. In this study, poly(2-isopropenyl-2-oxazoline) (PIPOx) is prepared through free-radical polymerization initiated with azobisisobutyronitrile. Reactive 2-oxazoline units in the side chain support an addition reaction with different compounds containing a carboxylic group, which facilitates the preparation of polymers labeled with two different fluorescent dyes. The cytotoxicities of 2-oxazoline monomers, PIPOx, and fluorescently labeled PIPOx are evaluated in vitro using an 3-(4,5-Dimethyldiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay and ex vivo using a cell proliferation assay with adenosine triphosphate bioluminescence. The cell uptake of labeled PIPOx is used to determine the colocalization of PIPOx with cell organelles that are part of the endocytic pathway. For the first time, it is shown that poly(2-isopropenyl-2-oxazoline) is a biocompatible material and is suitable for biomedical applications; further, its immunomodulative properties are evaluated. (Figure presented.).
KW - biocompatibility
KW - cell proliferation
KW - fluorescence
KW - functionalization of polymers
KW - poly(2-isopropenyl-2-oxazoline)
KW - splenocytes
UR - http://www.scopus.com/inward/record.url?scp=84982908292&partnerID=8YFLogxK
U2 - 10.1002/mabi.201600016
DO - 10.1002/mabi.201600016
M3 - Article
C2 - 27150385
AN - SCOPUS:84982908292
SN - 1616-5187
SP - 1200
EP - 1211
JO - Macromolecular Bioscience
JF - Macromolecular Bioscience
ER -