In vitro bio-immunological and cytotoxicity studies of poly(2-oxazolines).

J Mater Sci Mater Med

Polymer Institute, Slovak Academy of Sciences, Centre of Excellence GLYCOMED, Dúbravská cesta 9, 84541 Bratislava, Slovakia.

Published: July 2011

AI Article Synopsis

  • Poly(2-oxazolines) with different alkyl chain lengths were evaluated for their cell cytotoxicity using the MTT assay, showing that certain monomers like 2-methyl-2-oxazoline and 2-ethyl-2-oxazoline yield non-toxic polymers.
  • The study found that higher molar masses of poly(2-ethyl-2-oxazoline) (PETOX) correlate with increased cell viability, up to a molar mass of 15,000 g/mol, with aromatic and aliphatic variants demonstrating similar low cytotoxicity, making them promising for biomedical uses.
  • Fluorescence techniques revealed that polymer accumulation in cells depended on concentration, while immunological tests showed that the

Article Abstract

Poly(2-oxazolines) with varying alkyl chain lengths (e.g., methyl, ethyl, aryl) and molar masses have been tested for cell cytotoxicity in vitro. A standard 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was used for the estimation of cell viability. Two monomers, 2-methyl-2-oxazoline and 2-ethyl-2-oxazoline, were found to provide polymers with non-cytotoxic properties. The dependence of cell viability on molar mass confirmed the expected trend; the viability increased with the higher molar mass of poly(2-ethyl-2-oxazoline) (PETOX), up to 15,000 g/mol. The results obtained for the polymers with aliphatic side chains were compared with the analogues that possessed an aromatic moiety. All results confirmed low cytotoxicity of the polymers prepared by cationic polymerization of 2-alkyl- and 2-aryl-2-oxazolines, which supports their utilization in biomedical applications. Fluorescence microscopy and steady-state fluorescence were used to observe pyrene-labeled polymer interactions with living cells. Polymer accumulated within the cells was found to be dependent on polymer concentration in media. The immunoefficiency of aromatic and aliphatic oxazoline polymers and copolymers was also studied. Phagocytic and metabolic activities of macrophages were used to assess the immunosuppressive effects of the selected copolymers for possible applications in drug delivery and immunobiology. Overall, the tested polymers demonstrated no significant influences on the cellular immunological parameters.

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http://dx.doi.org/10.1007/s10856-011-4346-zDOI Listing

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