Journal
JOURNAL OF FUNCTIONAL BIOMATERIALS
Volume 13, Issue 4, Pages -Publisher
MDPI
DOI: 10.3390/jfb13040201
Keywords
conjugates; dopamine; SH-SY5Y cell viability; SNOM microscopy; antioxidant activity
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This study aimed to investigate the interactions between AlgOx-Da and SH-SY5Y neuronal cell lines, and evaluate their effects on cell structure and reactive oxygen species (ROS) production. The findings showed that AlgOx-Da reduced ROS production, which may have potential applications in PD treatment.
Background: We had previously synthetized a macromolecular prodrug consisting of oxidized Alginate and dopamine (AlgOx-Da) for a potential application in Parkinson disease (PD). Methods: In the present work, we aimed at gaining an insight into the interactions occurring between AlgOx-Da and SH-SY5Y neuronal cell lines in view of further studies oriented towards PD treatment. With the scope of ascertaining changes in the external and internal structure of the cells, multiple methodologies were adopted. Firstly, fluorescently labeled AlgOx-Da conjugate was synthetized in the presence of fluorescein 5(6)-isothiocyanate (FITC), providing FITC-AlgOx-Da, which did not alter SH-SY5Y cell viability according to the sulforhodamine B test. Furthermore, the uptake of FITC-AlgOx-Da by the SH-SY5Y cells was studied using scanning near-field optical microscopy and assessments of cell morphology over time were carried out using atomic force microscopy. Results: Notably, the AFM methodology confirmed that no relevant damage occurred to the neuronal cells. Regarding the effects of DA on the intracellular reactive oxygen species (ROS) production, AlgOx-Da reduced them in comparison to free DA, while AlgOx did almost not influence ROS production. Conclusions: these findings seem promising for designing in vivo studies aiming at administering Oxidized Alginate Dopamine Conjugate for PD treatment.
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