Polydopamine Coating of Graphitic Carbon Nitride, g-C 3 N 4 , Improves Biomedical Application.
Mehtap SahinerSahin DemirciNurettin SahinerPublished in: Biomedicines (2024)
Graphitic carbon nitride (g-C 3 N 4 ) is an intriguing nanomaterial that exhibits photoconductive fluorescence properties under UV-visible light. Dopamine (DA) coating of g-C 3 N 4 prepared from melamine was accomplished via self-polymerization of DA as polydopamine (PDA). The g-C 3 N 4 was coated with PDA 1, 3, and 5 times repeatedly as (PDA@g-C 3 N 4 ) in tris buffer at pH 8.5. As the number of PDA coatings was increased on g-C 3 N 4 , the peak intensity at 1512 cm -1 for N-H bending increased. In addition, the increased weight loss values of PDA@g-C 3 N 4 structures at 600 °C from TGA thermograms confirmed that the coating was accomplished. The band gap of g-C 3 N 4 , 2.72 eV, was reduced to 0.87 eV after five coatings with PDA. A pristine g-C 3 N 4 was found to have an isoelectric point (IEP) of 4.0, whereas the isoelectric points of 1PDA@g-C 3 N 4 and 3PDA@g-C 3 N 4 are close to each other at 3.94 and 3.91, respectively. On the other hand, the IEP of 5PDA@g-C 3 N 4 was determined at pH 5.75 assuming complete coating with g-C 3 N 4 . The biocompatibility of g-C 3 N 4 and PDA@g-C 3 N 4 against L929 fibroblast cell lines revealed that all PDA@g-C 3 N 4 coatings were found to be biocompatible up to a 1000 mg/mL concentration, establishing that PDA coatings did not adversely affect the biocompatibility of the composite materials. In addition, PDA@g-C 3 N 4 was screened for antioxidant potential via total phenol content (TPC) and total flavonoid content assays and it was found that PDA@g-C 3 N 4 has recognizable TPC values and increased linearly with an increased number of PDA coatings. Furthermore, blood compatibility of pristine g-C 3 N 4 is enhanced considerably upon PDA coating, affirmed by hemolysis and the blood clotting index%. Additionally, α-glucosidase inhibitory properties of PDA@g-C 3 N 4 structures revealed that 67.6 + 9.8% of this enzyme was evenly inhibited by 3PDA@g-C 3 N 4 structure.