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Beilstein J. Nanotechnol. 2019, 10, 1073–1088, doi:10.3762/bjnano.10.108
Figure 1: ATR-FTIR spectra of (a) chitosans: (i) precursor chitosan before modification, (ii) chitosan after ...
Scheme 1: The proposed mechanism of the modification of chitosan by phenolic compounds exemplified with galli...
Figure 2: TEM micrographs of (a) γ-Fe2O3, (c) γ-Fe2O3@Hep, (d) γ-Fe2O3@Hep-CS-H, (e) γ-Fe2O3@Hep-CS-G, and (f...
Figure 3: (a) ATR-FTIR spectra of (i) γ-Fe2O3, (ii) γ-Fe2O3@Hep, (iii) γ-Fe2O3@Hep-CS-G, (iv) γ-Fe2O3@Hep-CS-...
Figure 4: Free radical scavenging of the phenolic compound-modified particles. (a) Inhibition as a function o...
Figure 5: Cellular uptake of the phenolic compound-modified particles by (a) L-929 and (b) LN-229 cells. A ma...
Figure 6: Representative antioxidant activity of the phenolic compound-modified particles in (a–g) L-929 and ...
Figure 7: Flow cytometry analysis of the antioxidant activity of the phenolic compound-modified particles bas...
Figure 8: A schematic of the iron oxide nanoparticle coating with heparin and gallic acid-modified chitosan.