Figures & data
Table 1. Composition and manufacture of commercial materials used at the study.
Figure 1. Chemical structures of the two arylsulphonyl-ureido-benzenesulphonamides SULFA1 and SULFA2 and their inhibitory activity against S. mutans β-CA (SmuCA).
![Figure 1. Chemical structures of the two arylsulphonyl-ureido-benzenesulphonamides SULFA1 and SULFA2 and their inhibitory activity against S. mutans β-CA (SmuCA).](/cms/asset/e23497f4-bd4d-4947-af8c-902ec2fa386e/ienz_a_2150184_f0001_b.jpg)
Table 2. Relative fluorescence intensity emitted by the action of dentine gelatins.
Table 3. Average values (± DP) of bond strength after storage in distilled water (24 h and 12 months) and cariogenic challenge (CC) by microtensile bond strength assay (MPa).
Figure 2. Graphical representation of failure patterns (%) after storage in distilled water for 24 h, 12 months and after cariogenic challenge (CC).
![Figure 2. Graphical representation of failure patterns (%) after storage in distilled water for 24 h, 12 months and after cariogenic challenge (CC).](/cms/asset/a429f5e8-f096-4599-ad7a-3f51f1456963/ienz_a_2150184_f0002_c.jpg)
Figure 3. (A) Average values (±DP) of the contact angle. Slashes by different capital letters are statistically different (HSD of Tukey, p < 0.05). (B) Representative images of the groups: A-SULFA1; B-SULFA2; C-DMSO; D-PHEN; E-CTR. ↓ drop of adhesive in contact with the dentine, forming the contact angle.
![Figure 3. (A) Average values (±DP) of the contact angle. Slashes by different capital letters are statistically different (HSD of Tukey, p < 0.05). (B) Representative images of the groups: A-SULFA1; B-SULFA2; C-DMSO; D-PHEN; E-CTR. ↓ drop of adhesive in contact with the dentine, forming the contact angle.](/cms/asset/150f2af9-88c5-4910-aadc-572cfe2f3e36/ienz_a_2150184_f0003_c.jpg)