The study confirms the ability of ProRoot MTA to form a superficial layer of apatite within hours. The excellent bioactivity of ProRoot MTA might provide a significant clinical advantage over the traditional cements used for root-end or root-perforation repair.

Siboni F, Taddei P, Zamparini F, Prati C, Gandolfi MG. Properties of BioRoot RCS, a tricalcium silicate endodontic sealer modified with povidone and polycarboxylate.International Endodontic Journal, 50, e120-e136, 2017.Aim To evaluate the chemical and physical properties of a tricalcium silicate root canal sealer containing povidone and polycarboxylate (BioRoot RCS), a calcium silicate MTA-based sealer containing a salicylate resin (MTA Fillapex), a traditional eugenolcontaining sealer (Pulp Canal Sealer) and an epoxy resin-based root canal sealer (AH Plus). Methodology Calcium release, pH, setting time, water sorption, volume of open pores, volume of impervious portion, apparent porosity and weight loss were measured. The ability to nucleate calcium phosphates (CaP) after ageing 28 days in a simulated body fluid was evaluated using ESEM-EDX and microRaman spectroscopy. Data were statistically analysed (P = 0.05) using one-way ANOVA (setting time, radiopacity, solubility, water sorption, porosity) or two-way ANOVA (ion release tests). Results BioRoot RCS had a final setting time of 300 min and adequate radiopacity (5.2 mm Al). It demonstrated the highest (P < 0.05) and more prolonged ability to release calcium ions (721 ppm at 3 h) and to increase the pH (11-12) (P < 0.05); Btype carbonated apatite deposits were found on aged BioRoot RCS (biointeractivity-related CaP-forming ability). A final setting time of 270 min and good calcium release (17.4 ppm at 3 h) were measured for MTA Fillapex; apatite deposits were present on aged samples. No calcium release and no alkalizing activity were measured for Pulp Canal Sealer and AH Plus; no CaP nucleation was detected on aged Pulp Canal Sealer, and some apatite deposits were found on aged AH Plus (chemi/physisorption-related CaP-deposition). Higher and significantly different (P < 0.05) porosity, water sorption and solubility were measured for the two calcium silicate sealers, especially for BioRoot RCS. Conclusions BioRoot RCS had bioactivity with calcium release, strong alkalizing activity and apatiteforming ability, and adequate radiopacity.

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This study focuses on the conformational characterization of differently processedBombyx mori silk fibroin samples by Raman spectroscopy. The Raman spectra of silk fibroin film and liquid silk are discussed in comparison with those of the crystalline fractions of Bombyx mori silk fibroin (Cp, chymotryptic precipitate) with Silk I (Silk I-Cp) and Silk II (Silk II-Cp) structures. The complete 1800-200 cm −1 Raman spectrum of Silk I-Cp is reported for the first time. The amide I and amide III modes were found to be scarcely suitable for the spectroscopic characterization of silk fibroin in the Silk I form in the presence of a random coil conformation. Raman marker bands for the Silk I form were identified in other spectral ranges at about 1415, 950, 930, 865, 260 and 230 cm −1 . On the basis of the above findings, the comparison of the Raman spectra of film, liquid silk and Silk I-Cp in the range 1000-800 cm −1 clearly indicates that in addition to random coil, both film and liquid silk contain local domains of Silk I structure; their amount is higher in liquid silk, as indicated by the relative intensity of the bands at about 950, 930 and 865 cm −1 and by the I 1415 /I 1455 intensity ratio.The assignments of the bands at about 1275 and 1107 cm −1 are also discussed. These bands were previously assigned to the presence of a-helical conformation in Bombyx mori silk but, from the results reported, they should rather be attributed to the Silk I form.

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Commercial root end filling materials, namely two zinc oxide eugenol-based cements [intermediate restorative material (IRM), Superseal], a glass ionomer cement (Vitrebond) and three calcium-silicate mineral trioxide aggregate (MTA)-based cements (ProRoot MTA, MTA Angelus, and Tech Biosealer root end), were examined for their ability to: (a) release calcium (Ca(2+) ) and hydroxyl (OH(-) ) ions (biointeractivity) and (b) form apatite (Ap) and/or calcium phosphate (CaP) precursors. Materials were immersed in Hank's balanced salt solution (HBSS) for 1-28 days. Ca(2+) and OH(-) release were measured by ion selective probes, surface analysis was performed by environmental scanning electron microscopy/energy dispersive X-ray analysis, micro-Raman, and Fourier transform infrared spectroscopy. IRM and Superseal released small quantities of Ca(2+) and no OH(-) ions. Uneven sparse nonapatitic Ca-poor amorphous CaP (ACP) deposits were observed after 24 h soaking. Vitrebond did not release either Ca(2+) or OH(-) ions, but uneven nonapatitic Ca-poor CaP deposits were detected after 7 days soaking. ProRoot MTA, MTA Angelus, and Tech Biosealer root end released significant amounts of Ca(2+) and OH(-) ions throughout the experiment. After 1 day soaking, nanospherulites of CaP deposits formed by amorphous calcium/magnesium phosphate (ACP) Ap precursors were detected. A more mature ACP phase was present on ProRoot MTA and on Tech Biosealer root end at all times. In conclusion, zinc oxide and glass ionomer cements had little or no ability to release mineralizing ions: they simply act as substrates for the possible chemical bonding/adsorption of environmental ions and precipitation of nonapatitic Ca-poor ACP deposits. On the contrary, calcium-silicate cements showed a high calcium release and basifying effect and generally a pronounced formation of more mature ACP apatitic precursors correlated with their higher ion-releasing ability.

a b s t r a c tThis study was aimed at comparatively investigating the hydrolysis of crystalline and amorphous poly-(ethylene terephthalate) films by alkali and cutinase. Changes of surface properties were investigated by FTIR spectroscopy (ATR mode). The A 1341 /A 1410 and I 1120 /I 1100 absorbance ratios, and the full width at half maximum of the carbonyl stretching band (FWHM 1715 ) were used to evaluate the polymer crystallinity and its changes upon hydrolysis. The effect of different treatments on chain orientation was evaluated by calculating R ratios of appropriate bands. The spectroscopic indexes showed that both alkali and enzyme treatments induced structural and conformational rearrangements with a consequent increase in crystallinity in both amorphous and crystalline films. The crystalline PET film was modified more strongly by alkali than by cutinase, while the opposite occurred for the amorphous one. The trend of the water contact angle (WCA) clearly indicates that alkali is more effective than cutinase in enhancing hydrophilicity of PET films and that the effect is stronger on amorphous than on crystalline films. The values of WCA correlate well with the FTIR indexes calculated from the spectra of hydrolyzed crystalline PET films. The mechanism of the surface hydrolysis of PET by alkali and cutinase is discussed.

Crystalline 1,8-naphthalimide derivatives bearing a bromine atom at the 4-position and a 2-, 3-, or 4- methylpyridine at the imidic N-position have been synthesized, and their co-crystals with the coformer 1,4-diiodotetrafluorobenzene have been obtained via mechanochemistry. The structure of crystals and co-crystals has been characterized by means of X-ray diffraction and Raman and IR analysis. The luminescence properties of the derivatives have been explored both in solution and in their solid crystals and co-crystals. All of the compounds exhibit weak fluorescence in air-equilibrated solutions at room temperature and both fluorescence and phosphorescence at low temperature. In air-free solvent, all of the derivatives show phosphorescence at room temperature, at variance with the unsubstituted 1,8-naphthalimide model. Solid crystals display a red-shifted fluorescence with an increased emission quantum yield as compared to solution, whereas co-crystals show different behaviors. For all of the solid compounds, phosphorescence could be observed at room temperature by means of a gated detection. The dependence of the luminescence features of the solid materials on the intermolecular interactions that occur in the lattice is discussed.