Raúl A. Morales-Luckie

Mechanical, antibacterial and bond strength properties of nano-titanium-enriched glass ionomer cement

The use of nanoparticles (NPs) has become a significant area of research in Dentistry. Objective The aim of this study was to investigate the physical, antibacterial activity and bond strength properties of conventional base, core build and restorative of glass ionomer cement (GIC) compared to GIC supplemented with titanium dioxide (TiO2) nanopowder at 3% and 5% (w/w). Material and Methods Vickers microhardness was estimated with diamond indenter. Compressive and flexural strengths were analyzed in a universal testing machine. Specimens were bonded to enamel and dentine, and tested for shear bond strength in a universal testing machine. Specimens were incubated with S. mutans suspension for evaluating antibacterial activity. Surface analysis of restorative conventional and modified GIC was performed with SEM and EDS. The analyses were carried out with Kolmogorov-Smirnov, ANOVA (post-hoc), Tukey test, Kruskal-Wallis, and Mann Whitney. Results Conventional GIC and GIC modified with TiO2 nanopowder for the base/liner cement and core build showed no differences for mechanical, antibacterial, and shear bond properties (p>0.05). In contrast, the supplementation of TiO2 NPs to restorative GIC significantly improved Vickers microhardness (p<0.05), flexural and compressive strength (p<0.05), and antibacterial activity (p<0.001), without interfering with adhesion to enamel and dentin. Conclusion GIC supplemented with TiO2 NPs (FX-II) is a promising material for restoration because of its potential antibacterial activity and durable restoration to withstand the mastication force.

Synthesis of silver nanoparticles using aqueous extracts of Heterotheca inuloides as reducing agent and natural fibers as templates: Agave lechuguilla and silk.

Silver nanoparticles (Ag NPs) were synthesized using a one-pot green methodology with aqueous extract of Heterotheca inuloides as a reducing agent, and the support of natural fibers: Agave lechuguilla and silk. UV-Vis spectroscopy, X-Ray photoelectron spectroscopy XPS and transmission electron microscopy TEM were used to characterize the resulting bionanocomposite fibers. The average size of the Ag NPs was 16nm and they exhibited low polydispersity. XPS studies revealed the presence of only metallic Ag in the nanoparticles embedded in Agave. lechuguilla fibers. Significant antibacterial activities against gram-negative Escherichia coli and gram-positive Staphylococcus aureus were determined. AgO as well as metallic Ag phases were detected when silk threads were used as a substrates hinting at the active role of substrate during the nucleation and growth of Ag NPs. These bionanocomposites have excellent mechanical properties in tension which in addition to the antibacterial properties indicate the potential use of these modified natural fibers in surgical and biomedical applications.

Formation of silk-gold nanocomposite fabric using grapefruit aqueous extract

Gold nanostructures were synthesized by reduction of gold ions using aqueous extract of grapefruit pulp (Citrus paradisi). This eco-friendly bioreduction method allows the formation in solution and support of gold nanostructures on silk fibers. Bioreduction techniques involve biomolecules of grapefruit extract for reducing a gold precursor to obtain different kinds of nanostructures. Carbohydrates and organic acids, present in C. paradise, are believed to be responsible for the formation of nanoparticles. Analysis of gold–silk nanocomposites by electron microscopy shows gold nanostructures with quasi-spherical, hexagonal, and triangle shapes. The evolution of functional groups in the silk fibers before and after the bioreduction process was followed by infrared spectroscopy. Diffuse reflectance spectroscopy (DRS) and laser scanning confocal microscopy (LSCM) were used to probe surface plasmon resonance and fluorescent behavior in the silk–gold composite. This simple and novel methodology for obtaining these types of nanocomposite may have important applications in the development of functional fibers.

Size-controlled synthesis of Fe2O3 and Fe3O4 nanoparticles onto zeolite by means of a modified activated-coprecipitation method: effect of the HCl concentration during the activation

Synthetic sodium type A zeolite bearing Fe2O3 and Fe3O4 nanoparticles composites have been prepared by means of a coprecipitation method with two different activation methodologies, one using Sn and the other using Sn/Pd nanoparticles as activators. Sn activation generates hematite nanoparticles while Sn/Pd produces magnetite nanoparticles. Amount of HCl used during the activation of the zeolite with SnCl2 showed a correlation between the stannous activating species and the particle size. Both Sn and Sn–Pd activated nanocomposites show nearly narrow size distributions but only those iron oxides obtained with Sn–Pd showed supermagnetism.

Biosynthesis of Silver Nanoparticles on Orthodontic Elastomeric Modules: Evaluation of Mechanical and Antibacterial Properties

In the present study, silver nanoparticles (AgNPs) were synthesized in situ on orthodontic elastomeric modules (OEM) using silver nitrate salts as metal-ion precursors and extract of the plant Hetheroteca inuloides (H. inuloides) as bioreductant via a simple and eco-friendly method. The synthesized AgNPs were characterized by UV-visible spectroscopy; scanning electron microscopy-energy-dispersive spectroscopy (SEM-EDS) and transmission electron microscopy (TEM). The surface plasmon resonance peak found at 472 nm confirmed the formation of AgNPs. SEM and TEM images reveal that the particles are quasi-spherical. The EDS analysis of the AgNPs confirmed the presence of elemental silver. The antibacterial properties of OEM with AgNPs were evaluated against the clinical isolates Streptococcus mutans, Lactobacillus casei, Staphylococcus aureus and Escherichia coli using agar diffusion tests. The physical properties were evaluated by a universal testing machine. OEM with AgNPs had shown inhibition halos for all microorganisms in comparison with OEM control. Physical properties increased with respect to the control group. The results suggest the potential of the material to combat dental biofilm and in turn decrease the incidence of demineralization in dental enamel, ensuring their performance in patients with orthodontic treatment.

Facile Solventless Synthesis of a Nylon-6,6/Silver Nanoparticles Composite and Its XPS Study

Silver nanoparticles were synthesized and supported on thin nylon membranes by means of a simple method of impregnation and chemical reduction of Ag ions at ambient conditions. Particles of less than 10 nm were obtained using this methodology, in which the nylon fibers behave as constrained nanoreactors. Pores on nylon fibres along with oxygen and nitrogen from amide moieties in nylon provide effective sites for in situ reduction of silver ions and for the formation and stabilization of Ag nanoparticles. Transmission electron microscopy (TEM) analysis showed that silver nanoparticles are well dispersed throughout the nylon fibers. Furthermore, an interaction between nitrogen of amides moieties of nylon-6,6 and silver nanoparticles has been found by X-ray photoelectron spectroscopy (XPS).

Comparative study of fluoride released and recharged from conventional pit and fissure sealants versus surface prereacted glass ionomer technology.

Context: The fluoride release of sealants in vitro shows a marked decrease. Giomers are distinguishable from manufactured resin-based sealants and contain prereacted glass-ionomer particles (PRG). Aims: To compare the amounts of fluoride released from the main pit and fissure of a resin-based sealant with that from a Giomer and to assess the abilities of the sealant and the Giomer to recharge when exposed to regular use of fluoride rinse. Materials and Methods: The readings for the fluoride concentration were carried out for 60 days using a fluoride ion-specific electrode. After this period, the samples were recharged using a fluoride mouth rinse. The amount of fluoride released after this recharge was determined for 5 days. The data were analyzed using Student′s t- and analysis of variance tests. Results: In general, all materials presented higher fluoride release in the first 24 h; G1 and G4 showed a higher fluoride release in this period. On the other hand, G3 and G1 presented the most constant fluoride release until the 8 th day, wherein all the sealants considerably decreased in the amount of fluoride released. Conclusion: G1 and G3 released higher concentrations of fluoride, although no significant differences were found. Giomers recharged in the first 24 h after polymerization presented an improved and sustained fluoride release.

Synthesis, Characterization, and Catalytic Activity of Platinum Nanoparticles on Bovine-Bone Powder: A Novel Support

Pt nanoparticles supported on bovine-bone powder were obtained by a rather simple method consisting of immersing powder of bovine bone into a Pt+4 metal ion solution at room temperature and subsequent reduction by sodium borohydride. This method eliminates the calcination step of the usual catalyst preparation methods. The nanocomposite was characterized by transmission electron microscopy (TEM), which revealed uniformly dispersed platinum nanoparticles with average particle size of 2.2 nm ± 0.6 nm. The XPS studies exhibited the presence of 63% Pt° and 37% PtO. The catalytic activity was tested in the hydrogenation of 2-butyne-1,4-diol. The nanocomposite shows good catalytic performance with nearly 100% conversion and 83% selectivity towards 2-butene-1,4-diol.

1D and 3D supramolecular structures exhibiting weak ferromagnetism in three Cu(II) complexes based on malonato and di-alkyl-2,2’-bipyridines

Abstract Three new Cu(II) complexes composed of malonato (mal), methylmalonato (memal), 4,4′-di-tert-butyl-2,2′-bipyridine (tbpy) and 5,5′-dimethyl-2,2′-bipyridine (mebpy) ligands, Cu(H2O)(mal)(tbpy) (1), Cu(H2O)(memal)(tbpy) (2) and Cu4(H2O)4(memal)4(mebpy)4·11H2O (3) were synthesized by simple one-pot solution reactions at ambient conditions. Single-crystal X-ray diffraction analyses reveal that the Cu(II) ions exhibit a distorted five-coordinate square pyramidal geometry. These three complexes display supramolecular arrays due to hydrogen-bonding interactions. Complexes 1 and 2 show 1-D supramolecular structures; 1 forms a double-ion chain, unlike 2, which only generates a single-ion chain. In 3, there are two identical monomers in the asymmetric unit with Z″ = 2; its high number of noncoordinated water molecules, along with hydrogen-bonding interactions between aqua ligand and memal ligand, generate a supramolecular tetramer, which mimics to produce a 3-D supramolecular framework. Besides this fascinating and yet uncommon crystallographic phenomenon in 3, the structural differences found in these complexes arise from the substituted groups in the malonato dianion and in the bipyridine ligands. These compounds exhibit weak ferromagnetic-exchange interactions.

A comparative in vitro efficacy of conventional rotatory and chemomechanical caries removal: Influence on cariogenic flora, microhardness, and residual composition.

Background: Chemomechanical caries removal system is part of the minimal invasive dentistry; the aim of the study was to compare the amount of bacteria after caries removal with chemomechanical system and conventional rotatory instruments and to test the Vickers microhardness and micro-RAMAN analysis of residual dentin after excavation. Materials and Methods: Molars were induced for demineralization, confirmed with DIAGNOdent; Streptococcus mutans were inoculated into the cavities and filled. Caries removal was performed with rotatory instruments and chemomechanical system; surviving bacteria were cultured for 24 and 48 hours at 37°C. Vickers microhardness and micro-RAMAN analysis were tested after excavation. Data were analyzed with Wilcoxon, continuity correction, odds ratio, ANOVA post hoc Tukey test, and Spearman correlation. Results: Demineralization was significantly detectable at 240 hours of incubation; conventional rotatory instruments and chemomechanical caries removal were effective in 19.4%-22.6% and 25.8%-32.3%, respectively. Vickers microhardness of chemomechanical system was higher (P < 0.0001) than conventional rotatory instruments and comparable to healthy dentin. Micro-RAMAN analysis showed that healthy dentin is correlated to chemomechanical system (R2 = 0.683, P < 0.00001) and drilling with burs (R2 = 0.139, P < 0.00001). Conclusion: The chemomechanical system is effective for caries elimination, comparable to conventional rotatory instruments; the remaining Vickers microhardness and composition surface tissue are similar to healthy dentin.