Pharmaceutical Nanoplatforms Based on Self-nanoemulsifying Drug Delivery Systems for Optimal Transport and Co-delivery of siRNAs and Anticancer Drugs.

Small interfering RNAs (siRNAs) have the ability to induce selective gene silencing, although siRNAs are vulnerable to degradation in vivo. Various active pharmaceutical ingredients (APIs) are currently used as effective therapeutics in the treatment of cancer. However, routes of administration are limited due to their physicochemical and biopharmaceutical properties. This research aimed to develop oral pharmaceutical formulations based on self-nanoemulsifying drug delivery systems (SNEDDS) for optimal transport and co-delivery of siRNAs related to cancer and APIs. Formulations were developed using optimal mixing design (Design-Expert 11 software) for SNEDDS loading with siRNA (water/oil emulsion), API (oil/water emulsion), and siRNA-API (multiphase water/oil/water emulsion). The final formulations were characterized physicochemically and biologically. The nanosystems less than 50 nm in size had a drug loading above 48 %. The highest drug release occurred at intestinal pH, allowing drug protection in physiological fluids. SNEDDS-siRNA-APIs showed a twofold toxicity effect than APIs in solution and higher transfection and internalization of siRNA in cancer cells with respect to free siRNAs. In the duodenum, higher permeability was observed with SNEDDS-API than with the API solution, as determined by ex-vivo fluorescence microscopy. The multifunctional formulation based on SNEDDS was successfully prepared, siRNA, hydrophobic chemotherapeutics (doxorubicin, valrubicin and methotrexate) and photosensitizers (rhodamine b and protoporphyrin IX) agents were loaded, using a chitosan-RNA core, and Labrafil® M 1944 CS, Cremophor® RH40, phosphatidylcholine shell, forming stable hybrid SNEDDS as multiphasic emulsion, suitable as co-delivery system with a potent anticancer activity.

Antimicrobial Activity of Biogenic Silver Nanoparticles from Syzygium aromaticum against the Five Most Common Microorganisms in the Oral Cavity.

Syzygium aromaticum (clove) has been used as a dental analgesic, an anesthetic, and a bioreducing and capping agent in the formation of metallic nanoparticles. The main objective of this study was to evaluate the antimicrobial effect in oral microorganisms of biogenic silver nanoparticles (AgNPs) formed with aqueous extract of clove through an ecofriendly method "green synthesis". The obtained AgNPs were characterized by UV-Vis (ultraviolet-visible spectroscopy), SEM-EDS (scanning electron microscopy-energy dispersive X-ray spectroscopy), TEM (transmission electron microscopy), and ζ potential, while its antimicrobial effect was corroborated against oral Gram-positive and Gram-negative microorganisms, as well as yeast that is commonly present in the oral cavity. The AgNPs showed absorption at 400-500 nm in the UV-Vis spectrum, had an average size of 4-16 nm as observed by the high-resolution transmission electron microscopy (HR-TEM), and were of a crystalline nature and quasi-spherical form. The antimicrobial susceptibility test showed inhibition zones of 2-4 mm in diameter. Our results suggest that AgNPs synthesized with clove can be used as effective growth inhibitors in several oral microorganisms.

Effect of airborne-particle abrasion and, acid and alkaline treatments on shear bond strength of dental zirconia.

The surface roughness, morphology and shear bond strength (SBS) of dental zirconia using three different surface treatment techniques were evaluated. Three groups of sintered zirconia blocks were treated as follow, 1) Airborne-particle abrasion (APA) group (G1-APA), 50-µm Al2O3; 2) APA and 9% hydrofluoric acid etching (G2-HF); 3) APA and Sodium Hydroxide (G3-NaOH). The specimens were evaluated for roughness [atomic force microscope (AFM)], morphology [Scanning Electron Microscope (SEM)] and for SBS in the universal testing machine. The AFM revealed changes in the roughness after the surface treatments, however there was not Ra difference between groups, SEM analysis revealed changes in surface morphology for all surface treated specimens. For SBS, significant difference was found between G1-APA=8.4±2.7 MPa and G2-HF=3.3±0.6 MPa (p<0.05) and G2-HF and G3-NaOH=9.0±3.0 MPa (p<0.05). The main fracture mode was mixed failure (63%) for G1-APA and G3-NaOH groups. G2-HF showed 100% adhesive failure. SBS was improved with NaOH, however application of HF significantly decreased SBS.

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.

Chemical and morphological changes in human dentin after Er:YAGlaser irradiation: EDS and SEM analysis.

Sixty samples of human dentin were divided into six groups (n = 10) and were irradiated with Er:YAG laser at 100 mJ-19.9 J/cm(2), 150 mJ-29.8 J/cm(2), 100 mJ-35.3 J/cm(2), 150 mJ-53.0 J/cm(2), 200 mJ-70.7 J/cm(2), and 250 mJ-88.5 J/cm(2), respectively, at 7 Hz under a water spray. The atomic percentages of carbon, oxygen, magnesium, calcium, and phosphorus and the Ca-to-P molar ratio on the dentin were determined by energy dispersive X-ray spectroscopy. The morphological changes were observed using scanning electron microscopy. A paired t-test was used in statistical analysis before and after irradiation, and a one-way ANOVA was performed (P ≤ 0.05). The atomic percent of C tended to decrease in all of the groups after irradiation with statistically significant differences, O and Mg increased with significant differences in all of the groups, and the Ca-to-P molar ratio increased in groups IV, V, and VI, with statistically significant differences between groups II and VI. All the irradiated samples showed morphological changes. Major changes in the chemical composition of dentin were observed in trace elements. A significant increase in the Ca-to-P ratio was observed in the higher energy density groups. Morphological changes included loss of smear layer with exposed dentinal tubules. The changes produced by the different energy densities employed could have clinical implications, additional studies are required to clarify them.

An evaluation of the antibacterial properties and shear bond strength of copper nanoparticles as a nanofiller in orthodontic adhesive.

OBJECTIVES: To evaluate the antibacterial properties and effects of an orthodontic adhesive containing copper nanoparticles (NPs) on the material's shear bond strength. METHODS: Antimicrobial activity was analysed by a disk diffusion test against S. aureus, E. coli and S. mutans. The NPs were added to the orthodontic adhesive at 0.0100 wt%, 0.0075 wt%, and 0.0050 wt%. Sixty extracted bicuspids were divided into two groups and the enamel of all teeth was conditioned with phosphoric acid. A coat of moisture insensitive primer (MIP) was applied prior to the bonding of brackets with composite resin. Group I served as a control and the bonding procedure was performed according to the manufacturer's instructions. Group II comprised the test teeth, into which 0.0100 wt% copper NPs were included in the MIP. Samples were tested and statistically analysed (p ≤ 0.05). The adhesive remnant index (ARI) was also assessed microscopically. - RESULTS: The adhesive with copper NPs showed a bactericidal effect against the bacteria under study. A significantly higher bond strength was obtained with the orthodontic adhesive that included 0.0100 wt% of copper NPs (15.23 ± 6.8 MPa) in comparison with the control group (9.59 ± 4.3 MPa). The ARI scores indicated that the groups were significantly different and strengthened by the incorporation of NPs (p = 0.004). CONCLUSION: The results of the present study suggested that an orthodontic adhesive, which included copper NPs, significantly increased material shear bond strength without adverse side effects on colour and appearance. The adhesive interface was strengthened by homogeneously dispersed copper NPs added as a nanofiller.

Morphological and chemical changes of deciduous enamel produced by Er:YAG laser, fluoride, and combined treatment.

OBJECTIVE: The purpose of this study was to evaluate in vitro morphological and chemical changes on human deciduous enamel produced by Er:YAG laser irradiation, fluoride application, combined treatment, and acid dissolution. BACKGROUND DATA: Er:YAG laser has been proposed as a potential preventive dental caries strategy. There is scarce information regarding deciduous enamel. METHODS: Eighty enamel samples were assigned to eight groups (n=10): G1, control; G2, G3, and G4, Er:YAG laser irradiation at 7.5, 12.7, and 39.8 J/cm(2), respectively; G5, fluoride application; G6, G7, and G8, irradiation at previous densities plus fluoride application. Morphology was evaluated by scanning electron microscopy, and chemical composition was determined by energy dispersive X-ray spectroscopy before treatment (BT), after treatment (AT), and after acid dissolution (AAD). One way and repeated measures analysis of variance (ANOVA) were used (p≤0.05). RESULTS: Morphology of lased surfaces included craters, exposed prisms, fractures, and melting. No morphological modifications appeared after fluoride application, or AAD. Chemically, AT: C atomic percentage (at%) decreased in G3, G4, and G8; O at% decreased in G5-G8; F content was higher for G7; trace elements remained under 1.0 at%; Ca at % increased in G4, G7, and G8; there were increments in P at% in G4 and G8; and Ca/P increased in G4, G7, and G8. AAD: F at% dropped to 0.00 in G5-G8; and P at% increased in G7. CONCLUSIONS: Morphological changes of Er:YAG irradiated enamel represented mild to severe damages. Conditions employed in this study are not recommended for deciduous caries prevention. Er:YAG energy density influenced chemical changes in enamel to enhance its structure. Acid dissolution removed fluoride from enamel surface.

Chemical changes associated with increased acid resistance of Er:YAG laser irradiated enamel.

BACKGROUND: An increase in the acid resistance of dental enamel, as well as morphological and structural changes produced by Er:YAG laser irradiation, has been reported. PURPOSE: To evaluate the chemical changes associated with acid resistance of enamel treated with Er:YAG laser. Methods. Forty-eight enamel samples were divided into 4 groups (n = 12). Group I (control); Groups II, III, and IV were irradiated with Er:YAG at 100 mJ (12.7 J/cm(2)), 200 mJ (25.5 J/cm(2)), and 300 mJ (38.2 J/cm(2)), respectively. RESULTS: There were significant differences in composition of irradiated groups (with the exception of chlorine) and in the amount of calcium released. CONCLUSIONS: Chemical changes associated with an increase in acid resistance of enamel treated with Er:YAG laser showed a clear postirradiation pattern characterized by a decrease in C at.% and an increase in O, P, and Ca at.% and no changes in Cl at.%. An increased Ca/P ratio after Er:YAG laser irradiation was associated with the use of higher laser energy densities. Chemical changes produced by acid dissolution showed a similar trend among experimental groups. Stable or increased Ca/P ratio after acid dissolution was observed in the irradiated groups, with reduction of Ca released into the acid solution.

Morphological changes produced by acid dissolution in Er:YAG laser irradiated dental enamel.

Several scientific reports have shown the effects of Er:YAG laser irradiation on enamel morphology. However, there is lack of information regarding the morphological alterations produced by the acid attack on the irradiated surfaces. The aim of this study was to evaluate the morphological changes produced by acid dissolution in Er:YAG laser irradiated dental enamel. Forty-eight enamel samples were divided into four groups (n = 12). GI (control); Groups II, III, and IV were irradiated with Er:YAG at 100 mJ (12.7 J/cm(2) ), 200 mJ (25.5 J/cm(2) ), and 300 mJ (38.2 J/cm(2) ), respectively, at 10 Hz without water irrigation. Enamel morphology was evaluated before-irradiation, after-irradiation, and after-acid dissolution, by scanning electron microscopy (SEM). Sample coating was avoided and SEM analysis was performed in a low-vacuum mode. To facilitate the location of the assessment area, a reference point was marked. Morphological changes produced by acid dissolution of irradiated enamel were observed, specifically on laser-induced undesired effects. These morphological changes were from mild to severe, depending on the presence of after-irradiation undesired effects.

Evaluation of self-etching adhesive and Er:YAG laser conditioning on the shear bond strength of orthodontic brackets.

The purpose of this study was to evaluate the shear bond strength, the adhesive remnant index scores, and etch surface of teeth prepared for orthodontic bracket bonding with self-etching primer and Er:YAG laser conditioning. One hundred and twenty bovine incisors were randomly divided into four groups. In Group I (Control), the teeth were conditioned with 35% phosphoric acid for 15 seconds. In Group II the teeth were conditioned with Transbond Plus SEP (5 sec); III and IV were irradiated with the Er:YAG 150 mJ (11.0 J/cm²), 150 mJ (19.1 J/cm²), respectively, at 7-12 Hz with water spray. After surface preparation, upper central incisor stainless steel brackets were bonded with Transbond Plus Color Change Adhesive. The teeth were stored in water at 37°C for 24 hours and shear bond strengths were measured, and adhesive remnant index (ARI) was determined. The conditioned surface was observed under a scanning electron microscope. One-way ANOVA and chi-square test were used. Group I showed the significantly highest values of bond strength with a mean value of 8.2 megapascals (MPa). The lesser amount of adhesive remnant was found in Group III. The results of this study suggest that Er:YAG laser irradiation could not be an option for enamel conditioning.

Tribological properties of polymer nanohybrids containing gold nanoparticles obtained by laser ablation.

We have studied polystyrene (PS)+Au particles nanohybrids. Approximately spherical gold nanoparticles with the average diameter of 15 nm were obtained by laser ablation in a liquid environment. Thus any chemical residue on the particles was eliminated. Focused ion beam (FIB) milling plus scanning electron microscopy (SEM) observation show that Au particles are fairly well dispersed inside the polymer matrix, better than when PS is simply dissolved in a nanoparticle solution. The Au particles concentration as low as 0.15 wt% results in dramatic changes in tribological properties, namely dynamic friction and pin-on-disk wear. Both wear and dynamic friction results are explained in terms of high brittleness of PS, abrasion of Au particles against a ceramic indenter, and also effects of density of filler particles in the matrix on tribological properties. Effects of varying normal load on friction are small.

Morphological and structural changes on human dental enamel after Er:YAG laser irradiation: AFM, SEM, and EDS evaluation.

OBJECTIVE: The purpose of this study was to evaluate, using atomic force microscopy (AFM), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS), the morphological and structural changes of the enamel after irradiation with the Er:YAG laser. BACKGROUND DATA: A previous study showed that subablative Er:YAG laser irradiation produced undesirable morphological changes on the enamel surface, such as craters and cracks; however, the enamel acid resistance was not increased. METHODS: Fifty-two samples of human enamel were divided into four groups (n = 13): Group I was the control (no laser irradiation), whereas Groups II, III, and IV were irradiated with the Er:YAG 100 mJ (12.7 J/cm(2)), 100 mJ (7.5 J/cm(2)), and 150 mJ (11 J/cm(2)), respectively, at 10 Hz with water spray. The morphological changes were observed by AFM and SEM. The weight percentages (wt%) of calcium (Ca), phosphorus (P), oxygen (O) and chlorine (Cl) were determined in the resultant craters and their periphery using EDS. Kruskal-Wallis and Mann-Whitney U tests were performed (p ≤ 0.05) to distinguish significant differences among the groups. RESULTS: The AFM images showed cracks with depths between 250 nm and 750 nm for Groups II and IV, respectively, and the widths of these cracks were 5.37 µm and 2.58 µm. The interior of the cracks showed a rough surface. The SEM micrographs revealed morphological changes. Significant differences were detected in Ca, P, and Cl in the crater and its periphery. CONCLUSIONS: AFM observations showed triangular-shaped cracks, whereas craters and cracks were evident by SEM in all irradiated samples. It was not possible to establish a characteristic chemical pattern in the craters.

Wear resistance and wear mechanisms in polymer + metal composites.

We have investigated composites containing metallic micro-size and nano-sized particles as the 10 wt% dispersed phase. Branched low density polyethylene (LDPE) was the matrix. Microsized metals were Al, Ag and Ni; nanosized metals were Al and Ag. Several mechanisms of wear are observed in function of the kind and size of metal used: deformation, delamination, abrasion, adhesion and rolls formation. The presence of Ag particles increases the wear rate as compared to neat LDPE. The presence of Al particles lowers the wear of LDPE significantly; nanoparticles are more effective than microparticles.

Reinforcement of polymeric latexes by in situ polymerization.

Two silicas with different particle sizes have been synthesized by the Stöber method. The particles have been functionalized with methacryloyl groups. In situ emulsion polymerization of butyl acrylate and methyl methacrylate in the presence of functionalized silica particles was performed. The ratio of butyl acrylate to methyl methacrylate was varied in order to optimize the composition for improvement of tribological and thermophysical properties. The silica particles morphology and functionalization have been determined respectively by scanning electronic microscopy and infrared spectroscopy. The composites were characterized also by thermogravimetric analysis, differential scanning calorimetry, microscratch testing and static light scattering. The latex reinforced with the smallest functionalized silica exhibits higher thermal stability than the non reinforced latex, along with lower penetration depth and higher residual depth in progressive load scratch testing. Thus, the resistance to penetration is increased while viscoelastic healing is hampered by silica particles.