Use of resin-based restorative materials recently has become widely accepted for treatment of endodontically treated teeth. However, some solutions routinely used during endodontic treatment procedures may have an effect on bond strengths of adhesive materials to root canal dentin. The purpose of this in vitro study was to evaluate the effect of various medications on microtensile bond strength to root canal dentin. Fourteen extracted human single-rooted teeth were used. The crowns and the pulp tissues were removed. The root canals were then instrumented and widened to the same size. The teeth were randomly divided into seven groups of two teeth each. The root canal dentin walls of the roots were treated with 5% sodium hypochloride (NaOCI), 3% hydrogen peroxide (H2O2), the combination of H2O2 and NaOCl, or 0.2% chlorhexidine gluconate for 60 s; or calcium hydroxide or formocresol for 24 h. The teeth in control group were irrigated with water. The root canals were obturated using C&B Metabond. After 24 h of storage in distilled water, serial 1-mm-thick cross-sections were cut, and approximately 12 samples were obtained from each group. Microtensile bond strengths to root canal dentin were then measured by using an Instron machine. The data were recorded and expressed as MPa. The results indicated that NaOCI, H2O2, or a combination of NaOCl and H2O2 treatment decreased bond strength to root canal dentin significantly (p < 0.05). The teeth treated with chlorhexidine solution showed the highest bond strength values (p < 0.05). In conclusion, chlorhexidine is an appropriate irrigant solution for root canal treatment before adhesive post core applications.

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Manganese (Mn)- and yttrium (Y)-substituted Sr-nanohexaferrites (MYSNHFs) of composition Sr1−xMnxFe12−xYxO19 (with 0.0 ≤ x ≤ 0.5) were prepared by citrate sol-gel autocombustion method. As-prepared MYSNHFs were characterized via diverse analytical techniques to determine the influence of Mn and Y cosubstitution on their microstructures and magnetic properties. 57Fe Mössbauer spectra of the MYSNHFs were used to evaluate the variation in the line width, isomer shift, quadrupole splitting, and hyperfine magnetic field values. It was shown that the dopant ions could preferentially occupy the 12k, 4f2, and 2b sites. Furthermore, the observed shift in the blocking temperatures of the studied MYSNHFs towards lower values with rising Mn2+ and Y3+ contents was attributed to the overall particles size reduction. Meanwhile, the AC susceptibility of the proposed MYSNHFs revealed that the magnetic interactions were weakened with the increase in dopant contents which was ascribed to the replacement of both Sr2+ and Fe3+ ions by the Mn2+ and Y3+ dopants.

[Ni 0.4 Cu 0.2 Zn 0.4 ](Fe 2– x Dy x )O 4 spinel ferrite nanoparticles with different Dy 3+ concentrations (0.00 ≤ x ≤ 0.04) were prepared by a citrate sol–gel auto-combustion technique. A strong correlation among Dy concentration, structural parameters, and magnetic, electrical, and microwave properties was established. An increase in the Dy 3+ concentration is the reason for a rise in the crystal structure parameters (due to different ionic radii of Fe and Dy ions) and a slight increase in the average particle size with a minor reduction in the specific surface area. It was observed that Dy 3+ ions prefer to occupy the octahedral B site due to their large ionic radius (0.91 Å). The explanation of the electrical and magnetic properties was given in terms of the features of Dy 3+ –O 2– –Fe 3+ dysprosium–oxygen–iron indirect exchange. The occurrence of the intensive changes in amplitude–frequency characteristics was observed from 1.6 to 2.7 GHz. The explanation of electromagnetic absorption was given in terms of the peculiarities of the microstructure (resonance of domain boundaries). The results open perspectives in the utilization of [Ni 0.4 Cu 0.2 Zn 0.4 ](Fe 2– x Dy x )O 4 spinel ferrite nanoparticles as functional materials for targeted drug delivery and hyperthermia applications.

This paper reports the influence of dysprosium ion (Dy3+) substitution on the structural and magnetic properties of NiDyxFe2−xO4 (0.0 ≤ x ≤ 0.1) nanoparticles (NPs) prepared using a hydrothermal method. The structure and morphology of the as-synthesized NPs were characterized via X-ray diffraction (XRD), scanning and transmission electron microscope (SEM, and TEM) analyses. 57Fe Mössbauer spectra were recorded to determine the Dy3+ content dependent variation in the line width, isomer shift, quadrupole splitting, and hyperfine magnetic fields. Furthermore, the magnetic properties of the prepared NPs were also investigated by zero-field cooled (ZFC) and field cooled (FC) magnetizations and AC susceptibility measurements. The MZFC (T) results showed a blocking temperature (TB). Below TB, the products behave as ferromagnetic (FM) and act superparamagnetic (SPM) above TB. The MFC (T) curves indicated the existence of super-spin glass (SSG) behavior below Ts (spin-glass freezing temperature). The AC susceptibility measurements confirmed the existence of the two transition temperatures (i.e., TB and Ts). Numerous models, e.g., Neel–Arrhenius (N–A), Vogel–Fulcher (V–F), and critical slowing down (CSD), were used to investigate the dynamics of the systems. It was found that the Dy substitution enhanced the magnetic interactions.

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