The current applications of nano and biomaterials in drug delivery of dental implant.

BACKGROUND AND AIM: Dental implantology has revolutionized oral rehabilitation, offering a sophisticated solution for restoring missing teeth. Despite advancements, issues like infection, inflammation, and osseointegration persist. Nano and biomaterials, with their unique properties, present promising opportunities for enhancing dental implant therapies by improving drug delivery systems. This review discussed the current applications of nano and biomaterials in drug delivery for dental implants. METHOD: A literature review examined recent studies and advancements in nano and biomaterials for drug delivery in dental implantology. Various materials, including nanoparticles, biocompatible polymers, and bioactive coatings, were reviewed for their efficacy in controlled drug release, antimicrobial properties, and promotion of osseointegration. RESULTS: Nano and biomaterials exhibit considerable potential in improving drug delivery for dental implants. Nanostructured drug carriers demonstrate enhanced therapeutic efficacy, sustained release profiles, and improved biocompatibility. Furthermore, bioactive coatings contribute to better osseointegration and reduced risks of infections. CONCLUSION: Integrating current nano and biomaterials in drug delivery for dental implants holds promise for advancing clinical outcomes. Enhanced drug delivery systems can mitigate complications associated with dental implant procedures, offering improved infection control, reduced inflammation, and optimized osseointegration.

Shear Bond Strength of Zirconia Ceramic to Four Different Core Materials, An in vitro Study.

STATEMENT OF THE PROBLEM: Different materials can be used to reconstruct the core foundation in all-ceramic restorations. Bond strength of the core material to zirconia is an important factor in long-term restoration success. PURPOSE: The aim of this study was to assess shear bond strength (SBS) of zirconia to four different core materials. MATERIALS AND METHOD: In this experimental in vitro study, 40 zirconia ceramic disks (10×3 mm) were prepared and divided to four groups based on core material. Cylinder shaped core specimens (3×4 mm) of non-precious gold alloy (NPG), zirconia ceramic, natural dentin, and composite resin were prepared and bonded perpendicularly to the zirconia disks using Gillmore Needle Apparatus and dual cure resin cement. All samples were thermocycled for 2000 cycles. To evaluate SBS, the specimens were tested by universal testing machine. Data were analyzed using Kruskal-Wallis test followed by Dunn's test with Bonferroni correction. Statistical significance was set at p< 0.05. RESULTS: The highest values for SBS were achieved in composite resin group (11.58±1.74 MPa) followed by NPG (10.32±0.94 MPa), zirconia (7.3±1.11 MPa) and dentin group (6.53±0.56 MPa). SBS in composite resin and NPG core materials were significantly higher than other core materials (p< 0.05). CONCLUSION: Composite resin and NPG cores showed significant higher bond strength to zirconia in comparison to dentine and zirconia core materials.

A comparison between neurally induced bone marrow derived mesenchymal stem cells and olfactory ensheathing glial cells to repair spinal cord injuries in rat.

Cell therapy has proven to be a highly promising method in clinical applications, raising so much hope for the treatment of injured tissues with low, if any, self regeneration potential such as central and peripheral nervous system. Neurally induced bone marrow derived mesenchymal stem cells (NIMSCs) as well as olfactory ensheathing cells (OECs) were transplanted in a rat model of sub-acute spinal cord injury and the behavioral and histological analyses were conducted. A balloon-compression technique was used to produce an injury at T8-T9 level of spinal cord. After a week post injury, rats were injected with either NIMSCs or OECs at the center of developing lesion cavity, 3mm cranial and 3mm caudal to the cavity. Weekly behavioral assessment using BBB score was done over five-week period post transplantation and finally histological assessment was performed to locate labeled cells in the tissue in order to evaluate the reduction of cavity formation and axonal regeneration. Evaluation of locomotor performance showed significant behavioral improvement in NIMSC group over OEC and control groups. The histological analyses revealed the presence of transplanted cells in the spinal cord parenchyma. Volume of injured area that was occupied with syrinx cavity in NIMSC group was significantly less than control group. In addition, meanwhile neurofilament-positive axons significantly showed higher expression in rats receiving NIMSC compared to the other two groups. In conclusion NIMSC caused both behavioral and histological improvement that potentially makes them a promising candidate for cell therapy approaches of spinal cord injuries.