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1.
J Biomed Mater Res A ; 102(12): 4336-45, 2014 Dec.
Article in English | MEDLINE | ID: mdl-24497271

ABSTRACT

The physicochemical and biological properties of calcium silicate-based cement (CS) associated to microparticulated (micro) or nanoparticulated (nano) zirconium oxide (ZrO2 ) were compared with CS and bismuth oxide (BO) with CS. The pH, release of calcium ions, radiopacity, setting time, and compression strength of the materials were evaluated. The tissue reaction promoted by these materials in the subcutaneous was also investigated by morphological, immunohistochemical, and quantitative analyses. For this purpose, polyethylene tubes filled with materials were implanted into rat subcutaneous. After 7, 15, 30, and 60 days, the tubes surrounded by capsules were fixed and embedded in paraffin. In the H&E-stained sections, the number of inflammatory cells (ICs) in the capsule was obtained. Moreover, detection of interleukin-6 (IL-6) by immunohistochemistry and number of IL-6 immunolabeled cells were carried out. von Kossa method was also performed. The differences among the groups were subjected to Tukey test (p ≤ 0.05). The solutions containing the materials presented an alkaline pH and released calcium ions. The addition of radiopacifiers increased setting time and radiopacity of CS. A higher compressive strength in the CS + ZrO2 (micro and nano) was found compared with CS + BO. The number of IC and IL-6 positive cells in the materials with ZrO2 was significantly reduced in comparison with CS + BO. von Kossa-positive structures were observed adjacent to implanted materials. The ZrO2 associated to the CS provides satisfactory physicochemical properties and better biological response than BO. Thus, ZrO2 may be a good alternative for use as radiopacifying agent in substitution to BO.


Subject(s)
Bone Cements , Calcium Compounds , Materials Testing , Nanoparticles/chemistry , Silicates , Zirconium , Animals , Bone Cements/chemistry , Bone Cements/pharmacology , Calcium Compounds/chemistry , Calcium Compounds/pharmacology , Inflammation/chemically induced , Inflammation/metabolism , Inflammation/pathology , Interleukin-6/metabolism , Rats , Rats, Sprague-Dawley , Silicates/chemistry , Silicates/pharmacology , Zirconium/chemistry , Zirconium/pharmacology
2.
Lasers Med Sci ; 24(2): 195-201, 2009 Mar.
Article in English | MEDLINE | ID: mdl-18309458

ABSTRACT

The goal of this study was to analyze the role of cyclo-oxygenase-2 following bone repair in rats submitted to low-level laser therapy. A total of 48 rats underwent surgery to inflict bone defects in their tibias having been randomly distributed into two groups: negative control and laser exposed group, i.e., the animals were treated with low-level laser therapy by means of gallium arsenide laser at 16 J/cm(2). The animals were killed after 48 h, 7 days, 14 days, or 21 days. The tibias were removed for morphological, morphometric, and immunohistochemistry analysis for cyclo-oxygenase-2. Statistical significant differences (P < 0.05) were observed in the quality of bone repair and quantity of formed bone between groups 14 days after surgery in the laser exposed group. In the same way, cyclo-oxygenase-2 immunoreactivity was more intense in bone cells for intermediate periods evaluated in this group. Taken together, such results suggest that low-level laser therapy is able to improve bone repair in the tibia of rats after 14 days of surgery as a result of an up-regulation for cyclo-oxygenase-2 expression in bone cells.


Subject(s)
Cyclooxygenase 2/metabolism , Fracture Healing/radiation effects , Lasers, Semiconductor/therapeutic use , Low-Level Light Therapy , Tibial Fractures/enzymology , Tibial Fractures/radiotherapy , Animals , Disease Models, Animal , Fracture Healing/physiology , Male , Rats , Rats, Wistar , Tibial Fractures/pathology , Time Factors
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