Browsing by Subject "fracture toughness"

Now showing 1 - 3 of 3
  • Thumbnail Image
    Item
    The fracture toughness of small animal cortical bone measured using arc-shaped tension specimens: Effects of bisphosphonate and deproteinization treatments
    (Elsevier, 2017-12) Hunckler, Michael D.; Chu, Ethan D.; Baumann, Andrew P.; Curtis, Tyler E.; Ravosa, Matthew J.; Allen, Matthew R.; Roeder, Ryan K.; Department of Anatomy and Cell Biology, School of Medicine
    Small animal models, and especially transgenic models, have become widespread in the study of bone mechanobiology and metabolic bone disease, but test methods for measuring fracture toughness on multiple replicates or at multiple locations within a single small animal bone are lacking. Therefore, the objective of this study was to develop a method to measure cortical bone fracture toughness in multiple specimens and locations along the diaphysis of small animal bones. Arc-shaped tension specimens were prepared from the mid-diaphysis of rabbit ulnae and loaded to failure to measure the radial fracture toughness in multiple replicates per bone. The test specimen dimensions, crack length, and maximum load met requirements for measuring the plane strain fracture toughness. Experimental groups included a control group, bisphosphonate treatment group, and an ex vivo deproteinization treatment following bisphosphonate treatment (5 rabbits/group and 15 specimens/group). The fracture toughness of ulnar cortical bone from rabbits treated with zoledronic acid for six months exhibited no difference compared with the control group. Partially deproteinized specimens exhibited significantly lower fracture toughness compared with both the control and bisphosphonate treatment groups. The deproteinization treatment increased tissue mineral density (TMD) and resulted in a negative linear correlation between the measured fracture toughness and TMD. Fracture toughness measurements were repeatable with a coefficient of variation of 12–16% within experimental groups. Retrospective power analysis of the control and deproteinization treatment groups indicated a minimum detectable difference of 0.1 MPa·m1/2. Therefore, the overall results of this study suggest that arc-shaped tension specimens offer an advantageous new method for measuring the fracture toughness in small animal bones.
  • Thumbnail Image
    Item
    Physicomechanical properties of a zinc-reinforced glass ionomer restorative material
    (2014) Al-Angari, Sarah S.; Hara, Anderson T.; Chu, Tien-Min; Platt, Jeffrey; Eckert, George; Cook, N. Blaine; Department of Restorative Dentistry, School of Dentistry
    We compared a zinc-reinforced glass ionomer restorative material (ChemFil Rock) with three commercially available glass ionomer cements (GICs), namely, Fuji IX GP Extra, Ketac Molar Quick Aplicap, and EQUIA Fil, with respect to fracture toughness, microhardness, roughness, and abrasive wear. Fracture toughness (KIC) was tested according to ISO 13586 (n = 10). Hardness, roughness, and abrasive wear were also tested (n = 9). Data were analyzed using the Wilcoxon rank-sum test with adjustment for multiple comparisons (α = 0.05). As compared with the other GICs ChemFil Rock exhibited a greater increase in surface roughness (P < 0.05) and lower microhardness (P < 0.01). The wear resistance of ChemFil Rock was comparable to that of the other GICs (P > 0.05). ChemFil Rock had significantly lower fracture toughness as compared with EQUIA Fil (P = 0.01) and significantly higher fracture toughness as compared with the other GICs (P < 0.02). In conclusion, as compared with the three other commercially available GICs, ChemFil Rock had intermediate fracture toughness, the lowest microhardness, and the greatest change in surface roughness.
  • Thumbnail Image
    Item
    Thermoneutral Housing Did Not Impact the Combined Effects of External Loading and Raloxifene on Bone Morphology and Mechanical Properties in Growing Female Mice
    (2020-12) Tastad, Carli A.; Wallace, Joseph M.; Allen, Matthew R.; Li, Jiliang
    Raloxifene is an FDA-approved selective estrogen receptor modulator (SERM) that improves tissue quality by binding to collagen and increasing the bound water content in the bone matrix in a cell-independent manner. In this thesis, active tissue formation was induced by non-invasive external tibial loading in female mice and combined with raloxifene treatment to assess their combined effect on bone morphology and mechanical properties. Thermoregulation is an important factor that could have physiological consequences on research outcomes, and was introduced as an additional experimental factor in this study. We hypothesized that by removing the mild cold stress under which normal lab animals are housed, a metabolic boost would allow for further architectural and mechanical improvements as a result of the combination of tibial loading and raloxifene treatment. Ten week old female C57BL/6J mice were treated with raloxifene, underwent tibial loading to a strain level of 2050µε and were housed in thermoneutral conditions (32°C) for 6 weeks. We investigated bone morphology through microcomputed tomography (µCT) and mechanical properties via four-point bending and fracture toughness testing. Results indicated a combined improvement by external loading and raloxifene on geometry, particularly in the cancellous region of the bone, and also in bone mechanics leading to greater improvements than either treatment individually. Temperature did not have a robust impact on either bone architecture or mechanical integrity.