Department of Bioengineering, Karamanoglu Mehmetbey University, Karaman, 70200, Turkey
bDepartment of Biophysics, Faculty of Medicine, Karamanoglu Mehmetbey University, Karaman, 70200, Turkey
cDepartment of Orthopaedic Surgery, Vanderbilt University Medical Center, 1215 21st Ave. S, Suite 4200, Nashville, TN, 37232, USA
dVanderbilt Center for Bone Biology, Vanderbilt University Medical Center, 2215B Garland Ave, Nashville, TN, 37212, USA
eBiomedical Engineering Program, Systems Design Engineering, University of Waterloo, Waterloo, Ontario, Canada
fVanderbilt Center for Musculoskeletal Research, Vanderbilt University Medical Center, 2525 West End Avenue, Suite 1200, Nashville, TN, 37203, USA
gVanderbilt Center for Matrix Biology, Vanderbilt University Medical Center, 1611 21st Ave. S, Nashville, TN, 37212, USA
hDepartment of Veterans Affairs, Tennessee Valley Healthcare System, 1310 24th Ave. S, Nashville, TN, 37212, USA
iVanderbilt Center for Musculoskeletal Research, Vanderbilt University Medical Center, 2525 West End Avenue, Suite 1200, Nashville, TN, 37203, USA. Electronic address: jeffry.s.nyman@vumc.org
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Abstract
Raman spectroscopy (RS) is sensitive to the accumulation of glycation end-products (AGEs), and it measures matrix-sensitive properties that correlate with the fracture toughness of human cortical bone. However, it is unclear whether sugar-mediated accumulation of AGEs affects the fracture toughness of human cortical bone in a manner that is consistent with the negative correlations between amide I sub-peak ratios and fracture toughness. Upon machining 64 single-edge notched beam (SENB) specimens from cadaveric femurs (8 male and 7 female donors between 46 years and 61 years of age), pairs of SENB specimens were incubated in 15 mL of phosphate buffered saline with or without 0.1 M ribose for 4 weeks at 37 °C. After acquiring 10 Raman spectra per bone specimen (n=32 per incubation group), paired SENB specimens were loaded in three-point bending at a quasi-static or a high loading rate approximating 10−4 s−1 or 102 s−1, respectively (n=16 per incubation group per loading rate). While 2 amide I sub-peak ratios, I1670/I1640 and I1670/I1610, decreased by 3–5% with a 100% increase in AGE content, as confirmed by fluorescence measurements, the ribose incubation to accumulate AGEs in bone did not affect linear elastic (KIc) nor non-linear elastic (KJc) measurements of bone’s ability to resist crack growth. Moreover, AGE accumulation did not affect the change in these properties when the loading rate changed. Increasing the loading rate increased KIc but decreased KJc. Ribose incubation did not affect mineral-related RS properties such as mineral-to-matrix ratios, Type B carbonate substitutions, and crystallinity. It did however increase the thermal stability of demineralized bone (differential scanning calorimetry), without affecting the network connectivity of the organic matrix (i.e., maximum slope during a hydrothermal isometric tension test of demineralized bone). In conclusion, RS is sensitive to AGE accumulation via the amide I band (plus the hydroxyproline-to-proline ratio), but the increase in AGE content due to ribose incubation was not sufficient to affect the fracture toughness of human cortical bone.
TL;DRRaman spectroscopy is sensitive to AGE accumulation via the amide I band (plus the hydroxyproline-to-proline ratio), but the increase in AGE content due to ribose incubation was not sufficient to affect the fracture toughness of human cortical bone. (Semantic Scholar)