TY - JOUR
T1 - In vivo degradation of 14C-labeled porcine dermis biologic scaffold
AU - Carey, Lisa E.
AU - Dearth, Christopher L.
AU - Johnson, Scott A.
AU - Londono, Ricardo
AU - Medberry, Christopher J.
AU - Daly, Kerry A.
AU - Badylak, Stephen F.
N1 - Funding Information:
Funding for this research was provided, in part, by C. R. Bard. Lisa Carey was partially supported by the NIH-NHLBI training grant ( T32-HL76124-6 ) entitled “Cardiovascular Bioengineering Training Program” through the University of Pittsburgh, Department of Bioengineering. The authors would like to thank Deanna Rhoads and Lori Perez at the McGowan Histology Center for histologic section preparation. The authors would also like to thank Tim Keane, Denver Faulk, Peter Slivka, and Eve Simpson for their assistance with animal care and manuscript preparation.
PY - 2014/9
Y1 - 2014/9
N2 - Biologic scaffold materials are used for repair and reconstruction of injured or missing tissues. Such materials are often composed of allogeneic or xenogeneic extracellular matrix (ECM) manufactured by decellularization of source tissue, such as dermis. Dermal ECM (D-ECM) has been observed to degrade and remodel invivo more slowly than other biologic scaffold materials, such as small intestinal submucosa (SIS-ECM). Histologic examination is a common method for evaluating material degradation, but it lacks sensitivity and is subject to observer bias. Utilization of 14C-proline labeled ECM is a quantitative alternative for measuring degradation of ECM scaffolds. Using both methods, the amount of degradation of D-ECM and SIS-ECM was determined at 2, 4, and 24 weeks post-implantation in a rodent model. Results utilizing 14C liquid scintillation counting (LSC) analysis showed distinct differences in degradation at the three time points. D-ECM material in situ stayed the same at 76% remaining from 2 to 4 weeks post-implantation, and then decreased to 44% remaining at 24 weeks. In the same time period, implanted SIS-ECM material decreased from 72% to 13% to 0%. Visual examination of device degradation by histology overestimated degradation at 2 weeks and underestimated device degradation at 24 weeks, compared to the 14C method.
AB - Biologic scaffold materials are used for repair and reconstruction of injured or missing tissues. Such materials are often composed of allogeneic or xenogeneic extracellular matrix (ECM) manufactured by decellularization of source tissue, such as dermis. Dermal ECM (D-ECM) has been observed to degrade and remodel invivo more slowly than other biologic scaffold materials, such as small intestinal submucosa (SIS-ECM). Histologic examination is a common method for evaluating material degradation, but it lacks sensitivity and is subject to observer bias. Utilization of 14C-proline labeled ECM is a quantitative alternative for measuring degradation of ECM scaffolds. Using both methods, the amount of degradation of D-ECM and SIS-ECM was determined at 2, 4, and 24 weeks post-implantation in a rodent model. Results utilizing 14C liquid scintillation counting (LSC) analysis showed distinct differences in degradation at the three time points. D-ECM material in situ stayed the same at 76% remaining from 2 to 4 weeks post-implantation, and then decreased to 44% remaining at 24 weeks. In the same time period, implanted SIS-ECM material decreased from 72% to 13% to 0%. Visual examination of device degradation by histology overestimated degradation at 2 weeks and underestimated device degradation at 24 weeks, compared to the 14C method.
KW - Biomaterial degradation
KW - Dermis
KW - Extracellular matrix
UR - http://www.scopus.com/inward/record.url?scp=84904110396&partnerID=8YFLogxK
U2 - 10.1016/j.biomaterials.2014.06.015
DO - 10.1016/j.biomaterials.2014.06.015
M3 - Article
C2 - 24997479
AN - SCOPUS:84904110396
SN - 0142-9612
VL - 35
SP - 8297
EP - 8304
JO - Biomaterials
JF - Biomaterials
IS - 29
ER -