TY - GEN
T1 - Electroactive, multi-component scaffolds for skeletal muscle regeneration
AU - McKeon-Fischer, K. D.
AU - Flagg, D. H.
AU - Rossmeisl, J. H.
AU - Whittington, A. R.
AU - Freeman, J. W.
PY - 2013
Y1 - 2013
N2 - After loss of skeletal muscle function due to traumatic injuries, muscle healing may result in scar tissue formation and reduced function. A restoration method is needed to create a bioartificial muscle that supports cell growth. An electroactive, coaxial electrospun scaffold was created using PCL, MWCNT, and a PAA/PVA hydrogel. This scaffold was conductive and displayed an actuation response when electrically stimulated. Rat primary skeletal muscle cells were biocompatible with the scaffold and displayed multi-nucleated constructs with actin interaction. MWCNT toxicity was tested using a single exposure method on rat primary skeletal muscle cells. A decrease in cellular activity was found on day 14, but a recovering trend was observed on days 21 and 28. Scaffolds were implanted in the quadriceps muscle of rats for in vivo biocompatibility investigation. Muscle cells were found to have attached and infiltrated the PCL-MWCNT-PAA/PVA scaffolds over the 28 day period. Further development of this scaffold would lead to a viable option for a bioartificial muscle as it is biocompatible and may provide some functional movement to the patient.
AB - After loss of skeletal muscle function due to traumatic injuries, muscle healing may result in scar tissue formation and reduced function. A restoration method is needed to create a bioartificial muscle that supports cell growth. An electroactive, coaxial electrospun scaffold was created using PCL, MWCNT, and a PAA/PVA hydrogel. This scaffold was conductive and displayed an actuation response when electrically stimulated. Rat primary skeletal muscle cells were biocompatible with the scaffold and displayed multi-nucleated constructs with actin interaction. MWCNT toxicity was tested using a single exposure method on rat primary skeletal muscle cells. A decrease in cellular activity was found on day 14, but a recovering trend was observed on days 21 and 28. Scaffolds were implanted in the quadriceps muscle of rats for in vivo biocompatibility investigation. Muscle cells were found to have attached and infiltrated the PCL-MWCNT-PAA/PVA scaffolds over the 28 day period. Further development of this scaffold would lead to a viable option for a bioartificial muscle as it is biocompatible and may provide some functional movement to the patient.
UR - http://www.scopus.com/inward/record.url?scp=84890034637&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84890034637&partnerID=8YFLogxK
U2 - 10.1115/NEMB2013-93197
DO - 10.1115/NEMB2013-93197
M3 - Conference contribution
AN - SCOPUS:84890034637
SN - 9780791845332
T3 - ASME 2013 2nd Global Congress on NanoEngineering for Medicine and Biology, NEMB 2013
BT - ASME 2013 2nd Global Congress on NanoEngineering for Medicine and Biology, NEMB 2013
T2 - ASME 2013 2nd Global Congress on NanoEngineering for Medicine and Biology, NEMB 2013
Y2 - 4 February 2013 through 6 February 2013
ER -