Page 199 - Biodegradable Polyesters
P. 199

7.4  Applications  177





                   [40]     [158]     [47]         [159]     [160]

                   the  their  at  and  the        and
                   of           relation  at  the  spinal  that  with  greater
                   range  scaffolds  suggesting  number  in  modify  animal  supports  at  significantly  elongation,  showed  electrophysiological  fibers  scaffolds  were  regeneration

                   the          fibrosis  can  In  hemisection  graft  material
                   in  the addition,  lineage,  differentiation  macrophage  scaffolds  vitro.  in  scaffold  the  were  adhesion,  rats,  adult  the addition,  rate  PCL  scaffolds  nerve
                   (53.67 ± 3.48 MPa),  In  epidermal  regional  and  epidural  reduced  PLCL  that  cells  nerve  lateral complete  the  that  enter  to  seen  animals  grafted  cell  in  gap  nerve  similar achieving  In autografts.  regeneration  with compared  p-PCL (p-PCL).  cost-effective  a  is  peripheral  for







                   modulus  (15–150 MPa).  the  along  without The nanofibers were applied in animal models of spinal cord injury. The animals that  proliferation  more  a  indicate limit the scar formation and epidural fibrosis in spinal cord, preventing cicatrization  of growth  the  with  rats  demonstrated  were  axons  of  scores  Schwann  the  sciatic  regeneration,  as  such


                   elastic  skin  human  MSCs  of  regeneration  fibroblast  less  exhibited  results  initial  support  to  applied  findings  regenerating  sensory  vitro  in  8 mm  with  results,  matched  well  plasma  p-PCL  scaffolds,

                   showed  native  differentiation  skin  in  showed  animals  The  to  able  were  Histological  and  and  group  sustained  tests,  nerve  which  collagen/PCL  by  the  on  PCL/collagen

                   scaffolds  of modulus  the  application  scaffolds  These  site.  group.  were  scaffolds  level.  regeneration  Locomotor  control  the  fibers  vivo  In  supported  re-enervation  degraded,  with  made  modified  morphology  to


                   Coll/PLCL  elastic  supported  potential  received  injury  the  control  the  to  scaffolds  The  the  models,  T9–T10  axonal  sites.  injury  than  better  Collagen/PCL  proliferation.  scaffolds  the  muscle  and  gradually  Scaffolds  surface  their  normal  compared







                   and                             blend
                   collagen  (70 : 30)                       collagen/PCL  BMP-2, bone morphogenetic protein 2 and DBPs, demineralized bone powders.


                   of  poly(L-lactide-co-  caprolactone)  (Coll/PLACL)  Collagen/PCL  and
                   Blend    PLACL     PLGA                   PCL  blend



                   regeneration  cord              nerve




                   Skin     Spinal  regeneration   Peripheral  grafts
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