Literature DB >> 21803415

Comparison of polymer scaffolds in rat spinal cord: a step toward quantitative assessment of combinatorial approaches to spinal cord repair.

Bingkun K Chen1, Andrew M Knight, Nicolas N Madigan, LouAnn Gross, Mahrokh Dadsetan, Jarred J Nesbitt, Gemma E Rooney, Bradford L Currier, Michael J Yaszemski, Robert J Spinner, Anthony J Windebank.   

Abstract

The transected rat thoracic (T(9/10)) spinal cord model is a platform for quantitatively comparing biodegradable polymer scaffolds. Schwann cell-loaded scaffolds constructed from poly (lactic co-glycolic acid) (PLGA), poly(ɛ-caprolactone fumarate) (PCLF), oligo(polyethylene glycol) fumarate (OPF) hydrogel or positively charged OPF (OPF+) hydrogel were implanted into the model. We demonstrated that the mechanical properties (3-point bending and stiffness) of OPF and OPF + hydrogels closely resembled rat spinal cord. After one month, tissues were harvested and analyzed by morphometry of neurofilament-stained sections at rostral, midlevel, and caudal scaffold. All polymers supported axonal growth. Significantly higher numbers of axons were found in PCLF (P < 0.01) and OPF+ (P < 0.05) groups, compared to that of the PLGA group. OPF + polymers showed more centrally distributed axonal regeneration within the channels while other polymers (PLGA, PCLF and OPF) tended to show more evenly dispersed axons within the channels. The centralized distribution was associated with significantly more axons regenerating (P < 0.05). Volume of scar and cyst rostral and caudal to the implanted scaffold was measured and compared. There were significantly smaller cyst volumes in PLGA compared to PCLF groups. The model provides a quantitative basis for assessing individual and combined tissue engineering strategies.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21803415      PMCID: PMC3163757          DOI: 10.1016/j.biomaterials.2011.07.029

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  73 in total

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Journal:  J Neurotrauma       Date:  2004-06       Impact factor: 5.269

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  21 in total

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2.  Combinatorial tissue engineering partially restores function after spinal cord injury.

Authors:  Jeffrey S Hakim; Brian R Rodysill; Bingkun K Chen; Ann M Schmeichel; Michael J Yaszemski; Anthony J Windebank; Nicolas N Madigan
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3.  Long-term characterization of axon regeneration and matrix changes using multiple channel bridges for spinal cord regeneration.

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4.  Comparison of cellular architecture, axonal growth, and blood vessel formation through cell-loaded polymer scaffolds in the transected rat spinal cord.

Authors:  Nicolas N Madigan; Bingkun K Chen; Andrew M Knight; Gemma E Rooney; Eva Sweeney; Lisa Kinnavane; Michael J Yaszemski; Peter Dockery; Timothy O'Brien; Siobhan S McMahon; Anthony J Windebank
Journal:  Tissue Eng Part A       Date:  2014-08-11       Impact factor: 3.845

5.  Implantation of cauda equina nerve roots through a biodegradable scaffold at the conus medullaris in rat.

Authors:  Peter J Grahn; Sandeep Vaishya; Andrew M Knight; Bingkun K Chen; Ann M Schmeichel; Bradford L Currier; Robert J Spinner; Michael J Yaszemski; Anthony J Windebank
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6.  Tunable tissue scaffolds fabricated by in situ crosslink in phase separation system.

Authors:  Xifeng Liu; Wenjian Chen; Carl T Gustafson; A Lee Miller; Brian E Waletzki; Michael J Yaszemski; Lichun Lu
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Review 7.  Combination therapies in the CNS: engineering the environment.

Authors:  Dylan A McCreedy; Shelly E Sakiyama-Elbert
Journal:  Neurosci Lett       Date:  2012-02-17       Impact factor: 3.046

8.  Positively Charged Oligo[Poly(Ethylene Glycol) Fumarate] Scaffold Implantation Results in a Permissive Lesion Environment after Spinal Cord Injury in Rat.

Authors:  Jeffrey S Hakim; Melika Esmaeili Rad; Peter J Grahn; Bingkun K Chen; Andrew M Knight; Ann M Schmeichel; Nasro A Isaq; Mahrokh Dadsetan; Michael J Yaszemski; Anthony J Windebank
Journal:  Tissue Eng Part A       Date:  2015-07       Impact factor: 3.845

Review 9.  Non-viral gene therapy for spinal cord regeneration.

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10.  Hemisection spinal cord injury in rat: the value of intraoperative somatosensory evoked potential monitoring.

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