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Article

Dual-Component Gelatinous Peptide/Reactive Oligomer Formulations as Conduit Material and Luminal Filler for Peripheral Nerve Regeneration

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Institute of Pharmacy, Pharmaceutical Technology, Leipzig University, 04317 Leipzig, Germany
2
Collaborative Research Center (SFB-TR67), Matrixengineering Leipzig and Dresden, Germany
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New Jersey Center for Biomaterials, Rutgers, The State University of New Jersey, Piscataway, NJ 08854-8066, USA
4
Boston University School of Medicine, Boston University, Boston, MA 02118, USA
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Department of Dermatology, Venereology and Allergology of Medical Faculty of Leipzig University, 04317 Leipzig, Germany
*
Authors to whom correspondence should be addressed.
Academic Editor: Xiaofeng Jia
Int. J. Mol. Sci. 2017, 18(5), 1104; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18051104
Received: 3 March 2017 / Revised: 9 May 2017 / Accepted: 17 May 2017 / Published: 21 May 2017
(This article belongs to the Special Issue Peripheral Nerve Regeneration: From Bench to Bedside 2017)
Toward the next generation of nerve guidance conduits (NGCs), novel biomaterials and functionalization concepts are required to address clinical demands in peripheral nerve regeneration (PNR). As a biological polymer with bioactive motifs, gelatinous peptides are promising building blocks. In combination with an anhydride-containing oligomer, a dual-component hydrogel system (cGEL) was established. First, hollow cGEL tubes were fabricated by a continuous dosing and templating process. Conduits were characterized concerning their mechanical strength, in vitro and in vivo degradation and biocompatibility. Second, cGEL was reformulated as injectable shear thinning filler for established NGCs, here tyrosine-derived polycarbonate-based braided conduits. Thereby, the formulation contained the small molecule LM11A-31. The biofunctionalized cGEL filler was assessed regarding building block integration, mechanical properties, in vitro cytotoxicity, and growth permissive effects on human adipose tissue-derived stem cells. A positive in vitro evaluation motivated further application of the filler material in a sciatic nerve defect. Compared to the empty conduit and pristine cGEL, the functionalization performed superior, though the autologous nerve graft remains the gold standard. In conclusion, LM11A-31 functionalized cGEL filler with extracellular matrix (ECM)-like characteristics and specific biochemical cues holds great potential to support PNR. View Full-Text
Keywords: cross-linked gelatin; nerve regeneration; filler; maleic anhydride; oligomer; bioconjugation; LM11A-31; shear thinning; injectable hydrogel; human adipose-tissue derived stem cells cross-linked gelatin; nerve regeneration; filler; maleic anhydride; oligomer; bioconjugation; LM11A-31; shear thinning; injectable hydrogel; human adipose-tissue derived stem cells
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MDPI and ACS Style

Kohn-Polster, C.; Bhatnagar, D.; Woloszyn, D.J.; Richtmyer, M.; Starke, A.; Springwald, A.H.; Franz, S.; Schulz-Siegmund, M.; Kaplan, H.M.; Kohn, J.; Hacker, M.C. Dual-Component Gelatinous Peptide/Reactive Oligomer Formulations as Conduit Material and Luminal Filler for Peripheral Nerve Regeneration. Int. J. Mol. Sci. 2017, 18, 1104. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18051104

AMA Style

Kohn-Polster C, Bhatnagar D, Woloszyn DJ, Richtmyer M, Starke A, Springwald AH, Franz S, Schulz-Siegmund M, Kaplan HM, Kohn J, Hacker MC. Dual-Component Gelatinous Peptide/Reactive Oligomer Formulations as Conduit Material and Luminal Filler for Peripheral Nerve Regeneration. International Journal of Molecular Sciences. 2017; 18(5):1104. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18051104

Chicago/Turabian Style

Kohn-Polster, Caroline, Divya Bhatnagar, Derek J. Woloszyn, Matthew Richtmyer, Annett Starke, Alexandra H. Springwald, Sandra Franz, Michaela Schulz-Siegmund, Hilton M. Kaplan, Joachim Kohn, and Michael C. Hacker 2017. "Dual-Component Gelatinous Peptide/Reactive Oligomer Formulations as Conduit Material and Luminal Filler for Peripheral Nerve Regeneration" International Journal of Molecular Sciences 18, no. 5: 1104. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18051104

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