Matches in SemOpenAlex for { <https://semopenalex.org/work/W2023215998> ?p ?o ?g. }
- W2023215998 endingPage "3217" @default.
- W2023215998 startingPage "3217" @default.
- W2023215998 abstract "Promotion of peripheral nerve regeneration of a peptide compound hydrogel scaffold Guo-Jun Wei,1 Meng Yao,1 Yan-Song Wang,1 Chang-Wei Zhou,1 De-Yu Wan,1 Peng-Zhen Lei,1 Jian Wen,1 Hong-Wei Lei,2 Da-Ming Dong1 1Department of Orthopaedics, The 2nd Affiliated Hospital of Harbin Medical University, Harbin, People's Republic of China; 2Department of Rheumatology, The 2nd Affiliated Hospital of Harbin Medical University, Harbin, People's Republic of China Background: Peripheral nerve injury is a common trauma, but presents a significant challenge to the clinic. Silk-based materials have recently become an important biomaterial for tissue engineering applications due to silk’s biocompatibility and impressive mechanical and degradative properties. In the present study, a silk fibroin peptide (SF16) was designed and used as a component of the hydrogel scaffold for the repair of peripheral nerve injury. Methods: The SF16 peptide’s structure was characterized using spectrophotometry and atomic force microscopy, and the SF16 hydrogel was analyzed using scanning electron microscopy. The effects of the SF16 hydrogel on the viability and growth of live cells was first assessed in vitro, on PC12 cells. The in vivo test model involved the repair of a nerve gap with tubular nerve guides, through which it was possible to identify if the SF16 hydrogel would have the potential to enhance nerve regeneration. In this model physiological saline was set as the negative control, and collagen as the positive control. Walking track analysis and electrophysiological methods were used to evaluate the functional recovery of the nerve at 4 and 8 weeks after surgery. Results: Analysis of the SF16 peptide’s characteristics indicated that it consisted of a well-defined secondary structure and exhibited self-assembly. Results of scanning electron microscopy showed that the peptide based hydrogel may represent a porous scaffold that is viable for repair of peripheral nerve injury. Analysis of cell culture also supported that the hydrogel was an effective matrix to maintain the viability, morphology and proliferation of PC12 cells. Electrophysiology demonstrated that the use of the hydrogel scaffold (SF16 or collagen) resulted in a significant improvement in amplitude recovery in the in vivo model compared to physiological saline. Moreover, nerve cells in the SF16 hydrogel group displayed greater axon density, larger average axon diameter and thicker myelin compared to those of the group that received physiological saline. Conclusion: The SF16 hydrogel scaffold may promote excellent axonal regeneration and functional recovery after peripheral nerve injury, and the SF16 peptide may be a candidate for nerve tissue engineering applications. Keywords: peripheral nerve injury, silk fibroin, peptide, hydrogel, scaffold" @default.
- W2023215998 created "2016-06-24" @default.
- W2023215998 creator A5006402277 @default.
- W2023215998 creator A5010010207 @default.
- W2023215998 creator A5012749108 @default.
- W2023215998 creator A5015600863 @default.
- W2023215998 creator A5019745449 @default.
- W2023215998 creator A5025994085 @default.
- W2023215998 creator A5026785656 @default.
- W2023215998 creator A5048529238 @default.
- W2023215998 creator A5048912144 @default.
- W2023215998 date "2013-08-01" @default.
- W2023215998 modified "2023-10-14" @default.
- W2023215998 title "Promotion of peripheral nerve regeneration of a peptide compound hydrogel scaffold" @default.
- W2023215998 cites W1501126347 @default.
- W2023215998 cites W1968392514 @default.
- W2023215998 cites W1970787684 @default.
- W2023215998 cites W1972243157 @default.
- W2023215998 cites W1986841027 @default.
- W2023215998 cites W1988163495 @default.
- W2023215998 cites W2021550972 @default.
- W2023215998 cites W2027393834 @default.
- W2023215998 cites W2040776883 @default.
- W2023215998 cites W2047741707 @default.
- W2023215998 cites W2052068512 @default.
- W2023215998 cites W2066057481 @default.
- W2023215998 cites W2073254412 @default.
- W2023215998 cites W2077354973 @default.
- W2023215998 cites W2077386069 @default.
- W2023215998 cites W2087399647 @default.
- W2023215998 cites W2089401957 @default.
- W2023215998 cites W2097408970 @default.
- W2023215998 cites W2111699871 @default.
- W2023215998 cites W2112632147 @default.
- W2023215998 cites W2139053289 @default.
- W2023215998 cites W2325468551 @default.
- W2023215998 cites W4360630 @default.
- W2023215998 cites W8325258 @default.
- W2023215998 doi "https://doi.org/10.2147/ijn.s43681" @default.
- W2023215998 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3758218" @default.
- W2023215998 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24009419" @default.
- W2023215998 hasPublicationYear "2013" @default.
- W2023215998 type Work @default.
- W2023215998 sameAs 2023215998 @default.
- W2023215998 citedByCount "12" @default.
- W2023215998 countsByYear W20232159982014 @default.
- W2023215998 countsByYear W20232159982016 @default.
- W2023215998 countsByYear W20232159982018 @default.
- W2023215998 countsByYear W20232159982019 @default.
- W2023215998 countsByYear W20232159982020 @default.
- W2023215998 countsByYear W20232159982021 @default.
- W2023215998 countsByYear W20232159982022 @default.
- W2023215998 countsByYear W20232159982023 @default.
- W2023215998 crossrefType "journal-article" @default.
- W2023215998 hasAuthorship W2023215998A5006402277 @default.
- W2023215998 hasAuthorship W2023215998A5010010207 @default.
- W2023215998 hasAuthorship W2023215998A5012749108 @default.
- W2023215998 hasAuthorship W2023215998A5015600863 @default.
- W2023215998 hasAuthorship W2023215998A5019745449 @default.
- W2023215998 hasAuthorship W2023215998A5025994085 @default.
- W2023215998 hasAuthorship W2023215998A5026785656 @default.
- W2023215998 hasAuthorship W2023215998A5048529238 @default.
- W2023215998 hasAuthorship W2023215998A5048912144 @default.
- W2023215998 hasBestOaLocation W20232159981 @default.
- W2023215998 hasConcept C105702510 @default.
- W2023215998 hasConcept C122302759 @default.
- W2023215998 hasConcept C136229726 @default.
- W2023215998 hasConcept C159985019 @default.
- W2023215998 hasConcept C171056886 @default.
- W2023215998 hasConcept C178790620 @default.
- W2023215998 hasConcept C179253579 @default.
- W2023215998 hasConcept C185592680 @default.
- W2023215998 hasConcept C192562407 @default.
- W2023215998 hasConcept C2776880756 @default.
- W2023215998 hasConcept C2777230088 @default.
- W2023215998 hasConcept C2779281246 @default.
- W2023215998 hasConcept C2779560670 @default.
- W2023215998 hasConcept C2780431358 @default.
- W2023215998 hasConcept C2781149210 @default.
- W2023215998 hasConcept C3018498973 @default.
- W2023215998 hasConcept C55493867 @default.
- W2023215998 hasConcept C71924100 @default.
- W2023215998 hasConcept C86803240 @default.
- W2023215998 hasConcept C89429830 @default.
- W2023215998 hasConcept C95444343 @default.
- W2023215998 hasConceptScore W2023215998C105702510 @default.
- W2023215998 hasConceptScore W2023215998C122302759 @default.
- W2023215998 hasConceptScore W2023215998C136229726 @default.
- W2023215998 hasConceptScore W2023215998C159985019 @default.
- W2023215998 hasConceptScore W2023215998C171056886 @default.
- W2023215998 hasConceptScore W2023215998C178790620 @default.
- W2023215998 hasConceptScore W2023215998C179253579 @default.
- W2023215998 hasConceptScore W2023215998C185592680 @default.
- W2023215998 hasConceptScore W2023215998C192562407 @default.
- W2023215998 hasConceptScore W2023215998C2776880756 @default.
- W2023215998 hasConceptScore W2023215998C2777230088 @default.
- W2023215998 hasConceptScore W2023215998C2779281246 @default.
- W2023215998 hasConceptScore W2023215998C2779560670 @default.