Surface‐modified functionalized polycaprolactone scaffolds for bone repair: In vitro and in vivo experiments. Issue 9 (7th October 2013)
- Record Type:
- Journal Article
- Title:
- Surface‐modified functionalized polycaprolactone scaffolds for bone repair: In vitro and in vivo experiments. Issue 9 (7th October 2013)
- Main Title:
- Surface‐modified functionalized polycaprolactone scaffolds for bone repair: In vitro and in vivo experiments
- Authors:
- Jensen, Jonas
Rölfing, Jan Hendrik Duedal
Svend Le, Dang Quang
Kristiansen, Asger Albæk
Nygaard, Jens Vinge
Hokland, Lea Bjerre
Bendtsen, Michael
Kassem, Moustapha
Lysdahl, Helle
Bünger, Cody Eric - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <p>A porcine calvaria defect study was carried out to investigate the bone repair potential of three‐dimensional (3D)‐printed poly‐ε‐caprolactone (PCL) scaffolds embedded with nanoporous PCL. A microscopic grid network was created by rapid prototyping making a 3D‐fused deposition model (FDM‐PCL). Afterward, the FDM‐PCL scaffolds were infused with a mixture of PCL, water, and 1, 4‐dioxane and underwent a thermal‐induced phase separation (TIPS) followed by lyophilization. The TIPS process lead to a nanoporous structure shielded by the printed microstructure (NSP‐PCL). Sixteen Landrace pigs were divided into two groups with 8 and 12 weeks follow‐up, respectively. A total of six nonpenetrating holes were drilled in the calvaria of each animal. The size of the cylindrical defects was <italic>h</italic> 10 mm and Ø 10 mm. The defects were distributed randomly using following groups: (a) NSP‐PCL scaffold, (b) FDM‐PCL scaffold, (c) autograft, (d) empty defect, (a1) NSP‐PCL scaffold + autologous mononuclear cells, and (a2) NSP‐PCL scaffold + bone morphogenetic protein 2. Bone volume to total volume was analyzed using microcomputed tomography (µCT) and histomorphometry. The µCT and histological data showed significantly less bone formation in the NSP‐PCL scaffolds in all three variations after both 8 and 12 weeks compared to all other groups. The positive autograft control had significantly higher new bone formation compared to<abstract abstract-type="main"> <title>Abstract</title> <p>A porcine calvaria defect study was carried out to investigate the bone repair potential of three‐dimensional (3D)‐printed poly‐ε‐caprolactone (PCL) scaffolds embedded with nanoporous PCL. A microscopic grid network was created by rapid prototyping making a 3D‐fused deposition model (FDM‐PCL). Afterward, the FDM‐PCL scaffolds were infused with a mixture of PCL, water, and 1, 4‐dioxane and underwent a thermal‐induced phase separation (TIPS) followed by lyophilization. The TIPS process lead to a nanoporous structure shielded by the printed microstructure (NSP‐PCL). Sixteen Landrace pigs were divided into two groups with 8 and 12 weeks follow‐up, respectively. A total of six nonpenetrating holes were drilled in the calvaria of each animal. The size of the cylindrical defects was <italic>h</italic> 10 mm and Ø 10 mm. The defects were distributed randomly using following groups: (a) NSP‐PCL scaffold, (b) FDM‐PCL scaffold, (c) autograft, (d) empty defect, (a1) NSP‐PCL scaffold + autologous mononuclear cells, and (a2) NSP‐PCL scaffold + bone morphogenetic protein 2. Bone volume to total volume was analyzed using microcomputed tomography (µCT) and histomorphometry. The µCT and histological data showed significantly less bone formation in the NSP‐PCL scaffolds in all three variations after both 8 and 12 weeks compared to all other groups. The positive autograft control had significantly higher new bone formation compared to all other groups except the FDM‐PCL when analyzed using histomorphometry. The NSP‐PCL scaffolds were heavily infiltrated with foreign body giant cells suggesting an inflammatory response and perhaps active resorption of the scaffold material. The unmodified FDM‐PCL scaffold showed good osteoconductivity and osseointegration after both 8 and 12 weeks. © 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 102A: 2993–3003, 2014.</p> </abstract> … (more)
- Is Part Of:
- Journal of biomedical materials research. Volume 102:Issue 9(2014)
- Journal:
- Journal of biomedical materials research
- Issue:
- Volume 102:Issue 9(2014)
- Issue Display:
- Volume 102, Issue 9 (2014)
- Year:
- 2014
- Volume:
- 102
- Issue:
- 9
- Issue Sort Value:
- 2014-0102-0009-0000
- Page Start:
- 2993
- Page End:
- 3003
- Publication Date:
- 2013-10-07
- Subjects:
- Biomedical materials -- Periodicals
610.28 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1552-4965 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jbm.a.34970 ↗
- Languages:
- English
- ISSNs:
- 1549-3296
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4953.720000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3357.xml