## Abstract Standardized particulate bone constructs, obtained by expanding autologous mesenchymal stem cells (MSCs) onto coral granules in vitro, were transplanted into long‐bone, critical‐size defects in sheep. Control experiments were also performed in which autologous bone grafts were implanted
Long-bone critical-size defects treated with tissue-engineered polycaprolactone-co-lactide scaffolds: A pilot study on rats
✍ Scribed by Claudia Rentsch; Barbe Rentsch; Annette Breier; Kathrin Spekl; Roland Jung; Suzanne Manthey; Dieter Scharnweber; Hans Zwipp; Achim Biewener
- Book ID
- 102872675
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 599 KB
- Volume
- 95A
- Category
- Article
- ISSN
- 1549-3296
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✦ Synopsis
Abstract
The aim of this study was to evaluate the osteogenic potential of embroidered, tissue‐engineered polycaprolactone‐co‐lactide (trade name: PCL) scaffolds for the reconstruction of large bone defects. Ten piled‐up PCL scaffolds were implanted in femura with a critical size defect of immunodeficient nude rats for 12 weeks [n = 4, group 1: noncoated, group 2: collagen I (coll I), group 3: collagen I/chondroitin sulfate (coll I/CS), and group 4: collagen I/chondroitin sulfate/human mesenchymal stem cells (coll I/CS/hMSC)]. X‐ray examination, computer tomography, and histological analyses of the explanted scaffold pads were performed. The quantification of the bone volume ratio showed a significantly higher rate of new bone formation at coll I/CS‐coated scaffolds compared with the other groups. Histological investigations revealed that the defect reconstruction started from the peripheral bone ends and incorporated into the scaffold material. Additionally seeded hMSC on coll I/CS‐coated scaffolds showed a higher matrix deposition inside the implant but no higher bone formation was observed. These data imply that the coll I/CS‐coated PCL scaffolds have the highest potential for treating critical size defects. The scaffolds, being variable in size and structure, can be adapted to any bone defect. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2010.
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