The effect of platelet-rich plasma on healing in critical-size long-bone defects

Biomaterials ◽  
2008 ◽  
Vol 29 (29) ◽  
pp. 3983-3992 ◽  
Author(s):  
Philip Kasten ◽  
Julia Vogel ◽  
Florian Geiger ◽  
Philipp Niemeyer ◽  
Reto Luginbühl ◽  
...  
2009 ◽  
Vol 20 (1) ◽  
pp. 34-40 ◽  
Author(s):  
Kemal Findikcioglu ◽  
Fulya Findikcioglu ◽  
Reha Yavuzer ◽  
Cigdem Elmas ◽  
Kenan Atabay

Cytotherapy ◽  
2018 ◽  
Vol 20 (5) ◽  
pp. S14
Author(s):  
G. Nilsson Hall ◽  
L. Mendes ◽  
L. Geris ◽  
I. Papantoniou ◽  
F. Luyten

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Wai Long Tam ◽  
Luís Freitas Mendes ◽  
Xike Chen ◽  
Raphaëlle Lesage ◽  
Inge Van Hoven ◽  
...  

Abstract Background Bones have a remarkable capacity to heal upon fracture. Yet, in large defects or compromised conditions healing processes become impaired, resulting in delayed or non-union. Current therapeutic approaches often utilize autologous or allogeneic bone grafts for bone augmentation. However, limited availability of these tissues and lack of predictive biological response result in limitations for clinical demands. Tissue engineering using viable cell-based implants is a strategic approach to address these unmet medical needs. Methods Herein, the in vitro and in vivo cartilage and bone tissue formation potencies of human pluripotent stem cells were investigated. The induced pluripotent stem cells were specified towards the mesodermal lineage and differentiated towards chondrocytes, which subsequently self-assembled into cartilaginous organoids. The tissue formation capacity of these organoids was then challenged in an ectopic and orthotopic bone formation model. Results The derived chondrocytes expressed similar levels of collagen type II as primary human articular chondrocytes and produced stable cartilage when implanted ectopically in vivo. Upon targeted promotion towards hypertrophy and priming with a proinflammatory mediator, the organoids mediated successful bridging of critical size long bone defects in immunocompromised mice. Conclusions These results highlight the promise of induced pluripotent stem cell technology for the creation of functional cartilage tissue intermediates that can be explored for novel bone healing strategies.


2019 ◽  
Vol 36 (1) ◽  
pp. 145-151 ◽  
Author(s):  
Woonhyeok Jeong ◽  
Young Seok Kim ◽  
Tai Suk Roh ◽  
Eun Hye Kang ◽  
Bok Ki Jung ◽  
...  

Bone ◽  
2011 ◽  
Vol 48 ◽  
pp. S170
Author(s):  
S. Srouji ◽  
O. Fromigué ◽  
P. Vaudin ◽  
D. Ben-David ◽  
E. Livne ◽  
...  

Injury ◽  
2010 ◽  
Vol 41 (7) ◽  
pp. 717-723 ◽  
Author(s):  
M. Hakimi ◽  
P. Jungbluth ◽  
M. Sager ◽  
M. Betsch ◽  
M. Herten ◽  
...  

2016 ◽  
Vol 27 (5) ◽  
pp. 1367-1370 ◽  
Author(s):  
Nevra Seyhan ◽  
Suat Keskin ◽  
Murat Aktan ◽  
Mustafa Cihad Avunduk ◽  
Meltem Sengelen ◽  
...  

2009 ◽  
Vol 22 (06) ◽  
pp. 460-466 ◽  
Author(s):  
J.-G. Grand ◽  
E. Dalibert ◽  
B. Fellah ◽  
O. Gauthier ◽  
G.W. Niebauer ◽  
...  

SummaryThe aim of the study was to evaluate the bone healing properties of an osteopromotive platelet rich plasma (PRP) gel in combination with osteoconductive calcium phosphate (CaP) ceramic granules in a long-bone critical size defect in dogs. A standardised 2 cm long ulnar ostectomy was performed bilaterally in four dogs to compare new-bone formation by CaP matrix with and without association with PRP. Radiographic and histological evaluations were performed blindly. Radiographic evaluation was performed at three, six, nine, 12 and 16 weeks postoperatively. Quantitative measurements of new-bone formation were compared using statistical analysis. At explantation 16 weeks after surgery, no significant ossification was present, neither with CaP granules alone nor in association with PRP gel, and there was no difference of radiodensity between the groups. Qualitative histological evaluation demonstrated for both types of implants the presence of non-mineralised fibrous connective tissue around the CaP granules. New-bone formation was only present to a very small extent within the macropores of the CaP granules at the distal boneimplant interface. In our model which exhibited very limited osteoconduction, neither the CaP granules alone nor in association with PRP were sufficient to stimulate bone healing. In this canine model employing a critical size ulnar gap, the combination of CaP granules and PRP did not effectively promote bone regeneration.


2004 ◽  
Vol 65 (12) ◽  
pp. 1653-1657 ◽  
Author(s):  
Veronique Viateau ◽  
Genevieve Guillemin ◽  
Yu Chien Yang ◽  
Wassila Bensaid ◽  
Thierry Reviron ◽  
...  

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