A 3D-printed bioactive polycaprolactone scaffold assembled with core/shell microspheres as a sustained BMP2-releasing system for bone repair

Author(s):  
Weida Zhuang ◽  
Genlan Ye ◽  
Jiachang Wu ◽  
Leyu Wang ◽  
Guofan Fang ◽  
...  
Keyword(s):  
Author(s):  
Toshiyuki Kawai ◽  
Chi-chun Pan ◽  
Yaichiro Okuzu ◽  
Takayoshi Shimizu ◽  
Alexander Stahl ◽  
...  

2019 ◽  
Vol 84 ◽  
pp. 16-33 ◽  
Author(s):  
Lei Zhang ◽  
Guojing Yang ◽  
Blake N. Johnson ◽  
Xiaofeng Jia

2017 ◽  
Vol 214 (6) ◽  
pp. 1600887
Author(s):  
Waqas Amin Gill ◽  
Boo Hyun An ◽  
Ji Sung Lee ◽  
Dima Ali ◽  
Malathe Samir Khalil ◽  
...  

2020 ◽  
Vol 396 ◽  
pp. 125081 ◽  
Author(s):  
Hui Wang ◽  
Xiangqiong Zeng ◽  
Libin Pang ◽  
Haihang Wang ◽  
Bocai Lin ◽  
...  

2019 ◽  
Vol 22 (4) ◽  
pp. 1901065 ◽  
Author(s):  
Xibao Chen ◽  
Gang Chen ◽  
Gang Wang ◽  
Peizhi Zhu ◽  
Chunxia Gao

RSC Advances ◽  
2015 ◽  
Vol 5 (37) ◽  
pp. 29335-29345 ◽  
Author(s):  
KyoungHo Lee ◽  
Cho-Rong Seo ◽  
Jin-Mo Ku ◽  
Hyeongjin Lee ◽  
Hyeon Yoon ◽  
...  

A new composite scaffold consisting of poly(ε-caprolactone), alginate, and phenamil was manufactured by a combined process, 3D-printing and coating process, for hard tissue regeneration.


Author(s):  
Kenny Man ◽  
Mathieu Y. Brunet ◽  
Sophie Louth ◽  
Thomas E. Robinson ◽  
Maria Fernandez-Rhodes ◽  
...  

Extracellular Vesicles (EVs) are considered promising nanoscale therapeutics for bone regeneration. To date, EVs are typically procured from cells on 2D tissue culture plastic, an artificial environment that limits cell growth and does not replicate in situ biochemical or biophysical conditions. This study investigated the potential of 3D printed titanium scaffolds coated with hydroxyapatite to promote the therapeutic efficacy of osteoblast-derived EVs. Ti6Al4V titanium scaffolds with different pore sizes (500 and 1000 µm) and shapes (square and triangle) were fabricated by selective laser melting. A bone-mimetic nano-needle hydroxyapatite (nnHA) coating was then applied. EVs were procured from scaffold-cultured osteoblasts over 2 weeks and vesicle concentration was determined using the CD63 ELISA. Osteogenic differentiation of human bone marrow stromal cells (hBMSCs) following treatment with primed EVs was evaluated by assessing alkaline phosphatase activity, collagen production and calcium deposition. Triangle pore scaffolds significantly increased osteoblast mineralisation (1.5-fold) when compared to square architectures (P ≤ 0.001). Interestingly, EV yield was also significantly enhanced on these higher permeability structures (P ≤ 0.001), in particular (2.2-fold) for the larger pore structures (1000 µm). Furthermore osteoblast-derived EVs isolated from triangular pore scaffolds significantly increased hBMSCs mineralisation when compared to EVs acquired from square pore scaffolds (1.7-fold) and 2D culture (2.2-fold) (P ≤ 0.001). Coating with nnHA significantly improved osteoblast mineralisation (>2.6-fold) and EV production (4.5-fold) when compared to uncoated scaffolds (P ≤ 0.001). Together, these findings demonstrate the potential of harnessing bone-mimetic culture platforms to enhance the production of pro-regenerative EVs as an acellular tool for bone repair.


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