Development of functionalized multi-walled carbon nanotube-based polysaccharide–hydroxyapatite scaffolds for bone tissue engineering

RSC Advances ◽  
2016 ◽  
Vol 6 (85) ◽  
pp. 82385-82393 ◽  
Author(s):  
R. Rajesh ◽  
Y. Dominic Ravichandran ◽  
M. Jeevan Kumar Reddy ◽  
Sung Hun Ryu ◽  
A. M. Shanmugharaj

fMWCNT–amylopectin–HAP and fMWCNT–gellan gum–HAP were prepared and characterized and their in vitro cell proliferation and ALP activity were checked for the first time.

2019 ◽  
Vol 20 (9) ◽  
pp. 1869-1882 ◽  
Author(s):  
Hadi Tohidlou ◽  
Seyedeh Sara Shafiei ◽  
Shahsanam Abbasi ◽  
Mitra Asadi-Eydivand ◽  
Mehrnoosh Fathi-Roudsari

2016 ◽  
Vol 705 ◽  
pp. 297-303
Author(s):  
Shirin Ibrahim ◽  
Syazana Abu Bakar ◽  
Mohamad Azmirruddin Ahmad ◽  
Nurul Awanis Johan ◽  
Siti Farhana Hisham ◽  
...  

Osteogenesis and degradability of bioresorbable biphasic gypsum-carbonated apatite granules (BPG) were investigated. Three different sizes of gypsum, 300-600 μm (small), 600-1000 μm (medium) and 1000-2000 μm (large), denoted as S, M and L respectively, were developed through the crushing and sieving method. Exposure of gypsum granules in carbonate and phosphate sources formed BPG through dissolution and precipitation mechanism. BPG was firstly examined by X-ray Diffractometer (XRD) and Fourier Transform Infrared Spectrometer (FTIR) to confirm its phase and chemical composition respectively. In-vitro cell proliferation, alkaline phosphatase (ALP) activity and adhesion of human osteoblast (hFOB) were investigated for osteogenesis evaluation. Degradability in phosphate buffer saline (PBS) was characterized by weight loss whereas apatite mineralization on the BPG surface was examined using Scanning Electron Microscope (SEM). BPG with 300-600 μm and 600-1000 μm enhanced osteogenic differentiation of hFOB and accelerated differentiation process better than 1000-2000 μm as indicated by cell proliferation and ALP activity. Good hFOB adhesion was observed on all BPG surfaces. The weight loss of L and M was 68% and 59%, respectively, which are higher than S at only 32%, indicating faster degradation of large BPG compared to smaller granules upon immersion for 35 days. This in turn, suggested the ionic dissolution of BPG which has contributed to the apatite formation on its surface. The results suggest, the BPG mimicked the bone matrix, exhibited good osteogenesis and degradability, which might be used as a potential candidate for bone tissue engineering.


RSC Advances ◽  
2015 ◽  
Vol 5 (51) ◽  
pp. 41135-41143 ◽  
Author(s):  
R. Rajesh ◽  
Y. Dominic Ravichandran

GO–alginate–HAP, GO–amylopectin–HAP and GO–gellan gum–HAP were prepared and characterized and their osteoconductivity were checked for the first time.


2019 ◽  
Vol 2019 ◽  
pp. 1-8 ◽  
Author(s):  
Xiongfeng Tang ◽  
Yanguo Qin ◽  
Xinyu Xu ◽  
Deming Guo ◽  
Wenli Ye ◽  
...  

For bone tissue engineering, the porous scaffold should provide a biocompatible environment for cell adhesion, proliferation, and differentiation and match the mechanical properties of native bone tissue. In this work, we fabricated porous polyetherimide (PEI) scaffolds using a three-dimensional (3D) printing system, and the pore size was set as 800 μm. The morphology of 3D PEI scaffolds was characterized by the scanning electron microscope. To investigate the mechanical properties of the 3D PEI scaffold, the compressive mechanical test was performed via an electronic universal testing system. For the in vitro cell experiment, bone marrow stromal cells (BMSCs) were cultured on the surface of the 3D PEI scaffold and PEI slice, and cytotoxicity, cell adhesion, and cell proliferation were detected to verify their biocompatibility. Besides, the alkaline phosphatase staining and Alizarin Red staining were performed on the BMSCs of different samples to evaluate the osteogenic differentiation. Through these studies, we found that the 3D PEI scaffold showed an interconnected porous structure, which was consistent with the design. The elastic modulus of the 3D PEI scaffold (941.33 ± 65.26 MPa) falls in the range of modulus for the native cancellous bone. Moreover, the cell proliferation and morphology on the 3D PEI scaffold were better than those on the PEI slice, which revealed that the porous scaffold has good biocompatibility and that no toxic substances were produced during the progress of high-temperature 3D printing. The osteogenic differentiation level of the 3D PEI scaffold and PEI slice was equal and ordinary. All of these results suggest the 3D printed PEI scaffold would be a potential strategy for bone tissue engineering.


2011 ◽  
Vol 26 (1) ◽  
pp. 7-11 ◽  
Author(s):  
Taís Somacal Novaes Silva ◽  
Bruno Tochetto Primo ◽  
Aurelício Novaes Silva Júnior ◽  
Denise Cantarelli Machado ◽  
Christian Viezzer ◽  
...  

Purpose: To evaluate the ability of macroporous tricalcium phosphate cement (CPC) scaffolds to enable the adhesion, proliferation, and differentiation of mesenchymal stem cells derived from human bone marrow. Methods: Cells from the iliac crest of an adult human donor were processed and cultured on macroporous CPC discs. Paraffin spheres sized between 100 and 250µm were used as porogens. Cells were cultured for 5, 10, and 15 days. Next, we assessed cells' behavior and morphology on the biomaterial by scanning electron microscopy. The expression levels of the BGLA and SSP1 genes and the alkaline phosphatase (ALP) activity were quantified by the quantitative real-time polymerase chain reaction technique (QT-PCR) using the fluorophore SYBR GREEN®. Results: QT-PCR detected the expression of the BGLA and SSP1 genes and the ALP activity in the periods of 10 and 15 days of culture. Thus, we found out that there was cell proliferation and differentiation in osteogenic cells. Conclusion: Macroporous CPC, with pore sized between 100 and 250µm and developed using paraffin spheres, enables adhesion, proliferation, and differentiation of mesenchymal stem cells in osteogenic cells and can be used as a scaffold for bone tissue engineering.


2015 ◽  
Vol 10 (5) ◽  
pp. 055009 ◽  
Author(s):  
Yinglan Zhu ◽  
Ruiqiao Zhu ◽  
Juan Ma ◽  
Zhiqiang Weng ◽  
Yang Wang ◽  
...  

2017 ◽  
Vol 204 (3-4) ◽  
pp. 150-163 ◽  
Author(s):  
S. Pina ◽  
R.F. Canadas ◽  
G. Jiménez ◽  
M. Perán ◽  
J.A. Marchal ◽  
...  

The treatment and regeneration of bone defects caused by traumatism or diseases have not been completely addressed by current therapies. Lately, advanced tools and technologies have been successfully developed for bone tissue regeneration. Functional scaffolding materials such as biopolymers and bioresorbable fillers have gained particular attention, owing to their ability to promote cell adhesion, proliferation, and extracellular matrix production, which promote new bone growth. Here, we present novel biofunctional scaffolds for bone regeneration composed of silk fibroin (SF) and β-tricalcium phosphate (β-TCP) and incorporating Sr, Zn, and Mn, which were successfully developed using salt-leaching followed by a freeze-drying technique. The scaffolds presented a suitable pore size, porosity, and high interconnectivity, adequate for promoting cell attachment and proliferation. The degradation behavior and compressive mechanical strengths showed that SF/ionic-doped TCP scaffolds exhibit improved characteristics for bone tissue engineering when compared with SF scaffolds alone. The in vitro bioactivity assays using a simulated body fluid showed the growth of an apatite layer. Furthermore, in vitro assays using human adipose-derived stem cells presented different effects on cell proliferation/differentiation when varying the doping agents in the biofunctional scaffolds. The incorporation of Zn into the scaffolds led to improved proliferation, while the Sr- and Mn-doped scaffolds presented higher osteogenic potential as demonstrated by DNA quantification and alkaline phosphatase activity. The combination of Sr with Zn led to an influence on cell proliferation and osteogenesis when compared with single ions. Our results indicate that biofunctional ionic-doped composite scaffolds are good candidates for further in vivo studies on bone tissue regeneration.


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