scholarly journals Recent Developments in Nanofiber Fabrication and Modification for Bone Tissue Engineering

2019 ◽  
Vol 21 (1) ◽  
pp. 99 ◽  
Author(s):  
Nopphadol Udomluck ◽  
Won-Gun Koh ◽  
Dong-Jin Lim ◽  
Hansoo Park

Bone tissue engineering is an alternative therapeutic intervention to repair or regenerate lost bone. This technique requires three essential components: stem cells that can differentiate into bone cells, growth factors that stimulate cell behavior for bone formation, and scaffolds that mimic the extracellular matrix. Among the various kinds of scaffolds, highly porous nanofibrous scaffolds are a potential candidate for supporting cell functions, such as adhesion, delivering growth factors, and forming new tissue. Various fabricating techniques for nanofibrous scaffolds have been investigated, including electrospinning, multi-axial electrospinning, and melt writing electrospinning. Although electrospun fiber fabrication has been possible for a decade, these fibers have gained attention in tissue regeneration owing to the possibility of further modifications of their chemical, biological, and mechanical properties. Recent reports suggest that post-modification after spinning make it possible to modify a nanofiber’s chemical and physical characteristics for regenerating specific target tissues. The objectives of this review are to describe the details of recently developed fabrication and post-modification techniques and discuss the advanced applications and impact of the integrated system of nanofiber-based scaffolds in the field of bone tissue engineering. This review highlights the importance of nanofibrous scaffolds for bone tissue engineering.

2007 ◽  
Vol 5 (25) ◽  
pp. 899-907 ◽  
Author(s):  
M.A Wood ◽  
Y Yang ◽  
E Baas ◽  
D.O Meredith ◽  
R.G Richards ◽  
...  

A number of bone tissue engineering strategies use porous three-dimensional scaffolds in combination with bioreactor regimes. The ability to understand cell behaviour relative to strain profile will allow for the effects of mechanical conditioning in bone tissue engineering to be realized and optimized. We have designed a model system to investigate the effects of strain profile on bone cell behaviour. This simplified model has been designed with a view to providing insight into the types of strain distribution occurring across a single pore of a scaffold subjected to perfusion–compression conditioning. Local strains were calculated at the surface of the pore model using finite-element analysis. Scanning electron microscopy was used in secondary electron mode to identify cell morphology within the pore relative to local strains, while backscattered electron detection in combination with X-ray microanalysis was used to identify calcium deposition. Morphology was altered according to the level of strain experienced by bone cells, where cells subjected to compressive strains (up to 0.61%) appeared extremely rounded while those experiencing zero and tensile strain (up to 0.81%) were well spread. Osteoid mineralization was similarly shown to be dose dependent with respect to substrate strain within the pore model, with the highest level of calcium deposition identified in the intermediate zones of tension/compression.


2012 ◽  
Vol 2012 ◽  
pp. 1-25 ◽  
Author(s):  
Keith A. Blackwood ◽  
Nathalie Bock ◽  
Tim R. Dargaville ◽  
Maria Ann Woodruff

There remains a substantial shortfall in the treatment of severe skeletal injuries. The current gold standard of autologous bone grafting from the same patient has many undesirable side effects associated such as donor site morbidity. Tissue engineering seeks to offer a solution to this problem. The primary requirements for tissue-engineered scaffolds have already been well established, and many materials, such as polyesters, present themselves as potential candidates for bone defects; they have comparable structural features, but they often lack the required osteoconductivity to promote adequate bone regeneration. By combining these materials with biological growth factors, which promote the infiltration of cells into the scaffold as well as the differentiation into the specific cell and tissue type, it is possible to increase the formation of new bone. However due to the cost and potential complications associated with growth factors, controlling the rate of release is an important design consideration when developing new bone tissue engineering strategies. This paper will cover recent research in the area of encapsulation and release of growth factors within a variety of different polymeric scaffolds.


2022 ◽  
Vol 5 (1) ◽  
pp. 8
Author(s):  
Giorgia Borciani ◽  
Giorgia Montalbano ◽  
Nicola Baldini ◽  
Chiara Vitale-Brovarone ◽  
Gabriela Ciapetti

New biomaterials and scaffolds for bone tissue engineering (BTE) applications require to be tested in a bone microenvironment reliable model. On this assumption, the in vitro laboratory protocols with bone cells represent worthy experimental systems improving our knowledge about bone homeostasis, reducing the costs of experimentation. To this day, several models of the bone microenvironment are reported in the literature, but few delineate a protocol for testing new biomaterials using bone cells. Herein we propose a clear protocol to set up an indirect co-culture system of human-derived osteoblasts and osteoclast precursors, providing well-defined criteria such as the cell seeding density, cell:cell ratio, the culture medium, and the proofs of differentiation. The material to be tested may be easily introduced in the system and the cell response analyzed. The physical separation of osteoblasts and osteoclasts allows distinguishing the effects of the material onto the two cell types and to evaluate the correlation between material and cell behavior, cell morphology, and adhesion. The whole protocol requires about 4 to 6 weeks with an intermediate level of expertise. The system is an in vitro model of the bone remodeling system useful in testing innovative materials for bone regeneration, and potentially exploitable in different application fields. The use of human primary cells represents a close replica of the bone cell cooperation in vivo and may be employed as a feasible system to test materials and scaffolds for bone substitution and regeneration.


2019 ◽  
Vol 7 (5) ◽  
pp. 1973-1983 ◽  
Author(s):  
Qianmin Ou ◽  
Yingling Miao ◽  
Fanqiao Yang ◽  
Xuefeng Lin ◽  
Li-Ming Zhang ◽  
...  

In bone tissue engineering, it is important for biomaterials to promote the osteogenic differentiation of stem cells to achieve tissue regeneration.


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.


2009 ◽  
Vol 1235 ◽  
Author(s):  
Junping Wang ◽  
Xiaojun Yu

AbstractIn the previous studies, we have successfully developed a novel spiral structured nanofibrous scaffolds with improved osteoconductivity for bone tissue engineering. The spiral structure design facilitates the nutrient transport and waste removal, and allows uniform cellular growth and distribution within the scaffolds, thus enhanced the bioactivity of the scaffolds. In this chapter, HAP and BMP-2 were incorporated within the nanofibrous spiral scaffolds in order to enhance the osteoinductivity of the established system. The effect of the blending materials was evaluated through cell proliferation, cell differentiation of human osteoblast cells seeded on the scaffolds and cultured for 4 and 8 days. The results has demonstrated that the functionalization of PCL nanofibrous spiral scaffolds leads to higher ALP expression level and increased amount of mineralization level however lower cell proliferation rate.


2016 ◽  
Vol 695 ◽  
pp. 164-169 ◽  
Author(s):  
Woradej Pichaiaukrit ◽  
Wiriya Juwattanasamran ◽  
Teerasak Damrongrungruang

Scaffolds with mechanical properties that mimic the tissue to be restored are critical to maintain the morphology and function of a scaffold after implantation and during tissue regeneration. Silk fibroin (SF), a protein from the Bombyxmori silk worm cocoon, is currently employed in the biomedical field and tissue engineering. The objective of this study was to construct three-dimensional porous silk fibroin/alpha tricalcium phosphate scaffolds for bone tissue engineering application. The scaffolds were fabricated using a solvent casting and salt leaching technique. The hybrid strain of degummed Thai silk fibroin, Nangnoi Srisaket 1 x Mor, was dissolved in hexafluoroisopropanol at 16% (w/v). Alpha tricalcium phosphate (α-TCP) was incorporated to produce 4, 8, 12, and 16 wt% solution and sucrose (particle size 250-450 μm; sucrose/silk fibroin = 8.5/1 w/w) was used as a porogen. The microstructure and pore size, calcium and phosphorus contents, and compressive modulus were evaluated. The scanning electron microscope images revealed the microstructure of scaffolds to be square shaped with continuous interconnected pores. The average pore size of the scaffolds was 265.70 + 67.45 μm. The scaffolds containing 8% (w/w) α-TCP exhibited the highest compressive modulus (64.84 + 16.65 kPa) and the highest calcium content. The results suggested that the scaffolds containing α-TCP may be a potential candidate for application in bone tissue engineering applications.


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