A femoral shape porous scaffold bio-nanocomposite fabricated using 3D printing and freeze-drying technique for orthopedic application

2022 ◽  
Vol 275 ◽  
pp. 125302
Author(s):  
Xiaobiao Du ◽  
Mohammad Dehghani ◽  
Naif Alsaadi ◽  
Mazyar Ghadiri Nejad ◽  
Saeed Saber-Samandari ◽  
...  
2020 ◽  
Vol 21 (1) ◽  
pp. 315 ◽  
Author(s):  
Brian E. Grottkau ◽  
Zhixin Hui ◽  
Yang Yao ◽  
Yonggang Pang

Fused deposit modeling (FDM) 3D printing technology cannot generate scaffolds with high porosity while maintaining good integrity, anatomical-surface detail, or high surface area-to-volume ratio (S/V). Solvent casting and particulate leaching (SCPL) technique generates scaffolds with high porosity and high S/V. However, it is challenging to generate complex-shaped scaffolds; and solvent, particle and residual water removal are time consuming. Here we report techniques surmounting these problems, successfully generating a highly porous scaffold with the anatomical-shape characteristics of a human femur by polylactic acid polymer (PLA) and PLA-hydroxyapatite (HA) casting and salt leaching. The mold is water soluble and is easily removable. By perfusing with ethanol, water, and dry air sequentially, the solvent, salt, and residual water were removed 20 fold faster than utilizing conventional methods. The porosities are uniform throughout the femoral shaped scaffold generated with PLA or PLA-HA. Both scaffolds demonstrated good biocompatibility with the pre-osteoblasts (MC3T3-E1) fully attaching to the scaffold within 8 h. The cells demonstrated high viability and proliferation throughout the entire time course. The HA-incorporated scaffolds demonstrated significantly higher compressive strength, modulus and osteoinductivity as evidenced by higher levels of alkaline-phosphatase activity and calcium deposition. When 3D printing a 3D model at 95% porosity or above, our technology preserves integrity and surface detail when compared with FDM-generated scaffolds. Our technology can also generate scaffolds with a 31 fold larger S/V than FDM. We have developed a technology that is a versatile tool in creating personalized, patient-specific bone graft scaffolds efficiently with high porosity, good scaffold integrity, high anatomical-shaped surface detail and large S/V.


2021 ◽  
Vol 197 ◽  
pp. 109219
Author(s):  
Yuhao Zheng ◽  
Qing Han ◽  
Dongdong Li ◽  
Fan Sheng ◽  
Zhiming Song ◽  
...  

Biomaterials ◽  
2019 ◽  
Vol 197 ◽  
pp. 207-219 ◽  
Author(s):  
Yuxiao Lai ◽  
Ye Li ◽  
Huijuan Cao ◽  
Jing Long ◽  
Xinluan Wang ◽  
...  

2008 ◽  
Vol 368-372 ◽  
pp. 1224-1226
Author(s):  
Cheng Yun Ning ◽  
Hai Mei Cheng ◽  
Zhao Yi Yin ◽  
Wen Jun Zhu ◽  
Hao Chen ◽  
...  

The microstructure of scaffold was one of key factors for tissue engineering. Porous polycaprolactone (PCL) scaffolds were fabricated by combination of porogen-leaching and freeze-drying process. Ice particulates were used as porogen material, and PCL solutions in chloroform were mixed with ice particulates for 5minuture at zero temperature. Then the mixture was freezed in liquid nitrogen, and porous scaffold was prepared by freeze - drying finally. The microstructure and properties of the scaffolds were investigated. Porous structure of the scaffolds showed that good 3D microstructure and no porogen remained in the scaffold; pore size and porosity were determined by the size and mass fraction of ice particulates. The results demonstrated that the Scaffolds possessed open and interconnected pores with sizes ranging from several μm to more than 300μm and porosities of 50~80%.


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.


2014 ◽  
Vol 2 (4) ◽  
pp. 218-219 ◽  
Author(s):  
Yuxiao Lai ◽  
Long Li ◽  
Shukui Chen ◽  
Ming Zhang ◽  
Xinluan Wang ◽  
...  

2020 ◽  
Vol 20 (8) ◽  
pp. 5014-5018 ◽  
Author(s):  
Sunmi Zo ◽  
Soonmo Choi ◽  
Hyunduk Kim ◽  
Eunjoo Shin ◽  
Sungsoo Han

Bone tissue engineering has been rapidly developed in regenerative medicine field, which aims to induce new functional bone regeneration through the synergistic combination of biomaterials and cells. Porous biomaterials with sufficient mechanical properties and functional impregnating for bone substitutes have been imposed in the oncoming generation of bone reconstruction. In this study, we fabricated Carboxymethyl chitosan three dimensional (3D) porous scaffold modified with waterborne polyurethane (WPU) through freeze drying technique. In order to check its potential in bone tissue substitutes, osteoblast cells (hFOB 1.19) were seeded onto the fabricated scaffolds and then, SEM and proliferation assay were performed. The enhanced proliferation was contributed to 3D macroporous network structure, large surface area, and osteoconductive environments.


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