scholarly journals Enhanced Cartilaginous Tissue Formation with a Cell Aggregate-Fibrin-Polymer Scaffold Complex

Polymers ◽  
2017 ◽  
Vol 9 (12) ◽  
pp. 348 ◽  
Author(s):  
Soojin Lee ◽  
Kangwon Lee ◽  
Soo Kim ◽  
Youngmee Jung
2003 ◽  
Vol 85 ◽  
pp. 101-105 ◽  
Author(s):  
STEPHEN D. WALDMAN ◽  
CAROLINE G. SPITERI ◽  
MARC D. GRYNPAS ◽  
ROBERT M. PILLIAR ◽  
JASON HONG ◽  
...  

2007 ◽  
Vol 15 (1) ◽  
pp. 48-58 ◽  
Author(s):  
A. Marsano ◽  
S.J. Millward-Sadler ◽  
D.M. Salter ◽  
A. Adesida ◽  
T. Hardingham ◽  
...  

2004 ◽  
Vol 44 (supplement) ◽  
pp. S103
Author(s):  
H. Honda ◽  
T. Nagai ◽  
M. Tanemura

Author(s):  
Roberto Tarantino ◽  
Loraine L.Y. Chiu ◽  
Joanna F. Weber ◽  
M. Yat Tse ◽  
Davide D. Bardana ◽  
...  

2020 ◽  
Vol 48 (4) ◽  
pp. 1433-1445
Author(s):  
Mark Lemoine ◽  
Sarah M. Casey ◽  
John M. O'Byrne ◽  
Daniel J. Kelly ◽  
Fergal J. O'Brien

Due to the limited regenerative capacity of cartilage, untreated joint defects can advance to more extensive degenerative conditions such as osteoarthritis. While some biomaterial-based tissue-engineered scaffolds have shown promise in treating such defects, no scaffold has been widely accepted by clinicians to date. Multi-layered natural polymer scaffolds that mimic native osteochondral tissue and facilitate the regeneration of both articular cartilage (AC) and subchondral bone (SCB) in spatially distinct regions have recently entered clinical use, while the transient localized delivery of growth factors and even therapeutic genes has also been proposed to better regulate and promote new tissue formation. Furthermore, new manufacturing methods such as 3D bioprinting have made it possible to precisely tailor scaffold micro-architectures and/or to control the spatial deposition of cells in requisite layers of an implant. In this way, natural and synthetic polymers can be combined to yield bioactive, yet mechanically robust, cell-laden scaffolds suitable for the osteochondral environment. This mini-review discusses recent advances in scaffolds for osteochondral repair, with particular focus on the role of natural polymers in providing regenerative templates for treatment of both AC and SCB in articular joint defects.


2021 ◽  
Author(s):  
Seunggyu Jeon ◽  
Se-Hwan Lee ◽  
Saeed B. Ahmed ◽  
Jonghyeuk Han ◽  
Su-Jin Heo ◽  
...  

Abstract Various cell aggregate culture technologies have been developed and actively applied to tissue engineering and organ-on-a-chip. However, the conventional culture technologies are labor-intensive, and their outcomes are highly user dependent. In addition, the technologies cannot be used to produce three-dimensional (3D) complex tissues. In this regard, 3D cell aggregate printing technology has attracted increased attention from many researchers owing to its 3D processability. The technology allows the fabrication of 3D freeform constructs using multiple types of cell aggregates in an automated manner. Technological advancement has resulted in the development of a printing technology with a high resolution of approximately 20 μm in 3D space. A high-speed printing technology that can print a cell aggregate in milliseconds has also been introduced. The developed aggregate printing technologies are being actively applied to produce various types of engineered tissues. Although various types of high-performance printing technologies have been developed, there are still some technical obstacles in the fabrication of engineered tissues that mimic the structure and function of native tissues. This review highlights the central importance and current technical level of 3D cell aggregate printing technology, and their applications to tissue/disease models, artificial tissues, and drug-screening platforms. The paper also discusses the remaining hurdles and future directions of the printing processes.


2011 ◽  
Vol 133 (8) ◽  
Author(s):  
Yuhang Chen ◽  
Michiel Schellekens ◽  
Shiwei Zhou ◽  
Joseph Cadman ◽  
Wei Li ◽  
...  

Tissue scaffolds aim to provide a cell-friendly biomechanical environment for facilitating cell growth. Existing studies have shown significant demands for generating a certain level of wall shear stress (WSS) on scaffold microstructural surfaces for promoting cellular response and attachment efficacy. Recently, its role in shear-induced erosion of polymer scaffold has also drawn increasing attention. This paper proposes a bi-directional evolutionary structural optimization (BESO) approach for design of scaffold microstructure in terms of the WSS uniformity criterion, by downgrading highly-stressed solid elements into fluidic elements and/or upgrading lowly-stressed fluidic elements into solid elements. In addition to this, a computational model is presented to simulate shear-induced erosion process. The effective stiffness and permeability of initial and optimized scaffold microstructures are characterized by the finite element based homogenization technique to quantify the variations of mechanical properties of scaffold during erosion. The illustrative examples show that a uniform WSS is achieved within the optimized scaffold microstructures, and their architectural and biomechanical features are maintained for a longer lifetime during shear-induced erosion process. This study provides a mathematical means to the design optimization of cellular biomaterials in terms of the WSS criterion towards controllable shear-induced erosion.


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