Characterization of Particle Packing in an Injected Molded Green Body

1995 ◽  
Vol 78 (11) ◽  
pp. 3107-3109 ◽  
Author(s):  
Keizo Uematsu ◽  
Hiroshige Ito ◽  
Shigeru Ohsaka ◽  
Hideo Takahashi ◽  
Nobuhiro Shinohara ◽  
...  
Keyword(s):  
2004 ◽  
Vol 264-268 ◽  
pp. 189-192 ◽  
Author(s):  
Satoshi Tanaka ◽  
Yoshiyuki Saito ◽  
Katsushi Tanaka ◽  
Nozomu Uchida ◽  
Keizo Uematsu

2003 ◽  
Vol 40 (3) ◽  
pp. 163-168 ◽  
Author(s):  
Hiroya Abe ◽  
Kenji Okamoto ◽  
Tadashi Hotta ◽  
Makio Naito ◽  
Keizo Uematsu

2014 ◽  
Vol 925 ◽  
pp. 442-449 ◽  
Author(s):  
Suriani Shamsudin ◽  
Mat Ghani Suhaida ◽  
Sudirman Sahid ◽  
Wan Ruzaini Wan Sulaiman ◽  
Salina Sabudin ◽  
...  

There are many challenges in designing and fabrication of synthetic tissue scaffold for osteochondral tissue engineering. A promising scaffolding material such as 45S5 Bioglass® has been extensively considered to construct scaffolds for this purpose. The 45S5 Bioglass® scaffold was fabricated using foam replication technique. The polyurethane foam was immersed in slurry of 45S5 Bioglass® and poly vinyl alcohol (PVA). The obtained green body was exposed for 1 hour at room temperature before oven dried at 60°C for 24 hours. The 45S5 Bioglass® composite scaffold was prepared by sintering the green body at 1050 °C for 2 hours, followed by dipping in PDLLA solution and dried at room temperature for 12 hours. Characterisations of the above scaffold were carried out using Extended Pressure Scanning Electron Microscope (SEM), Universal Tensile Machine (UTM) and X-ray diffraction (XRD). The SEM micrographs revealed the porous structure of the scaffold. The X-ray diffraction (XRD) spectrum showed the presence of Na2Ca2Si3O9 and (Na2Ca4(PO4)2SiO4 phases in the sintered scaffold. The result showed that the 45S5® Bioglass scaffold has compressive strength of 0.40 MPa with porosity of 88%. Bioactivity assessment in Simulated Body Fluid (SBF) for 7, 14 and 28 hours gave the formation of apatite layer on the scaffold.


1997 ◽  
Vol 17 (2-3) ◽  
pp. 177-181 ◽  
Author(s):  
Keizo Uematsu ◽  
S. Ohsak ◽  
H. Takahashi ◽  
N. Shinohara ◽  
M. Okumiy ◽  
...  

Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


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