Mathematical modeling of elastodynamics and cell growth inside a deformable scaffold fitted to the periphery of a bioreactor

2021 ◽  
Author(s):  
Prakash Kumar ◽  
G. P. Raja Sekhar
Keyword(s):  
Mathematical Modeling ◽  
Cell Growth

Mathematical modeling of cell growth in a 3D scaffold and validation of static and dynamic cultures

2016 ◽  
Vol 16 (3) ◽  
pp. 290-298 ◽  
Author(s):  
Fatemeh Mokhtari-Jafari ◽  
Ghassem Amoabediny ◽  
Nooshin Haghighipour ◽  
Reza Zarghami ◽  
Alireza Saatchi ◽  
...  
Keyword(s):  
Mathematical Modeling ◽  
Cell Growth ◽  
3D Scaffold

Kinetic analysis and mathematical modeling of cell growth and canthaxanthin biosynthesis by Dietzia natronolimnaea HS-1 on waste molasses hydrolysate

RSC Advances ◽  
2013 ◽  
Vol 3 (45) ◽  
pp. 23495 ◽  
Author(s):  
Seyed Mohammad Taghi Gharibzahedi ◽  
Seyed Hadi Razavi ◽  
Mohammad Mousavi
Keyword(s):  
Mathematical Modeling ◽  
Cell Growth ◽  
Kinetic Analysis

Mathematical Model of the Cell Growth for Methane-Oxidizing Bacteria

2015 ◽  
Vol 731 ◽  
pp. 345-348
Author(s):  
Jing Dong ◽  
He Teng Wang ◽  
Ying Xin Zhang
Keyword(s):  
Mathematical Modeling ◽  
Experimental Data ◽  
Mathematical Model ◽  
Cell Growth ◽  
Living Cell ◽  
Fermentation Process ◽  
Logistic Curve ◽  
Cell Content ◽  
Methane Oxidizing Bacteria

The dynamic trends of living cell content of methane-oxidizing bacteria during its fermentation process were analyzed. According to the experimental data, mathematical modeling of methane-oxidizing bacteria cell growth was simulated. The results showed that the logistic curve could be used to describe the mathematical modeling of methane-oxidizing bacteria cell growth well. The establishment of the model is the theoretic basis in optimizing the fermentable parameters and analyzing the fermented metabolites.

scholarly journals Mathematical Modeling Reveals That Changes to Local Cell Density Dynamically Modulate Baseline Variations in Cell Growth and Drug Response

2016 ◽  
Vol 76 (10) ◽  
pp. 2882-2890 ◽  
Author(s):  
James M. Greene ◽  
Doron Levy ◽  
Sylvia P. Herrada ◽  
Michael M. Gottesman ◽  
Orit Lavi
Keyword(s):  
Mathematical Modeling ◽  
Cell Growth ◽  
Cell Density ◽  
Drug Response ◽  
Local Cell

Electron Microscopic Study of the Epithelium of the Seminal Vesicle of Aging Rats

1974 ◽  
Vol 32 ◽  
pp. 138-139
Author(s):  
V. F. Allison ◽  
G. C. Fink ◽  
G. W. Cearley
Keyword(s):  
Cell Growth ◽  
Epithelial Cell ◽  
Epithelial Cells ◽  
Seminal Vesicle ◽  
Seminal Vesicles ◽  
Epithelial Layer ◽  
Epithelial Hyperplasia ◽  
Electron Microscopic ◽  
Aging Rats ◽  
Pseudostratified Epithelium

It is well known that epithelial hyperplasia (benign hypertrophy) is common in the aging prostate of dogs and man. In contrast, little evidence is available for abnormal epithelial cell growth in seminal vesicles of aging animals. Recently, enlarged seminal vesicles were reported in senescent mice, however, that enlargement resulted from increased storage of secretion in the lumen and occurred concomitant to epithelial hypoplasia in that species.The present study is concerned with electron microscopic observations of changes occurring in the pseudostratified epithelium of the seminal vescles of aging rats. Special attention is given to certain non-epithelial cells which have entered the epithelial layer.

Rotary Beveling for In Situ Thin-Section Microscopy of Cell Cultures

1981 ◽  
Vol 39 ◽  
pp. 550-551
Author(s):  
Dean A. Handley ◽  
Jack T. Alexander ◽  
Shu Chien
Keyword(s):  
Cell Growth ◽  
Cell Cultures ◽  
Molecular Interactions ◽  
Convenient Method ◽  
Petri Dish ◽  
Simple Method ◽  
Thin Section Microscopy ◽  
Thin Sectioning ◽  
Organic Fluids

In situ preparation of cell cultures for ultrastructural investigations is a convenient method by which fixation, dehydration and embedment are carried out in the culture petri dish. The in situ method offers the advantage of preserving the native orientation of cell-cell interactions, junctional regions and overlapping configurations. In order to section after embedment, the petri dish is usually separated from the polymerized resin by either differential cryo-contraction or solvation in organic fluids. The remaining resin block must be re-embedded before sectioning. Although removal of the petri dish may not disrupt the native cellular geometry, it does sacrifice what is now recognized as an important characteristic of cell growth: cell-substratum molecular interactions. To preserve the topographic cell-substratum relationship, we developed a simple method of tapered rotary beveling to reduce the petri dish thickness to a dimension suitable for direct thin sectioning.

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