Modeling process-induced cell damage in the biodispensing process.

Tissue Eng Part C Methods

Department of Mechanical Engineering, University of Saskatchewan, Saskatoon, Canada.

Published: June 2010

Emerging biomanufacturing processes involve incorporation of living cells into various processes and systems by employing different cell manipulation techniques. Among them, biodispensing, in which the cell suspension is extruded via a fine needle under pressurized air, is a promising technique because of its high efficiency. Cells in this process are continually subjected to mechanical forces and may be damaged if the force or manipulation time exceeds certain levels. Modeling cell injury incurred in these processes is lacking in the literature. This article presents a method to quantify the force-induced cell damage in the biodispensing process. This method consists of two steps: first is to establish cell damage laws to relate cell damage to hydrostatic pressure/shear stress; and the second is to represent the process-induced forces experienced by cells during the biodispensing process and apply the established cell damage law to represent the percentage of cell damage. Schwann cells and 3T3 fibroblasts were used to validate the model and the comparisons of experimental and simulation results show the effectiveness of the method presented in this article.

Download full-text PDF

Source
http://dx.doi.org/10.1089/ten.TEC.2009.0178DOI Listing

Publication Analysis

Top Keywords

cell damage
24
biodispensing process
12
cell
9
damage biodispensing
8
damage
6
modeling process-induced
4
process-induced cell
4
biodispensing
4
process
4
process emerging
4

Similar Publications

Background: Dexamethasone has proven life-saving in severe acute respiratory syndrome (SARS) and COVID-19 cases. However, its systemic administration is accompanied by serious side effects. Inhalation delivery of dexamethasone (Dex) faces challenges such as low lung deposition, brief residence in the respiratory tract, and the pulmonary mucus barrier, limiting its clinical use.

View Article and Find Full Text PDF

Background: Myocardial ischemia-reperfusion (I/R) injury refers to cell damage that occurs as a consequence of the restoration of blood circulation following reperfusion therapy for cardiovascular diseases, and it is a primary cause of myocardial infarction. The search for nove therapeutic targets in the context of I/R injury is currently a highly active area of research. p70 ribosomal S6 kinase (S6K1) plays an important role in I/R induced necrosis, although the specific mechanisms remain unclear.

View Article and Find Full Text PDF

Background: Androgenic anabolic steroids (AASs) are synthetic drugs structurally related to testosterone, with the ability to bind to androgen receptors. Their uncontrolled use by professional and recreational sportspeople is a widespread problem. AAS abuse is correlated with severe damage to the cardiovascular system, including changes in homeostasis and coagulation disorders.

View Article and Find Full Text PDF

Background: Rheumatic heart disease (RHD), which is caused mainly by Group A Streptococcus, leads to fibrotic damage to heart valves. Recently, endothelial‒mesenchymal transition (EndMT), in which activin plays an important role, has been shown to be an important factor in RHD valvular injury. However, the mechanism of activin activity and EndMT in RHD valvular injury is not clear.

View Article and Find Full Text PDF

The Role of NF-κB/MIR155HG in Regulating the Stemness and Radioresistance in Breast Cancer Stem Cells.

Front Biosci (Landmark Ed)

January 2025

Department of Chemoradiotherapy, Ningbo No 2 Hospital, 315000 Ningbo, Zhejiang, China.

Background: Breast cancer stem cells (BCSCs) are instrumental in treatment resistance, recurrence, and metastasis. The development of breast cancer and radiation sensitivity is intimately pertinent to long non-coding RNA (lncRNA). This work is formulated to investigate how the lncRNA affects the stemness and radioresistance of BCSCs.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!