Plate Electroporation: A Numerical Study of Factors Affecting Thermal Damage

Author(s):  
S. M. Becker ◽  
A. V. Kuznetsov

Electroporation is an approach used to enhance the transport of large molecules to cell cytosol in which a targeted tissue region is exposed to a series of electric pulses. The cell membrane, which normally acts as a barrier to large molecule transport into the cell interior, is temporarily destabilized due to the development of pores in the cell membrane. Consequently agents that are ordinarily unable enter the cell are able to pass through the cell membrane. Of possible concern when exposing biological tissue to an electric field is thermal tissue damage associated with joule heating. This paper explores the thermal effects of various geometric, biological, and electroporation pulse parameters including the blood vessel presence and size, plate electrode configuration, and pulse duration and frequency. A three-dimensional transient finite volume model of in vivo parallel plate electroporation of liver tissue is used to develop a better understanding of the underlying relationships between the physical parameters involved with tissue electroporation and resulting thermal damage potential.

2005 ◽  
Vol 128 (1) ◽  
pp. 76-84 ◽  
Author(s):  
S. M. Becker ◽  
A. V. Kuznetsov

Electroporation is an approach used to enhance the transport of large molecules to the cell cytosol in which a targeted tissue region is exposed to a series of electric pulses. The cell membrane, which normally acts as a barrier to large molecule transport into the cell interior, is temporarily destabilized due to the development of pores in the cell membrane. Consequently, agents that are ordinarily unable enter the cell are able to pass through the cell membrane. Of possible concern when exposing biological tissue to an electric field is thermal tissue damage associated with joule heating. This paper explores the thermal effects of various geometric, biological, and electroporation pulse parameters including the blood vessel presence and size, plate electrode configuration, and pulse duration and frequency. A three-dimensional transient finite volume model of in vivo parallel plate electroporation of liver tissue is used to develop a better understanding of the underlying relationships between the physical parameters involved with tissue electroporation and resulting thermal damage potential.


2006 ◽  
Vol 129 (3) ◽  
pp. 330-340 ◽  
Author(s):  
S. M. Becker ◽  
A. V. Kuznetsov

Electroporation is an approach used to enhance transdermal transport of large molecules in which the skin is exposed to a series of electric pulses. The structure of the transport inhibiting outer layer, the stratum corneum, is temporarily destabilized due to the development of microscopic pores. Consequently agents that are ordinarily unable to pass into the skin are able to pass through this outer barrier. Of possible concern when exposing biological tissue to an electric field is thermal tissue damage associated with Joule heating. This paper shows the importance of using a composite model in calculating the electrical and thermal effects associated with skin electroporation. A three-dimensional transient finite-volume model of in vivo skin electroporation is developed to emphasize the importance of representing the skin’s composite layers and to illustrate the underlying relationships between the physical parameters of the composite makeup of the skin and resulting thermal damage potential.


2011 ◽  
Vol 219-220 ◽  
pp. 1211-1214
Author(s):  
Wei Jiang

Finite element simulation is an efficient method for studying factors affecting weld-induced residual stress distributions. In this paper, a validated three-dimensional finite element model consisting of sequentially coupled thermal and structural analyses was developed. Three possible symmetrical welding sequences, i.e. one-welder, two-welder and four-welder sequence, which were perceived to generate the least distortion in actual welding circumstances, were proposed and their influences on the residual stress fields in a thick-walled tee joint were investigated. Appropriate conclusions and recommendations regarding welding sequences are presented.


2012 ◽  
Vol 47 (3-4) ◽  
pp. 238-251 ◽  
Author(s):  
Jun Zhao ◽  
Yerubandi R. Rao ◽  
Jinyu Sheng

A nested-grid hydrodynamic modeling system is used to examine the circulation and dispersion in Lake Huron and adjacent areas with specific attention to physical parameters pertinent to the estimation of hydrodynamic connectivity of near-surface waters. The nested system is forced by monthly mean surface heat flux and 12-hourly wind stress computed from wind speeds extracted from the National Centers for Environmental Prediction of the National Center for Atmospheric Research (NCEP/NCAR) 40-year reanalysis data. The three-dimensional model currents are used to calculate the retention and dispersion of conservative, near-surface particles carried by the currents. The near-surface dispersion is relatively low in Saginaw Bay, eastern Georgian Bay and the eastern North Channel; and relatively high over the western part of the main lake and the coastal region of south Lake Huron. The hydrodynamic connectivity in the surface water and connectivity matrices are calculated from particle movements carried passively by model currents superposed by a random walk process. The model results demonstrate that the hydrodynamic connectivity in the North Channel and Georgian Bay (ranging from 0.9 to 2.2%) is much weaker than those in the main lake (5.3 to 21.9%).


Molecules ◽  
2019 ◽  
Vol 24 (4) ◽  
pp. 675 ◽  
Author(s):  
Yi Zhao ◽  
Ranjith Kankala ◽  
Shi-Bin Wang ◽  
Ai-Zheng Chen

With advantageous features such as minimizing the cost, time, and sample size requirements, organ-on-a-chip (OOC) systems have garnered enormous interest from researchers for their ability for real-time monitoring of physical parameters by mimicking the in vivo microenvironment and the precise responses of xenobiotics, i.e., drug efficacy and toxicity over conventional two-dimensional (2D) and three-dimensional (3D) cell cultures, as well as animal models. Recent advancements of OOC systems have evidenced the fabrication of ‘multi-organ-on-chip’ (MOC) models, which connect separated organ chambers together to resemble an ideal pharmacokinetic and pharmacodynamic (PK-PD) model for monitoring the complex interactions between multiple organs and the resultant dynamic responses of multiple organs to pharmaceutical compounds. Numerous varieties of MOC systems have been proposed, mainly focusing on the construction of these multi-organ models, while there are only few studies on how to realize continual, automated, and stable testing, which still remains a significant challenge in the development process of MOCs. Herein, this review emphasizes the recent advancements in realizing long-term testing of MOCs to promote their capability for real-time monitoring of multi-organ interactions and chronic cellular reactions more accurately and steadily over the available chip models. Efforts in this field are still ongoing for better performance in the assessment of preclinical attributes for a new chemical entity. Further, we give a brief overview on the various biomedical applications of long-term testing in MOCs, including several proposed applications and their potential utilization in the future. Finally, we summarize with perspectives.


Cells ◽  
2019 ◽  
Vol 8 (11) ◽  
pp. 1470 ◽  
Author(s):  
Dettin ◽  
Sieni ◽  
Zamuner ◽  
Marino ◽  
Sgarbossa ◽  
...  

Tumor electroporation (EP) refers to the permeabilization of the cell membrane by means of short electric pulses thus allowing the potentiation of chemotherapeutic drugs. Standard plate adhesion 2D cell cultures can simulate the in vivo environment only partially due to lack of cell–cell interaction and extracellular matrix (ECM). In this study, we assessed a novel 3D scaffold for cell cultures based on hyaluronic acid and ionic-complementary self-assembling peptides (SAPs), by studying the growth patterns of two different breast carcinoma cell lines (HCC1569 and MDA-MB231). This 3D scaffold modulates cell shape and induces extracellular matrix deposit around cells. In the MDA-MB 231 cell line, it allows three-dimensional growth of structures known as spheroids, while in HCC1569 it achieves a cell organization similar to that observed in vivo. Interestingly, we were able to visualize the electroporation effect on the cells seeded in the new scaffold by means of standard propidium iodide assay and fluorescence microscopy. Thanks to the presence of cell–cell and cell–ECM interactions, the new 3D scaffold may represent a more reliable support for EP studies than 2D cancer cell cultures and may be used to test new EP-delivered drugs and novel EP protocols.


Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 5196-5196
Author(s):  
Mario Gimona ◽  
Rokhsareh Rohban ◽  
Thomas Lener ◽  
Doris Peckl-Schmid ◽  
Michaela Oeller ◽  
...  

Abstract Abstract 5196 Background and rationale Human mesenchymal stem/progenitor cells (MSPCs) are important tools for tissue repair and regenerative approaches. Co-application of autologous pairs of human MSPCs and endothelial colony forming progenitor cells (ECFCs) drives vessel formation in a mouse model. However, a more detailed mechanistic insight into the contribution of MSPCs to vasculogenesis is required prior to a potential application in clinical trials. The formation of perfused blood vessels following the co-injection of MSPC/ECFC pairs requires directed migration of these cell types through the extracellular matrix. For this, cells must interpret and respond to both biochemical cues and physical parameters of the matrix. Here we aimed at identifying changes in early signaling molecules that could potentially mediate these complex behaviors in ECFCs and MSPCs. Results By antibody array analysis of biopsies from vasculogenic regions we identified the levels of the discoidin domain receptor 2 (DDR2) to be upregulated about twofold in MSPCs in an MSPC/ECFC mixture compared to MSPC-only implants. Expression of DDR2 was confirmed by flow cytometry analysis. Employing immunofluorescence microscopy we showed components of the mechanotransduction and cytoskeleton machinery (Paxillin, ILK, Src, h1CaP, and cortactin) to be abundantly expressed and correctly localized in MSPCs. MSPCs also responded to manipulation of cytoskeletal integrity with phorbol dibutyrate or Y-27632, demonstrating the presence of a tissue transmigration machinery in MSPCs. Applying various three dimensional cell culture strategies we identified significant alterations in MSPC morphology, as well as in the mRNA levels for DDR1 and DDR2, and for miRNAs 29b, 199a, 331 in response to different matrix conditions. Conclusions Our data suggest a mechanosensitive regulation of MSPC function and we thus conclude that direct or indirect (miRNA-mediated) regulation of the collagen receptors DDR1/2 could have a role in modulating MSPC function during stem-cell induced neo-vascularization in vivo. Disclosures: No relevant conflicts of interest to declare.


2018 ◽  
Vol 67 (4) ◽  
pp. 045101
Author(s):  
Li Han-Wei ◽  
Sun An-Bang ◽  
Zhang Xing ◽  
Yao Cong-Wei ◽  
Chang Zheng-Shi ◽  
...  

Author(s):  
Mumtaz Khan ◽  
Amer Rasheed

The current article presents a comprehensive investigation of MHD viscous flow of hybrid-nanofluids (Al2O3 − Ag/ water and (Al2O3 − Cu/) over a horizontally irregular 3D plane with non-uniform thickness combined with slip effects. The foremost aim of conducting this study is to enhance thermal transportation. Based on the following novelties, the subject study holds tremendous significance: i. A comparative analysis of two hybrid nanofluids with hybrid-base fluid together with slip effects ii. An exclusive study where the Tiwari and Das nanofluid model is employed combined with Fourier's heat flux model iii. Development of finite-difference code which implements the three-stage Lobatto IIIa approach for the designed problem. We have used suitable scaling transformations to convert the three-dimensional conservation equations of mass, momentum, and energy into a dimensionless system of boundary layer equations. The numerical solution of the coupled non-linear boundary layer problem is determined using the built-in finite-difference code designed to employ the three-stage Lobatto IIIa formula. A comprehensive assessment is carried out in how the velocity components, temperature, skin friction, and heat transfer rate are affected by the physical parameters of interest. The same is presented through graphs and in tabular form to offer a pictorial overview. The fluctuating trends of skin friction coefficients (x, y-directions) and Nusselt number are investigated to explore the physical landscape of the current study. The findings of this study offer a noticeable contrast to their existing counterparts.


Author(s):  
D. Reis ◽  
B. Vian ◽  
J. C. Roland

Wall morphogenesis in higher plants is a problem still open to controversy. Until now the possibility of a transmembrane control and the involvement of microtubules were mostly envisaged. Self-assembly processes have been observed in the case of walls of Chlamydomonas and bacteria. Spontaneous gelling interactions between xanthan and galactomannan from Ceratonia have been analyzed very recently. The present work provides indications that some processes of spontaneous aggregation could occur in higher plants during the formation and expansion of cell wall.Observations were performed on hypocotyl of mung bean (Phaseolus aureus) for which growth characteristics and wall composition have been previously defined.In situ, the walls of actively growing cells (primary walls) show an ordered three-dimensional organization (fig. 1). The wall is typically polylamellate with multifibrillar layers alternately transverse and longitudinal. Between these layers intermediate strata exist in which the orientation of microfibrils progressively rotates. Thus a progressive change in the morphogenetic activity occurs.


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