In Vitro Biological SystemsIn vitro methods have provided a valuable tool for toxicological research over the years. Historically, these methods have made significant contributions to our understanding of toxic mechanisms of action and xenobiotic metabolism and, in this context, have provided an indispensable resource for investigative toxicology. More recently, the value of in vitro systems as toxicity tests for chemical safety and hazard evaluation has been recognized and explored. Whether the in vitro approach is employed as a model system for investigative research or as a toxicity test for risk assessment, a critical component is the biological system. Selection and successful culturing of the appropriate cell, tissue or organ for a particular scientific purpose is essential for a satisfactory outcome. The objective of this volume is to provide both beginning and established researchers with basic techniques employed by widely recognized scientists to prepare and maintain the biological components of in vitro model systems. The compilation is not intended to be exhaustive but to provide a set of pivotal methods of value to researchers in the field of toxicology. The methods have been organized by organ systems for easy reference. |
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Page 223
TISSUE SLICE TECHNOLOGY Precision Tissue Slicing This newly developed
technology includes a mechanical slicing apparatus in which it is possible to
produce slices of nearly identical dimensions in a controlled environment with
minimal ...
TISSUE SLICE TECHNOLOGY Precision Tissue Slicing This newly developed
technology includes a mechanical slicing apparatus in which it is possible to
produce slices of nearly identical dimensions in a controlled environment with
minimal ...
Page 224
The individual tissue cores ( A ) are placed into a matching cylindrical tissue
holder ( B ) and lightly compressed with a piston ( C ) holding adjustable weights
. The combination of the distance between an adjustable base plate ( D ) and the
...
The individual tissue cores ( A ) are placed into a matching cylindrical tissue
holder ( B ) and lightly compressed with a piston ( C ) holding adjustable weights
. The combination of the distance between an adjustable base plate ( D ) and the
...
Page 268
Smaller wedges ( 10 g ) can be perfused with a single cannula ; the larger
wedges ( 25 – 50 g ) may need two cannulas per tissue piece . 5 . The flow rate of
the pump should be set to approximately 10 to 20 ml / min , depending on the
size of ...
Smaller wedges ( 10 g ) can be perfused with a single cannula ; the larger
wedges ( 25 – 50 g ) may need two cannulas per tissue piece . 5 . The flow rate of
the pump should be set to approximately 10 to 20 ml / min , depending on the
size of ...
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In Vitro Biological Systems: Methods in Toxicology, Volume 1 Charles A. Tyson,John M. Frazier Limited preview - 2016 |
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acid activity added addition agents aliquots allow animals approximately attached Biochem Biol buffer cell cultures cell suspension cellular centrifuge changes chemical collagenase collected concentration containing deionized water density described determined developed digestion dish dissociation effects enzyme epithelial experiments explants factors Figure filter final flask forceps fraction function glucose growth hepatocytes HEPES human important increased incubated isolated kidney laboratory layer levels liver maintained material measured mechanisms medium method neurons obtained organ Percoll perfusion period pipette placed plastic plates preparation Press primary procedure protein proximal tubule rabbit reaggregates removed renal segments separate serum Sigma skin slices solution specific step sterile stored studies surface technique tion tissue toxicity TOXICOLOGY transferred trypsin tube tubules vessel vitro vivo volume washed yield