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 360
tion cocktail and digested for a total of 50 min at 37°C in an orbital shaking water
bath ( 150 rpm ) under a 95 % 02 / 5 % CO2 atmosphere . Harvesting Tissue
during Digestion To prevent excessive enzymatic digestion and to improve the
yield ...
tion cocktail and digested for a total of 50 min at 37°C in an orbital shaking water
bath ( 150 rpm ) under a 95 % 02 / 5 % CO2 atmosphere . Harvesting Tissue
during Digestion To prevent excessive enzymatic digestion and to improve the
yield ...
Page 544
... 288 – 289 materials and reagents for , 281 - 283 procedures for , 283 – 288
reagents and medium for , preparation of , 281 - 282 selective metabolic
induction or inhibi . tion of , 290 spleen cell preparation for , 286 surgery and liver
perfusion ...
... 288 – 289 materials and reagents for , 281 - 283 procedures for , 283 – 288
reagents and medium for , preparation of , 281 - 282 selective metabolic
induction or inhibi . tion of , 290 spleen cell preparation for , 286 surgery and liver
perfusion ...
Page 567
... 159 Vascular cells loss of differentiated functions , as func . tion of time in
cultures , 166 – 167 structure of , 159 – 168 Vascular smooth muscle excitation /
contraction coupling in , sources of calcium involved in , 178 – 179 optimal length
for ...
... 159 Vascular cells loss of differentiated functions , as func . tion of time in
cultures , 166 – 167 structure of , 159 – 168 Vascular smooth muscle excitation /
contraction coupling in , sources of calcium involved in , 178 – 179 optimal length
for ...
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In Vitro Biological Systems: Methods in Toxicology, Volume 1 Charles A. Tyson,John M. Frazier Limited preview - 2016 |
Common terms and phrases
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