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 47
22 g glucose 500 ml sterile water Filter , store at 4°C for up to 12 months . Media
stock ( MS ) 900 ml sterile water , in a one liter bottle ( GIBCO , Grand Island , NY
) 100 ml 10 % MEM ( Eagle ' s minimal essential medium , Earle ' s salts , GIBCO
...
22 g glucose 500 ml sterile water Filter , store at 4°C for up to 12 months . Media
stock ( MS ) 900 ml sterile water , in a one liter bottle ( GIBCO , Grand Island , NY
) 100 ml 10 % MEM ( Eagle ' s minimal essential medium , Earle ' s salts , GIBCO
...
Page 59
Media glucose utilization can be substantial in dense older cultures , so one
advantage of a high glucose concentration is better maintenance of glucose
availability between feedings . Our plating and growth media contain only the
glutamate ...
Media glucose utilization can be substantial in dense older cultures , so one
advantage of a high glucose concentration is better maintenance of glucose
availability between feedings . Our plating and growth media contain only the
glutamate ...
Page 518
Viability is assessed by real - time monitoring of arterial pressure , flow , perfusate
pH , and glucose utilization calculated from the product of glucose extraction ( mg
/ dl ) and the flow rate ( ml / min ) at each observation time . IPPSFs are ...
Viability is assessed by real - time monitoring of arterial pressure , flow , perfusate
pH , and glucose utilization calculated from the product of glucose extraction ( mg
/ dl ) and the flow rate ( ml / min ) at each observation time . IPPSFs are ...
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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