Regular articleBiotransformation activity in vitrified human liver slices
References (26)
- et al.
Factors influencing renal preservation. I. Effects of three vehicle solutions and the permeation kinetics of three cryoprotectants assessed with rabbit cortical slices
Cryobiology
(1984) - et al.
The influence of temperature on the function of renal cortical slices frozen in various cryoprotectants
Cryobiology
(1985) - et al.
Vitrification solutions: Molecular and biological aspects
Cryobiology
(1986) - et al.
Some emerging principles underlying the physical properties, biological actions and utility of vitrification solutions
Cryobiology
(1987) - et al.
The influence of cooling rate and warming rate on the response of renal cortical slices frozen to −40 °C in the presence of 2. 1 M cryoprotectant (ethylene glycol, glycerol, or dimethyl sulfoxide)
Cryobiology
(1985) - et al.
Vitrification of human islets of Langerhans
Cryobiology
(1987) - et al.
Cryopreservation of rat blastocysts by vitrification
Cryobiology
(1988) A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples
Anal. Biochem
(1978)- et al.
Preliminary experiments on vitrification of isolated rat islets of Langerhans
Cryobiol. Abstr
(1985) - et al.
Organ culture of precision-cut liver slices for in vitro toxicology
Life Sci
(1985)
Vitrification of human monocytes
Cryobiology
(1986)
Factors influencing renal preservation. II Toxic effects of three cryoprotectants in combination with three vehicle solutions in nonfrozen rabbit cortical slices
Cryobiology
(1984)
Hepatotoxicity of dichlorobenzene isomers in rat liver slices
Toxicologist
(1986)
Cited by (46)
Cryobiology
2008, Tissue EngineeringCryopreservation of rat hippocampal slices by vitrification
2006, CryobiologyOrgan slices for the evaluation of human drug toxicity
2004, Chemico-Biological InteractionsCitation Excerpt :Further refinement is needed to ensure that the function of cold or cryopreserved tissue is truly equivalent to freshly prepared tissue, in order for the methodologies to become common practice. Cryopreservation of slices by vitrification, a process which prevents the formation of both intra- and extracellular ice crystals while an amorphous glass is formed of the slice liquid constituents, has shown success and may become the best suited method for slices [49–51]. A promising goal for in vitro models is the ability to identify cellular markers which could be used in vivo to monitor the development or progression of a drug-induced side-effect or toxicity.
High-throughput optimization by statistical designs: Example with rat liver slices cryopreservation
2003, Analytical Biochemistry
Copyright © 1991 Published by Elsevier Inc.