Literature DB >> 3535871

Cryopreservation of rabbit corneas: assessment by microscopy and transplantation.

L P Fong, C J Hunt, M J Taylor, D E Pegg.   

Abstract

Rabbit corneas were frozen and thawed by three methods and compared by full thickness transplantation as well as specular microscopy, histology, and transmission electron microscopy. Two of the methods used a recently described technique, in which the excised cornea was immersed in a potassium-rich buffered solution containing the cryoprotectant dimethyl sulphoxide (Me2SO, 2 mol/l). This solution was designed to restrict the loss of intracellular potassium and to prevent cell swelling at low temperatures. In one group the corneas were frozen and thawed surrounded by 5 ml of medium, while in the second group corneas were drained of excess fluid and frozen in air. The third group consisted of corneas cryopreserved by Capella and colleagues' method. All the cryopreserved corneas were damaged, but those that had been frozen in air after exposure to the new medium showed better structure and function than corneas frozen by either of the other two techniques.

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Year:  1986        PMID: 3535871      PMCID: PMC1040821          DOI: 10.1136/bjo.70.10.751

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  33 in total

1.  TECHNIQUES FOR FULL-THICKNESS KERATOPLASTY IN RABBITS USING FRESH AND FROZEN CORNEAL TISSUE.

Authors:  F O MUELLER
Journal:  Br J Ophthalmol       Date:  1964-07       Impact factor: 4.638

2.  The mechanism of the protective action of glycerol against haemolysis by freezing and thawing.

Authors:  J E LOVELOCK
Journal:  Biochim Biophys Acta       Date:  1953-05

3.  The haemolysis of human red blood-cells by freezing and thawing.

Authors:  J E LOVELOCK
Journal:  Biochim Biophys Acta       Date:  1953-03

4.  A multirate small-volume cooling machine.

Authors:  A R Hayes; D E Pegg; R E Kingston
Journal:  Cryobiology       Date:  1974-08       Impact factor: 2.487

5.  Experimental rehydration of cryopreserved corneal tissue.

Authors:  H F Edelhauser; D L Van Horn; A B Gallun; R O Schultz
Journal:  Invest Ophthalmol       Date:  1971-02

6.  Cell preservation in a programmed cooling machine: the effect of variations in supercooling.

Authors:  J Foreman; D E Pegg
Journal:  Cryobiology       Date:  1979-08       Impact factor: 2.487

7.  Dual staining of corneal endothelium with trypan blue and alizarin red S: importance of pH for the dye-lake reaction.

Authors:  M J Taylor; C J Hunt
Journal:  Br J Ophthalmol       Date:  1981-12       Impact factor: 4.638

8.  Assessment and interpretation of corneal endothelial cell morphology and function following cryopreservation.

Authors:  P W Madden; D L Easty
Journal:  Br J Ophthalmol       Date:  1982-02       Impact factor: 4.638

9.  Preservation of viable corneal tissue.

Authors:  J A Capella; H E Kaufman; J E Robbins
Journal:  Cryobiology       Date:  1965 Nov-Dec       Impact factor: 2.487

10.  The role of pH and buffer capacity in the recovery of function of smooth muscle cooled to -13 degrees C in unfrozen media.

Authors:  M J Taylor
Journal:  Cryobiology       Date:  1982-12       Impact factor: 2.487

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  3 in total

1.  Osmotic properties of the rabbit corneal endothelium and their relevance to cryopreservation.

Authors:  D E Pegg; C J Hunt; L P Fong
Journal:  Cell Biophys       Date:  1987-04

2.  Latent endothelial cell damage after experimental corneal cryopreservation.

Authors:  M Hagenah; M Böhnke
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1993-09       Impact factor: 3.117

3.  Thermal expansion of the cryoprotectant cocktail DP6 combined with synthetic ice modulators in presence and absence of biological tissues.

Authors:  David P Eisenberg; Michael J Taylor; Yoed Rabin
Journal:  Cryobiology       Date:  2012-05-03       Impact factor: 2.487

  3 in total

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