Literature DB >> 9367610

Vitrification properties of solutions of ethylene glycol in saline containing PVP, Ficoll, or dextran.

J M Shaw1, L L Kuleshova, D R MacFarlane, A O Trounson.   

Abstract

Vitrification solutions which are used for cells or embryos generally contain cryoprotectant, physiological saline, and one or more macromolecular solutes. The macromolecules modify the vitrification tendencies of these solutions, but there is little detailed information on the vitrification properties of ethylene glycol solutions containing the additives PVP, Ficoll, and dextran. This study therefore added ethylene glycol to 0.9% NaCl in water (saline) and used differential scanning calorimetry to determine the lowest concentration at which the solution would remain vitreous when a warming rate of 10 degrees C/min was used. In the absence of other additives 59 wt% ethylene glycol (EG) in saline formed a stable glass. When ethylene glycol was replaced by the polymers Ficoll and/or dextran on a weight for weight basis, the resulting solution vitrified less readily than an EG-saline solution even though the total solute concentration was kept constant. The total solute concentration required to form a stable vitreous solution increased as the Ficoll 70,000 and 400,000 MW or dextran 78,000 MW content increased (5, 10, and 20 wt%). Ficoll and dextran had little or no effect on the glass transition and melting points of the solutions. In the presence of PVP vitrification occurred at a total solute concentration of 59 wt% (PVP 360,000 MW) or 60 wt% (PVP 40,000 MW) for all three tested PVP concentrations (5, 10, and 20 wt%). Although this indicates that PVP and EG have comparable vitrification properties, the melting and the glass transition temperature of the solutions rose as the PVP content increased. When 1 m sucrose was added to saline and 0, 5, 10, or 20 wt% PVP 40,000 MW vitrification was achieved with 31, 26, 23, and 15% EG, respectively, indicating that the total solute concentration required for vitrification could be estimated with reasonable accuracy from the sum of the individual components. We conclude that the tested polymers differ in how they interact with ethylene glycol-based vitrification solutions. Copyright 1997 Academic Press.

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Year:  1997        PMID: 9367610     DOI: 10.1006/cryo.1997.2043

Source DB:  PubMed          Journal:  Cryobiology        ISSN: 0011-2240            Impact factor:   2.487


  13 in total

1.  Effect of warming rate on the survival of vitrified mouse oocytes and on the recrystallization of intracellular ice.

Authors:  Shinsuke Seki; Peter Mazur
Journal:  Biol Reprod       Date:  2008-06-18       Impact factor: 4.285

2.  Cytotoxicity effects of cryoprotectants as single-component and cocktail vitrification solutions.

Authors:  Alison Lawson; Hajira Ahmad; Athanassios Sambanis
Journal:  Cryobiology       Date:  2011-01-22       Impact factor: 2.487

3.  Hydroxypropyl cellulose supplementation in vitrification solutions: a prospective study with donor oocytes.

Authors:  Miguel Gallardo; María Hebles; Beatriz Migueles; Mónica Dorado; Laura Aguilera; Mercedes González; Paloma Piqueras; Alejandro Lucas; Lorena Montero; Pascual Sánchez-Martín; Fernando Sánchez-Martín; Ramón Risco
Journal:  J Assist Reprod Genet       Date:  2016-12-27       Impact factor: 3.412

4.  Effect of vitrification on mitochondrial membrane potential in human metaphase II oocytes.

Authors:  Cui Chen; Shubiao Han; Weiwei Liu; Yaping Wang; Guoning Huang
Journal:  J Assist Reprod Genet       Date:  2012-08-23       Impact factor: 3.412

5.  Principles of Ice-Free Cryopreservation by Vitrification.

Authors:  Gregory M Fahy; Brian Wowk
Journal:  Methods Mol Biol       Date:  2021

6.  Hydrogel Encapsulation Facilitates Rapid-Cooling Cryopreservation of Stem Cell-Laden Core-Shell Microcapsules as Cell-Biomaterial Constructs.

Authors:  Gang Zhao; Xiaoli Liu; Kaixuan Zhu; Xiaoming He
Journal:  Adv Healthc Mater       Date:  2017-11-27       Impact factor: 9.933

7.  The effect of minimal concentration of ethylene glycol (EG) combined with polyvinylpyrrolidone (PVP) on mouse oocyte survival and subsequent embryonic development following vitrification.

Authors:  Yao Wang; Osamu Okitsu; Xiao-Ming Zhao; Yun Sun; Wen Di; Ri-Cheng Chian
Journal:  J Assist Reprod Genet       Date:  2013-11-21       Impact factor: 3.412

8.  An improved cryopreservation method for a mouse embryonic stem cell line.

Authors:  Corinna M Kashuba Benson; James D Benson; John K Critser
Journal:  Cryobiology       Date:  2007-12-10       Impact factor: 2.487

9.  Synthetic polymers improve vitrification outcomes of macaque ovarian tissue as assessed by histological integrity and the in vitro development of secondary follicles.

Authors:  Alison Y Ting; Richard R Yeoman; Maralee S Lawson; Mary B Zelinski
Journal:  Cryobiology       Date:  2012-04-28       Impact factor: 2.487

10.  Efficient production of live offspring from mouse oocytes vitrified with a novel cryoprotective agent, carboxylated ε-poly-L-lysine.

Authors:  Hitomi Watanabe; Natsuki Kohaya; Maki Kamoshita; Katsuyoshi Fujiwara; Kazuaki Matsumura; Suong-Hyu Hyon; Junya Ito; Naomi Kashiwazaki
Journal:  PLoS One       Date:  2013-12-23       Impact factor: 3.240

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