determination of cell membrane transport
properties. Biophys J 71:443–450
87. Mullen SF, Rosenbaum M, Critser JK (2007)
The effect of osmotic stress on the cell volume, metaphase ii spindle and developmental
potential of in vitro matured porcine oocytes.
Cryobiology 54:281–289
88. Zhao G, Zhang Z, Zhang Y, Chen Z, Niu D,
Cao Y, He X (2017) A microfluidic perfusion
approach for on-chip characterization of the
transport properties of human oocytes. Lab
Chip 17:1297–1305
89. Mbogba MK, Haider Z, Hossain SM,
Huang D, Memon K, Panhwar F, Lei Z,
Zhao G (2018) The application of convolution neural network based cell segmentation
during
cryopreservation.
Cryobiology
85:95–104.
https://doi.org/10.1016/j.
cryobiol.2018.09.003
90. Chaveiro A, Liu J, Engel B, Critser JK,
Woelders H (2006) Significant variability
among bulls in the sperm membrane permeability for water and glycerol: possible implications for semen freezing protocols for
individual males. Cryobiology 53:349–359
91. Fry AK, Higgins AZ (2012) Measurement of
cryoprotectant permeability in adherent
endothelial cells and applications to cryopreservation. Cell Mol Bioeng 5:287–298
92. Zhurova M, Olivieri A, Holt A, Acker JP
(2014) A method to measure permeability of
red blood cell membrane to water and solutes
using intrinsic fluorescence. Clin Chim Acta
Int J Clin Chem 431C:103–110. https://doi.
org/10.1016/j.cca.2014.01.045
93. Toner M, Cravalho EG, Karel M (1993)
Cellular-response of mouse oocytes to freezing stress - prediction of intracellular ice formation. J Biomech Eng Trans ASME
115:169–174
94. Karlsson JOM, Cravalho EG, Toner M
(1994) A model of diffusion–limited ice
growth inside biological cells during freezing.
J Appl Phy 75:4442–4455
95. Karlsson JOM (2010) Effects of solution
composition on the theoretical prediction of
ice nucleation kinetics and thermodynamics.
Cryobiology 60:43–51
96. Glazar AI, Mullen SF, Liu J, Benson JD, Critser JK, Squires EL, Graham JK (2009)
Osmotic tolerance limits and membrane permeability characteristics of stallion spermatozoa treated with cholesterol. Cryobiology
59:201–206
97. Yoshimori T, Takamatsu H (2009) 3-D measurement of osmotic dehydration of isolated
and adhered PC-3 cells. Cryobiology
58:52–61.
http://dx.doi.org/10.1016/j.
cryobiol.2008.10.128
98. Blanco JM, Long JA, Gee G, Donoghue AM,
Wildt DE (2008) Osmotic tolerance of avian
spermatozoa: influence of time, temperature,
cryoprotectant and membrane ion pump
function on sperm viability. Cryobiology
56:8–14
99. Salinas-Flores L, Adams SL, Lim MH (2008)
Determination of the membrane permeability
characteristics of pacific oyster, crassostrea
gigas, oocytes and development of optimized
methods to add and remove ethylene glycol.
Cryobiology 56:43–52
100. Si W, Benson J, Men H, Critser J (2006)
Osmotic tolerance limits and effects of cryoprotectants on the motility, plasma membrane
integrity and acrosomal integrity of rat sperm.
Cryobiology 53:336–348
101. Agca Y, Mullen S, Liu J, Johnson-Ward J,
Gould K, Chan A, Critser J (2005) Osmotic
tolerance and membrane permeability characteristics of rhesus monkey (Macaca mulatta)
spermatozoa. Cryobiology 50:1–14
102. Walters EM, Men H, Agca Y, Mullen SF,
Critser ES, Critser JK (2005) Osmotic tolerance of mouse spermatozoa from various
genetic backgrounds: acrosome integrity,
membrane integrity, and maintenance of
motility. Cryobiology 50:193–205
103. Hunt C, Armitage S, Pegg D (2003) Cryopreservation of umbilical cord blood: 2. Tolerance of CD34(+) cells to multimolar dimethyl
sulphoxide and the effect of cooling rate on
recovery after freezing and thawing. Cryobiology 46:76–87
104. Guthrie H, Liu J, Critser J (2002) Osmotic
tolerance limits and effects of cryoprotectants
on motility of bovine spermatozoa. Biol
Reprod
67.
https://doi.org/10.1095/
biolreprod67.6.1811
105. Koshimoto C, Mazur P (2002) The effect of
the osmolality of sugar-containing media, the
type of sugar, and the mass and molar concentration of sugar on the survival of frozenthawed mouse sperm. Cryobiology 45:80–90
106. Liu J, Christian J, Critser J (2002) Canine
RBC osmotic tolerance and membrane permeability. Cryobiology 44:258–268
107. Koshimoto C, Gamliel E, Mazur P (2000)
Effect of osmolality and oxygen tension on
the survival of mouse sperm frozen to various
temperatures in various concentrations of
glycerol
and
raffinose.
Cryobiology
41:204–231
108. Gao DY, Liu J, Liu C, McGann LE, Watson
PF, Kleinhans FW, Mazur P, Critser ES,
Mathematical Modeling and Optimization of Cryopreservation in Single Cells
171
properties. Biophys J 71:443–450
87. Mullen SF, Rosenbaum M, Critser JK (2007)
The effect of osmotic stress on the cell volume, metaphase ii spindle and developmental
potential of in vitro matured porcine oocytes.
Cryobiology 54:281–289
88. Zhao G, Zhang Z, Zhang Y, Chen Z, Niu D,
Cao Y, He X (2017) A microfluidic perfusion
approach for on-chip characterization of the
transport properties of human oocytes. Lab
Chip 17:1297–1305
89. Mbogba MK, Haider Z, Hossain SM,
Huang D, Memon K, Panhwar F, Lei Z,
Zhao G (2018) The application of convolution neural network based cell segmentation
during
cryopreservation.
Cryobiology
85:95–104.
https://doi.org/10.1016/j.
cryobiol.2018.09.003
90. Chaveiro A, Liu J, Engel B, Critser JK,
Woelders H (2006) Significant variability
among bulls in the sperm membrane permeability for water and glycerol: possible implications for semen freezing protocols for
individual males. Cryobiology 53:349–359
91. Fry AK, Higgins AZ (2012) Measurement of
cryoprotectant permeability in adherent
endothelial cells and applications to cryopreservation. Cell Mol Bioeng 5:287–298
92. Zhurova M, Olivieri A, Holt A, Acker JP
(2014) A method to measure permeability of
red blood cell membrane to water and solutes
using intrinsic fluorescence. Clin Chim Acta
Int J Clin Chem 431C:103–110. https://doi.
org/10.1016/j.cca.2014.01.045
93. Toner M, Cravalho EG, Karel M (1993)
Cellular-response of mouse oocytes to freezing stress - prediction of intracellular ice formation. J Biomech Eng Trans ASME
115:169–174
94. Karlsson JOM, Cravalho EG, Toner M
(1994) A model of diffusion–limited ice
growth inside biological cells during freezing.
J Appl Phy 75:4442–4455
95. Karlsson JOM (2010) Effects of solution
composition on the theoretical prediction of
ice nucleation kinetics and thermodynamics.
Cryobiology 60:43–51
96. Glazar AI, Mullen SF, Liu J, Benson JD, Critser JK, Squires EL, Graham JK (2009)
Osmotic tolerance limits and membrane permeability characteristics of stallion spermatozoa treated with cholesterol. Cryobiology
59:201–206
97. Yoshimori T, Takamatsu H (2009) 3-D measurement of osmotic dehydration of isolated
and adhered PC-3 cells. Cryobiology
58:52–61.
http://dx.doi.org/10.1016/j.
cryobiol.2008.10.128
98. Blanco JM, Long JA, Gee G, Donoghue AM,
Wildt DE (2008) Osmotic tolerance of avian
spermatozoa: influence of time, temperature,
cryoprotectant and membrane ion pump
function on sperm viability. Cryobiology
56:8–14
99. Salinas-Flores L, Adams SL, Lim MH (2008)
Determination of the membrane permeability
characteristics of pacific oyster, crassostrea
gigas, oocytes and development of optimized
methods to add and remove ethylene glycol.
Cryobiology 56:43–52
100. Si W, Benson J, Men H, Critser J (2006)
Osmotic tolerance limits and effects of cryoprotectants on the motility, plasma membrane
integrity and acrosomal integrity of rat sperm.
Cryobiology 53:336–348
101. Agca Y, Mullen S, Liu J, Johnson-Ward J,
Gould K, Chan A, Critser J (2005) Osmotic
tolerance and membrane permeability characteristics of rhesus monkey (Macaca mulatta)
spermatozoa. Cryobiology 50:1–14
102. Walters EM, Men H, Agca Y, Mullen SF,
Critser ES, Critser JK (2005) Osmotic tolerance of mouse spermatozoa from various
genetic backgrounds: acrosome integrity,
membrane integrity, and maintenance of
motility. Cryobiology 50:193–205
103. Hunt C, Armitage S, Pegg D (2003) Cryopreservation of umbilical cord blood: 2. Tolerance of CD34(+) cells to multimolar dimethyl
sulphoxide and the effect of cooling rate on
recovery after freezing and thawing. Cryobiology 46:76–87
104. Guthrie H, Liu J, Critser J (2002) Osmotic
tolerance limits and effects of cryoprotectants
on motility of bovine spermatozoa. Biol
Reprod
67.
https://doi.org/10.1095/
biolreprod67.6.1811
105. Koshimoto C, Mazur P (2002) The effect of
the osmolality of sugar-containing media, the
type of sugar, and the mass and molar concentration of sugar on the survival of frozenthawed mouse sperm. Cryobiology 45:80–90
106. Liu J, Christian J, Critser J (2002) Canine
RBC osmotic tolerance and membrane permeability. Cryobiology 44:258–268
107. Koshimoto C, Gamliel E, Mazur P (2000)
Effect of osmolality and oxygen tension on
the survival of mouse sperm frozen to various
temperatures in various concentrations of
glycerol
and
raffinose.
Cryobiology
41:204–231
108. Gao DY, Liu J, Liu C, McGann LE, Watson
PF, Kleinhans FW, Mazur P, Critser ES,
Mathematical Modeling and Optimization of Cryopreservation in Single Cells
171