The effects of different cryoprotectants and the temperature of addition on the survival of red deer epididymal spermatozoa

With the aim of finding an ideal cryoprotectant in a suitable concentration for red deer epididymal spermatozoa conservation, we evaluated the effects of four most commonly used cryoprotectants (CPAs), Glycerol (G), Ethylene glycol (EG), Propylene glycol (PG), and Dimethyl sulfoxide (DMSO), on the sperm survival. Besides, the effects of two temperatures of CPA addition--22 degrees C (ambient temperature) and 5 degrees C--on sperm quality were also tested. For each temperature tested, sperm samples were evaluated after 0, 15, 30 and 60 min of spermatozoa exposition to CPAs. Thus, sperm quality was in vitro judged by microscopic assessments of individual sperm motility (SMI), and of plasma membrane (Viability) and acrosome (NAR) integrities. Overall, DMSO showed the highest toxicity for red deer epididymal spermatozoa, and glycerol the lowest. Thus, at 60 min of incubation SMI results showed that the toxicity to red deer epididymal spermatozoa of the four CPAs are in the following sequence: G approximately = EG approximately = PG < DMSO ('less than' symbol means P < 0.05, and approximate symbol means P = 0.08). Furthermore, our results also showed a differential response of acrosome membrane to temperature of CPAs addition. Regardless of the CPA used, statistically significant variations (P < 0.05) were found between the two temperatures of addition of CPAs for acrosome integrity, the best being 22 degrees C (NAR = 83.8% vs. 69.8%). These data indicate that sperm quality of red deer epididymal spermatozoa, in addition to be affected by the cryoprotectant, can also be influenced by the temperature at which CPAs are added prior to freezing.     

Vitrification of zebrafish embryo blastomeres in microvolumes

Cryopreservation of fish embryos may play an important role in biodiversity preservation and in aquaculture, but it is very difficult. In addition, the cryopreservation of fish embryo blastomeres makes conservation strategies feasible when they are used in germ-line chimaerism, including interspecific chimaerism. Fish embryo blastomere cryopreservation has been achieved by equilibrium procedures, but to our knowledge, no data on vitrification procedures are available. In the present work, zebrafish embryo blastomeres were successfully vitrified in microvolumes: a number of 0.25 microl drops, sufficient to contain all the blastomeres of an embryo at blastula stage (from 1000-cell stage to oblong stage), were placed over a 2.5 cm loop of nylon filament. In this procedure, where intracellular cryoprotectant permeation is not required, blastomeres were exposed to cryoprotectants for a maximum of 25 sec prior vitrification. The assayed cryoprotectants (ethylene glycol, propylene glycol, dimethyl sulphoxide, glycerol and methanol) are all frequently used in fish embryo and blastomere cryopreservation. Methanol was finally rejected because of the excessive concentration required for the vitrification (15M). All other cryoprotectants were prepared (individually) at 5 M in Hanks' buffered salt solution (sigma) plus 20% FBS (vitrification solutions: vs). After direct thawing in Hanks' buffered salt solution plus 20% FBS, acceptable survival rates were obtained with ethylene glycol: 82.8%, propylene glycol: 87.7%, dimethyl sulphoxide: 93.4%, and glycerol: 73.9% (p < 0.05). Dimethyl sulphoxide showed the highest blastomere survival rate and allowed the rescue of as much as 20% of the total blastomeres from each zebrafish blastula embryo.     

Topological alterations in human spermatozoa associated with the polyelectrolytic effect of RISUG

A new method of male contraception has been developed which results in long-term infertility and has the potential advantage of being reversible. The contraceptive, given the name RISUG (an acronym for Reversible Inhibition of Sperm Under Guidance) is a polyelectrolytic compound and when injected into the lumen of the vas deferens, induces a surface charge imbalance on the sperm membrane system leading to its destabilization. In the present study, morphological and topological alterations in human spermatozoa induced by RISUG have been investigated using atomic force microscopy (AFM). Complete disintegration of the plasma membrane with subsequent rupture and dispersion of the acrosomal contents is observed on treatment with RISUG in vitro. Considerable damage to the midpiece region with significant clustering of the mitochondria and its fusion with the head region is also observed. These observations are in agreement with the significant increase in the volume of RISUG-treated sperm-head region. Topological alterations in the flagellar and midpiece region of RISUG-treated spermatozoa have also been studied.     

The Characteristic Cooling Rate and Vitrification of Liquids

Doklady Physics - This work is devoted to analysis and generalization of the kinetic criteria of vitrification using the model of delocalized atoms. The generalized criterion of a...     

Vitrification of a monatomic 2D simple liquid

A monatomic simple liquid in two dimensions, where atoms interact isotropically through the Lennard-Jones-Gauss potential [M. Engel, H.-R. Trebin, Phys. Rev. Lett. 98, 225505 (2007)], is vitrified by the use of a rapid cooling technique in a molecular dynamics simulation. Transformation to a crystalline state is investigated at various temperatures and the time-temperature-transformation (TTT) curve is determined. It is found that the transformation time to a crystalline state is the shortest at a temerature 14% below the melting temperature T _m and that at temperatures below T _v ≡ 0:6T _m the transformation time is much longer than the available CPU time. This indicates that a long-lived glassy state is realized for T ≤ T _v .      

Amidic and acetonic cryoprotectants improve cryopreservation of volvocine green algae

A number of volvocalean green algae species were subjected to a two-step cryopreservation protocol with various cryoprotectants. Potential cryoprotectants were methanol (DMSO), N,N-dimethylformamide (DMF), N,N-dimethylacetamide, N-methylformamide, and hydroxyacetone (HA). We confirmed prior reports that MeOH was effective for cryopreserving Chlamydomonas, but did not work well for larger volvocaleans such as Volvox. In contrast, DMF and HA were effective for both unicellular and multicellular representatives. When we used a cold-inducible transposon to probe Southern blots of Volvox DNA samples taken before and after storage for one month in LN, we could detect no differences, indicating that the genome had remained relatively stable and that the transposon had not been induced by the cryopreservation procedure. We believe these methods will facilitate long-term storage of several volvocine algal species, including Volvox strains harboring transposon-induced mutations of developmental interest.     

Fluorescent Microscopy Analysis of Mammalian Oocyte Viability after Vitrification

Optics and Spectroscopy - The paper reports the results of a fluorescent microscopy analysis of the viability of oocytes from cattle and pigs after vitrification. Oocytes were frozen in a...     

Vitrification, encapsulation-vitrification and droplet-vitrification: a review

This paper discusses the importance of the successive steps of the vitrification technique and reviews the current development and use of vitrification and of the two derived protocols, encapsulation-vitrification and droplet-vitrification. Vitrification refers to the physical process by which a highly concentrated cryoprotective solution supercools to very low temperatures and finally solidifies into a metastable glass, without undergoing crystallization at a practical cooling rate. Samples are thus cryopreserved without detrimental intracellular ice formation. In a standard vitrification protocol, excised explants are precultured on medium enriched with sucrose, treated (loaded) with a loading solution composed of 2 M glycerol + 0.4 M sucrose, dehydrated with a highly concentrated vitrification solution [e.g. the PVS2 vitrification solution, which contains 30 percent (w/v) glycerol, 15 percent (w/v) ethylene glycol and 15 percent (w/v) DMSO and 0.4 M sucrose], frozen and rewarmed rapidly, unloaded with basal culture medium supplemented with 1.2 M sucrose, and then transferred to standard culture conditions. In the encapsulation-vitrification technique, the explants are encapsulated in alginate beads, loaded and dehydrated with a vitrification solution before rapid immersion in liquid nitrogen. In the droplet-freezing technique, excised explants are loaded, treated with the vitrification solution and frozen in individual microdroplets of vitrification solution placed on aluminium foils, which are immersed rapidly in liquid nitrogen. These three techniques have been applied to different tissues of over 100 plant species from temperate and tropical origins and the number of cases where they are being tested on a large scale or applied routinely is increasing.     

Vitrification of caudal fin explants from zebrafish adult specimens

No data on vitrification of tissue samples are available in fishes. Three vitrification solutions were compared: V1: 20% ethylene glycol and 20% dimethyl sulphoxide; V2: 25% propylene glycol and 20% dimethyl sulphoxide, and; V3: 20% propylene glycol and 13% methanol, all three prepared in Hanks' buffered salt solution plus 20 percent FBS, following the same one step vitrification procedure developed in mammals. Caudal fin tissue pieces were vitrified into 0.25 ml plastic straws in 30s and stored in liquid nitrogen for 3 days minimum, warmed (10s in nitrogen vapour and 5s in a 25 degree C water bath) and cultured (L-15 plus 20% FBS at 28.5 degree C). At the third day of culture, both attachment and outgrowing rates were recorded. V3 led to the worst results (8% of attachment rate). V1 and V2 allow higher attachment rates (V1: 63% vs V2: 50%. P < 0.05) but not significantly different outgrowing rates (83% to 94%). Vitrification of caudal fin pieces is advantageous in fish biodiversity conservation, particularly in the wild, due to the simplicity of procedure and equipment.     

Vitrification and transport properties in AgBr-doped chalcogenide systems

Vitrification and transport properties measurements for (AgBr)_x(As₂Se₃)_1−x glasses have been carried out in order to investigate the ion conduction phenomena of these systems. Glass samples were successfully obtained in a composition range of 0 ≤ x ≤ 0.65. The addition of AgBr leads these systems to an exponential increase of electrical conductivity. The ionic component of the electrical conductivity is dominant in highly AgBr-doped glasses. The vitrification brings the fast ion conduction to the present glass systems.     

Vitrification of encapsulated hepatocytes with reduced cooling and warming rates

We have used microencapsulated hepatocytes as model to develop a method of vitreous cryopreservation of large quantities of cell-containing constructs. The method included a pre-equilibration procedure in which the amount of penetrating cryoprotectant was gradually increased by 15% in each step. The optimal vitrification solution consists of 40% ethylene glycol and 0.6M sucrose. The concentration of 1M sucrose used for the first dilution solution with subsequent decrease of sucrose concentration to 0.7 M sucrose and by 0.2-0.15M for each subsequent step. This sucrose dilution procedure had no adverse effect on cell functions. Three cooling rates (400 degrees C/min and above) and three warming rates (650 degrees C/min and above), in combination with the proposed vitrification solution, were equally effective. The optimization of the procedure and solutions allow microencapsulated hepatocytes to be preserved with almost 100% retention of cell functions and no detectable damage to the fragile microcapsules. The de-linking of the cooling/warming rates with the effectiveness of vitrification potentially paves the way for large scale cryopreservation of complex tissue engineered constructs.     

Patchy胶体粒子的结晶、玻璃化和凝胶化问题

本文探讨了中性多缔合位点Patchy胶体粒子系统的相图及其相关问题. 在研究中,计入了分子间的硬芯Lennard-Jones势和缔合作用,进而阐明了系统的流体相(F),无规密积相(RCP)和面心立方相(FCC)之间转变的相态结构. 在体系丰富的相结构中,F-F,F-RCP及F-FCC相转变以及描述粒子间联结性的溶胶-凝胶转变相互影响,致使一些相态在不同相互作用强度时可以呈现亚稳态和稳态. 同时,本文重点阐述了缔合能量以及patch数目对体系的临界温度、临界密度、临界三相点以及溶胶-凝胶转变等的调控机制.     

Vitrification of cultured and non-cultured expanded and hatched porcine blastocysts

The aim of this experiment was to examine the survival of porcine embryos following exposure or vitrification in EFS solution. The work was carried out on cultured and non-cultured expanded and hatched blastocysts. The viability of treated embryos was assessed by their ability to develop in in vitro culture. The results showed a higher viability of cultured expanded blastocyst (35.1 percent) vitrified in EFS medium compared to those non-cultured (12.5 percent). The proportion of cultured hatched blastocyst vitrified in this medium was 13.2 percent, while none of the non-cultured hatched blastocyst survived vitrification. It is concluded that: 1. The EFS solution was more toxic to hatched blastocyst than expanded blastocyst 2. The expanded blastocyst was a more suitable developmental stage for vitrification than hatched blastocyst. Moreover, we demonstrated that the survival rate of vitrified cultured pig blastocyst was higher compared to non-cultured.     

地下玻璃固化体中元素垂直迁移规律初探

利用上升气流模型模拟研究了地下玻璃固化体中As, Cs和Sr元素的迁移行为。 利用中子活化分析（INAA）技术检测了玻璃固化体中元素迁出量, 用原子力显微镜观察了迁出物质的形态。 实验结果表明: 在上升气流作用下, 被玻璃固化的元素会以纳米微粒的形式迁移出来, 迁移方向是垂直向上的, 迁出的元素会在玻璃固化体上方的吸附物中不断积累; 上升气流作用时间越长, 固化体中元素迁出的量越大; 玻璃固化体处置点与地表的温差越大, 元素迁出的速度越快。 The transporting behavior of As, Cs, Sr in vitrification form has been studied using a simulating model of ascending flows.Instrumental Neutron Activation Analysis (INAA) was used to determine the quantity of elements transportation. The results of simulating experiment show that the elements can be transported vertically from the vitrification form by ascending flows in the form of nano scale particles. Then these elements accumulate continuously in the adsorber above the vitrification form. In addition, when the temperature difference between the ground surface and the environment where the vitrification form disposed increases, the transportation speed of these elements will increase too.     

NMR Insights into Wasteforms for the Vitrification of High-Level Nuclear Waste

Magic-angle spinning nuclear magnetic resonance of ¹¹B, ²⁹Si and ²⁷Al has been used to study the distribution of nonbridging oxygen atoms (NBO) in an alkali borosilicate glass to which surrogate oxides for high-level radioactive waste have been added. The properties of such glasses are shown to depend on the fraction N ₄ of four-coordinated boron atoms (B4) and on the fraction of silicate tetrahedra possessing one NBO, Q³. The aqueous corrosion rate increases with Q³ content, as does weight loss due to evaporation from the melt. The activation energy for direct current conduction scales with N ₄. Values of N ₄ obtained for these glasses deviate from those predicted by the currently accepted model and are strongly affected by the modifier or intermediate nature of the surrogate oxide and also by its effect on the distribution of NBO between the silicate and borate polyhedra. Authors' address: Diane Holland, Department of Physics, University of Warwick, Coventry CV4 7AL, UK     

Vitrification in a 2D Ising model with mobile bonds

A bond-disordered two-dimensional Ising model is used to simulate Kauzmann's mechanism of vitrification in liquids, by a Glauber Monte Carlo simulation. The rearrangement of configurations is achieved by allowing impurity bonds to hop to nearest neighbors at the same rate as the spins flip. For slow cooling, the theoretical minimum energy configuration is approached, characterized by an amorphous distribution of locally optimally arranged impurity bonds. Rapid cooling to low temperatures regularly finds bond configurations of higher energy, which are both a priori rare and severely restrictive to spin movement, providing a simple realization of kinetic vitrification. A supercooled liquid regime is also found, and characterized by a change in sign of the field derivative of the spin-glass susceptibility at a finite temperature. Received 3 August 2000 and Received in final form 9 March 2001     

Energy of Atom Delocalization and Thermal Motion in the Region of Vitrification

Russian Physics Journal - A linear correlation has been established between the empirical parameter D of the Enkel equation for the viscosity and the vitrification temperature Tg of inorganic...     

Vitrification and glass transition of water: insights from spin probe ESR

Three long-standing problems related to the physics of water, viz., the possibility of vitrifying bulk water by rapid quenching, its glass transition, and the supposed impossibility of obtaining supercooled water between 150 and 233 K, the so-called "no man's land" of its phase diagram, are studied using the highly sensitive technique of spin probe ESR. Our results suggest that water can indeed be vitrified by rapid quenching; it undergoes a glass transition at approximately 135 K, and the relaxation behavior studied using this method between 165 K and 233 K closely follows the predictions of the Adam-Gibbs model.     

The mechanical point impedance of the human head, with and without skin penetration

The fact that a titanium screw can be implanted into the mastoid portion of the human skull, at the same time establishing a permanent, reaction-free skin penetration, has made it possible to attach a new bone conduction hearing aid directly to the skull. To understand and improve this new method of bone stimulation, the mechanical point impedance of the titanium screw-skull system was measured. The conventional point impedance of the skin-covered mastoid portion of the temporal bone was also measured and the difference in magnitude between the two impedances was calculated. An impedance head (Brüel & Kjaer 8001) and an FFT analyzer (Hewlett-Packard 5423) were used for mechanical point impedance measurements. Seven patients have been investigated. The magnitude of the impedance for the screw-skull system was found to be generally between 10 and 30 dB higher than that for the conventional skin-covered mastoid bone. One conclusion is that the conventional point impedance of the skin-covered mastoid portion of the human skull is essentially due to the properties of the skin and subcutaneous soft tissue. Another conclusion is that a much lower stimulation velocity is needed, with skin penetration, to produce a given hearing sensation.