Search results for "vitrification"

showing 10 items of 47 documents

Direct transfer of vitrified rabbit embryos.

1994

In this study we looked at the feasibility of transferring vitrified rabbit embryos directly into recipient does. Compacted morulae were vitrified in a solution of 20% ethylene glycol and 20% dimethyl sulfoxide. After thawing, and without step-wise diluted solution, the vitrified embryos were transferred into the recipient's uterine horns. Survival rate at birth differed from fresh rabbit embryos (40% vs 55%, P0.05). However, the percentage of does that delivered (94%) and the survival rate suggested this method is suitable for both storage and simple transfer of rabbit morulae.

animal structuresEquineChemistryDimethyl sulfoxideUterine hornsEmbryoRabbit (nuclear engineering)AnatomyDirect transferAndrologychemistry.chemical_compoundFood Animalsembryonic structuresAnimal Science and ZoologyVitrificationSmall AnimalsEthylene glycolTheriogenology
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Closed vs. Open Oocyte Vitrification Methods Are Equally Effective for Blastocyst Embryo Transfers: Prospective Study from a Sibling Oocyte Donation …

2020

<b><i>Purpose:</i></b> To assess whether open and closed vitrification protocols are equally effective for sibling-oocyte cycles when performing blastocyst embryo transfers. <b><i>Materials and Methods:</i></b> A prospective study was set up comparing the open and the closed vitrification techniques in oocyte recipients sharing sibling oocytes between 2014 and 2016. Sibling oocytes were randomly and equally assigned into the closed group (oocytes vitrified in a closed system) or the open group (oocytes vitrified in an open system). Intracytoplasmic sperm injection was performed on all cases. Embryo transfers were performed on day 5. Power anal…

AdultPregnancy Ratemedicine.medical_treatmentIntracytoplasmic sperm injectionAndrology03 medical and health sciences0302 clinical medicineHuman fertilizationPregnancymedicineHumansVitrificationBlastocystAdult Birth RateEmbryo ImplantationProspective StudiesSperm Injections IntracytoplasmicBirth RateSurvival rateCryopreservation030219 obstetrics & reproductive medicineOocyte Donationbusiness.industryObstetrics and GynecologyEmbryoOocyteEmbryo TransferVitrificationInfertility; Oocyte donation; Vitrificationmedicine.anatomical_structureBlastocystReproductive Medicine030220 oncology & carcinogenesisInfertilityOocytesFemaleLive birthbusinessGynecologic and obstetric investigation
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Factors affecting shoot proliferation and vitrification inDigitalis obscura cultures

1992

Variations of composition and consistency of the culture medium and time of exposure to growth regulators were assayed to optimize normal caulogenic response ofDigitalis obscura hypocotyls cultured in vitro. The effects of the culture conditions on physiologic changes related to vitrification of the regenerated plants were also investigated. Liquid medium increased the bud-forming capacity of the explants but induced buds failed to develop into shoots and showed symptoms of vitrification. On agar-solidified media, maximum multiplication rates were achieved with 0.7% agar. Increasing agar concentration reduced vitrification but lowered the propagation rate. Changes in the strength of the mac…

food.ingredientbiologyDigitalis obscuraPlant Sciencebiology.organism_classificationHypocotylchemistry.chemical_compoundHorticulturefoodchemistryShootBotanyCardenolideAgarDry matterVitrificationBiotechnologyExplant cultureIn Vitro Cellular & Developmental Biology - Plant
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Viability and function of the cryopreserved whole rat ovary: comparison between slow-freezing and vitrification

2011

Objective To investigate four different protocols for cryopreservation of the whole rat ovary with intact vasculature to evaluate whether differences exist in post-thawing viability of the ovary after either vitrification or slow freezing. Design Experimental study. Setting Obstetrics and gynecology department. Animal(s) Immature Sprague-Dawley female rats. Intervention(s) Ovaries were isolated with the vascular tree intact up to the bifurcation of the abdominal aorta and were subsequently cannulated. The ovaries were flushed with increasing concentrations of the cryoprotectant dimethyl sulfoxide (DMSO) to either 1.5 or 7 M. The ovaries underwent cryopreservation by vitrification or passive…

medicine.medical_specialtyNeutral redTime FactorsCryoprotectantApoptosisOvaryBiologyCryopreservationRats Sprague-DawleyTissue Culture TechniquesAndrologychemistry.chemical_compoundCryoprotective AgentsOvarian FollicleFreezingFollicular phasemedicineAnimalsDimethyl SulfoxideVitrificationIncubationCryopreservationTissue SurvivalGynecologyDose-Response Relationship DrugEstradiolCaspase 3Dimethyl sulfoxideOvaryFertility PreservationObstetrics and GynecologyOrgan PreservationImmunohistochemistryVitrificationRatsPerfusionmedicine.anatomical_structureReproductive MedicinechemistryFemaleFertility and Sterility
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P–446 Controlled ovarian stimulation protocols for oocyte vitrification induce differential gene expression profiles in primary tumours of breast can…

2021

Abstract Study question Could controlled ovarian stimulation (COS) protocols used in fertility preservation (FP) impact on malignant cell proliferation and tumour molecular profiling of breast cancer (BC) patients? Summary answer Letrozole supplementation during ovarian stimulation for oocyte vitrification could be considered as a safe procedure in estrogen-dependent BC patients undergoing FP. What is known already High estradiol levels associated to COS could promote changes in gene expression in estrogen-positive BC tumors. Estradiol levels reached during the ovarian stimulation could aggressively promote malignant cell proliferation and cell migration to adjacent organs. Aromatase inhibi…

business.industryRehabilitationObstetrics and GynecologyStimulationmedicine.diseaseOocyteBreast cancermedicine.anatomical_structureReproductive MedicineGene expressionCancer researchMedicineVitrificationbusinessHuman Reproduction
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Cryopreservation of Hazelnut (Corylus avellana L.) Axillary Buds from In Vitro Shoots Using the Droplet Vitrification Method

2021

Cryopreservation by droplet vitrification was applied to hazelnut (Corylus avellana L.). axillary buds of the Italian cultivated variety Tonda Gentile Romana, which were collected from in vitro growing shoots, immersed in ice cooled PVS2 or PVS3 for 60 or 90 min, then transferred to a droplet of vitrification solution, placed on a strip of aluminium foil, and plunged into liquid nitrogen (LN). Additionally, the effect on the recovery of the mother plant after cryopreservation was evaluated, following a cold pre-treatment at 4 °C for 3 months. The highest regrowth percentage (56.7%) was obtained after applying PVS3 for 60 min, while the application of PVS2 for the same amount of time reduced…

rootingChemistrylength of dehydrationPlant cultureregrowthPlant ScienceHorticultureLiquid nitrogen<i>in vitro</i> cultureCryopreservationSB1-1110Settore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreeHorticultureAluminium foilAxillary budin vitro cultureShootPVS3PVS2VitrificationHorticulturae
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Cryopreservation of Limonium serotinum apical meristems from in vitro plantlets using droplet-vitrification

2011

Abstract In this study in vitro shoot tips of a Sicilian genotype of Limonium serotinum were successfully cryopreserved using the droplet-vitrification technique. Growth recovery of cryopreserved shoot tips was possible only when samples were pretreated for 16 h in liquid medium with 0.3 M sucrose, then for 5 h in liquid medium with 0.7 M sucrose before performing the cryopreservation protocol. Optimal conditions included treatment for 20 min in a loading solution containing 1.9 M glycerol + 0.5 M sucrose, treatment with vitrification solution B5 (glycerol 40.0%, sucrose 40.0%, w/v) for 60 and 90 min or vitrification solution A9 (glycerol 30.0%, dimethylsulfoxide 20.0%, ethylene glycol 20.0…

CryopreservationSucroseChromatographyCallus formationLimoniumSettore AGR/04 - Orticoltura E FloricolturaHorticultureBiologyLimonium serotinumVitrification solutionbiology.organism_classificationCryopreservationchemistry.chemical_compoundCryopreservation Droplet-vitrification Limonium serotinum Statice Sucrose pretreatment Vitrification solutionchemistryDroplet-vitrificationShootBotanyGlycerolStaticeSucrose pretreatmentVitrificationEthylene glycol
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Vitrification of human mature oocytes in clinical practice.

2009

Oocyte cryopreservation has long been the focus of unsuccessful efforts to perfect its clinical application. Lately, vitrification has been shown to provide high degrees of success by different research groups. This review attempts to address the efficiency of oocyte vitrification in clinical practice through an analysis of reports of IVF cycles in which embryo transfers have been conducted with vitrified metaphase-II human oocytes.

CryopreservationResearch groupsCell SurvivalObstetrics and GynecologyOocyte cryopreservationFertilization in VitroBiologyOocyteEmbryo TransferClinical PracticeAndrologymedicine.anatomical_structureTreatment OutcomeReproductive MedicinePregnancymedicineOocytesHumansVitrificationFemaleDevelopmental BiologyReproductive biomedicine online
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Vitrification of human oocytes.

2018

In recent years, growing evidence for the safety and efficiency of oocyte vitrification has made this technique be increasingly proposed for fertility preservation (FP). The populations who could benefit from FP include oncological patients who need the option to preserve their gametes before undergoing potential sterilizing treatment, patients with non-oncologic conditions requiring gonadotoxic chemotherapy and women who wish to delay their motherhood for a variety of reasons. By vitrifying oocytes, women have the chance to conceive in the future, have their own genetic offspring and maintain their reproductive autonomy. This review focuses on describing current knowledge on oocyte vitrifi…

0301 basic medicineCryopreservationmedicine.medical_specialtybusiness.industryReproductive autonomymedia_common.quotation_subjectObstetrics and GynecologyFertility PreservationFertilityVitrification03 medical and health sciences030104 developmental biologyOocytesMedicineHumansVitrificationFemaleFertility preservationbusinessIntensive care medicinemedia_commonMinerva ginecologica
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Hydrophilic membranes based on poly(vinyl methyl ether-crosslinked-polystyrene) semi-interpenetrating networks

1991

Microporous membranes were prepared from poly(vinyl methyl ether - crosslinked-polystyrene) (PVME-cross-PS) semi-IPN's by extraction of poly(vinyl methyl ether) (PVME) with water. Membrane morphology and properties are fixed during the process of swelling, phase separation, PVME extraction and vitrification which occurs upon immersing the samples in water. The membranes are characterized by swelling (water uptake), the relative amounts of free and bound water, and their permselectivity towards KCI solution.

Materials sciencePolymers and PlasticsOrganic ChemistryExtraction (chemistry)technology industry and agriculturePoly(vinyl methyl ether)EtherCondensed Matter Physicschemistry.chemical_compoundMembranechemistryPolymer chemistryMaterials ChemistrymedicineBound waterVitrificationPolystyreneSwellingmedicine.symptomMakromolekulare Chemie. Macromolecular Symposia
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