Search results for "Preservation"

showing 10 items of 484 documents

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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Comparing encapsulation-dehydration and droplet-vitrification for cryopreservation of sugarcane (Saccharum spp.) shoot tips

2011

Abstract In this study, in vitro shoot tips of two sugarcane clones were successfully cryopreserved using encapsulation-dehydration and droplet-vitrification with two vitrification solutions, PVS2 and PVS3. For both clones, encapsulation-dehydration induced significantly higher recovery, reaching 60% for clone H70-144 and 53% for clone CP68-1026, compared with droplet-vitrification in which recovery was 33–37% for clone H70-144 and 20–27% for clone CP68-1026. Optimal conditions included preculture of encapsulated shoot apices for 24 h in liquid medium with 0.75 M sucrose and dehydration with silica gel to 20% moisture content (fresh weight basis) before direct immersion in liquid nitrogen. …

CryopreservationSucrosebiologyChemistrySilica gelSugarcaneHorticultureLiquid nitrogenmedicine.diseasebiology.organism_classificationCryopreservationSaccharumHorticulturechemistry.chemical_compoundDroplet-vitrificationBotanyShootmedicineEncapsulation-dehydrationVitrificationDehydrationScientia Horticulturae
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Ultrastructure of preimplantation genetic diagnosis-derived human blastocysts grown in a coculture system after vitrification

2006

Objective To evaluate ultrastructural features of preimplantation genetic diagnosis (PGD) blastocysts before and after vitrification. Design Descriptive study of both vitrified and fresh hatching blastocysts. Setting PGD program at the Instituto Universitario, Instituto Valenciano de Infertilidad. Patient(s) Patients undergoing PGD donated their abnormal embryos for research (n = 26). Intervention(s) Biopsied embryos were cultured in the presence of human endometrial cells until day 6. Sixteen blastocysts were vitrified. A total of 11 high-scored hatching blastocysts, 6 warmed and 5 fresh, were fixed for ultrastructure. Main Outcome Measure(s) The cytoskeleton structure, type of intercellul…

CryopreservationTight junctionHatchingObstetrics and GynecologyEmbryoAnatomyBiologyPreimplantation genetic diagnosisCoculture TechniquesCryopreservationAndrologyBlastocystmedicine.anatomical_structureReproductive MedicineCytogenetic Analysisembryonic structuresmedicineUltrastructureHumansInner cell massBlastocystCells CulturedPreimplantation DiagnosisFertility and Sterility
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Histologic effects of university of wisconsin two-layer method preservation of rat pancreas.

2013

Marginal donors represent a poorly utilized source of organs for transplantation despite their availability. The key is to reduce the ischemic damage in the effort to improve organ quality. This study investigated the histologic effects after in situ perfusion of preservation with a two-layer method compared with the classic University of Wisconsin preservation in term of tissue integrity and number of viable exocrine cells in the rat pancreas both after exsanguination and at 8 weeks of cryopreservation. Pancreata harvested from 60 rats were collected using 3 methods: two-layer method following University of Wisconsin perfusion; exsanguination; and classic University of Wisconsin perfusion/…

CryopreservationTransplantationPathologymedicine.medical_specialtybusiness.industryIn situ perfusionTwo layerOxygenationCryopreservationRatsTransplantationSettore MED/18 - Chirurgia Generalemedicine.anatomical_structureTwo-layer method; organ preservationMedicineRat PancreasAnimalsSurgeryRats Wistarorgan preservationbusinessPancreasTwo-layer methodPerfusionPancreas
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Neonatal Outcomes and Long-Term Follow-Up of Children Born from Frozen Embryo, a Narrative Review of Latest Research Findings

2022

In recent years, the growing use of ART (assisted reproductive techniques) has led to a progressive improvement of protocols; embryo freezing is certainly one of the most important innovations. This technique is selectively offered as a tailored approach to reduce the incidence of multiple pregnancies and, most importantly, to lower the risk of developing ovarian hyperstimulation syndrome when used in conjunction with an ovulation-triggering GnRH antagonist. The increase in transfer cycles with frozen embryos made it possible to study the effects of the technique in children thus conceived. Particularly noteworthy is the increase in macrosomal and LGA (large for gestational age) newborns, i…

Cryopreservationfresh embryo transferReproductive Techniques Assistedcryopreservation; fresh embryo transfer; frozen embryo transfer; neonatal outcomes; vitrificationInfant NewbornGeneral MedicineEmbryo TransferSettore MED/40 - Ginecologia E OstetriciavitrificationGonadotropin-Releasing HormonePregnancyneonatal outcomesHumansFemalefrozen embryo transferChildFollow-Up StudiesMedicina
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Long- and short-term in vitro D-dimer stability measured with INNOVANCE D-Dimer.

2009

Summary In vitro D-dimer stability in plasma is widely assumed, but has not yet been documented by systematic studies using samples covering a wide range of D-dimer. We investigated the short- and long-term stability of D-dimer in clinical citrated plasma samples with normal and pathological levels. The short-term stability was analysed by measuring D-dimer fresh, after storage of plasma for 4 hours at room temperature (RT) and after an additional 24 h storage at +2 to +8°C (n=40). Long-term stability samples (n=40) were measured fresh and after storage for 19, 25 and 36 months at ≤-60°C. The effect of repeated freezing was analysed by measuring samples (n=50) fresh and after four consecuti…

Cryopreservationmedicine.medical_specialtyTime FactorsPlasma samplesChemistryProtein StabilityHematologyAntifibrinolytic AgentsSurgeryFibrin Fibrinogen Degradation ProductsAnimal scienceProtein stabilityBlood PreservationAntifibrinolytic agentD-dimerFreezingmedicineHumansFrozen storageReagent Kits DiagnosticThrombosis and haemostasis
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A comparative study of mechanical properties of fresh and frozen-thawed porcine intervertebral discs in a bioreactor environment

2016

Abstract Limited availability of fresh intervertebral discs (IVDs) necessitates the use of frozen-thawed samples in biomechanical investigations. Several authors have reported the mechanical properties of frozen-thawed IVDs, but few studies have investigated the effects of storage temperature and cooling rate. The validity and reliability of the applied freezing-thawing procedures are still relatively unknown. The study aims to compare the mechanical responses of fresh porcine IVDs and porcine IVDs, which were frozen at different freezing temperatures with a controlled-rate cooling process and then thawed. The specimens were obtained from pigs aged 6 months. A total of 18 functional spine u…

Cryopreservationmusculoskeletal diseasesLumbar VertebraeMaterials scienceSwine0206 medical engineeringBiomedical EngineeringReproducibility of Results02 engineering and technologymusculoskeletal system020601 biomedical engineeringBiomechanical PhenomenaBiomaterials03 medical and health sciencesBioreactors0302 clinical medicineCooling rateMechanics of MaterialsFreezingBioreactorAnimalsFrozen storageIntervertebral Disc030217 neurology & neurosurgeryBiomedical engineeringJournal of the Mechanical Behavior of Biomedical Materials
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Cryopreserved primary hepatocytes as a constantly available in vitro model for the evaluation of human and animal drug metabolism and enzyme inductio…

2000

The use of primary hepatocytes is now well established for both studies of drug metabolism and enzyme induction. Cryopreservation of primary hepatocytes decreases the need for fresh liver tissue. This is especially important for research with human hepatocytes because availability of human liver tissue is limited. In this review, we summarize our research on optimization and validation of cryopreservation techniques. The critical elements for successful cryopreservation of hepatocytes are (1) the freezing protocol, (2) the concentration of the cryoprotectant [10% dimethyl-sulfoxide (DMSO)], (3) slow addition and removal of DMSO, (4) carbogen equilibration during isolation of hepatocytes and…

CryoprotectantLiver cytologyBiologyCryopreservationMiceDogsmedicineCytochrome P-450 CYP1A1AnimalsHumansPharmacology (medical)General Pharmacology Toxicology and PharmaceuticsEnzyme inducerEpoxide hydrolaseCryopreservationRatsmedicine.anatomical_structureBiochemistryLiverPharmaceutical PreparationsHepatocyteEnzyme Inductionbiology.proteinPercollDrug metabolismNADPDrug metabolism reviews
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Lactic acid bacteria strains for bioprotection application with cells entrapment in biopolymeric matrices

2013

Among the various methods to control foodborne pathogenic and/or food spoilage microorganisms in food chain, bioprotective lactic acid bacteria (LAB) appear to be promising tools for food biopreservation. This collaborative study, between PAPC (Agrosup Dijon, University of Burgundy) and BioDyMIA (University Lyon1-Lyon Isara) laboratories, concerned the development of sodium alginate/sodium caseinate polymeric matrices intended to entrap LAB cells selected for their anti-Listeria spp. activity. First, 4 LAB strains from 19 LAB strains were selected for their anti-Listeria spp. activity: this screening was performed by the method of agar diffusion against three Listeria spp strains. Then, ant…

Cultivabilité[SDV.SA] Life Sciences [q-bio]/Agricultural sciencesGelBiopréservationCaséinate de sodium[ SDV.AEN ] Life Sciences [q-bio]/Food and NutritionActivité anti-ListeriaAlginate de sodiumBiopreservationCulturability[SDV.AEN] Life Sciences [q-bio]/Food and NutritionBactéries lactiquesSodium caseinate[CHIM.OTHE] Chemical Sciences/OtherSéparation de phase[ CHIM.OTHE ] Chemical Sciences/OtherLactic acid bacteriaAqueous two-phase systemAnti-listerial activitySodium alginateEntrapment[ SDV.SA ] Life Sciences [q-bio]/Agricultural sciencesConfinement
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DIAGNOSTICS FOR CULTURAL HERITAGE: ANALYTICAL APPROACH FOR AN EFFECTIVE CONSERVATION

2014

Cultural Heritage C.H. conservation C.H. preservation C.H. restoration
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