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Influence of Zinc Nanocomplexes on Health of Model Animals Organism

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62156489%3A43210%2F19%3A43916830" target="_blank" >RIV/62156489:43210/19:43916830 - isvavai.cz</a>

  • Výsledek na webu

  • DOI - Digital Object Identifier

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Influence of Zinc Nanocomplexes on Health of Model Animals Organism

  • Popis výsledku v původním jazyce

    The experiment was carried out in the experimental facility of the Institute of Animal Nutrition and Forage Production at MENDELU in Brno (in accordance with the Animal Protection Act No. 246/1992 Coll.). Throughout the experiment, microclimatic conditions were monitored in the laboratory, which were mainly limited by the temperature measured by the &quot;DATALOGER S 3120&quot; instrument and maintained at 23 o C +- 1 o C. The photoperiod was artificially controlled according to the 12 h day and 12 h night schedule with a maximum illumination intensity of 200 lx. Male Wistar albino rats were divided into 7 groups of 10 each as the model animal for this experiment. The average rat weight at the start of the experiment was 144 +- 2 grams. Zinc was not increased to control group (C). Four phosphate nanoparticles were fed to the four rats (ZnA; ZnB; ZnC; ZnD) in a dose (2000 mg Zn / kg diet). A group of rats (ZnO-N) received commercial zinc nanoparticles (Sigma Aldrich (C), Germany) at a dose of 2000 mg Zn / kg diets. A group of rats (ZnO) was fed zinc oxide at a dose of 2000 mg Zn / kg diets. The last group served as control (C) without the addition of zinc to the diet. All rats were fed a monodietic (wheat) containing 21.7 mg Zn / kg diet. The feeding experiment lasted 30 days. At the end of the experiment, animals were sacrificed (according to Section 16a of Act No. 246/1992 Coll., On the protection of animals against cruelty) and samples of whole blood, liver, kidneys were collected and processed and subjected to appropriate analyzes immediately after collection. Next, a small intestine sample (1/3 of the duodenum) and a liver were taken for histological analysis. Samples were fixed with 10% formaldehyde. The total zinc content was determined by atomic absorption spectrometry and the concentration of oxidized and reduced glutathione was determined by high performance liquid chromatography.

  • Název v anglickém jazyce

    Influence of Zinc Nanocomplexes on Health of Model Animals Organism

  • Popis výsledku anglicky

    The experiment was carried out in the experimental facility of the Institute of Animal Nutrition and Forage Production at MENDELU in Brno (in accordance with the Animal Protection Act No. 246/1992 Coll.). Throughout the experiment, microclimatic conditions were monitored in the laboratory, which were mainly limited by the temperature measured by the &quot;DATALOGER S 3120&quot; instrument and maintained at 23 o C +- 1 o C. The photoperiod was artificially controlled according to the 12 h day and 12 h night schedule with a maximum illumination intensity of 200 lx. Male Wistar albino rats were divided into 7 groups of 10 each as the model animal for this experiment. The average rat weight at the start of the experiment was 144 +- 2 grams. Zinc was not increased to control group (C). Four phosphate nanoparticles were fed to the four rats (ZnA; ZnB; ZnC; ZnD) in a dose (2000 mg Zn / kg diet). A group of rats (ZnO-N) received commercial zinc nanoparticles (Sigma Aldrich (C), Germany) at a dose of 2000 mg Zn / kg diets. A group of rats (ZnO) was fed zinc oxide at a dose of 2000 mg Zn / kg diets. The last group served as control (C) without the addition of zinc to the diet. All rats were fed a monodietic (wheat) containing 21.7 mg Zn / kg diet. The feeding experiment lasted 30 days. At the end of the experiment, animals were sacrificed (according to Section 16a of Act No. 246/1992 Coll., On the protection of animals against cruelty) and samples of whole blood, liver, kidneys were collected and processed and subjected to appropriate analyzes immediately after collection. Next, a small intestine sample (1/3 of the duodenum) and a liver were taken for histological analysis. Samples were fixed with 10% formaldehyde. The total zinc content was determined by atomic absorption spectrometry and the concentration of oxidized and reduced glutathione was determined by high performance liquid chromatography.

Klasifikace

  • Druh

    D - Stať ve sborníku

  • CEP obor

  • OECD FORD obor

    40401 - Agricultural biotechnology and food biotechnology

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2019

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název statě ve sborníku

    Proceedings Conference of Agronomy Students

  • ISBN

  • ISSN

    2334-9883

  • e-ISSN

  • Počet stran výsledku

    7

  • Strana od-do

    332-338

  • Název nakladatele

    University of Kragujevac

  • Místo vydání

    Čačak

  • Místo konání akce

    Čačak

  • Datum konání akce

    14. 8. 2019

  • Typ akce podle státní příslušnosti

    EUR - Evropská akce

  • Kód UT WoS článku