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TRANSPORT AND INTERACTIONS OF SULFAPYRIDINE IN AGAROSE HYDROGELS ENRICHED BY HUMIC ACIDS

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26310%2F21%3APU147740" target="_blank" >RIV/00216305:26310/21:PU147740 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://www.scopus.com/record/display.uri?eid=2-s2.0-85127239244&origin=inward&txGid=42faca9b28f9ea1280cac078116a5e67" target="_blank" >https://www.scopus.com/record/display.uri?eid=2-s2.0-85127239244&origin=inward&txGid=42faca9b28f9ea1280cac078116a5e67</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.37904/nanocon.2021.4368" target="_blank" >10.37904/nanocon.2021.4368</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    TRANSPORT AND INTERACTIONS OF SULFAPYRIDINE IN AGAROSE HYDROGELS ENRICHED BY HUMIC ACIDS

  • Popis výsledku v původním jazyce

    Knowledge of behaviour of pharmaceuticals as contaminants in nature is essential for their mobility and toxicity in the soils and surface- and ground-water environments. Their migration ability and toxicity can be affected by their interactions with organic matter. In this contribution, sulfapyridine (a sulfanilamide drug used for antibacterial medication) is studied from the point of view of its transport in hydrogels containing humic substances. Agarose hydrogel was used as a model medium for the transport experiments. Standard Elliot soil humic acid (4S102H) purchased from International Humic Substances Society was incorporated into the hydrogel as an active nanomaterial for interactions with drug and potential suppression of their migration and toxicity in soil systems. The method of diffusion couple was applied on the diffusion experiments. Donor part was saturated by sulfapyridine and acceptor part was free of drug. After connecting of both parts, the time development of concentration profiles in the couple was monitored. The effective diffusion coefficients for the transport of sulfapyridine in hydrogel enriched by humic acids and pure agarose hydrogel were determined and compared. It was found that the transport of drug is influenced by interactions with humic acids which can immobilize partially sulfapyridine in humic structure. Simultaneously, sorption/desorption experiments were realized. Their results confirmed high degree of drug immobilization (60 - 90 % in the dependence on drug concentration).

  • Název v anglickém jazyce

    TRANSPORT AND INTERACTIONS OF SULFAPYRIDINE IN AGAROSE HYDROGELS ENRICHED BY HUMIC ACIDS

  • Popis výsledku anglicky

    Knowledge of behaviour of pharmaceuticals as contaminants in nature is essential for their mobility and toxicity in the soils and surface- and ground-water environments. Their migration ability and toxicity can be affected by their interactions with organic matter. In this contribution, sulfapyridine (a sulfanilamide drug used for antibacterial medication) is studied from the point of view of its transport in hydrogels containing humic substances. Agarose hydrogel was used as a model medium for the transport experiments. Standard Elliot soil humic acid (4S102H) purchased from International Humic Substances Society was incorporated into the hydrogel as an active nanomaterial for interactions with drug and potential suppression of their migration and toxicity in soil systems. The method of diffusion couple was applied on the diffusion experiments. Donor part was saturated by sulfapyridine and acceptor part was free of drug. After connecting of both parts, the time development of concentration profiles in the couple was monitored. The effective diffusion coefficients for the transport of sulfapyridine in hydrogel enriched by humic acids and pure agarose hydrogel were determined and compared. It was found that the transport of drug is influenced by interactions with humic acids which can immobilize partially sulfapyridine in humic structure. Simultaneously, sorption/desorption experiments were realized. Their results confirmed high degree of drug immobilization (60 - 90 % in the dependence on drug concentration).

Klasifikace

  • Druh

    D - Stať ve sborníku

  • CEP obor

  • OECD FORD obor

    20700 - Environmental engineering

Návaznosti výsledku

  • Projekt

  • Návaznosti

    S - Specificky vyzkum na vysokych skolach

Ostatní

  • Rok uplatnění

    2021

  • 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

    NANOCON Conference Proceedings - International Conference on Nanomaterials

  • ISBN

    9788088365006

  • ISSN

  • e-ISSN

  • Počet stran výsledku

    7

  • Strana od-do

    389-395

  • Název nakladatele

    Neuveden

  • Místo vydání

    neuveden

  • Místo konání akce

    Brno

  • Datum konání akce

    20. 10. 2021

  • Typ akce podle státní příslušnosti

    WRD - Celosvětová akce

  • Kód UT WoS článku