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Chitosan-alginate hydrogels for simultaneous and sustained releases of ciprofloxacin, amoxicillin and vancomycin for combination therapy

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70883521%3A28610%2F21%3A63526429" target="_blank" >RIV/70883521:28610/21:63526429 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://www.sciencedirect.com/science/article/pii/S1773224720314155" target="_blank" >https://www.sciencedirect.com/science/article/pii/S1773224720314155</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jddst.2020.102126" target="_blank" >10.1016/j.jddst.2020.102126</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Chitosan-alginate hydrogels for simultaneous and sustained releases of ciprofloxacin, amoxicillin and vancomycin for combination therapy

  • Popis výsledku v původním jazyce

    A set of chitosan-alginic acid hydrogels were prepared for multiple encapsulation and release of antibiotics for future application in combination therapy. Vancomycin, ciprofloxacin and amoxicillin were used as models, as widely used in therapy, either individually and in combination. The hydrogels were prepared by a simple, low cost and solventfree approach based on complexation between chitosan and alginic acid followed by crosslinking with CaCl2 to enhance structural properties. The antibiotics were loaded during the gelification process to maximize efficiency, and to reduce the loss of material. All the formulations were analyzed by scanning electron microscope to investigate the surface morphology, the inner structure, and the effect of the drugs loading. The swelling behavior, the cytotoxicityand the antibacterial activity, were evaluated. The investigation of the impact of simultaneous loading of the antibiotics along with the variation in the surrounding pH, on the release trend, represents a key part of work. The results revealed that the physicochemical properties of the combination of the drugs-loaded play an essential role in the morphology, structural changes and release profile.

  • Název v anglickém jazyce

    Chitosan-alginate hydrogels for simultaneous and sustained releases of ciprofloxacin, amoxicillin and vancomycin for combination therapy

  • Popis výsledku anglicky

    A set of chitosan-alginic acid hydrogels were prepared for multiple encapsulation and release of antibiotics for future application in combination therapy. Vancomycin, ciprofloxacin and amoxicillin were used as models, as widely used in therapy, either individually and in combination. The hydrogels were prepared by a simple, low cost and solventfree approach based on complexation between chitosan and alginic acid followed by crosslinking with CaCl2 to enhance structural properties. The antibiotics were loaded during the gelification process to maximize efficiency, and to reduce the loss of material. All the formulations were analyzed by scanning electron microscope to investigate the surface morphology, the inner structure, and the effect of the drugs loading. The swelling behavior, the cytotoxicityand the antibacterial activity, were evaluated. The investigation of the impact of simultaneous loading of the antibiotics along with the variation in the surrounding pH, on the release trend, represents a key part of work. The results revealed that the physicochemical properties of the combination of the drugs-loaded play an essential role in the morphology, structural changes and release profile.

Klasifikace

  • Druh

    J<sub>SC</sub> - Článek v periodiku v databázi SCOPUS

  • CEP obor

  • OECD FORD obor

    20903 - Bioproducts (products that are manufactured using biological material as feedstock) biomaterials, bioplastics, biofuels, bioderived bulk and fine chemicals, bio-derived novel materials

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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 periodika

    Journal of Drug Delivery Science and Technology

  • ISSN

    1773-2247

  • e-ISSN

  • Svazek periodika

    61

  • Číslo periodika v rámci svazku

    Neuveden

  • Stát vydavatele periodika

    NL - Nizozemsko

  • Počet stran výsledku

    13

  • Strana od-do

  • Kód UT WoS článku

    000619147200002

  • EID výsledku v databázi Scopus

    2-s2.0-85092917562