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Biocompatible Delivery System for Metformin: Characterization, Radiolabeling and In Vitro Studies

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389005%3A_____%2F20%3A00534009" target="_blank" >RIV/61389005:_____/20:00534009 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.2174/1871520620666200423081235" target="_blank" >https://doi.org/10.2174/1871520620666200423081235</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2174/1871520620666200423081235" target="_blank" >10.2174/1871520620666200423081235</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Biocompatible Delivery System for Metformin: Characterization, Radiolabeling and In Vitro Studies

  • Original language description

    Background: In recent years, the uses of nanotechnology in medicine have an increasing potential as an effective nanocarrier system. These systems are improved with the purpose of maximizing therapeutic activity and minimizing undesirable side-effects. Moreover, radiolabeled nanoparticles can be used as agents for diagnosis and therapeutic purposes in clinical applications. They have three main components: the core, the targeting biomolecule, and the radionuclide.nnObjective: It is aimed to synthesize Metformin (MET) loaded Solid Lipid Nanoparticles (MET-SLN) and radiolabeled with technetium-99m tricarbonyl core.nnMethods: The structure of synthesized nanoparticles was characterized by Fourier Transform Infrared Spectroscopy (FTIR). The particle size and morphology of nanoparticles were examined by Dynamic Light Scattering (DLS), and Scanning Electron Microscope (SEM). Quality control studies of radiolabeled MET-SLN [Tc-99m(CO)(3)-MET-SLN] were performed by High-Performance Liquid Radiochromatography (HPLRC) and Thin Layer Radiochromatography (TLRC).nnResults: The radiolabeling yield of [Tc-99m(CO)(3)-MET-SLN] was found to be 88%. In vitro studies have been performed on cancer lines(MCF7, MDA-MD-231 breast, and HEPG2 liver cancer cells) to determine the biological behavior of Tc-99m(CO)3-MET-SLNs.nnConclusion: The results showed that higher uptake values were observed on estrogen-positive MCF7 breast cancer cell line according to estrogen negative MDA-MB-231 breast cancer and HEPG2 liver cancer cell lines.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30224 - Radiology, nuclear medicine and medical imaging

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Anti-Cancer Agents in Medicinal Chemistry

  • ISSN

    1871-5206

  • e-ISSN

  • Volume of the periodical

    20

  • Issue of the periodical within the volume

    13

  • Country of publishing house

    AE - UNITED ARAB EMIRATES

  • Number of pages

    9

  • Pages from-to

    1626-1634

  • UT code for WoS article

    000573095600002

  • EID of the result in the Scopus database

    2-s2.0-85088953120