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Preučevanje toksikološkega profila izbranih nanodelcev na celični liniji HepG2
ID Cundrič, Sandra (Author), ID Žgur Bertok, Darja (Mentor) More about this mentor... This link opens in a new window, ID Žegura, Bojana (Comentor)

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MD5: 0E31840264BDCB9D7E9CAA242FE4D133
PID: 20.500.12556/rul/44d6cae4-e128-4a5a-9986-184608fd2f40

Abstract
Nanodelci imajo velik potencial za uporabo v medicini in farmaciji, predvsem kot sistemi za dostavo zdravilnih učinkovin za boj proti rakavim obolenjem. Prednost je, da izbrano učinkovino/spojino lahko zaščitijo, stabilizirajo in selektivno dostavijo na tarčno mesto. Vendar je pred uporabo nanodelcev potrebno opredeliti njihovo toksično delovanje. Cilj magistrske naloge je bil preveriti morebiten toksičen učinek s poli-glutaminsko kislino (PGA) obdanih nanodelcev (ND) poli-epsilon- kaprolaktona (PCL), ND poli-(mlečne-ko-glikolne) kisline (PLGA) z inkapsuliranimi ND selena (Se) ter z govejim serumskim albuminom (BSA) obdanih ND Se. Po izpostavitvi celic HepG2 raztopini testiranih ND, smo s testom MTT določali citotoksičnost vzorcev, s testom DCFH-DA merili nastanek reaktivnih kisikovih spojin (ROS) in s tem vpliv na oksidativni stres, ter s testom komet preučevali genotoksično delovanje ND. Ugotovili smo, da noben od testiranih vzorcev ne izkazuje toksičnih učinkov na celicah človeškega hepatoma (HepG2). Največji porast ROS in prelomov DNA smo opazili pri celicah, ki so bile izpostavljene ND PCL brez PGA.

Language:Slovenian
Keywords:nanodelci, PCL, PLGA, Se, citotoksičnost, ROS, genotoksičnost, HepG2
Work type:Master's thesis/paper
Typology:2.09 - Master's Thesis
Organization:BF - Biotechnical Faculty
Publisher:[S. Cundrič]
Year:2017
PID:20.500.12556/RUL-91989 This link opens in a new window
UDC:606:61:57.083.36(043.2)
COBISS.SI-ID:8717945 This link opens in a new window
Publication date in RUL:05.05.2017
Views:2093
Downloads:471
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Secondary language

Language:English
Title:Study of toxicological profile of selected nanoparticles on cell line HepG2
Abstract:
Nanoparticles have a high potential for use in medicine and pharmacy, especially as nanodelivery systems used in anti-cancer therapy. Their advantage is protection, stabilization and selective delivery of a compound to a target site. Although, potential toxicity of nanoparticles need to be evaluated before their use. The goal of our master thesis was to investigate potential toxic effect of poly-epsilon-caprolactone (PCL) nanoparticles coated with poly-glutamic acid (PGA), poly-(lactic-co-glycolic) acid (PLGA) with encapsulated selenium (Se) nanoparticles and selenium (Se) nanoparticles coated with bovine serum albumin (BSA). After exposure to solutions of tested nanoparticles we evaluated their cytotoxicity with MTT assay, reactive oxygen species (ROS) production and subsequent oxidative stress with DCFH-DA assay and genotoxic effects of nanoparticles with Comet assay. Our results showed no biologically relevant toxic effects on human hepatoma (HepG2) cell line in all tested samples of nanoparticles although slightly increased ROS production and DNA strand breaks was detected in cells, which were exposed to ND PCL without PGA.

Keywords:nanoparticles, PCL, PLGA, Se, cytotoxicity, ROS, genotoxicity, HepG2

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