About: Modulation of induced cytotoxicity of doxorubicin by using apoferritin and liposomal cages     Goto   Sponge   NotDistinct   Permalink

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  • Doxorubicin is an effective chemotherapeutic drug, however, its toxicity is a significant limitation in therapy. Encapsulation of doxorubicin inside liposomes or ferritin cages decreases cardiotoxicity while maintaining anticancer potency. We synthesized novel apoferritin- and liposome-encapsulated forms of doxorubicin (“Apodox” and “lip-8-dox”) and compared its toxicity with doxorubicin and Myocet on prostate cell lines. Three different prostatic cell lines PNT1A, 22Rv1, and LNCaP were chosen. The toxicity of the modified doxorubicin forms was compared to conventional doxorubicin using the MTT assay, real-time cell impedance-based cell growth method (RTCA), and flow cytometry. The efficiency of doxorubicin entrapment was 56% in apoferritin cages and 42% in the liposome carrier. The accuracy of the RTCA system was verified by flow-cytometric analysis of cell viability. The doxorubicin half maximal inhibition concentrations (IC50) were determined as 170.5, 234.0, and 169.
  • Doxorubicin is an effective chemotherapeutic drug, however, its toxicity is a significant limitation in therapy. Encapsulation of doxorubicin inside liposomes or ferritin cages decreases cardiotoxicity while maintaining anticancer potency. We synthesized novel apoferritin- and liposome-encapsulated forms of doxorubicin (“Apodox” and “lip-8-dox”) and compared its toxicity with doxorubicin and Myocet on prostate cell lines. Three different prostatic cell lines PNT1A, 22Rv1, and LNCaP were chosen. The toxicity of the modified doxorubicin forms was compared to conventional doxorubicin using the MTT assay, real-time cell impedance-based cell growth method (RTCA), and flow cytometry. The efficiency of doxorubicin entrapment was 56% in apoferritin cages and 42% in the liposome carrier. The accuracy of the RTCA system was verified by flow-cytometric analysis of cell viability. The doxorubicin half maximal inhibition concentrations (IC50) were determined as 170.5, 234.0, and 169. (en)
Title
  • Modulation of induced cytotoxicity of doxorubicin by using apoferritin and liposomal cages
  • Modulation of induced cytotoxicity of doxorubicin by using apoferritin and liposomal cages (en)
skos:prefLabel
  • Modulation of induced cytotoxicity of doxorubicin by using apoferritin and liposomal cages
  • Modulation of induced cytotoxicity of doxorubicin by using apoferritin and liposomal cages (en)
skos:notation
  • RIV/00216224:14110/14:00078586!RIV15-MSM-14110___
http://linked.open...avai/riv/aktivita
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  • I, P(GA14-18344S)
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  • 12
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  • 30222
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  • RIV/00216224:14110/14:00078586
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  • Apoferritin; Cancer; Cardiotoxicity; Doxorubicin; Encapsulation; Liposome; Modification (en)
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  • CH - Švýcarská konfederace
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  • [1354BEC49C23]
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  • International Journal of Molecular Sciences
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  • 15
http://linked.open...iv/tvurceVysledku
  • Adam, Vojtěch
  • Babula, Petr
  • Gumulec, Jaromír
  • Knopfová, Lucia
  • Kizek, Rene
  • Masařík, Michal
  • Sztalmachová, Markéta
  • Kopel, Pavel
  • Raudenská, Martina
  • Nejdl, Lukáš
  • Stiborova, Marie
  • Skalickova, Sylvie
  • Fojtů, Michaela
  • Skotáková, Anna
  • Vlachova, Jana
http://linked.open...ain/vavai/riv/wos
  • 000346797400083
issn
  • 1422-0067
number of pages
http://bibframe.org/vocab/doi
  • 10.3390/ijms151222960
http://localhost/t...ganizacniJednotka
  • 14110
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