About: HPMA copolymer-doxorubicin conjugates: the effects of molecular weight and architecture on biodistribution and in vivo activity     Goto   Sponge   Distinct   Permalink

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  • The molecular weight and molecular architecture of soluble polymer drug carriers significantly influence the biodistribution and anti-tumour activities of their doxorubicin (DOX) conjugates in tumour-bearing mice. Biodistribution of N-(2-hydroxypropyl)methacrylamide (HPMA) copolymer-DOX conjugates of linear and star architectures were compared in EL4 T-cell lymphoma-bearing mice. Biodistribution, including tumour accumulation, and anti-tumour activity of the conjugates strongly depended on conjugate molecular weight (MW), polydispersity, hydrodynamic radius (Rh) and molecular architecture. With increasing MW, renal clearance decreased, and the conjugates displayed extended blood circulation and enhanced tumour accumulation. The linear conjugates with flexible polymer chains were eliminated by kidney clearance more quickly than the highly branched star conjugates with comparable MWs. Interestingly, the data suggested different mechanisms of renal filtration for star and linear conjugates.
  • The molecular weight and molecular architecture of soluble polymer drug carriers significantly influence the biodistribution and anti-tumour activities of their doxorubicin (DOX) conjugates in tumour-bearing mice. Biodistribution of N-(2-hydroxypropyl)methacrylamide (HPMA) copolymer-DOX conjugates of linear and star architectures were compared in EL4 T-cell lymphoma-bearing mice. Biodistribution, including tumour accumulation, and anti-tumour activity of the conjugates strongly depended on conjugate molecular weight (MW), polydispersity, hydrodynamic radius (Rh) and molecular architecture. With increasing MW, renal clearance decreased, and the conjugates displayed extended blood circulation and enhanced tumour accumulation. The linear conjugates with flexible polymer chains were eliminated by kidney clearance more quickly than the highly branched star conjugates with comparable MWs. Interestingly, the data suggested different mechanisms of renal filtration for star and linear conjugates. (en)
Title
  • HPMA copolymer-doxorubicin conjugates: the effects of molecular weight and architecture on biodistribution and in vivo activity
  • HPMA copolymer-doxorubicin conjugates: the effects of molecular weight and architecture on biodistribution and in vivo activity (en)
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  • HPMA copolymer-doxorubicin conjugates: the effects of molecular weight and architecture on biodistribution and in vivo activity
  • HPMA copolymer-doxorubicin conjugates: the effects of molecular weight and architecture on biodistribution and in vivo activity (en)
skos:notation
  • RIV/61388971:_____/12:00383776!RIV13-GA0-61388971
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  • I, P(GAP301/11/0325), P(IAAX00500803), Z(AV0Z40500505), Z(AV0Z50200510)
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  • 3
http://linked.open...vai/riv/dodaniDat
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  • 139739
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  • RIV/61388971:_____/12:00383776
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  • drug delivery; tumour accumulation; body distribution (en)
http://linked.open.../riv/klicoveSlovo
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  • NL - Nizozemsko
http://linked.open...ontrolniKodProRIV
  • [7B59D6D3D3C1]
http://linked.open...i/riv/nazevZdroje
  • Journal of Controlled Release
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  • 164
http://linked.open...iv/tvurceVysledku
  • Etrych, Tomáš
  • Strohalm, Jiří
  • Ulbrich, Karel
  • Říhová, Blanka
  • Šírová, Milada
  • Šubr, Vladimír
http://linked.open...ain/vavai/riv/wos
  • 000312947600014
http://linked.open...n/vavai/riv/zamer
issn
  • 0168-3659
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.jconrel.2012.06.029
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