About: Combination chemotherapy using core-shell nanoparticles through the self-assembly of HPMA-based copolymers and degradable polyester     Goto   Sponge   NotDistinct   Permalink

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  • The preparation of core-shell polymeric nanoparticles simultaneously loaded with docetaxel (DTXL) and doxorubicin (DOX) is reported herein. The self-assembly of the aliphatic biodegradable copolyester PBS/PBDL (poly(butylene succinate-co-butylene dilinoleate)) and HPMA-based copolymers (N-(2-hydroxypropyl)methacrylamide-based copolymers) hydrophobically modified by the incorporation of cholesterol led to the formation of narrow-size-distributed (PDI<0.10) sub-200-nm polymeric nanoparticles suitable for passive tumor-targeting drug delivery based on the size-dependent EPR (enhanced permeability and retention) effect. The PHPMA provided to the self-assembled nanoparticle stability against aggregation as evaluated in vitro. Additionally, the obtained self-assembled nanoparticles enable further development of targeting strategies based on the use of multiple ligands attached to an HPMA copolymer on the particle surface for simultaneous passive and active targeting and different combination therapies.
  • The preparation of core-shell polymeric nanoparticles simultaneously loaded with docetaxel (DTXL) and doxorubicin (DOX) is reported herein. The self-assembly of the aliphatic biodegradable copolyester PBS/PBDL (poly(butylene succinate-co-butylene dilinoleate)) and HPMA-based copolymers (N-(2-hydroxypropyl)methacrylamide-based copolymers) hydrophobically modified by the incorporation of cholesterol led to the formation of narrow-size-distributed (PDI<0.10) sub-200-nm polymeric nanoparticles suitable for passive tumor-targeting drug delivery based on the size-dependent EPR (enhanced permeability and retention) effect. The PHPMA provided to the self-assembled nanoparticle stability against aggregation as evaluated in vitro. Additionally, the obtained self-assembled nanoparticles enable further development of targeting strategies based on the use of multiple ligands attached to an HPMA copolymer on the particle surface for simultaneous passive and active targeting and different combination therapies. (en)
Title
  • Combination chemotherapy using core-shell nanoparticles through the self-assembly of HPMA-based copolymers and degradable polyester
  • Combination chemotherapy using core-shell nanoparticles through the self-assembly of HPMA-based copolymers and degradable polyester (en)
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  • Combination chemotherapy using core-shell nanoparticles through the self-assembly of HPMA-based copolymers and degradable polyester
  • Combination chemotherapy using core-shell nanoparticles through the self-assembly of HPMA-based copolymers and degradable polyester (en)
skos:notation
  • RIV/61388971:_____/13:00385103!RIV13-AV0-61388971
http://linked.open...avai/riv/aktivita
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  • I, P(GA202/09/2078), P(GPP207/11/P551), P(IAAX00500803), Z(AV0Z40500505), Z(AV0Z50200510)
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  • 2
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  • 65953
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  • RIV/61388971:_____/13:00385103
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  • combination therapy; polymeric core-shell nanoparticles; docetaxel (en)
http://linked.open.../riv/klicoveSlovo
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  • NL - Nizozemsko
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  • [0E556EF29DB4]
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  • Journal of Controlled Release
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  • 165
http://linked.open...iv/tvurceVysledku
  • Chytil, Petr
  • Etrych, Tomáš
  • Ulbrich, Karel
  • Říhová, Blanka
  • Štěpánek, Petr
  • Giacomelli, F. C.
  • Jäger, Alessandro
  • Jäger, Eliezer
http://linked.open...ain/vavai/riv/wos
  • 000315679100008
http://linked.open...n/vavai/riv/zamer
issn
  • 0168-3659
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.jconrel.2012.11.009
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