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Journal Abstract Search

549 related items for PubMed ID: 25531063

  • 1. Synthesis of amphiphilic copolymers containing zwitterionic sulfobetaine as pH and redox responsive drug carriers.
    Cai M, Leng M, Lu A, He L, Xie X, Huang L, Ma Y, Cao J, Chen Y, Luo X.
    Colloids Surf B Biointerfaces; 2015 Feb 01; 126():1-9. PubMed ID: 25531063
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  • 2. pH/redox dual-responsive amphiphilic zwitterionic polymers with a precisely controlled structure as anti-cancer drug carriers.
    Wu Z, Gan Z, Chen B, Chen F, Cao J, Luo X.
    Biomater Sci; 2019 Aug 01; 7(8):3190-3203. PubMed ID: 31145392
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  • 3. pH and redox-responsive mixed micelles for enhanced intracellular drug release.
    Cai M, Zhu K, Qiu Y, Liu X, Chen Y, Luo X.
    Colloids Surf B Biointerfaces; 2014 Apr 01; 116():424-31. PubMed ID: 24549044
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  • 4. Ligand-directed reduction-sensitive shell-sheddable biodegradable micelles actively deliver doxorubicin into the nuclei of target cancer cells.
    Zhong Y, Yang W, Sun H, Cheng R, Meng F, Deng C, Zhong Z.
    Biomacromolecules; 2013 Oct 14; 14(10):3723-30. PubMed ID: 23998942
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  • 5. Computer simulations on the pH-sensitive tri-block copolymer containing zwitterionic sulfobetaine as a novel anti-cancer drug carrier.
    Min W, Zhao D, Quan X, Sun D, Li L, Zhou J.
    Colloids Surf B Biointerfaces; 2017 Apr 01; 152():260-268. PubMed ID: 28119221
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  • 8. Comb-like amphiphilic copolymers bearing acetal-functionalized backbones with the ability of acid-triggered hydrophobic-to-hydrophilic transition as effective nanocarriers for intracellular release of curcumin.
    Zhao J, Wang H, Liu J, Deng L, Liu J, Dong A, Zhang J.
    Biomacromolecules; 2013 Nov 11; 14(11):3973-84. PubMed ID: 24107101
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  • 11. Protein adsorption and macrophage uptake of zwitterionic sulfobetaine containing micelles.
    Lu A, Wu Z, Luo X, Li S.
    Colloids Surf B Biointerfaces; 2018 Jul 01; 167():252-259. PubMed ID: 29674293
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  • 12. Fine tuning micellar core-forming block of poly(ethylene glycol)-block-poly(ε-caprolactone) amphiphilic copolymers based on chemical modification for the solubilization and delivery of doxorubicin.
    Yan J, Ye Z, Chen M, Liu Z, Xiao Y, Zhang Y, Zhou Y, Tan W, Lang M.
    Biomacromolecules; 2011 Jul 11; 12(7):2562-72. PubMed ID: 21598958
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  • 13. Exogenous Vitamin C-Triggered Surface Charge Conversion of pH/Reduction-Responsive Micelles for the Enhanced Tumor-Specific Activity of Loaded Doxorubicin.
    Wu Z, Chen B, Gan Z, Chen F, Luo X.
    Mol Pharm; 2020 Mar 02; 17(3):954-964. PubMed ID: 31977226
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  • 15. Redox and pH-responsive degradable micelles for dually activated intracellular anticancer drug release.
    Chen W, Zhong P, Meng F, Cheng R, Deng C, Feijen J, Zhong Z.
    J Control Release; 2013 Aug 10; 169(3):171-9. PubMed ID: 23306022
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  • 16. Polymeric micelles with citraconic amide as pH-sensitive bond in backbone for anticancer drug delivery.
    Cao J, Su T, Zhang L, Liu R, Wang G, He B, Gu Z.
    Int J Pharm; 2014 Aug 25; 471(1-2):28-36. PubMed ID: 24836667
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  • 19. Tumor-targeting, pH-responsive, and stable unimolecular micelles as drug nanocarriers for targeted cancer therapy.
    Yang X, Grailer JJ, Pilla S, Steeber DA, Gong S.
    Bioconjug Chem; 2010 Mar 17; 21(3):496-504. PubMed ID: 20163170
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