An intelligent drug delivery system that exhibits a thermosensitive phase transition from a soluble to insoluble state was developed to deliver drugs into a tumor. Cyclotriphosphazene-Pt-DACH (trans(+/-)-1,2-diaminocyclohexane) conjugates with dipeptide spacers were synthesized by successive reaction steps. The conjugates exhibited a reversible and thermosensitive phase transition with lower critical solution temperature in aqueous media that was varied by the substitution of different hydrophilic/hydrophobic side groups. The conjugate had similar cytotoxicity as cisplatin, but much greater than carboplatin against various human cancer cell lines. The conjugate was much more potent than cisplatin against the cisplatin-resistant cell line, A...
ii The aim of my Ph. D. thesis is to generalize a method for targeted anti-cancer drug delivery. Hyd...
The aim of my Ph. D. thesis is to generalize a method for targeted anti-cancer drug delivery. Hydrop...
Flurbiprofen, a hydrophobic COX inhibitor, was coordinated axially with oxoplatin to form a new conj...
Reduction-responsive nano-carriers have been confirmed to be promising for intracellular drug delive...
In this study, we suggest a novel strategy of constituting an in situ-formed hydrogel composed of po...
This paper describes the synthesis of a polymer–prodrug conjugate, its aqueous self-assembly, noncov...
The preparation of novel macromolecular prodrugs via the conjugation of two platinum(IV) complexes t...
Cell-penetrating peptide [WR]5 has been previously shown to be an efficient molecular transporter fo...
This research focuses on the synthesis of new polymeric platinum conjugated drugs which were designe...
The design and study of efficient polymer-based drug delivery systems for the controlled release of ...
The synthesis of polymer-drug conjugate (PDC) capable of convenient preparation and controlled relea...
We present here a novel camptothecin (CPT) prodrug based on polyethylene glycol monomethyl ether-blo...
In this study, to enhance the therapeutic function and reduce the side-effects of doxorubicin (DOX),...
Within this work we aimed to improve the pharmacodynamics and toxicity profile of organoruthenium an...
The synthesis of selectively oxidized cellulose, 2,3-dicarboxycellulose (DCC), is optimized for prep...
ii The aim of my Ph. D. thesis is to generalize a method for targeted anti-cancer drug delivery. Hyd...
The aim of my Ph. D. thesis is to generalize a method for targeted anti-cancer drug delivery. Hydrop...
Flurbiprofen, a hydrophobic COX inhibitor, was coordinated axially with oxoplatin to form a new conj...
Reduction-responsive nano-carriers have been confirmed to be promising for intracellular drug delive...
In this study, we suggest a novel strategy of constituting an in situ-formed hydrogel composed of po...
This paper describes the synthesis of a polymer–prodrug conjugate, its aqueous self-assembly, noncov...
The preparation of novel macromolecular prodrugs via the conjugation of two platinum(IV) complexes t...
Cell-penetrating peptide [WR]5 has been previously shown to be an efficient molecular transporter fo...
This research focuses on the synthesis of new polymeric platinum conjugated drugs which were designe...
The design and study of efficient polymer-based drug delivery systems for the controlled release of ...
The synthesis of polymer-drug conjugate (PDC) capable of convenient preparation and controlled relea...
We present here a novel camptothecin (CPT) prodrug based on polyethylene glycol monomethyl ether-blo...
In this study, to enhance the therapeutic function and reduce the side-effects of doxorubicin (DOX),...
Within this work we aimed to improve the pharmacodynamics and toxicity profile of organoruthenium an...
The synthesis of selectively oxidized cellulose, 2,3-dicarboxycellulose (DCC), is optimized for prep...
ii The aim of my Ph. D. thesis is to generalize a method for targeted anti-cancer drug delivery. Hyd...
The aim of my Ph. D. thesis is to generalize a method for targeted anti-cancer drug delivery. Hydrop...
Flurbiprofen, a hydrophobic COX inhibitor, was coordinated axially with oxoplatin to form a new conj...