Research graph
References from Facile Strategies to Synthesize Dual Location Dual Acidic pH/Reduction-Responsive Degradable Block Copolymers Bearing Acetal/Disulfide Block Junctions and Disulfide Pendants. Local targets link to admitted publications; unresolved targets remain external evidence.
Nano-engineering block copolymer aggregates for drug delivery
10.1016/s0927-7765(99)00058-2 · 1999 · External reference
Block copolymer micelles for delivery of cancer therapy: Transport at the whole body, tissue and cellular levels
10.1016/j.jconrel.2009.04.010 · 2009 · External reference
Engineering of amphiphilic block copolymers for polymeric micellar drug and gene delivery
10.1016/j.jconrel.2011.04.028 · 2011 · External reference
Nanostructured devices based on block copolymer assemblies for drug delivery: designing structures for enhanced drug function
10.1007/12_025 · 2006 · External reference
Nanoporous materials from block copolymer precursors
10.1007/12_002 · 2005 · External reference
Block copolymer assembly via kinetic control
10.1126/science.1141768 · 2007 · External reference
Cylindrical block copolymer micelles and co-micelles of controlled length and architecture
10.1126/science.1141382 · 2007 · External reference
Ion-induced morphological changes in “crew-cut” aggregates of amphiphilic block copolymers
10.1126/science.272.5269.1777 · 1996 · External reference
Aqueous Dispersion Polymerization: A New Paradigm for in Situ Block Copolymer Self-Assembly in Concentrated Solution
10.1021/ja205887v · 2011 · External reference
Hierarchical Interfacial Assembly of ABC Triblock Copolymer
10.1021/ja075201i · 2008 · External reference
Nanoparticles with targeting, triggered release, and imaging functionality for cancer applications
10.1039/c0sm00534g · 2011 · External reference
Triggered destabilization of polymeric micelles and vesicles by changing polymers polarity: An attractive tool for drug delivery
10.1016/j.jconrel.2007.03.023 · 2007 · External reference
Making polymeric nanoparticles stimuli-responsive with dynamic covalent bonds
10.1039/c2py20727c · 2013 · External reference
Acid-degradable polymers for drug delivery: a decade of innovation
10.1039/c2cc36589h · 2013 · External reference
Light-Responsive Block Copolymer Micelles
10.1021/ma300094t · 2012 · External reference
Tuning the Amphiphilicity of Building Blocks: Controlled Self-Assembly and Disassembly for Functional Supramolecular Materials
10.1002/adma.200803276 · 2009 · External reference
Enzyme-responsive polymer assemblies constructed through covalent synthesis and supramolecular strategy
10.1039/c4cc05878j · 2015 · External reference
Encapsulation and Enzyme-Mediated Release of Molecular Cargo in Polysulfide Nanoparticles
10.1021/nn201477y · 2011 · External reference
Designing Dendron-Polymer Conjugate Based Targeted Drug Delivery Platforms with a “Mix-and-Match” Modularity
10.1021/acs.bioconjchem.7b00595 · 2017 · External reference
pH degradable dendron-functionalized poly(2-ethyl-2-oxazoline) prepared by a cascade “double-click” reaction
10.1039/c3py00258f · 2013 · External reference
Stimuli-responsive nanocarriers for drug delivery
10.1038/nmat3776 · 2013 · External reference
Design and development of polymeric micelles with cleavable links for intracellular drug delivery
10.1016/j.progpolymsci.2012.07.002 · 2013 · External reference
Smart drug delivery systems: from fundamentals to the clinic
10.1039/c4cc01429d · 2014 · External reference
Functional block copolymer assemblies responsive to tumor and intracellular microenvironments for site-specific drug delivery and enhanced imaging performance
10.1039/c3cs60048c · 2013 · External reference
Biodegradable polymeric micelles for targeted and controlled anticancer drug delivery: Promises, progress and prospects
10.1016/j.nantod.2012.08.005 · 2012 · External reference
Glutathione-responsive polymeric micelles formed by a biodegradable amphiphilic triblock copolymer for anticancer drug delivery and controlled release
10.1021/acsbiomaterials.5b00119 · 2015 · External reference
Disulfide-Cleavage-Triggered Chemosensors and Their Biological Applications
10.1021/cr300358b · 2013 · External reference
o-Nitrobenzyl Alcohol Derivatives: Opportunities in Polymer and Materials Science
10.1021/ma201924h · 2012 · External reference
Polymeric assemblies and nanoparticles with stimuli-responsive fluorescence emission characteristics
10.1039/c2cc17695e · 2012 · External reference
Responsive Polymers for Detection and Sensing Applications: Current Status and Future Developments
10.1021/ma1005815 · 2010 · External reference
Stimuli-responsive polymers and their applications
10.1039/c6py01585a · 2017 · External reference
Recent advances in stimuli-responsive degradable block copolymer micelles: synthesis and controlled drug delivery applications
10.1039/c2cc32408c · 2012 · External reference
Molecular Precision and Enzymatic Degradation: From Readily to Undegradable Polymeric Micelles by Minor Structural Changes
10.1021/jacs.6b10624 · 2017 · External reference
Dual and multi-stimuli responsive polymeric nanoparticles for programmed site-specific drug delivery
10.1016/j.biomaterials.2013.01.084 · 2013 · External reference
Multiresponsive polymers: nano-sized assemblies, stimuli-sensitive gels and smart surfaces
10.1039/c0py00424c · 2011 · External reference
Multi-stimuli responsive polymers – the all-in-one talents
10.1039/c3py00880k · 2014 · External reference
Controlled micellar disassembly of photo- and pH-cleavable linear-dendritic block copolymers
10.1039/c5py00792e · 2015 · External reference
Dual-stimuli-responsive glycopolymer bearing a reductive and photo-cleavable unit at block junction
10.1039/c6ra22207b · 2016 · External reference
Dual-Stimuli-Responsive Micelle of an ABC Triblock Copolymer Bearing a Redox-Cleavable Unit and a Photocleavable Unit at Two Block Junctions
10.1021/la404493n · 2014 · External reference
Design and synthesis of redox and oxidative dual responsive block copolymer micelles for intracellular drug delivery
10.1016/j.eurpolymj.2016.09.047 · 2016 · External reference
Biodegradable Block Copolymer Micelles with Thiol-Responsive Sheddable Coronas
10.1021/bm2011032 · 2011 · External reference
A dual location stimuli-responsive degradation strategy of block copolymer nanocarriers for accelerated release
10.1039/c3cc44200d · 2013 · External reference
Dual location disulfide degradable interlayer-crosslinked micelles with extended sheddable coronas exhibiting enhanced colloidal stability and rapid release
10.1039/c3py00852e · 2014 · External reference
Glutathione-Triggered Disassembly of Dual Disulfide Located Degradable Nanocarriers of Polylactide-Based Block Copolymers for Rapid Drug Release
10.1021/bm5008508 · 2014 · External reference
Stimulus-Responsive Degradable Polylactide-Based Block Copolymer Nanoassemblies for Controlled/Enhanced Drug Delivery
10.1021/acs.molpharmaceut.7b00284 · 2017 · External reference
Dual location reduction-responsive degradable nanocarriers: A new strategy for intracellular anticancer drug delivery with accelerated release
10.1021/bk-2015-1188.ch017 · 2015 · External reference
Redox and pH-responsive degradable micelles for dually activated intracellular anticancer drug release
10.1016/j.jconrel.2013.01.001 · 2013 · External reference
Dually pH/reduction-responsive vesicles for ultrahigh-contrast fluorescence imaging and thermo-chemotherapy-synergized tumor ablation
10.1021/acsnano.5b02843 · 2015 · External reference
Construction of Targeting-Clickable and Tumor-Cleavable Polyurethane Nanomicelles for Multifunctional Intracellular Drug Delivery
10.1021/bm401342t · 2013 · External reference
Dual Location, Dual Acidic pH/Reduction-Responsive Degradable Block Copolymer: Synthesis and Investigation of Ketal Linkage Instability under ATRP Conditions
10.1021/acs.macromol.7b02070 · 2017 · External reference
Dual Location Dual Reduction/Photoresponsive Block Copolymer Micelles: Disassembly and Synergistic Release
10.1002/marc.201500306 · 2015 · External reference
Quadruple-Stimuli-Sensitive Polymeric Nanocarriers for Controlled Release under Combined Stimulation
10.1021/ma502003v · 2014 · External reference
Atom Transfer Radical Polymerization
10.1021/cr940534g · 2001 · External reference
10.1002/0471220450
10.1002/0471220450 · 2002 · External reference
Polymers prepared using cleavable initiators: Synthesis, characterization and degradation
10.1016/j.progpolymsci.2011.01.004 · 2011 · External reference
Degradable vinyl polymers for biomedical applications
10.1038/nchem.2343 · 2015 · External reference
Opportunities for dual RDRP agents in synthesizing novel polymeric materials
10.1039/c7py00344g · 2017 · External reference
Synthesis of Well-Defined Poly(vinyl acetate)-b-Polystyrene by Combination of ATRP and RAFT Polymerization
10.1021/ma800799x · 2008 · External reference
Neuron-Targeted Copolymers with Sheddable Shielding Blocks Synthesized Using a Reducible, RAFT-ATRP Double-Head Agent
10.1021/ja3085803 · 2012 · External reference
Concurrent ATRP/RAFT of styrene and methyl methacrylate with dithioesters catalyzed by copper(I) complexes
10.1021/ma801502s · 2008 · External reference
Dibromotrithiocarbonate Iniferter for Concurrent ATRP and RAFT Polymerization. Effect of Monomer, Catalyst, and Chain Transfer Agent Structure on the Polymerization Mechanism
10.1021/ma800539v · 2008 · External reference
ATRP with Alkyl Pseudohalides Acting as Initiators and Chain Transfer Agents: When ATRP and RAFT Polymerization Become One
10.1002/ijch.201100124 · 2012 · External reference
Dual Concurrent ATRP/RAFT of Methyl Acrylate Co-initiated by Alkyl Halides
10.1021/ma200263w · 2011 · External reference
Acid-Labile Poly(glycidyl methacrylate)-Based Star Gene Vectors
10.1021/acsami.5b02733 · 2015 · External reference
Activators regenerated by electron transfer for atom transfer radical polymerization of styrene
10.1021/ma0522716 · 2006 · External reference
Diminishing catalyst concentration in atom transfer radical polymerization with reducing agents
10.1073/pnas.0602675103 · 2006 · External reference
Non-heme Iron(II) Complexes Containing Tripodal Tetradentate Nitrogen Ligands and Their Application in Alkane Oxidation Catalysis
10.1021/ic0509229 · 2005 · External reference
Thiol-responsive block copolymer nanocarriers exhibiting tunable release with morphology changes
10.1039/c2py20582c · 2013 · External reference
