Backbone-Degradable (Co-)Polymers for Light-Triggered Drug Delivery

[1]  Saji Uthaman,et al.  Photo- and pH-Responsive Polycarbonate Block Copolymer Prodrug Nanomicelles for Controlled Release of Doxorubicin. , 2020, Macromolecular bioscience.

[2]  Li-Fang Wang,et al.  Strategy to design a smart photocleavable and pH sensitive chitosan based hydrogel through a novel crosslinker: a potential vehicle for controlled drug delivery , 2020, RSC advances.

[3]  D. Kuckling,et al.  Synthesis and characterization of light-degradable bromocoumarin functionalized polycarbonates , 2020 .

[4]  D. Kuckling,et al.  Light-Responsive Serinol-Based Polyurethane Nanocarrier for Controlled Drug Release. , 2019, Macromolecular rapid communications.

[5]  D. Kuckling,et al.  In vitro evaluation of innovative light-responsive nanoparticles for controlled drug release in intestinal PDT. , 2019, International journal of pharmaceutics.

[6]  D. Kuckling,et al.  Light-Responsive Serinol-Based Polycarbonate and Polyester as Degradable Scaffolds. , 2019, ACS applied bio materials.

[7]  D. Kuckling,et al.  Preparation of Light-Responsive Aliphatic Polycarbonate via Versatile Polycondensation for Controlled Degradation , 2019, Macromolecular Chemistry and Physics.

[8]  D. Kuckling,et al.  Light‐responsive nanoparticles based on new polycarbonate polymers as innovative drug delivery systems for photosensitizers in PDT , 2019, International journal of pharmaceutics.

[9]  W. Tan,et al.  Self-Assembled Aptamer-Grafted Hyperbranched Polymer Nanocarrier for Targeted and Photoresponsive Drug Delivery. , 2018, Angewandte Chemie.

[10]  D. Kuckling,et al.  Use of Light-Degradable Aliphatic Polycarbonate Nanoparticles As Drug Carrier for Photosensitizer. , 2018, Biomacromolecules.

[11]  F. Wurm,et al.  Functional biodegradable polymers via ring-opening polymerization of monomers without protective groups. , 2018, Chemical Society reviews.

[12]  Jun Hee Lee,et al.  Diphenyl Carbonate: A Highly Reactive and Green Carbonyl Source for the Synthesis of Cyclic Carbonates. , 2018, The Journal of organic chemistry.

[13]  To Ngai,et al.  Hybrid nanodiamond quantum sensors enabled by volume phase transitions of hydrogels , 2018, Nature Communications.

[14]  Xuequan Zhang,et al.  Tumor-pH-Sensitive PLLA-Based Microsphere with Acid Cleavable Acetal Bonds on the Backbone for Efficient Localized Chemotherapy. , 2018, Biomacromolecules.

[15]  Hao Tan,et al.  Acid- and reduction-sensitive micelles for improving the drug delivery efficacy for pancreatic cancer therapy. , 2018, Biomaterials science.

[16]  Seungil Kim,et al.  Smart and Biostable Polyurethanes for Long-Term Implants. , 2018, ACS biomaterials science & engineering.

[17]  B. Amsden,et al.  Synthesis of cinnamoyl and coumarin functionalized aliphatic polycarbonates , 2017 .

[18]  Ghislaine Vantomme,et al.  A Rewritable, Reprogrammable, Dual Light‐Responsive Polymer Actuator , 2017, Angewandte Chemie.

[19]  Couturaud Benoit,et al.  Dual thermo- and light-responsive coumarin-based copolymers with programmable cloud points , 2017 .

[20]  H. Sardón,et al.  Temperature responsive PEG-based polyurethanes “à la carte” , 2017 .

[21]  Yafei Luan,et al.  Comparison of the Responsivity of Solution-Suspended and Surface-Bound Poly(N-isopropylacrylamide)-Based Microgels for Sensing Applications. , 2017, ACS applied materials & interfaces.

[22]  D. Kuckling,et al.  Synthesis of hyperbranched polymers from vegetable oil based monomers via ozonolysis pathway , 2017 .

[23]  Michel Armand,et al.  Polycondensation as a Versatile Synthetic Route to Aliphatic Polycarbonates for Solid Polymer Electrolytes , 2017 .

[24]  María Vallet-Regí,et al.  Self-immolative polymers as novel pH-responsive gate keepers for drug delivery , 2017 .

[25]  L. Tayebi,et al.  Wound dressing application of pH-sensitive carbon dots/chitosan hydrogel , 2017 .

[26]  K. Langer,et al.  Polymeric nanoparticles - Influence of the glass transition temperature on drug release. , 2017, International journal of pharmaceutics.

[27]  Yong Wang,et al.  Ultrasensitive GSH-Responsive Ditelluride-Containing Poly(ether-urethane) Nanoparticles for Controlled Drug Release. , 2016, ACS applied materials & interfaces.

[28]  A. Kasko,et al.  Shape-Changing Photodegradable Hydrogels for Dynamic 3D Cell Culture. , 2016, ACS applied materials & interfaces.

[29]  Yi Wang,et al.  Biomimicking Nano-Micro Binary Polymer Brushes for Smart Cell Orientation and Adhesion Control. , 2016, Small.

[30]  Huabing Chen,et al.  Rational Design of Multi-Stimuli-Responsive Nanoparticles for Precise Cancer Therapy. , 2016, ACS nano.

[31]  A. Khademhosseini,et al.  A robust super-tough biodegradable elastomer engineered by supramolecular ionic interactions. , 2016, Biomaterials.

[32]  Michael R Hamblin,et al.  Smart micro/nanoparticles in stimulus-responsive drug/gene delivery systems. , 2016, Chemical Society reviews.

[33]  D. Kuckling,et al.  Synthesis of high-molecular-weight aliphatic polycarbonates by organo-catalysis , 2016 .

[34]  O. Farokhzad,et al.  Degradable Controlled-Release Polymers and Polymeric Nanoparticles: Mechanisms of Controlling Drug Release. , 2016, Chemical reviews.

[35]  Mauro Ferrari,et al.  Principles of nanoparticle design for overcoming biological barriers to drug delivery , 2015, Nature Biotechnology.

[36]  Zhiyuan Zhong,et al.  Micelles Based on Acid Degradable Poly(acetal urethane): Preparation, pH-Sensitivity, and Triggered Intracellular Drug Release. , 2015, Biomacromolecules.

[37]  J. Feijen,et al.  Enzymatically and reductively degradable α-amino acid-based poly(ester amide)s: synthesis, cell compatibility, and intracellular anticancer drug delivery. , 2015, Biomacromolecules.

[38]  Jing Wang,et al.  Ring-opening polymerization of prodrugs: a versatile approach to prepare well-defined drug-loaded nanoparticles. , 2015, Angewandte Chemie.

[39]  C. Tonda-Turo,et al.  Biomimetic polyurethanes in nano and regenerative medicine. , 2014, Journal of materials chemistry. B.

[40]  A. Kasko,et al.  Complex Dynamic Substrate Control: Dual‐Tone Hydrogel Photoresists Allow Double‐Dissociation of Topography and Modulus , 2014, Advanced materials.

[41]  Zhiyuan Zhong,et al.  Dual and multi-stimuli responsive polymeric nanoparticles for programmed site-specific drug delivery. , 2013, Biomaterials.

[42]  P. Nagy Kinetics and mechanisms of thiol-disulfide exchange covering direct substitution and thiol oxidation-mediated pathways. , 2013, Antioxidants & redox signaling.

[43]  Jung Jae Lee,et al.  Preparation of High-Molecular-Weight Aliphatic Polycarbonates by Condensation Polymerization of Diols and Dimethyl Carbonate , 2013 .

[44]  L. Mespouille,et al.  Synthesis and post-polymerisation modifications of aliphatic poly(carbonate)s prepared by ring-opening polymerisation. , 2013, Chemical Society reviews.

[45]  R. Givens,et al.  Photoremovable Protecting Groups in Chemistry and Biology: Reaction Mechanisms and Efficacy , 2012, Chemical reviews.

[46]  Adah Almutairi,et al.  A Single UV or Near IR Triggering Event Leads to Polymer Degradation into Small Molecules. , 2012, ACS macro letters.

[47]  K. Landfester,et al.  Photo-sensitive PMMA microgels: light-triggered swelling and degradation , 2011 .

[48]  Jiehua Li,et al.  Synthesis and Characterization of pH-Sensitive Biodegradable Polyurethane for Potential Drug Delivery Applications , 2011 .

[49]  Kristi S Anseth,et al.  Tunable Hydrogels for External Manipulation of Cellular Microenvironments through Controlled Photodegradation , 2010, Advanced materials.

[50]  Motohiro Uo,et al.  Microparticle formation and its mechanism in single and double emulsion solvent evaporation. , 2004, Journal of controlled release : official journal of the Controlled Release Society.

[51]  B. Trathnigg,et al.  Quantitation in liquid chromatography of polymers: size-exclusion chromatography with dual detection , 1997 .

[52]  J. Smedinga,et al.  Biodegradable lysine diisocyanate-based poly(glycolide-co-epsilon-caprolactone)-urethane network in artificial skin. , 1990, Biomaterials.

[53]  H. Maeda,et al.  A new concept for macromolecular therapeutics in cancer chemotherapy: mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs. , 1986, Cancer research.

[54]  E. Kretschmann Die Bestimmung optischer Konstanten von Metallen durch Anregung von Oberflächenplasmaschwingungen , 1971 .

[55]  K. Frisch,et al.  Isocyanate–catalyst and hydroxyl–catalyst complex formation , 1970 .

[56]  D. Kuckling,et al.  Responsive polymers as smart carriers in tunable catalytic processes , 2019, Smart Polymer Catalysts and Tunable Catalysis.

[57]  Patrick Theato,et al.  Multi-stimuli responsive polymers – the all-in-one talents , 2014 .