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