Diazonaphthoquinone-based amphiphilic polymer assemblies for NIR/UV light- and pH-responsive controlled release
Literature Information
Qingwei Li, Ziquan Cao, Guojie Wang
Here, a novel near-infrared (NIR)/ultraviolet (UV) light-, pH- and temperature-responsive amphiphilic polymer, poly(ethylene glycol)-block-poly(dimethylaminoethyl methacrylate)@2-diazo-1,2-naphthoquinone (PEG-PDMAEMA@DNQ), is synthesized via an atom transfer radical polymerization (ATRP) and quaternization reaction. In aqueous solution, this amphiphilic polymer could self-assemble into spherical assemblies with hydrophobic NIR/UV light and base responsive DNQ moieties as the core and hydrophilic PEG and pH/temperature-responsive PDMAEMA as the corona. The NIR/UV light- and pH-sensitive absorbances of the polymer were characterized by UV-vis spectroscopy. Under 365 nm UV or 808 nm NIR irradiation, the characteristic absorption intensity of DNQ gradually decreased, indicating that DNQ converted to 3-indenecarboxylic acid (3-IC) via the Wolff rearrangement. Under acidic conditions, the absorption spectra changed little, while the absorption peak at around 400 nm decreased and a new absorption peak at 350 nm appeared under basic conditions. The morphological changes of the assemblies, which could be dissociated after UV/NIR irradiation, swollen under acidic conditions, while turned into nanocapsules under basic conditions and shrunk above the lower critical solution temperature (LCST), were revealed by transmission electron microscopy (TEM) and dynamic light scattering (DLS). The loaded hydrophobic model molecules coumarin 102 could be released from the assemblies in response to NIR, UV light and pH. More importantly, the release efficiency could be enhanced dramatically under combined stimulation. The reported NIR/UV light- and pH-responsive polymer assemblies would have great potential as nanocarriers for controlled release.
Related Literature
Reduction of carbonyl groups to the corresponding methylenes with Ni–Al alloy in water
Keiko Ishimoto, Yoshiharu Mitoma, Satoko Nagashima, Hideki Tashiro, G. K. Surya Prakash, George A. Olah, Masashi Tashiro
DOI: 10.1039/B211571A
Crown-ether functionalised second coordination sphere palladiumcatalysts by molecular imprinting
Florian Viton, Peter S. White, Michel R. Gagné
DOI: 10.1039/B309072H
Novel alignment technique for LCD-biosensors
Johan Hoogboom, Joost Clerx, Matthijs B. J. Otten, Alan E. Rowan, Theo Rasing, Roeland J. M. Nolte
DOI: 10.1039/B310860K
The key intermediates that interact with the fluorophores in the peroxyoxalate chemiluminescence reaction of 2,4,6-trichlorophenyl N-aryl-N-tosyloxamates
Ryu Koike, Jiro Motoyoshiya, Yutaka Takaguchi, Hiromu Aoyama
DOI: 10.1039/B300079F
A supramolecular approach to lithium ion solvation at nanostructured dye sensitised inorganic/organic heterojunctions
Taiho Park, Saif A. Haque, Robert J. Potter, Andrew B. Holmes, James R. Durrant
DOI: 10.1039/B306604E
Designed layer assembly: a three-dimensional framework with 74% extra-framework volume by connection of infinite two-dimensional sheets
T. J. Prior, D. Bradshaw, S. J. Teat, M. J. Rosseinsky
DOI: 10.1039/B211124C
Cell-permeable small molecule probes for site-specific labeling of proteins
Dawn S. Y. Yeo, Rajavel Srinivasan, Mahesh Uttamchandani, Qing Zhu
DOI: 10.1039/B309196A
Functional analysis of the biomimetic silica precipitating activity of the R5 peptide from Cylindrotheca fusiformis
Marc R. Knecht, David W. Wright
DOI: 10.1039/B309074D
Photomodulated molecular recognition of the guanidinium cation
Christopher A. Hunter, Mahmut Togrul, Salvador Tomas
DOI: 10.1039/B311060E
First high thermally stable organo–inorganic 3D polymer scandium derivative as a heterogeneous Lewis acid catalyst
Josefina Perles, Marta Iglesias, Caridad Ruiz-Valero, Natalia Snejko
DOI: 10.1039/B210034G
You might also like
What precautions should be taken when handling lithium chloride hydrate (1:1:1) (CAS: 16712-20-2)?
When handling lithium chloride hydrate (1:1:1) (CAS: 16712-20-2), it is importan...
Is 4-(4H-1,2,4-Triazol-4-yl)piperidine (CAS: 690261-92-8) safe?
4-(4H-1,2,4-Triazol-4-yl)piperidine is generally considered safe for use in phar...
How should waste containing 1,3-Thiazole-2-carboxamide (CAS: 16733-85-0) be handled?
Waste containing 1,3-Thiazole-2-carboxamide (CAS: 16733-85-0) should be collecte...
What regulatory guidelines apply to 5-(Difluoromethyl)-2-fluorobenzonitrile (CAS: 934175-58-3)?
5-(Difluoromethyl)-2-fluorobenzonitrile (CAS: 934175-58-3) is subject to regulat...
How is Methyl 3-acetamido-2-thiophenecarboxylate (CAS: 22288-79-5) typically synthesized?
Methyl 3-acetamido-2-thiophenecarboxylate can be synthesized by the reaction of ...
What is 4-Isoquinolinecarbonitrile (CAS: 34846-65-6)?
4-Isoquinolinecarbonitrile is a chemical compound with the CAS number 34846-65-6...
How should Methyl 1H-1,2,3-triazole-4-carboxylate (CAS: 877309-59-6) be stored?
Store Methyl 1H-1,2,3-triazole-4-carboxylate (CAS: 877309-59-6) in a cool, dry p...
What regulatory guidelines apply to 6-Bromo[1,3]thiazolo[5,4-b]pyridin-2-amine (CAS: 1160791-13-8)?
6-Bromo[1,3]thiazolo[5,4-b]pyridin-2-amine (CAS: 1160791-13-8) is subject to the...
Is (2S,3S)-2-Ammonio-3-(3,4-dihydroxyphenyl)-3-hydroxypropanoate (CAS: 23651-95-8) safe?
(2S,3S)-2-Ammonio-3-(3,4-dihydroxyphenyl)-3-hydroxypropanoate (CAS: 23651-95-8) ...
What are the physical and chemical properties of 7-bromo-3-methyl-3,4-dihydroquinazolin-4-one (CAS: 1293987-84-4)?
7-Bromo-3-methyl-3,4-dihydroquinazolin-4-one is a solid with a crystalline form....
Source Journal
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.










![1-[4-(4-Methyl-1H-imidazol-1-yl)phenyl]ethanone structure 1-[4-(4-Methyl-1H-imidazol-1-yl)phenyl]ethanone structure](https://static.chemtradehub.com/structs/142/142161-53-3-7f55.webp)

![(1R,5R)-3-{[(2-Methyl-2-propanyl)oxy]carbonyl}-3-azabicyclo[3.1.0]hexane-1-carboxylic acid structure (1R,5R)-3-{[(2-Methyl-2-propanyl)oxy]carbonyl}-3-azabicyclo[3.1.0]hexane-1-carboxylic acid structure](https://static.chemtradehub.com/structs/116/1165450-63-4-bfe1.webp)
![(R)-N-[(S)-1-[2-(Diphenylphosphino)phenyl]ethyl]-2-methylpropane-2-sulfinamide structure (R)-N-[(S)-1-[2-(Diphenylphosphino)phenyl]ethyl]-2-methylpropane-2-sulfinamide structure](https://static.chemtradehub.com/structs/159/1595319-98-4-33e7.webp)
