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By combining controlled experiments on single interfaces with measurements on solitary bubbles and liquid foams, we show that poly( N-isopropylacrylamide) (PNIPAM) microgels assembled at air/water interfaces exhibit a solid to liquid transition changing the temperature, and that this is associated with the change in the interfacial microstructure of the PNIPAM particles around their volume phase transition temperature. We show that the solid behaves as a soft 2D colloidal glass, and that the existence of this solid/liquid transition offers an ideal platform to tune the permeability of air bubbles covered by PNIPAM and to control macroscopic foam properties such as drainage, stability, and foamability. PNIPAM particles on fluid interfaces allow new tunable materials, for example foam structures with variable mechanical properties upon small temperature changes.
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http://dx.doi.org/10.1021/acs.langmuir.7b03879 | DOI Listing |
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December 2024
Key Laboratory of Bionic Engineering, Ministry of Education, Jilin University, Changchun, 130012, China.
Traditional microneedle (MN) technology offers unique advantages in treating wound infections; however, its single-function design lacks the capability for real-time monitoring of wound conditions, often resulting in uncontrolled drug release. Herein, an anti-infective and intelligent MN patch (SP-CSMN) integrating three functional modules is developed, including temperature monitoring, Bluetooth wireless communication, and responsive drug release. The patch employed chitosan (CS) as a porous substrate, filled with temperature-sensitive poly(N-isopropylacrylamide) (PNIPAM) to encapsulate and release the antibiotic rifampicin.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
School of Biomedical and Pharmaceutical Sciences, Guangdong University of Technology, Guangzhou 510006, China; Department of Traditional Chinese Medicine, Institute of Guangdong Geriatric, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou 510080, China.
Thermosensitive hydrogels show great potential in healing diabetic wounds, but they are still challenged by the long healing time, risk of infectivity, and accumulation of melanin. Herein, a dual network hydrogel is designed, which consists of chlorogenic acid (CA) modified chitosan (CS) (CA@CS), poly(N-isopropylacrylamide) (PNIPAm), and glabridin liposomes (GL). The gelation transition temperature of the hydrogel is 32-34 °C, which thus endows it with superior injectability at ambient temperature.
View Article and Find Full Text PDFACS Appl Polym Mater
December 2024
Department of NanoEngineering, University of California San Diego, La Jolla, California 92093, United States.
Microgel suspensions have garnered significant interest in fundamental research due to their phase transition between liquid-like to paste-like behaviors stemming from tunable interparticle and particle-solvent interactions. Particularly, stimuli-responsive microgels undergo faster volume changes in response to external stimuli in comparison to their bulk counterparts, while maintaining their structural integrity. Here, concentrated and diluted suspensions of poly(-isopropylacrylamide) (PNIPAm) microgels are dispersed to different packing fractions in water for the characterizations of temperature-responsive rheological responses.
View Article and Find Full Text PDFPolymers (Basel)
December 2024
Vinča Institute of Nuclear Sciences, National Institute of the Republic of Serbia, University of Belgrade, Mike Petrovića Alasa 12-14, Vinča, 11351 Belgrade, Serbia.
Hydrogel nanocomposites that respond to external stimuli and possess switchable electrical properties are considered as emerging materials with potential uses in electrical, electrochemical, and biological devices. This work reports the synthesis and characterization of thermo-responsive and electroconductive hydrogel nanocomposites based on poly(-isopropylacrylamide) (PNiPAAm) and gold nanoparticles (nanospheres-AuNPs and nanorods-AuNRs) using two different synthetic techniques. Method I involved γ-irradiation-induced crosslinking of a polymer matrix (hydrogel), followed by radiolytic formation of gold nanoparticles, while Method II included the chemical synthesis of nanoparticles, followed by radiolytic formation of a polymer matrix around the gold nanoparticles.
View Article and Find Full Text PDFPolymers (Basel)
November 2024
División de Física Aplicada, Centro de Investigación Científica y Educación Superior de Ensenada, Ensenada 22860, Mexico.
A series of copolymers containing a thermo-responsive biocompatible first block of poly[di(ethylene glycol) methyl ether methacrylate)--(oligo(ethylene glycol) methyl ether methacrylate], P(DEGMA--OEGMA) were chain-extended to incorporate either poly(-isopropylacrylamide), PNIPAAm or poly(-isopropylacrylamide--butyl acrylate), P(NIPAAm-co-BA) as second thermo-responsive block using reversible addition-fragmentation chain transfer (RAFT) polymerization. P(DEGMA--OEGMA)--PNIPAAm copolymers showed two response temperatures at 33 and 43 °C in an aqueous solution forming stable aggregates at 37 °C. In contrast, P(DEGMA--OEGMA)--P(NIPAAm--BA) copolymers showed aggregation below room temperature due to the shift in response temperature provoked by the presence of hydrophobic butyl acrylate (BA) units, and shrinkage upon heating up to body temperature, while maintaining the second response temperature above 40 °C.
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