Self-assembly and multi-stimuli responsive behavior of PAA-b-PAzoMA-b-PNIPAM triblock copolymers

2017 ◽  
Vol 8 (48) ◽  
pp. 7529-7536 ◽  
Author(s):  
Fei Gao ◽  
Yaohui Xing ◽  
Yuan Yao ◽  
Liuying Sun ◽  
Yao Sun ◽  
...  
Keyword(s):  
Self Assembly ◽  
Triblock Copolymer ◽  
Triblock Copolymers ◽  
Temperature Sensitive ◽  
Stimuli Responsive ◽  
Responsive Behavior ◽  
Spherical Micelles

A PAA-b-PAzoMA-b-PNIPAM triblock copolymer containing pH, photo and temperature sensitive groups could self-assemble into spherical micelles or vesicles with multi-stimuli responsiveness.

Sticky ends in a self-assembling ABA triblock copolymer: the role of ureas in stimuli-responsive hydrogels

2019 ◽  
Vol 4 (1) ◽  
pp. 91-102 ◽  
Author(s):  
Ryan T. Shafranek ◽  
Joel D. Leger ◽  
Song Zhang ◽  
Munira Khalil ◽  
Xiaodan Gu ◽  
...  
Keyword(s):  
Self Assembly ◽  
Viscoelastic Properties ◽  
Triblock Copolymer ◽  
Thermal Response ◽  
Stimuli Responsive ◽  
Self Assembling ◽  
Polymeric Hydrogels ◽  
Aba Triblock Copolymer ◽  
Responsive Hydrogels

Directed self-assembly in polymeric hydrogels allows tunability of thermal response and viscoelastic properties.

Self-assembly of dual-responsive amphiphilic POEGMA-b-P4VP-b-POEGMA triblock copolymers: Effect of temperature, pH, and complexation with Cu2+

2021 ◽  
Author(s):  
Daniela M. Zanata ◽  
Maria Isabel Felisberti
Keyword(s):  
Smart Materials ◽  
Self Assembly ◽  
Triblock Copolymers ◽  
Critical Micellar Concentration ◽  
Effect Of Temperature ◽  
Important Class ◽  
Stimuli Responsive ◽  
Dual Responsive

Amphiphilic and stimuli-responsive triblock copolymers are an important class of smart materials due to their low critical micellar concentration in solution and capacity of self-assembly into different structures depending on...

Main-chain PPEGMEMA-b-PBTFVPP-b-PPEGMEMA perfluorocyclobutyl aryl ether-based amphiphilic ABA triblock copolymer: synthesis and self-assembly

RSC Advances ◽  
2015 ◽  
Vol 5 (94) ◽  
pp. 77388-77398 ◽  
Author(s):  
Chun Feng ◽  
Wenqiang Yao ◽  
Guolin Lu ◽  
Yongjun Li ◽  
Xiaoyu Huang
Keyword(s):  
Self Assembly ◽  
Triblock Copolymer ◽  
Main Chain ◽  
Triblock Copolymers ◽  
Aryl Ether ◽  
Step Growth ◽  
Aba Triblock Copolymer ◽  
Transformation Strategy

A novel perfluorocyclobutyl aryl ether-based amphiphilic ABA triblock copolymers were synthesized via the site transformation strategy using sequential thermal [2π + 2π] step-growth cycloaddition polymerization and ATRP.

SELF-ASSEMBLY OF SILVER NANOCLUSTERS ON TRIBLOCK COPOLYMER TEMPLATES

2005 ◽  
Vol 19 (15n17) ◽  
pp. 2792-2797
Author(s):  
ZHONG-TAO SHI ◽  
MIN HAN ◽  
SHI-FENG ZHAO ◽  
LU ZHANG ◽  
XUE-FEI LI ◽  
...  
Keyword(s):  
Self Assembly ◽  
Triblock Copolymer ◽  
Triblock Copolymers ◽  
Quartz Substrate ◽  
Low Energy ◽  
Silver Nanoclusters ◽  
Disorder Phase Transition ◽  
Fused Quartz ◽  
Low Coverage ◽  
Beam Deposition

Poly (styrene-b-butadiene-b-styrene) (SBS) triblock copolymer templates have been prepared by solvent-induced order-disorder phase transition method. Silver nanoclusters have been deposited onto the SBS copolymer templates by low energy clusters beam deposition (LECBD) method. The microstructures of the template and cluster deposits have been characterized by AFM with tapping-mode. It is shown that the triblock copolymers are self-assembled to form an in-plane cylinder ordered microstructure. In the case of low coverage (<50%), silver nanaoclusters deposited on the template tend to aggregate along with the pattern of the template and coalesce into larger nanoparticles. Optical absorption spectra reveal that the surface plasmon resonance (SPR) of silver nanoclusters deposited on the template occurs at 545nm, being a red shift of ~75nm compared to that silver nanoclusters deposited on the fused quartz substrate.

Synthesis and Self-Assembly of CO2–Temperature Dual Stimuli-Responsive Triblock Copolymers

2014 ◽  
Vol 47 (9) ◽  
pp. 2938-2946 ◽  
Author(s):  
Bo-wen Liu ◽  
Hang Zhou ◽  
Si-tong Zhou ◽  
Hui-juan Zhang ◽  
An-Chao Feng ◽  
...  
Keyword(s):  
Self Assembly ◽  
Triblock Copolymers ◽  
Stimuli Responsive

Synthesis, self-assembly and self-healing properties of organic–inorganic ABA triblock copolymers with poly(POSS acrylate) endblocks

2019 ◽  
Vol 10 (19) ◽  
pp. 2424-2435 ◽  
Author(s):  
Bingjie Zhao ◽  
Sen Xu ◽  
Sixun Zheng
Keyword(s):  
Self Assembly ◽  
Triblock Copolymer ◽  
Chain Transfer ◽  
Triblock Copolymers ◽  
Raft Polymerization ◽  
Self Healing ◽  
Reversible Addition ◽  
Aba Triblock Copolymer

A novel organic–inorganic ABA triblock copolymer with a poly(acrylate amide) (PAA) midblock and poly(POSS acrylate) [P(POSS)] endblocks was synthesized via sequential reversible addition–fragmentation chain transfer (RAFT) polymerization.

Synthesis and Self-Assembly Study of Biodegradable Amphiphilic Triblock Copolymers with PEG Block

2014 ◽  
Vol 998-999 ◽  
pp. 95-98
Author(s):  
Xu Du ◽  
Qin Wang ◽  
Chuan Dong Wang ◽  
Yang Liu
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solution ◽  
Ethylene Glycol ◽  
Self Assembly ◽  
Triblock Copolymers ◽  
Poly Ethylene Glycol ◽  
Chemical Structures ◽  
Transmission Electron ◽  
Spherical Micelles ◽  
Poly Ethylene

Three biodegradable amphiphilic triblock copolymers: polylactide-poly (ethylene glycol)-polylactide (PLA-PEG-PLA), poly (ε-caprolactone)-poly (ethylene glycol)-poly (ε-caprolactone) (PCL-PEG-PCL) and poly (lactide-glycolide)-poly (ethylene glycol)-poly (lactide-glycolide) (PLGA-PEG-PLGA) were synthesized. Their chemical structures were characterized. In aqueous solution, their self-assembly and degradation were studied by dynamic light scattering (DLS) and transmission electron microscopy (TEM). Spherical micelles were formed in aqueous solution via self-assembly of the amphiphilic triblock copolymers. After degradation, the PLA-PEG-PLA and PCL-PEG-PCL micelles became smaller and the PLGA-PEG-PLGA micelles change to vesicles, which should mainly attribute to their different degradation speed.

scholarly journals One-pot synthesis of oxidation-sensitive supramolecular gels and vesicles

2021 ◽  
Author(s):  
Aroa Duro-Castano ◽  
Laura Rodriguez-Arco ◽  
Lorena Ruiz-Perez ◽  
Cesare De Pace ◽  
Gabriele Marchello ◽  
...  
Keyword(s):  
Self Assembly ◽  
Biomedical Applications ◽  
Stimuli Responsive ◽  
Sustained Drug Release ◽  
One Pot ◽  
Physiological Conditions ◽  
One Pot Synthesis ◽  
Wide Range ◽  
Spherical Micelles ◽  
The One

Polypeptide-based nanoparticles offer unique advantages from a nanomedicine perspective such as biocompatibility, biodegradability and stimuli-responsive properties to (patho)physiological conditions. Conventionally, self-assembled polypeptide nanostructures are prepared by first synthesizing their constituent amphiphilic polypeptides followed by post-polymerization self-assembly. Herein, we describe the one-pot synthesis of oxidation-sensitive supramolecular micelles and vesicles. This was achieved by polymerization-induced self-assembly (PISA) of the N-carboxyanhydride (NCA) precursor of methionine using polyethylene oxide as stabilizing and hydrophilic block in dimethyl sulfoxide (DMSO). By adjusting the hydrophobic block length and concentration we obtained a range of morphologies from spherical to worm-like micelles, to vesicles. Remarkably, the secondary structure of polypeptides greatly influenced the final morphology of the assemblies. Surprisingly, worm-like micellar morphologies were obtained for a wide range of methionine block lengths and solid contents, with spherical micelles restricted to very short hydrophobic lengths. Worm-like micelles further assembled into oxidation-sensitive, self-standing gels in the reaction pot. Both vesicles and worm-like micelles obtained using this method demonstrated to degrade under controlled oxidant conditions which would expand their biomedical applications such as in sustained drug release or as cellular scaffolds in tissue engineering.

Synthesis and Characterization of pH and Temperature-Sensitive Semi-IPN Hydrogels

2014 ◽  
Vol 1053 ◽  
pp. 224-230
Author(s):  
Shan Jiang ◽  
Xia Qian Li ◽  
Qiang Yu
Keyword(s):  
Temperature Sensitive ◽  
Stimuli Responsive ◽  
Swelling Properties ◽  
Dimethyl Ammonium ◽  
Swelling Rate ◽  
Ph And Temperature Sensitivity ◽  
Responsive Behavior ◽  
Radical Solution ◽  
Diallyl Dimethyl Ammonium Chloride

A series of novel cross-linked poly N-isopropylacrylamide (PNIPAM)/poly diallyl dimethyl ammonium chloride (PDMDAAC) semi-IPN hydrogels were synthesized through free radical solution polymerization in water at 30°C. FTIR was used to characterize the structure of resultant hydrogels. The pH and temperature sensitivity of hydrogels were systematicly studied, and the swelling properties of hydrogels were also explored. The results show that the semi-IPN hydrogels have both temperature and pH sensitivities. The hydrogels exhibit fast swelling rate and excellent stimuli-responsive behavior.

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