Molecular captain: A light-sensitive linker molecule in poly(ethylene glycol)-poly(L-alanine)-poly(ethylene glycol) triblock copolymer directs molecular nano-assembly, conformation, and sol-gel transition

2012 ◽  
Vol 50 (15) ◽  
pp. 3184-3191 ◽  
Author(s):  
So Young Jeong ◽  
Hyo Jung Moon ◽  
Min Hee Park ◽  
Min Kyung Joo ◽  
Byeongmoon Jeong
Keyword(s):  
Ethylene Glycol ◽  
Triblock Copolymer ◽  
Sol Gel ◽  
Poly Ethylene Glycol ◽  
Sol Gel Transition ◽  
Poly Ethylene ◽  
Gel Transition

Controlled Hierarchical Pore Structures in Ethylene-Bridged Polysilsesquioxane Gels

2003 ◽  
Vol 788 ◽  
Author(s):  
Yuki Kobayashi ◽  
Kazuki Nakanishi ◽  
Kazuyuki Hirao
Keyword(s):  
Phase Separation ◽  
Ethylene Glycol ◽  
Triblock Copolymers ◽  
Sol Gel ◽  
Poly Ethylene Glycol ◽  
Bridged Polysilsesquioxane ◽  
Sol Gel Transition ◽  
Poly Ethylene ◽  
Hierarchical Pore ◽  
Gel Transition

ABSTRACTFormation of hierarchical macropores and mesopores in ethylene-bridged polysilsesquioxane sol-gel systems via concurrent sol-gel transition and phase separation induced by the incorporation of supramolecular templats has been investigated. A series of poly(ethylene-glycol)-poly(propyleneglycol)- poly(ethyleneglycol) triblock copolymers, EOPOEOs, have been employed as supramolecular templates, while 1,2-bis(trimethoxysilyl)ethane was used as a polysilsesquioxane source. Successful combination of templated mesopores and well-defined macropores due to phase-separation has been found in the system with EOPOEOs having 70 PO units and respective 20 EO units. Although similar macroporous morphology has been obtained for all the EOPOEOs with EO chain longer or shorter than 20 units, the optimum composition for the co-continuous macropores and that for templated mesopores deviated from each other, resulting in the failure of producing hierarchical macropores and mesopores.

Biomolecularly stimuli-responsive tetra-poly(ethylene glycol) that undergoes sol–gel transition in response to a target biomolecule

2017 ◽  
Vol 8 (41) ◽  
pp. 6378-6385 ◽  
Author(s):  
Chisa Norioka ◽  
Kazuma Okita ◽  
Miho Mukada ◽  
Akifumi Kawamura ◽  
Takashi Miyata
Keyword(s):  
Phase Transition ◽  
Ethylene Glycol ◽  
Sol Gel ◽  
Stimuli Responsive ◽  
Poly Ethylene Glycol ◽  
Stimuli Responsive Polymers ◽  
Responsive Polymers ◽  
Sol Gel Transition ◽  
Poly Ethylene ◽  
Gel Transition

We designed biotin-conjugated four-armed poly(ethylene glycol) (biotinylated Tetra-PEG) as biomolecularly stimuli-responsive polymers that underwent the phase transition from a sol to a gel state in response to avidin as a target biomolecule.

scholarly journals ‘Reverse’ Hofmeister effects on the sol–gel transition rates for an α-helical peptide–PEG bioconjugate

2018 ◽  
Vol 20 (30) ◽  
pp. 20287-20295 ◽  
Author(s):  
Sean C. O’Neill ◽  
Ankit D. Kanthe ◽  
Jacob A. Weber ◽  
Raymond S. Tu
Keyword(s):  
Ethylene Glycol ◽  
Sol Gel ◽  
Transition Rates ◽  
Poly Ethylene Glycol ◽  
Helical Peptide ◽  
Aqueous Environments ◽  
Sol Gel Transition ◽  
Poly Ethylene ◽  
Gel Transition

We examine the dynamics of the sol–gel transition for end-functionalized linear- and 4-arm-peptides bioconjugated to poly-ethylene glycol (PEG) in aqueous environments with increasingly chaotropic (Cl− < Br− < I−) anions.

scholarly journals Application of Thermosensitive Peptide Copolymer Gels to Removal of Endocrine Disruptor

2009 ◽  
Vol 2009 ◽  
pp. 1-4 ◽  
Author(s):  
Satoshi Tanimoto ◽  
Naoto Yagi ◽  
Hitoshi Yamaoka
Keyword(s):  
Bisphenol A ◽  
Ring Opening ◽  
Endocrine Disruptor ◽  
Sol Gel ◽  
Chloroform Solution ◽  
Poly Ethylene Glycol ◽  
Sol Gel Transition ◽  
Poly Ethylene ◽  
Peptide Segments ◽  
Gel Transition

Poly(L-leucine)-block-poly(ethylene glycol)-block-poly(L-leucine) triblock copolymers were synthesized by a ring-opening polymerization ofα-amino acid N-carboxyanhydride with amino-terminated PEG as an initiator. The chloroform solution of these peptide copolymers showed a thermo-sensitive sol-gel transition. The transition temperature varied as a function of the length of peptide segments. Additionally, we used these peptide copolymers to remove an endocrine disruptor such as bisphenol A from its aqueous solution. As a result, it became clear that the peptide copolymer gel used in this study could capture bisphenol A efficiently.

Thermal Gelation and Stability of Pectin Grafted with PEPE

2012 ◽  
Vol 1403 ◽  
Author(s):  
Harshal D. Santan ◽  
Axel T. Neffe ◽  
Stefan Kamlage ◽  
Andreas Lendlein
Keyword(s):  
Transition Temperature ◽  
Ethylene Glycol ◽  
Uv Spectroscopy ◽  
Sol Gel ◽  
Thermal Gelation ◽  
Mechanistic Investigation ◽  
Sol Gel Transition ◽  
Poly Ethylene ◽  
Stimuli Sensitive ◽  
Gel Transition

ABSTRACTStimuli-sensitive materials can change properties upon exposure to an external stimulus. Thermoreversible gelation upon heating is one example for such a stimuli sensitivity. Here, it is of significance to tailor the transition temperature and to achieve large changes of G’ and the viscosity. Grafting of the thermosensitive poly(ethylene glycol-b-propylene glycol-b-ethylene glycol)s (PEPEs) to pectin was performed in order to investigate if tailoring of the sol-gel-transition temperature can be achieved by adjusting the grafting ratio. PEPEs were aminated and grafted to the polysaccharide via EDC coupling as shown by FTIR. The sol-gel transition of the pectin, PEPE, and the grafted system (PGP) was investigated by rheology. The gelation temperature (Tgel) of the system could be adjusted by varying the grafting density of PEPE onto pectin as well as by the concentration of the thermosensitive polymer in aqueous solution. A concentration of 15 – 20 wt% of the grafted system in water led to gelation temperatures in the range of 25 – 33 °C and the critical micelle concentration (CMC) and critical micelle temperature (CMT) of the grafted systems were determined by UV spectroscopy. The viscosity and the G’ increased by four orders of magnitudes at Tgel, which is comparable to PEPEs alone, but could be reached at lower PEPE concentrations. In the future, a thorough mechanistic investigation of the gelation process would be of interest.

Reversibly cross-linked poly(ethylene glycol)–poly(amino acid)s copolymer micelles: a promising approach to overcome the extracellular stability versus intracellular drug release challenge

RSC Advances ◽  
2015 ◽  
Vol 5 (26) ◽  
pp. 20025-20034 ◽  
Author(s):  
Yuling Li ◽  
Sai Wang ◽  
Dandan Zhu ◽  
Yuling Shen ◽  
Baixiang Du ◽  
...  
Keyword(s):  
Amino Acid ◽  
Drug Release ◽  
Ethylene Glycol ◽  
Lipoic Acid ◽  
Triblock Copolymer ◽  
Intracellular Delivery ◽  
Poly Ethylene Glycol ◽  
Copolymer Micelles ◽  
Poly Ethylene ◽  
Copolymer Poly

Reversibly shell cross-linked micelles based on a lipoic acid (LA) decorated triblock copolymer poly(ethylene glycol)-b-poly(γ-benzyl-l-glutamate)-b-poly(l-phenylalanine) have been developed for efficient intracellular delivery of DOX.

Preparation of thermo-responsive drug carrier consisting of biocompatible triblock copolymer and fullerene

2021 ◽  
Author(s):  
Kohei Kitano ◽  
Kazuhiko Ishihara ◽  
Shinichi Yusa
Keyword(s):  
Ethylene Glycol ◽  
Radical Polymerization ◽  
Triblock Copolymer ◽  
Drug Carrier ◽  
Controlled Radical Polymerization ◽  
Poly Ethylene Glycol ◽  
Poly Ethylene

A triblock copolymer (PEG-b-PUEM-b-PMPC; EUM) comprising poly(ethylene glycol) (PEG), thermo-responsive poly(2-ureidoethyl methacrylate) (PUEM), and poly(2-(methacryloyloxy)ethyl phosphorylcholine) (PMPC) blocks was synthesized via controlled radical polymerization. PEG and PMPC blocks exhibit hydrophilicity...

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