930741
Poly(oligoethylene glycol methacrylate)
Sinonimo/i:
POEGMA, Poly(oligo(ethylene glycol)methacrylate)
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About This Item
Formula condensata:
C6H8NO2[C4H5O2(C2H4O)x]nOH
Codice UNSPSC:
12352104
NACRES:
NA.21
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Descrizione generale
Poly(oligo(ethylene glycol) methacrylate) (POEGMA) is a family of polymers consisting of a hydrophobic methacrylate backbone and hydrophilic ethylene oxide (EO) side groups with highly branched architecture. The highly branched architecture with a high density of oligo EO moities enhances the solubility of the polymer in water.
Applicazioni
- Drug delivery- enhances the stability and delivery of siRNA and eliminates PEG antigenicity
- Biosensor coatings- provides an anti-fouling surface
- Stimuli-responsive hydrogels for tissue engineering, drug delivery, and other biomedical applications
Poly(oligo(ethylene glycol) methyl ether methacrylate) (POEGMA) is a family of polymers consisting of a hydrophobic methacrylate backbone and hydrophilic ethylene oxide (EO) side groups with highly branched architecture[1] . The side chain EO segments enhance the solubility of the polymer in water [2], exhibiting many interesting properties such as non-fouling [3], stealth, anti-PEG antibodies [4] & thermo-responsive [5] behaviors.
Caratteristiche e vantaggi
- Highly branched architecture and high density of oligo ethylene oxide moieties
- Water soluble
- Nonfouling and thermo-responsive behaviors
- Viable alternative to PEG in biological and biomaterial applications
Codice della classe di stoccaggio
10 - Combustible liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
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I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
Rafael Pires-Oliveira et al.
Langmuir : the ACS journal of surfaces and colloids, 36(49), 15018-15029 (2020-12-05)
Understanding of the temperature-induced phase transition of poly(oligo(ethylene glycol) methyl ether methacrylate) (POEGMA) random copolymers with varied composition remains largely incomplete. Upon heating they can form either macroscopically phase-separated aggregates or micelles. We examined the effect of polymer architecture by
Yizhi Qi et al.
Nature biomedical engineering, 1 (2016-01-01)
The delivery of therapeutic peptides and proteins is often challenged by a short half-life, and thus the need for frequent injections that limit efficacy, reduce patient compliance and increase treatment cost. Here, we demonstrate that a single subcutaneous injection of
In Pursuit of Zero 2.0: Recent Developments in Nonfouling Polymer Brushes for Immunoassays
Heggestad J., et al.
Advanced Materials, 32 (2020)
(Co)polymers of oligo(ethylene glycol) methacrylates?temperature-induced aggregation in aqueous solution.
Trzebicka B, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 51, 614?623-614?623 (2013)
Fei Xu et al.
ACS biomaterials science & engineering, 7(9), 4258-4268 (2021-02-12)
Reactive electrospinning is demonstrated as a viable method to create fast-responsive and degradable macroporous thermoresponsive hydrogels based on poly(oligoethylene glycol methacrylate) (POEGMA). Hydrazide- and aldehyde-functionalized POEGMA precursor polymers were coelectrospun to create hydrazone cross-linked nanostructured hydrogels in a single processing
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