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Poly ethylene glycol methyl ether methacrylate pegma

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Poly(ethylene glycol)methyl ether methacrylate (PEGMA) is a water-soluble, biocompatible polymer used in various laboratory applications. It serves as a versatile building block for the synthesis of polymeric materials. PEGMA exhibits physical and chemical properties that make it suitable for use in a range of research and development activities.

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Lab products found in correlation

Methacrylic acid, by Thermo Fisher Scientific (1 mentions) N n methylenebisacrylamide, by Thermo Fisher Scientific (1 mentions) 2 2 azo bis isobutyronitrile, by Thermo Fisher Scientific (1 mentions) Acetonitrile, by Merck Group (1 mentions) Neodymium 3 oxide, by Merck Group (1 mentions) Methacrylic acid, by Merck Group (1 mentions) Ethylene glycol dimethacrylate, by Merck Group (1 mentions) 2 hydroxyethyl methacrylate, by Merck Group (1 mentions) Phosphate buffered saline solution pbs, by Merck Group (1 mentions) 4 4 azobis 4 cyanovaleric acid acva, by Merck Group (1 mentions) 4 cyano 4 phenylcarbonothioylthio pentanoic acid cpa, by Merck Group (1 mentions) Diethyl ether dee, by Merck Group (1 mentions) Tetrahydrofuran thf, by Merck Group (1 mentions) Deuterated chloroform cdcl3, by Merck Group (1 mentions) Tween 80, by Merck Group (1 mentions) ε caprolactone, by Merck Group (1 mentions) Fetal bovine serum (fbs), by Lonza (1 mentions) 2 2 azodiisobutyramidinedihydrochloride aiba, by Merck Group (1 mentions) Qpcr reagents, by Thermo Fisher Scientific (1 mentions) 2 vinylpyridine, by Merck Group (1 mentions)

Close spelling variants of this product

Poly(ethylene glycol) methyl ether methacrylate Poly (ethylene glycol) methacrylate (PEGMA, Poly(ethylene glycol) methyl ether Poly(ethylene glycol) methacrylate Methyl ether methacrylate Ethylene glycol Methyl methacrylate PEGMA

5 protocols using poly ethylene glycol methyl ether methacrylate pegma

1

Synthesis and Characterization of Polymers

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Water (18.2 MΩ·cm) was deionized with Merck Millipore (Darmstadt, Germany) purification system. 2-(1-Isobutyl)sulfanylthiocarbonylsulfanyl-2-methyl propionic acid was prepared as reported previously34 (link). 2,2′-Azobis[2-(2-imidazolin-2-yl) propane] (VA-061) was purchased from Wako Pure Chemical Industries (Tokyo, Japan). The inhibitors, poly(ethylene glycol)methyl ether methacrylate (PEGMA, Mn = 500 and 2,000 g/mol), and all other reagents were purchased from Sigma-Aldrich (St. Louis, MO) and used without further purification.
Morimoto N., Takei R., Wakamura M., Oishi Y., Nakayama M., Suzuki M., Yamamoto M, & Winnik F.M. (2018). Fast and effective mitochondrial delivery of ω-Rhodamine-B-polysulfobetaine-PEG copolymers. Scientific Reports, 8, 1128.
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2

Synthesis of Stimuli-Responsive Polymeric Nanocarriers

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Methacrylic acid (MAA, 99%), 2,2′-Azobisisobutyronitrile (AIBN, 98%) and N,N′-methylenebisacrylamide (MBA, 96%) were purchased from Acros. N,N-dimetilaminoethylethacrylate (DMAEMA), Poly(ethyleneglycol)methylethermethacrylate (PEGMA; Mn = 475) and acetonitrile (ACN) were obtained from Sigma-Aldrich., N′-bis(acryloyl)cystamine (BAC, 98%) was purchased from Alfa Aesar. Daunorubicin HCl (DNR) was provided by Pharmacia & Upjohn.
Toniolo G., Efthimiadou E.K., Kordas G, & Chatgilialoglu C. (2018). Development of multi-layered and multi-sensitive polymeric nanocontainers for cancer therapy: in vitro evaluation. Scientific Reports, 8, 14704.
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3

Synthesis of Methacrylate-based Nanocomposites

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For the reagents used in this study, including 2-hydroxyethyl methacrylate (HEMA) and azobisisobutyronitrile (AIBN), the products of Junsei were used, and methacrylic acid (MA), ethylene glycol dimethacrylate (EGDMA), Poly (ethylene glycol) methyl ether methacrylate (PEGMA), and Neodymium (III) oxide nanoparticles were purchased from Sigma-Aldrich (Saint Louis, MO, USA) and used without purification.
Lee M.J., Park S.Y, & Sung A.Y. (2021). Characterization of Biocompatible Hydrogel Lenses Using Methacrylic Acid with Neodymium Oxide Nanoparticles. Polymers, 13(10), 1575.
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4

Biodegradable Polymer Synthesis and Characterization

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ε-Caprolactone (CL, Acros, 99% purity), 2-ethylhexanoic acid tin(II) salt (Sn(Oct)2; Sigma-Aldrich, St. Louis, MO, USA, purity ≥95%), 4,4′-Azobis(4-cyanovaleric acid) (ACVA; Sigma-Aldrich, purity ≥ 98%), 4-Cyano-4-(phenylcarbonothioylthio)pentanoic acid (CPA; Sigma-Aldrich, purity ≥ 97%), poly(ethylene glycol) methyl ether methacrylate (PEGMA; Sigma-Aldrich, Mn 950 Da), Tween80 (Sigma-Aldrich), Diethyl ether (DEE, Sigma-Aldrich, ≥99%), Deuterated chloroform (CDCl3, Sigma-Aldrich, 99.8%), Ethanol (EtOH, Sigma-Aldrich, 99.8%), acetonitrile (ACN, Sigma-Aldrich, 99.9%), 6-hydroxycaproic acid (HCA, ABCR, Karlsruhe, Germany, 95%) were used as received without further treatments. The cell medium is composed by high glucose DMEM/F12 (Biowest, Nuaillé, France) supplemented with 10% fetal bovine serum (Lonza, Basel, Switzerland). Phosphate-buffered saline solution (PBS) was purchased from Sigma-Aldrich. For gel permeation chromatography (SEC) analysis Tetrahydrofuran (THF, Sigma-Aldrich, purity ≥ 99.7%) was used as eluent.
Gatti S., Agostini A., Ferrari R, & Moscatelli D. (2017). Synthesis and Nanoprecipitation of HEMA-CLn Based Polymers for the Production of Biodegradable Nanoparticles. Polymers, 9(9), 389.
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5

Synthesis of Functionalized Polymers

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2-Vinylpyridine (97%,
2VP; Sigma-Aldrich,
U.K.) and divinylbenzene (80 mol % 1,4-divinyl content, DVB; Sigma-Aldrich,
U.K.) were passed through a column of activated basic alumina to remove
inhibitors and impurities before use. 2,2′-Azodiisobutyramidine
dihydrochloride (AIBA; 97%) was purchased from Sigma-Aldrich (U.K.)
and used as received. Aliquat 336 surfactant (Thermo Fisher, U.K.)
was used as received. Poly(ethylene glycol) methyl ether methacrylate
(PEGMA, average Mn 2000 g mol–1, Sigma-Aldrich, U.K.) was supplied as a 50 wt % solution in H2O. PCR reagents were used as received. DNA extraction and
purification kits (Qiagen, U.K.) were used as per manufacturer’s
instructions. qPCR reagents (Thermo Fisher, U.K.) and viral extraction
reagents (Invitrogen, U.K.) were used as received.
Trinh E., Batt L.J., Yue Q., Du R., Jones S.T, & Fielding L.A. (2024). Bridging Flocculation of a Sterically Stabilized Cationic Latex as a Biosensor for the Detection of Microbial DNA after Amplification via PCR. Biomacromolecules, 25(3), 1629-1636.
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