[go: up one dir, main page]
Wikipedia

Polyethylene glycol

(Redirected from Carbowax)
Not to be confused with Ethylene glycol or Diethylene glycol or Polypropylene glycol or Propylene glycol.
For medical uses of polyethylene glycol, see Macrogol.

Polyethylene glycol (PEG; /ˌpɒliˈɛθəlˌiːn ˈɡlaɪˌkɒl, -ˈɛθɪl-, -ˌkɔːl/) is a polyether compound derived from petroleum with many applications, from industrial manufacturing to medicine. PEG is also known as polyethylene oxide (PEO) or polyoxyethylene (POE), depending on its molecular weight. The structure of PEG is commonly expressed as H−(O−CH2−CH2)n−OH.[3]

Polyethylene glycol
Polyethylene glycol 400
Names
IUPAC names
poly(oxyethylene) {structure-based},
poly(ethylene oxide) {source-based}[1]
Other names
Kollisolv, Carbowax, GoLYTELY, GlycoLax, Fortrans, TriLyte, Colyte, Halflytely, macrogol, MiraLAX, MoviPrep
Identifiers
Abbreviations PEG
ChEMBL
ChemSpider
  • none
ECHA InfoCard 100.105.546 Edit this at Wikidata
E number E1521 (additional chemicals)
UNII
Properties
C2nH4n+2On+1
Molar mass 44.05n + 18.02 g/mol
Density 1.125[2]
Pharmacology
A06AD15 (WHO)
Hazards
Flash point 182–287 °C; 360–549 °F; 455–560 K
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Uses

edit

Medical uses

edit
Main articles: Macrogol and PEGylation
  • Pharmaceutical-grade PEG is used as an excipient in many pharmaceutical products, in oral, topical, and parenteral dosage forms.[4]
  • PEG is the basis of a number of laxatives (as MiraLax, RestoraLAX, MoviPrep, etc.).[5] Whole bowel irrigation with polyethylene glycol and added electrolytes is used for bowel preparation before surgery or colonoscopy or for children with constipation.[6] Macrogol (with brand names such as Laxido, Movicol and Miralax) is the generic name for polyethylene glycol used as a laxative. The name may be followed by a number that represents the average molecular weight (e.g. macrogol 3350, macrogol 4000, or macrogol 6000).
  • The possibility that PEG could be used to fuse axons is being explored by researchers studying peripheral nerve and spinal cord injury.[5]
  • An example of PEG hydrogels (see Biological uses section) in a therapeutic has been theorized by Ma et al. They propose using the hydrogel to address periodontitis (gum disease) by encapsulating stem cells in the gel that promote healing in the gums.[7] The gel with encapsulated stem cells was to be injected into the site of disease and crosslinked to create the microenvironment required for the stem cells to function.
  • PEGylation of adenoviruses for gene therapy can help prevent adverse reactions due to pre-existing adenovirus immunity.[8]
  • A PEGylated lipid is used as an excipient in both the Moderna and Pfizer–BioNTech vaccines for SARS-CoV-2. Both RNA vaccines consist of messenger RNA, or mRNA, encased in a bubble of oily molecules called lipids. Proprietary lipid technology is used for each. In both vaccines, the bubbles are coated with a stabilizing molecule of polyethylene glycol.[9] PEG could trigger allergic reaction,[10] and allergic reactions are the driver for both the United Kingdom and Canadian regulators to issue an advisory, noting that: two "individuals in the U.K. ... were treated and have recovered" from anaphylactic shock.[11][12] The US CDC stated that in their jurisdiction six cases of "severe allergic reaction" had been recorded from more than 250,000 vaccinations, and of those six only one person had a "history of vaccination reactions".[13]

Chemical uses

edit
 
The remains of the 16th century carrack Mary Rose undergoing conservation treatment with PEG in the 1980s
 
Terra cotta warrior, showing traces of original color
  • Polyethylene glycol is also commonly used as a polar stationary phase for gas chromatography, as well as a heat transfer fluid in electronic testers.
  • PEG is frequently used to preserve waterlogged wood and other organic artifacts that have been salvaged from underwater archaeological contexts, as was the case with the warship Vasa in Stockholm,[14] and similar cases. It replaces water in wooden objects, making the wood dimensionally stable and preventing the warping or shrinking of the wood when it dries.[5] In addition, PEG is used when working with green wood as a stabilizer, and to prevent shrinkage.[15]
  • PEG has been used to preserve the painted colors on Terracotta Warriors unearthed at a UNESCO World Heritage site in China.[16] These painted artifacts were created during the Qin Shi Huang (first emperor of China) era. Within 15 seconds of the terra-cotta pieces being unearthed during excavations, the lacquer beneath the paint begins to curl after being exposed to the dry Xi'an air. The paint would subsequently flake off in about four minutes. The German Bavarian State Conservation Office developed a PEG preservative that when immediately applied to unearthed artifacts has aided in preserving the colors painted on the pieces of clay soldiers.[17]
  • PEG is often used (as an internal calibration compound) in mass spectrometry experiments, with its characteristic fragmentation pattern allowing accurate and reproducible tuning.
  • PEG derivatives, such as narrow range ethoxylates, are used as surfactants.
  • PEG has been used as the hydrophilic block of amphiphilic block copolymers used to create some polymersomes.[18]
  • PEG is a component of the propellent used in UGM-133M Trident II Missiles, in service with the United States Navy.[19]
  • PEG has been used as a solvent for aryl thioether synthesis.[20]

Biological uses

edit
  • An example study was done using PEG-diacrylate hydrogels to recreate vascular environments with the encapsulation of endothelial cells and macrophages. This model furthered vascular disease modeling and isolated macrophage phenotype's effect on blood vessels.[21]
  • PEG is commonly used as a crowding agent in in vitro assays to mimic highly crowded cellular conditions.[22] Although polyethylene glycol is considered biologically inert, it can form non-covalent complexes with monovalent cations such as Na+, K+, Rb+, and Cs+, affecting equilibrium constants of biochemical reactions.[23][24]
  • PEG is commonly used as a precipitant for plasmid DNA isolation and protein crystallization. X-ray diffraction of protein crystals can reveal the atomic structure of the proteins.
  • PEG is used to fuse two different types of cells, most often B-cells and myelomas to create hybridomas. César Milstein and Georges J. F. Köhler originated this technique, which they used for antibody production, winning a Nobel Prize in Physiology or Medicine in 1984.[5]
  • In microbiology, PEG precipitation is used to concentrate viruses. PEG is also used to induce complete fusion (mixing of both inner and outer leaflets) in liposomes reconstituted in vitro.
  • Gene therapy vectors (such as viruses) can be PEG-coated to shield them from inactivation by the immune system and to de-target them from organs where they may build up and have a toxic effect.[25] The size of the PEG polymer is important, with larger polymers achieving the best immune protection.
  • PEG is a component of stable nucleic acid lipid particles (SNALPs) used to package siRNA for use in vivo.[26][27]
  • In blood banking, PEG is used as a potentiator to enhance detection of antigens and antibodies.[5][28]
  • When working with phenol in a laboratory situation, PEG 300 can be used on phenol skin burns to deactivate any residual phenol.[29]
  • In biophysics, polyethylene glycols are the molecules of choice for the functioning ion channel diameter studies, because in aqueous solutions they have a spherical shape and can block ion channel conductance.[30][31]

Commercial uses

edit

Industrial uses

edit
  • A nitrate ester-plasticized polyethylene glycol (NEPE-75) is used in Trident II submarine-launched ballistic missile solid rocket fuel.[36]
  • Dimethyl ethers of PEG are the key ingredient of Selexol, a solvent used by coal-burning, integrated gasification combined cycle (IGCC) power plants to remove carbon dioxide and hydrogen sulfide from the syngas stream.
  • PEG has been used as the gate insulator in an electric double-layer transistor to induce superconductivity in an insulator.[37]
  • PEG is used as a polymer host for solid polymer electrolytes. Although not yet in commercial production, many groups around the globe are engaged in research on solid polymer electrolytes involving PEG, to improve their properties, and in permitting their use in batteries, electro-chromic display systems, and other products in the future.
  • PEG is injected into industrial processes to reduce foaming in separation equipment.
  • PEG is used as a binder in the preparation of technical ceramics.[38]
  • PEG was used as an additive to silver halide photographic emulsions.

Entertainment uses

edit

Human health effects

edit

PEO's[clarification needed] have "very low single dose oral toxicity", on the order of tens of grams per kilogram of human body weight when ingested by mouth.[3] Because of its low toxicity, PEO is used in a variety of edible products.[39] It is also used as a lubricating coating for various surfaces in aqueous and non-aqueous applications.[40]

The precursor to PEGs is ethylene oxide, which is hazardous.[41] Ethylene glycol and its ethers are nephrotoxic (poisonous to the kidneys) if applied to damaged skin.[42]

The United States Food and Drug Administration (FDA or US FDA) regards PEG as biologically inert and safe.[citation needed]

A 2015 study appears to challenge the FDA's conclusion. In the study, a high-sensitivity ELISA assay detected anti-PEG antibodies in 72% of random blood plasma samples collected from 1990 to 1999. According to the study's authors, this result suggests that anti-PEG antibodies may be present, typically at low levels, in people who were never treated with PEGylated drugs.[43][44] Due to its ubiquity in many products and the large percentage of the population with antibodies to PEG, which indicates an allergic reaction, hypersensitive reactions to PEG are an increasing health concern.[45][46] Allergy to PEG is usually discovered after a person has been diagnosed with an allergy to several seemingly unrelated products—including processed foods, cosmetics, drugs, and other substances—that contain or were manufactured with PEG.[45]

Available forms and nomenclature

edit

PEG, PEO, and POE refer to an oligomer or polymer of ethylene oxide. The three names are chemically synonymous, but historically PEG is preferred in the biomedical field, whereas PEO is more prevalent in the field of polymer chemistry. Because different applications require different polymer chain lengths, PEG has tended to refer to oligomers and polymers with a molecular mass below 20,000 g/mol, PEO to polymers with a molecular mass above 20,000 g/mol, and POE to a polymer of any molecular mass.[47] PEGs are prepared by polymerization of ethylene oxide and are commercially available over a wide range of molecular weights from 300 g/mol to 10,000,000 g/mol.[48]

PEG and PEO are liquids or low-melting solids, depending on their molecular weights. While PEG and PEO with different molecular weights find use in different applications and have different physical properties (e.g. viscosity) due to chain length effects, their chemical properties are nearly identical. Different forms of PEG are also available, depending on the initiator used for the polymerization process – the most common initiator is a monofunctional methyl ether PEG, or methoxypoly(ethylene glycol), abbreviated mPEG. Lower-molecular-weight PEGs are also available as purer oligomers, referred to as monodisperse, uniform, or discrete. Very high-purity PEG has recently been shown to be crystalline, allowing the determination of a crystal structure by x-ray crystallography.[48] Since purification and separation of pure oligomers is difficult, the price for this type of quality is often 10–1000 fold that of polydisperse PEG.

PEGs are also available with different geometries.

  • Branched PEGs have three to ten PEG chains emanating from a central core group.
  • Star PEGs have 10 to 100 PEG chains emanating from a central core group.
  • Comb PEGs have multiple PEG chains normally grafted onto a polymer backbone.

The numbers that are often included in the names of PEGs indicate their average molecular weights (e.g. a PEG with n = 9 would have an average molecular weight of approximately 400 daltons, and would be labeled PEG 400). Most PEGs include molecules with a distribution of molecular weights (i.e. they are polydisperse). The size distribution can be characterized statistically by its weight average molecular weight (Mw) and its number average molecular weight (Mn), the ratio of which is called the polydispersity index (ĐM). Mw and Mn can be measured by mass spectrometry.

PEGylation is the act of covalently coupling a PEG structure to another larger molecule, for example, a therapeutic protein, which is then referred to as a PEGylated protein. PEGylated interferon alfa-2a or alfa-2b are commonly used injectable treatments for hepatitis C infection.

PEG is soluble in water, methanol, ethanol, acetonitrile, benzene, and dichloromethane, and is insoluble in diethyl ether and hexane. It is coupled to hydrophobic molecules to produce non-ionic surfactants.[49]

 
Polyethylene oxide (PEO, Mw 4 kDa) nanometric crystallites (4 nm)

PEG and related polymers (PEG phospholipid constructs) are often sonicated when used in biomedical applications. However, as reported by Murali et al., PEG is very sensitive to sonolytic degradation and PEG degradation products can be toxic to mammalian cells. It is, thus, imperative to assess potential PEG degradation to ensure that the final material does not contain undocumented contaminants that can introduce artifacts into experimental results.[50]

PEGs and methoxypolyethylene glycols are manufactured by Dow Chemical under the trade name Carbowax for industrial use, and Carbowax Sentry for food and pharmaceutical use. They vary in consistency from liquid to solid, depending on the molecular weight, as indicated by a number following the name. They are used commercially in numerous applications, including foods, cosmetics, pharmaceutics, biomedicine, dispersing agents, solvents, ointments, suppository bases, as tablet excipients, and as laxatives. Some specific groups are lauromacrogols, nonoxynols, octoxynols, and poloxamers.

Production

edit
 
Polyethylene glycol 400, pharmaceutical quality
 
Polyethylene glycol 4000, pharmaceutical quality

The production of polyethylene glycol was first reported in 1859. Both A. V. Lourenço and Charles Adolphe Wurtz independently isolated products that were polyethylene glycols.[51] Polyethylene glycol is produced by the interaction of ethylene oxide with water, ethylene glycol, or ethylene glycol oligomers.[52] The reaction is catalyzed by acidic or basic catalysts. Ethylene glycol and its oligomers are preferable as a starting material instead of water because they allow the creation of polymers with a low polydispersity (narrow molecular weight distribution). Polymer chain length depends on the ratio of reactants.

HOCH2CH2OH + n(CH2CH2O) → HO(CH2CH2O)n+1H

Depending on the catalyst type, the mechanism of polymerization can be cationic or anionic. The anionic mechanism is preferable because it allows one to obtain PEG with a low polydispersity. Polymerization of ethylene oxide is an exothermic process. Overheating or contaminating ethylene oxide with catalysts such as alkalis or metal oxides can lead to runaway polymerization, which can end in an explosion after a few hours.

Polyethylene oxide, or high-molecular-weight polyethylene glycol, is synthesized by suspension polymerization. It is necessary to hold the growing polymer chain in solution in the course of the polycondensation process. The reaction is catalyzed by magnesium-, aluminium-, or calcium-organoelement compounds. To prevent coagulation of polymer chains from solution, chelating additives such as dimethylglyoxime are used.

Alkaline catalysts such as sodium hydroxide (NaOH), potassium hydroxide (KOH), or sodium carbonate (Na2CO3) are used to prepare low-molecular-weight polyethylene glycol.[53]

See also

edit

References

edit
  1. ^ Kahovec J, Fox RB, Hatada K (2002). "Nomenclature of regular single-strand organic polymers". Pure and Applied Chemistry. 74 (10): 1921–1956. doi:10.1351/pac200274101921.
  2. ^ "Poly(ethylene glycol)". ChemSrc. 7 January 2020.
  3. ^ a b "Polyoxyalkylenes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. 2000. doi:10.1002/14356007.a21_579. ISBN 978-3527306732.
  4. ^ "Polyethylene Glycol as Pharmaceutical Excipient". pharmaceutical.basf.com. Retrieved 27 April 2021.
  5. ^ a b c d e f Kean S (2017). "Chemical Hope". Distillations. 2 (4): 5. Retrieved 22 March 2018.
  6. ^ "Polyethyleneglycol (PEG 4000 ) | Laxolite | Medical Dialogues". Medical Dialogues. 19 January 2021. Retrieved 19 January 2021.
  7. ^ Ma Y, Ji Y, Zhong T, Wan W, Yang Q, Li A, et al. (December 2017). "Bioprinting-Based PDLSC-ECM Screening for in Vivo Repair of Alveolar Bone Defect Using Cell-Laden, Injectable and Photocrosslinkable Hydrogels". ACS Biomaterials Science & Engineering. 3 (12): 3534–3545. doi:10.1021/acsbiomaterials.7b00601. PMID 33445388.
  8. ^ Seregin SS, Amalfitano A (2009). "Overcoming pre-existing adenovirus immunity by genetic engineering of adenovirus-based vectors". Expert Opinion on Biological Therapy. 9 (12): 1521–1531. doi:10.1517/14712590903307388. PMID 19780714. S2CID 21927486.
  9. ^ "Moderna COVID-19 Vaccine Standing Orders for Administering Vaccine to Persons 18 Years of Age and Older" (PDF). Centers for Disease Control and Prevention (CDC). 11 July 2022. Archived from the original (PDF) on 14 August 2021. Retrieved 23 October 2024.
  10. ^ Cabanillas B, Akdis CA, Novak N (June 2021). "Allergic reactions to the first COVID-19 vaccine: A potential role of polyethylene glycol?". Allergy. 76 (6): 1617–1618. doi:10.1111/all.14711. PMID 33320974. S2CID 229284320.
  11. ^ Bostock N (9 December 2020). "MHRA warning after allergic reactions in NHS staff given COVID-19 vaccine". GP. Archived from the original on 9 December 2020. Retrieved 9 December 2020.
  12. ^ "Pfizer-BioNTech COVID-19 vaccine: Health Canada recommendations for people with serious allergies". Health Canada. 12 December 2020.
  13. ^ Furtula A, Jordans F (21 December 2020). "EU regulator gives conditional approval to Pfizer-BioNTech COVID-19 vaccine". The Globe and Mail Inc. Reuters.
  14. ^ Kvarning LÅ, Ohrelius B (1998). The Vasa – The Royal Ship. Atlantis. pp. 133–141. ISBN 91-7486-581-1.
  15. ^ "Anti-Freeze is Not a Green Wood Stabilizer – Buzz Saw". The Rockler Blog. 2 May 2006. Archived from the original on 17 January 2022. Retrieved 30 November 2012.
  16. ^ Reiffert S (18 March 2015). "Conservators preserve the paint layers of the Terracotta Army". tum.de. Technische Universität München. Archived from the original on 22 December 2015. Retrieved 19 December 2015.
  17. ^ Larmer B (June 2012). "Terra-Cotta Warriors in Color". National Geographic. 221 (6): 74–87.
  18. ^ Rameez S, Alosta H, Palmer AF (May 2008). "Biocompatible and biodegradable polymersome encapsulated hemoglobin: a potential oxygen carrier". Bioconjugate Chemistry. 19 (5): 1025–32. doi:10.1021/bc700465v. PMID 18442283.
  19. ^ "Facts: Polaris Poseidon Trident". Strategic Systems Programs. U.S. Navy.
  20. ^ Firouzabadi H, Iranpoor N, Gholinejad M (January 2010). "One-Pot Thioetherification of Aryl Halides Using Thiourea and Alkyl Bromides Catalyzed by Copper(I) Iodide Free from Foul-Smelling Thiols in Wet Polyethylene Glycol (PEG 200)". Advanced Synthesis & Catalysis. 352 (18): 119–24. doi:10.1002/adsc.200900671.
  21. ^ Moore EM, Ying G, West JL (March 2017). "Macrophages Influence Vessel Formation in 3D Bioactive Hydrogels". Advanced Biosystems. 1 (3): 1600021. doi:10.1002/adbi.201600021. S2CID 102369711.
  22. ^ Ganji M, Docter M, Le Grice SF, Abbondanzieri EA (September 2016). "DNA binding proteins explore multiple local configurations during docking via rapid rebinding". Nucleic Acids Research. 44 (17): 8376–8384. doi:10.1093/nar/gkw666. PMC 5041478. PMID 27471033.
  23. ^ Bielec K, Kowalski A, Bubak G, Witkowska Nery E, Hołyst R (January 2022). "Ion Complexation Explains Orders of Magnitude Changes in the Equilibrium Constant of Biochemical Reactions in Buffers Crowded by Nonionic Compounds". The Journal of Physical Chemistry Letters. 13 (1): 112–117. doi:10.1021/acs.jpclett.1c03596. PMC 8762655. PMID 34962392.
  24. ^ Breton MF, Discala F, Bacri L, Foster D, Pelta J, Oukhaled A (3 July 2013). "Exploration of Neutral Versus Polyelectrolyte Behavior of Poly(ethylene glycol)s in Alkali Ion Solutions using Single-Nanopore Recording". The Journal of Physical Chemistry Letters. 4 (13): 2202–2208. doi:10.1021/jz400938q. ISSN 1948-7185.
  25. ^ Kreppel F, Kochanek S (January 2008). "Modification of adenovirus gene transfer vectors with synthetic polymers: a scientific review and technical guide". Molecular Therapy. 16 (1): 16–29. doi:10.1038/sj.mt.6300321. PMID 17912234.
  26. ^ Rossi JJ (April 2006). "RNAi therapeutics: SNALPing siRNAs in vivo". Gene Therapy. 13 (7): 583–584. doi:10.1038/sj.gt.3302661. PMID 17526070. S2CID 7232293.
  27. ^ Geisbert TW, Lee AC, Robbins M, Geisbert JB, Honko AN, Sood V, et al. (May 2010). "Postexposure protection of non-human primates against a lethal Ebola virus challenge with RNA interference: a proof-of-concept study". Lancet. 375 (9729): 1896–1905. doi:10.1016/S0140-6736(10)60357-1. PMC 7138079. PMID 20511019. (free with registration)
  28. ^ Harmening DM (2005). Modern Blood Banking & Transfusion Practices. F. A. Davis Company. ISBN 978-0-8036-1248-8.
  29. ^ Monteiro-Riviere NA, Inman AO, Jackson H, Dunn B, Dimond S (May 2001). "Efficacy of topical phenol decontamination strategies on severity of acute phenol chemical burns and dermal absorption: in vitro and in vivo studies in pig skin". Toxicology and Industrial Health. 17 (4): 95–104. Bibcode:2001ToxIH..17...95M. doi:10.1191/0748233701th095oa. PMID 12479505. S2CID 46229131.
  30. ^ Krasilnikov OV, Sabirov RZ, Ternovsky VI, Merzliak PG, Muratkhodjaev JN (September 1992). "A simple method for the determination of the pore radius of ion channels in planar lipid bilayer membranes". FEMS Microbiology Immunology. 5 (1–3): 93–100. doi:10.1016/0378-1097(92)90079-4. PMID 1384601.
  31. ^ Bárcena-Uribarri I, Thein M, Maier E, Bonde M, Bergström S, Benz R (2013). "Use of nonelectrolytes reveals the channel size and oligomeric constitution of the Borrelia burgdorferi P66 porin". PLOS ONE. 8 (11): e78272. Bibcode:2013PLoSO...878272B. doi:10.1371/journal.pone.0078272. PMC 3819385. PMID 24223145.
  32. ^ "Tattoo to monitor diabetes". BBC News. 1 September 2002.
  33. ^ US Government – Food and Drug Agency "Food Additive Status List". Food and Drug Administration. Retrieved 2 May 2017.
  34. ^ "Codex Alimentarius". codexalimentarius.net. Archived from the original on 7 January 2012.{{cite web}}: CS1 maint: unfit URL (link)
  35. ^ "Current EU approved additives and their E Numbers". UK Government – Food Standards Agency. Retrieved 21 October 2010.
  36. ^ Spinardi G (1994). From Polaris to Trident: the development of US fleet ballistic missile technology. Cambridge: Cambridge Univ. Press. p. 159. ISBN 978-0-521-41357-2.
  37. ^ Ueno K, Nakamura S, Shimotani H, Ohtomo A, Kimura N, Nojima T, et al. (November 2008). "Electric-field-induced superconductivity in an insulator". Nature Materials. 7 (11): 855–8. Bibcode:2008NatMa...7..855U. doi:10.1038/nmat2298. PMID 18849974.
  38. ^ Schneider, Samuel J. (1991) Engineered Materials Handbook: Ceramics and Glasses, Vol. 4. ASM International. ISBN 0-87170-282-7. p. 49.
  39. ^ Sheftel VO (2000). Indirect Food Additives and Polymers: Migration and Toxicology. CRC. pp. 1114–1116. Archived from the original on 9 August 2007. Retrieved 22 August 2007.
  40. ^ Nalam PC, Clasohm JN, Mashaghi A, Spencer ND (2009). "Macrotribological Studies of Poly(L-lysine)-graft-Poly(ethylene glycol) in Aqueous Glycerol Mixtures" (PDF). Tribology Letters (Submitted manuscript). 37 (3): 541–552. doi:10.1007/s11249-009-9549-9. hdl:20.500.11850/17055. S2CID 109928127.
  41. ^ Center for Food Safety and Applied Nutrition. "Potential Contaminants - 1,4-Dioxane A Manufacturing Byproduct". fda.gov. Retrieved 26 May 2017.
  42. ^ Andersen FA (1999). "Special Report: Reproductive and Developmental Toxicity of Ethylene Glycol and Its Ethers". International Journal of Toxicology. 18 (3): 53–67. doi:10.1177/109158189901800208. S2CID 86231595.
  43. ^ Yang Q, Lai SK (2015). "Anti-PEG immunity: emergence, characteristics, and unaddressed questions". Wiley Interdisciplinary Reviews. Nanomedicine and Nanobiotechnology. 7 (5): 655–77. doi:10.1002/wnan.1339. PMC 4515207. PMID 25707913.
  44. ^ Yang, Qi; Jacobs, Timothy M.; McCallen, Justin D.; Moore, Dominic T.; Huckaby, Justin T.; Edelstein, Jasmine N.; Lai, Samuel K. (16 November 2016). "Analysis of Pre-existing IgG and IgM Antibodies against Polyethylene Glycol (PEG) in the General Population". Analytical Chemistry. 88 (23): 11804–11812. doi:10.1021/acs.analchem.6b03437. eISSN 1520-6882. ISSN 0003-2700. PMC 6512330. PMID 27804292.
  45. ^ a b Wenande E, Garvey LH (July 2016). "Immediate-type hypersensitivity to polyethylene glycols: a review". Clinical and Experimental Allergy. 46 (7): 907–22. doi:10.1111/cea.12760. PMID 27196817. S2CID 1247758.
  46. ^ Stone CA, Liu Y, Relling MV, Krantz MS, Pratt AL, Abreo A, et al. (May 2019). "Immediate Hypersensitivity to Polyethylene Glycols and Polysorbates: More Common Than We Have Recognized". The Journal of Allergy and Clinical Immunology. In Practice. 7 (5): 1533–1540.e8. doi:10.1016/j.jaip.2018.12.003. PMC 6706272. PMID 30557713.
  47. ^ For example, in the online catalog Archived 29 December 2006 at the Wayback Machine of Scientific Polymer Products, Inc., poly(ethylene glycol) molecular weights run up to about 20,000, while those of poly(ethylene oxide) have six or seven digits.
  48. ^ a b French AC, Thompson AL, Davis BG (2009). "High-purity discrete PEG-oligomer crystals allow structural insight" (PDF). Angewandte Chemie. 48 (7): 1248–52. doi:10.1002/anie.200804623. PMID 19142918.
  49. ^ Winger M, De Vries AH, Van Gunsteren WF (2009). "Force-field dependence of the conformational properties of α,ω-dimethoxypolyethylene glycol". Molecular Physics. 107 (13): 1313–1321. Bibcode:2009MolPh.107.1313W. doi:10.1080/00268970902794826. hdl:10072/37876. S2CID 97215923.
  50. ^ Murali VS, Wang R, Mikoryak CA, Pantano P, Draper R (September 2015). "Rapid detection of polyethylene glycol sonolysis upon functionalization of carbon nanomaterials". Experimental Biology and Medicine. 240 (9): 1147–51. doi:10.1177/1535370214567615. PMC 4527952. PMID 25662826.
  51. ^ Bailey FE, Koleske JV (1990). Alkylene oxides and their polymers. New York: Dekker. pp. 27–28. ISBN 9780824783846. Retrieved 17 July 2017.
  52. ^ Polyethylene glycol, Chemindustry.ru
  53. ^ "PEG 4000, 6000, 8000, 12000 | Polyethylene glycol". www.venus-goa.com. Retrieved 19 January 2023.
edit
 
Wikimedia Commons has media related to Poly(ethylene glycol).
 
Wikimedia Commons has media related to Polyethylene glycols.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Polyethylene_glycol&oldid=1256872265"