"Acrylates" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Derivatives of acrylic acid (the structural formula CH2=CHCO2H), including its salts and esters.
Descriptor ID |
D000179
|
MeSH Number(s) |
D02.241.081.069
|
Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Acrylates".
Below are MeSH descriptors whose meaning is more specific than "Acrylates".
This graph shows the total number of publications written about "Acrylates" by people in this website by year, and whether "Acrylates" was a major or minor topic of these publications.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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2004 | 1 | 0 | 1 |
2005 | 0 | 1 | 1 |
2007 | 0 | 2 | 2 |
2008 | 1 | 1 | 2 |
2010 | 1 | 0 | 1 |
2014 | 0 | 1 | 1 |
2016 | 1 | 0 | 1 |
2017 | 0 | 1 | 1 |
2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Acrylates" by people in Profiles.
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Klep O, Jones HW, Reukov V, Foulger SH. Control of Vancomycin Activity through the Encapsulation and Controlled Release from a Propargyl Acrylate-Poloxamer Nanocomposite System. Langmuir. 2020 12 08; 36(48):14607-14613.
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He H, Markoutsa E, Li J, Xu P. Repurposing disulfiram for cancer therapy via targeted nanotechnology through enhanced tumor mass penetration and disassembly. Acta Biomater. 2018 03 01; 68:113-124.
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Jenkins R, Bandera YP, Daniele MA, Ledford LL, Tietje A, Kelso AA, Sehorn MG, Wei Y, Chakrabarti M, Ray SK, Foulger SH. Sequestering survivin to functionalized nanoparticles: a strategy to enhance apoptosis in cancer cells. Biomater Sci. 2016 Apr; 4(4):614-26.
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Sivaraman S, Ostendorff R, Fleishman B, Nagatomi J. Tetronic(®)-based composite hydrogel scaffolds seeded with rat bladder smooth muscle cells for urinary bladder tissue engineering applications. J Biomater Sci Polym Ed. 2015; 26(3):196-210.
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Aulich D, Hoy O, Luzinov I, Brücher M, Hergenröder R, Bittrich E, Eichhorn KJ, Uhlmann P, Stamm M, Esser N, Hinrichs K. In situ studies on the switching behavior of ultrathin poly(acrylic acid) polyelectrolyte brushes in different aqueous environments. Langmuir. 2010 Aug 03; 26(15):12926-32.
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Yu M, Urban MW, Sheng Y, Leszczynski J. Molecular recognition at methyl methacrylate/n-butyl acrylate (MMA/nBA) monomer unit boundaries of phospholipids at p-MMA/nBA copolymer surfaces. Langmuir. 2008 Sep 16; 24(18):10382-9.
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Rasal RM, Bohannon BG, Hirt DE. Effect of the photoreaction solvent on surface and bulk properties of poly(lactic acid) and poly(hydroxyalkanoate) films. J Biomed Mater Res B Appl Biomater. 2008 May; 85(2):564-72.
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Kutty JK, Cho E, Soo Lee J, Vyavahare NR, Webb K. The effect of hyaluronic acid incorporation on fibroblast spreading and proliferation within PEG-diacrylate based semi-interpenetrating networks. Biomaterials. 2007 Nov; 28(33):4928-38.
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Sandoval HP, Fernández de Castro LE, Vroman DT, Solomon KD. Comparison of visual outcomes, photopic contrast sensitivity, wavefront analysis, and patient satisfaction following cataract extraction and IOL implantation: aspheric vs spherical acrylic lenses. Eye (Lond). 2008 Dec; 22(12):1469-75.
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Bae WS, Lestage DJ, Proia M, Heinhorst S, Urban MW. Film formation from colloidal dispersions stabilized by sugar derivatives and their controllable release for selective protein adsorption. Biomacromolecules. 2005 Sep-Oct; 6(5):2615-21.