2021
DOI: 10.1002/mabi.202000379
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Electron Beam Sterilization of Poly(Methyl Methacrylate)—Physicochemical and Biological Aspects

Abstract: Electron beam (E‐beam) irradiation is an attractive and efficient method for sterilizing clinically implantable medical devices made of natural and/or synthetic materials such as poly(methyl methacrylate) (PMMA). As ionizing irradiation can affect the physicochemical properties of PMMA, understanding the consequences of E‐beam sterilization on the intrinsic properties of PMMA is vital for clinical implementation. A detailed assessment of the chemical, optical, mechanical, morphological, and biological properti… Show more

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Cited by 14 publications
(20 citation statements)
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“…Cell viability. The viability of cells was assessed using a commercial kit (LIVE/DEAD™ viability/cytotoxicity kit, for mammalian cells, (Thermofisher Scientific; Cambridge, MA), as previously described 60 , 61 . Briefly, cells were double-stained with calcein acetoxymethyl and ethidium homodimer for 30 min and imaged by inverted fluorescent microscopy (Zeiss Axio Observer Z1; Thornwood, NY) with a 10X objective.…”
Section: Methodsmentioning
confidence: 99%
“…Cell viability. The viability of cells was assessed using a commercial kit (LIVE/DEAD™ viability/cytotoxicity kit, for mammalian cells, (Thermofisher Scientific; Cambridge, MA), as previously described 60 , 61 . Briefly, cells were double-stained with calcein acetoxymethyl and ethidium homodimer for 30 min and imaged by inverted fluorescent microscopy (Zeiss Axio Observer Z1; Thornwood, NY) with a 10X objective.…”
Section: Methodsmentioning
confidence: 99%
“…This is crucially important in the radiation chemistry of the polymer and leads to the industrial application of the radiation processing of polymer. Although cross-linking and degradation may take place to some extent at the same time, one of them must predominate [46][47][48][49].…”
Section: The Application Field Of Ebi In the Textile Industrymentioning
confidence: 99%
“…To evaluate the cytotoxicity of the (G-GMA and H0−H5) constructs and their interactions with human corneal epithelial cells (HCEp) (kind gift of Dr. M. Griffith, University of Montreal) and corneal stromal cells (HCs) (kind gift of Dr. J. Jester, UC-Irvine), we performed a standard Live−Dead assay. 36 After hydration of dried composites and cutting them to a disc shape, they were treated with a 3X antibiotic solution containing 300 unit/mL penicillin and 300 μg/mL streptomycin solution. The culture discs were washed and used as substrates for culturing (10000 cells), followed by the addition of appropriate media 37,38 (400 μL) and incubation at 37 °C in 5% CO 2 .…”
Section: ■ Experimental Sectionmentioning
confidence: 99%