2020
DOI: 10.1167/tvst.9.13.41
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Sputter Deposition of Titanium on Poly(Methyl Methacrylate) Enhances Corneal Biocompatibility

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Cited by 14 publications
(15 citation statements)
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“…Then, 20 μL of the cell dispersion was transferred to polydimethylsiloxane (PDMS) mold (diameter = 8 mm, thickness = 0.2 mm) and exposed to photoirradiation for a varying period. Those cell-laden gels were immediately washed 3 times with PBS and incubated in 200 μL culture medium (DMEM/F-12 50/50, 1 × media (Corning, VA, USA) at 37°C 59 . For mesenchymal stems cells, after resuspending (2 × 10 5 cells per mL) in the hydrogel precursor solution containing (10% GelMA, 0.05 mM EY, 1% (w/v) TEOA, and 1% (w/v), the suspension (20 μL) was transferred to PDMS mold and exposed to photoirradiation for a 4 and 10 min.…”
Section: Methodsmentioning
confidence: 99%
“…Then, 20 μL of the cell dispersion was transferred to polydimethylsiloxane (PDMS) mold (diameter = 8 mm, thickness = 0.2 mm) and exposed to photoirradiation for a varying period. Those cell-laden gels were immediately washed 3 times with PBS and incubated in 200 μL culture medium (DMEM/F-12 50/50, 1 × media (Corning, VA, USA) at 37°C 59 . For mesenchymal stems cells, after resuspending (2 × 10 5 cells per mL) in the hydrogel precursor solution containing (10% GelMA, 0.05 mM EY, 1% (w/v) TEOA, and 1% (w/v), the suspension (20 μL) was transferred to PDMS mold and exposed to photoirradiation for a 4 and 10 min.…”
Section: Methodsmentioning
confidence: 99%
“…Nonproliferative surfaces can induce ECM-related stress in cultured cells and lead to myofibroblasts differentiation and α-SMA overexpression, which are involved in pro-inflammatory and fibrotic responses. 51 When cultured on constructs, HCS did not express α-SMA. These data suggest that GM-VP construct is biocompatible and promotes cell adhesion and proliferation, while preserving the phenotypic characteristics of HCS.…”
Section: ■ Results and Discussionmentioning
confidence: 98%
“…After 1, 4, and 7 days of cell culture, the specimens were stained with standard Live–Dead staining kit (LIVE/DEAD viability/cytotoxicity kit, for mammalian cells, Thermofisher Scientific, Cambridge, MA) and imaged by inverted fluorescent microscopy (Zeiss Axio Observer Z1; Thornwood, NY). Cell viabilities were quantified by using ImageJ software from multiple images acquired from each sample ( n = 4) and compared to those cultured on TCP as a control and as described elsewhere. , …”
Section: Methodsmentioning
confidence: 99%
“…Cell viabilities were quantified by using ImageJ software from multiple images acquired from each sample (n = 4) and compared to those cultured on TCP as a control and as described elsewhere. 39,40 The alamarBlue Assay. To assess the metabolic activity of the cultured cells (HCEp and HCS) when grown on the constructs, we used a standard alamarBlue assay.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%