2020
DOI: 10.1016/j.jmrt.2020.11.036
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Preparation, structural and microstructural characterization of Ti–30Nb–10Ta–5Zr alloy for biomedical applications

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Cited by 21 publications
(16 citation statements)
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“…The number of cells in a state of mitosis was determined using fluorescence microscopy using in-vitro staining with the Hoechst 33342 fluorescent dye (Sigma, Saint-Louis, MO, USA) [ 31 ]. The density of the culture was assessed using the approaches developed earlier [ 32 ].…”
Section: Methodsmentioning
confidence: 99%
“…The number of cells in a state of mitosis was determined using fluorescence microscopy using in-vitro staining with the Hoechst 33342 fluorescent dye (Sigma, Saint-Louis, MO, USA) [ 31 ]. The density of the culture was assessed using the approaches developed earlier [ 32 ].…”
Section: Methodsmentioning
confidence: 99%
“…For analysis, at least 500 cells were counted on the each sample surface. The mitotic index (MI) was calculated by the formula MI = (P + M + A + T) / N × 100%, where (P + M + A + T) is the number of cells at the stage of prophase, metaphase, anaphase, and telophase, respectively, and N is the total number of analyzed cells [36].…”
Section: Cell Culturementioning
confidence: 99%
“…SH-SY5Y cells are also interesting in that they can grow not only in monolayers but also form cell aggregates, which also take root on substrates SH-SY5Y usually used in the study of cells proliferation and differentiation in different conditions. For example, SH-SY5Y cells can spontaneously divide into one of two phenotypes, similar to "neuroblast" or "epithelial" phenotypes [65]. The SH-SY5Y cells were cultured by standard protocol in DMEM (Biolot, Moscow, Russia) supplemented with 10% fetal bovine serum (Gibco, USA) and 30 µg/mL gentamicin in a CO 2 incubator (Binder, Tuttlingen, Germany).…”
Section: Assay Of Biocompatibility With Mammalial Cellsmentioning
confidence: 99%