2021
DOI: 10.1016/j.bioactmat.2020.11.029
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The development of laminin-alginate microspheres encapsulated with Ginsenoside Rg1 and ADSCs for breast reconstruction after lumpectomy

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Cited by 18 publications
(12 citation statements)
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“…If the concentration of cells in microspheres is too high, it can easily cause cell death due to hypoxia and nutrient deficiency; meanwhile, if the concentration of cells in microspheres is too low, cell survival and cell functions can be affected, resulting in reduced function of cellular microspheres. Previous studies have shown that a cell density of 10 6 /mL in sodium alginate microspheres exhibits good survival rates and functions [55,56]. As observed in our study, HepG2 cells preserved their viability no less than 80% over a course of 14 days and maintained biological functionality such as albumin generation and urea secretion (Figs.…”
Section: Discussionsupporting
confidence: 84%
“…If the concentration of cells in microspheres is too high, it can easily cause cell death due to hypoxia and nutrient deficiency; meanwhile, if the concentration of cells in microspheres is too low, cell survival and cell functions can be affected, resulting in reduced function of cellular microspheres. Previous studies have shown that a cell density of 10 6 /mL in sodium alginate microspheres exhibits good survival rates and functions [55,56]. As observed in our study, HepG2 cells preserved their viability no less than 80% over a course of 14 days and maintained biological functionality such as albumin generation and urea secretion (Figs.…”
Section: Discussionsupporting
confidence: 84%
“…Aluminum oxide (Al 2 O 3 , Sigma-Aldrich) and zinc diethyldithiocarbamate (ZDEC, Sigma-Aldrich) were used as negative and positive controls, respectively. The extracted medium was cultured with C2C12 myoblasts for 24 h. Thereafter, 100 μL WST-1 solution was added to the wells and incubated for 2 h. The absorbance values of each well were measured at 450 nm using an ELISA plate reader (Molecular Devices) [ 18 , 19 ].…”
Section: Methodsmentioning
confidence: 99%
“…Cytotoxicity was evaluated using the LIVE/DEAD staining kit (L3224, Invitrogen, USA) according to the manufacturer’s instructions [ 19 ]. C2C12 myoblasts were cultured in a 24-well plate at a density of 3 × 10 4 cells/well and incubated for 24 h for full adhesion.…”
Section: Methodsmentioning
confidence: 99%
“…The unique three-dimensional gel structure provides comfortable stereo space for the growth of the seed cells, and the shape is regular and the surface is smooth, which can avoid secondary damage to the injured site when the implant of irregular shape is implanted. It has been used in the cartilage [ 120 ], hard bone [ 121 ], nerve tissue repair [ 122 , 123 ] and other aspects [ 124 ].…”
Section: Biomedical Applicationsmentioning
confidence: 99%