2011
DOI: 10.1016/j.ijpharm.2011.04.042
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Cytotoxicity and biocompatibility evaluation of a poly(magnesium acrylate) hydrogel synthesized for drug delivery

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Cited by 30 publications
(16 citation statements)
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“…The in vitro cytotoxicity of the gels was evaluated by using a direct contact method according to ISO 10933 . The hydrogel samples were cut into 100 µm thickness disks with vibroslicer (752M Vibroslice, Campden Instruments, UK).…”
Section: Methodsmentioning
confidence: 99%
“…The in vitro cytotoxicity of the gels was evaluated by using a direct contact method according to ISO 10933 . The hydrogel samples were cut into 100 µm thickness disks with vibroslicer (752M Vibroslice, Campden Instruments, UK).…”
Section: Methodsmentioning
confidence: 99%
“…In addition, cytotoxicity studies in human cells were carried out. For this purpose, we used the MTT ((3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay and a cytofluorometric analysis to determine their impact on human neutrophil apoptosis and survival [24][25][26]. All of them were devoid of any toxic effect in these in vitro assays.…”
Section: Introductionmentioning
confidence: 99%
“…The increased viscosity may be the reason for the slight toxicity demonstrated at these polymer concentrations, as also suggested by others, studying the cytotoxicity of hydrogels. 52 Indeed, we have seen in many cases that dispersions of large multilamellar liposomes demonstrate significant toxicity toward various cell types, whereas small unilamellar liposomes incubated at the same lipidic concentrations do not. This is explained by the hypothesis that the toxicity demonstrated (in the case of the MLV liposomes) is not directly caused by the lipid components of the liposomes but by their size and perhaps the fact that dispersions of large liposomes have higher viscosity compared with dispersions of nanosized ones (of identical composition and lipid concentration).…”
Section: ' Results and Discussionmentioning
confidence: 98%