2015
DOI: 10.1186/s12893-015-0111-4
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Safety of bioabsorbable implants in vitro

Abstract: BackgroundThe aim of the present study was to investigate the safety of bioabsorbable plates and screws in humans.MethodsFor this purpose, an implant system based on [poly(lactic-co-glycolic acids)(85:15)] was designed. The system was tested for pH, temperature, and swelling and then its surface morphology was analyzed for surface porosity using environmental electron microscopy. Then, the effects of this bioabsorbable system on the viability and profileration of osteocytes were examined on a molecular level v… Show more

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Cited by 12 publications
(14 citation statements)
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“…However, as is known, the sensitivity of human and animal tissues differs greatly, and may therefore generate misleading results. Additionally, as cell lines use single-type cells and do not have complex coordination mechanisms regarding the micro environments of cells and inhibit cell interactions, such as in the extracellular matrix, in vitro test results, which are already difficult to compare with in vivo conditions, become more controversial (7,8,15).…”
Section: █ Discussionmentioning
confidence: 99%
“…However, as is known, the sensitivity of human and animal tissues differs greatly, and may therefore generate misleading results. Additionally, as cell lines use single-type cells and do not have complex coordination mechanisms regarding the micro environments of cells and inhibit cell interactions, such as in the extracellular matrix, in vitro test results, which are already difficult to compare with in vivo conditions, become more controversial (7,8,15).…”
Section: █ Discussionmentioning
confidence: 99%
“…MTT analyses were evaluated in accordance with commercial kit bulletins on the 1st, 7th, 14th, and 21st days [1520, 24, 26]. …”
Section: Methodsmentioning
confidence: 99%
“…The supernatant was removed, and the cells were resuspended in an assay buffer and analyzed with a flow cytometer. Results were evaluated using the BD FACSCalibur Cell Quest software (Becton Dickinson, Palo Alto, CA, USA) [ 11 , 14 , 15 ].…”
Section: Methodsmentioning
confidence: 99%
“…The glutaraldehyde solution was then removed, and cells were maintained at room temperature for 2 h, prior to three washes using cacodylate buffer. After the last wash, the cells were covered with cacodylate buffer and stored at 4°C prior to analysis [ 14 , 15 , 17 , 18 ]. Images of the extracellular matrix and characteristic cellular structures were obtained.…”
Section: Methodsmentioning
confidence: 99%