2009
DOI: 10.1016/j.msec.2008.12.019
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Biocompatibility of pure iron: In vitro assessment of degradation kinetics and cytotoxicity on endothelial cells

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Cited by 162 publications
(104 citation statements)
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“…During in vitro tests a layer of precipitated degradation products forms, which usually exhibits a brownish color and consists of hydroxides originating from the reactions above [71,72].…”
Section: Degradation Mechanismmentioning
confidence: 99%
“…During in vitro tests a layer of precipitated degradation products forms, which usually exhibits a brownish color and consists of hydroxides originating from the reactions above [71,72].…”
Section: Degradation Mechanismmentioning
confidence: 99%
“…The average weight loss of the specimen in 40 mL SBF solution was 17.15×10 −5 g cm -2 day −1 , so the 25% of the 24 h immersion is 0.0429 mg mL −1 . Zhu et al [31] reported that approximately a release of 0.05 mg mL −1 Fe ion is considered safe for the human body. Therefore, our results suggest that the concentration of Fe ions released from the specimen is within the safety level.…”
Section: Tensilementioning
confidence: 99%
“…However, the mechanical properties of such alloys, i.e., strength and the elongation to fracture are not always acceptable which combined to the development of signiicant quantities of hydrogen limits their widespread use. Some studies [53][54][55] have reported as alternative solution the use of Fe-based alloys. However, the implants realized using such alloys reveal some reactions like those developed in longterm uses which is predominantly due to the low-degradation rate of pure Fe in biological atmosphere [56].…”
Section: Outlinementioning
confidence: 99%