2021
DOI: 10.1049/nbt2.12032
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In vitro degradation, haemolysis and cytotoxicity study of Mg‐0.4Ce/ZnO 2 nanocomposites

Abstract: Magnesium is an ideal candidate for biodegradable implants, but the major concern is its uncontrollable degradation for application as a biomaterial. The in vitro corrosion and cytotoxicity of Mg-0.4Ce/ZnO 2 (magnesium nanocomposites) were studied to determine its suitability as a biodegradable material. The polycrystalline nature of Mg-0.4Ce/ZnO 2 was assessed using an optical microscope. The hydrophobic nature of Mg-0.4Ce/ZnO 2 was determined by contact angle measurements. The corrosion resistance of magnesi… Show more

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Cited by 8 publications
(4 citation statements)
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References 32 publications
(41 reference statements)
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“…Another report stated that ZnO nanoparticles in concentrations up to 20 mg/l have no adverse effect on HeLa cells [78]. Our previous findings demonstrated the results of the MTT assay for the Mg 0.4Ce/ZnO 2 surface appear to have a cytotoxicity effect after one day due to an increase in pH [71]. The % viability of Mg Ni/ Ti nanocomposite was found to be 136.18%.…”
Section: Cytotoxicity Assessmentsupporting
confidence: 62%
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“…Another report stated that ZnO nanoparticles in concentrations up to 20 mg/l have no adverse effect on HeLa cells [78]. Our previous findings demonstrated the results of the MTT assay for the Mg 0.4Ce/ZnO 2 surface appear to have a cytotoxicity effect after one day due to an increase in pH [71]. The % viability of Mg Ni/ Ti nanocomposite was found to be 136.18%.…”
Section: Cytotoxicity Assessmentsupporting
confidence: 62%
“…From the third to the fourteenth day, the surface of pure Mg suffers from localized pitting corrosion. The protective film rupture mechanism dominated the cracking and further dissolving of the sample surfaces, and the pure Mg was more susceptible to cracking[71]. Figures4(e)-(h) show macroscopic pictures of corroded Mg Ni/Ti surfaces on days 3, 5, 7, and 14, respectively.…”
mentioning
confidence: 99%
“…The hemolysis and cytotoxicity were calculated using the following formulas: hemolysis (%) = {[OD 540 (optical density at 540 nm) sample − OD 540 buffer]/[OD 540 max − OD 540 buffer]} × 100 and cytotoxicity (%) = (OD 490 sample − OD 490 negative control)/(OD 490 max − OD 490 buffer) × 100, calculated based on the average of replicates ( 86 ). Approximately 20% was regarded as the minimal hemolysis value compared to the positive control for hemolytic activity of FX-compounds ( 87 ), and because lactate dehydrogenase release over 20% has been used to evaluate the chemotherapy effect of advanced non-small cell lung cancer patients with platinum-based chemotherapy ( 88 ), 20% was listed as the cutoff for evaluating hemolysis and cytotoxicity in this study.…”
Section: Methodsmentioning
confidence: 99%
“…[33] Hemolysis assays were performed as described by Prabakaran et al. [34] Defibrinated sheep blood (5 mL) was washed repeatedly with PBS until the supernatant no longer showed any red color. A 2 % (v/v) mixture of the red blood cell suspension was prepared in PBS.…”
Section: Analysis Of Cytotoxicity and Hemolytic Activitymentioning
confidence: 99%