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Ion release from magnesium materials in physiological solutions under different oxygen tensions

Research output: Journal contributions › Journal articles › Research › peer-review

Standard

Ion release from magnesium materials in physiological solutions under different oxygen tensions. / Feyerabend, Frank; Drücker, Heiko; Laipple, Daniel et al.
In: Journal of Materials Science: Materials in Medicine, Vol. 23, No. 1, 01.2012, p. 9-24.

Research output: Journal contributions › Journal articles › Research › peer-review

Harvard

Feyerabend, F, Drücker, H, Laipple, D, Vogt, C, Stekker, M, Hort, N & Willumeit, R 2012, 'Ion release from magnesium materials in physiological solutions under different oxygen tensions', Journal of Materials Science: Materials in Medicine, vol. 23, no. 1, pp. 9-24. https://doi.org/10.1007/s10856-011-4490-5

APA

Feyerabend, F., Drücker, H., Laipple, D., Vogt, C., Stekker, M., Hort, N., & Willumeit, R. (2012). Ion release from magnesium materials in physiological solutions under different oxygen tensions. Journal of Materials Science: Materials in Medicine, 23(1), 9-24. https://doi.org/10.1007/s10856-011-4490-5

Vancouver

Feyerabend F, Drücker H, Laipple D, Vogt C, Stekker M, Hort N et al. Ion release from magnesium materials in physiological solutions under different oxygen tensions. Journal of Materials Science: Materials in Medicine. 2012 Jan;23(1):9-24. doi: 10.1007/s10856-011-4490-5

Bibtex

@article{4bd662ff48fd44fc80b839739e9defe3,
title = "Ion release from magnesium materials in physiological solutions under different oxygen tensions",
abstract = "Although magnesium as degradable biomaterial already showed clinical proof of concepts, the design of new alloys requires predictive in vitro methods, which are still lacking. Incubation under cell culture conditions to obtain {"}physiological{"} corrosion may be a solution. The aim of this study was to analyse the influence of different solutions, addition of proteins and of oxygen availability on the corrosion of different magnesium materials (pure Mg, WE43, and E11) with different surface finishing. Oxygen content in solution, pH, osmolality and ion release were determined. Corrosion led to a reduction of oxygen in solution. The influence of oxygen on pH was enhanced by proteins, while osmolality was not influenced. Magnesium ion release was solution-dependent and enhanced in the initial phase by proteins with delayed release of alloying elements. The main corrosion product formed was magnesium carbonate. Therefore, cell culture conditions are proposed as first step toward physiological corrosion.",
keywords = "Engineering",
author = "Frank Feyerabend and Heiko Dr{\"u}cker and Daniel Laipple and Carla Vogt and Michael Stekker and Norbert Hort and Regine Willumeit",
year = "2012",
month = jan,
doi = "10.1007/s10856-011-4490-5",
language = "English",
volume = "23",
pages = "9--24",
journal = "Journal of Materials Science: Materials in Medicine",
issn = "0957-4530",
publisher = "Springer",
number = "1",

}

RIS

TY - JOUR

T1 - Ion release from magnesium materials in physiological solutions under different oxygen tensions

AU - Feyerabend, Frank

AU - Drücker, Heiko

AU - Laipple, Daniel

AU - Vogt, Carla

AU - Stekker, Michael

AU - Hort, Norbert

AU - Willumeit, Regine

PY - 2012/1

Y1 - 2012/1

N2 - Although magnesium as degradable biomaterial already showed clinical proof of concepts, the design of new alloys requires predictive in vitro methods, which are still lacking. Incubation under cell culture conditions to obtain "physiological" corrosion may be a solution. The aim of this study was to analyse the influence of different solutions, addition of proteins and of oxygen availability on the corrosion of different magnesium materials (pure Mg, WE43, and E11) with different surface finishing. Oxygen content in solution, pH, osmolality and ion release were determined. Corrosion led to a reduction of oxygen in solution. The influence of oxygen on pH was enhanced by proteins, while osmolality was not influenced. Magnesium ion release was solution-dependent and enhanced in the initial phase by proteins with delayed release of alloying elements. The main corrosion product formed was magnesium carbonate. Therefore, cell culture conditions are proposed as first step toward physiological corrosion.

AB - Although magnesium as degradable biomaterial already showed clinical proof of concepts, the design of new alloys requires predictive in vitro methods, which are still lacking. Incubation under cell culture conditions to obtain "physiological" corrosion may be a solution. The aim of this study was to analyse the influence of different solutions, addition of proteins and of oxygen availability on the corrosion of different magnesium materials (pure Mg, WE43, and E11) with different surface finishing. Oxygen content in solution, pH, osmolality and ion release were determined. Corrosion led to a reduction of oxygen in solution. The influence of oxygen on pH was enhanced by proteins, while osmolality was not influenced. Magnesium ion release was solution-dependent and enhanced in the initial phase by proteins with delayed release of alloying elements. The main corrosion product formed was magnesium carbonate. Therefore, cell culture conditions are proposed as first step toward physiological corrosion.

KW - Engineering

UR - http://www.scopus.com/inward/record.url?scp=84857626243&partnerID=8YFLogxK

U2 - 10.1007/s10856-011-4490-5

DO - 10.1007/s10856-011-4490-5

M3 - Journal articles

C2 - 22138756

AN - SCOPUS:84857626243

VL - 23

SP - 9

EP - 24

JO - Journal of Materials Science: Materials in Medicine

JF - Journal of Materials Science: Materials in Medicine

SN - 0957-4530

IS - 1

ER -

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Research output: Contributions to collected editions/works › Article in conference proceedings › Research › peer-review

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Research output: Contributions to collected editions/works › Article in conference proceedings › Research › peer-review

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