In vivo degradation of magnesium alloy LA63 scaffolds for temporary stabilization of biological myocardial grafts in a swine model

Publikation: Beitrag in FachzeitschriftÜbersichtsarbeitForschungPeer-Review

Autorschaft

  • Tobias Schilling
  • Gudrun Brandes
  • Igor Tudorache
  • Serghei Cebotari
  • Andres Hilfiker
  • Tanja Meyer
  • Christian Biskup
  • Michael Bauer
  • Karl Heinz Waldmann
  • Friedrich Wilhelm Bach
  • Axel Haverich
  • Thomas Hassel

Organisationseinheiten

Externe Organisationen

  • Stiftung Tierärztliche Hochschule Hannover
  • Medizinische Hochschule Hannover (MHH)
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)407-416
Seitenumfang10
FachzeitschriftBiomedizinische Technik
Jahrgang58
Ausgabenummer5
Frühes Online-Datum29 Aug. 2013
PublikationsstatusVeröffentlicht - 1 Okt. 2013

Abstract

Synthetic or biological patch materials used for surgical myocardial reconstruction are often fragile. Therefore, a transient support by degradable magnesium scaffolds can reduce the risk of dilation or rupture of the patch until physiological remodeling has led to a sufficient mechanical durability. However, there is evidence that magnesium implants can influence the growth and physiological behavior of the host's cells and tissue. Hence, we epicardially implanted scaffolds of the magnesium fluoride-coated magnesium alloy LA63 in a swine model to assess biocompatibility and degradation kinetics. Chemical analysis of the pigs' organs revealed no toxic accumulation of magnesium ions in the skeletal muscle, myocardium, liver, kidney, and bone of the pigs 1, 3, and 6 months postimplantation. The implants were surrounded by a fibrous granulation tissue, but no signs of necrosis were histologically evaluable. A sufficiently slow degradation rate of the magnesium alloy scaffold can be demonstrated via micro-computed tomography investigation. We conclude that stabilizing scaffolds of the magnesium fluoride-coated magnesium alloy LA63 can be used for epicardial application because no significant adverse effects to myocardial tissue were noted. Thus, degradable stabilizing scaffolds of this magnesium alloy with a slow degradation rate can extend the indication of innovative biological and synthetic patch materials.

ASJC Scopus Sachgebiete

Zitieren

In vivo degradation of magnesium alloy LA63 scaffolds for temporary stabilization of biological myocardial grafts in a swine model. / Schilling, Tobias; Brandes, Gudrun; Tudorache, Igor et al.
in: Biomedizinische Technik, Jahrgang 58, Nr. 5, 01.10.2013, S. 407-416.

Publikation: Beitrag in FachzeitschriftÜbersichtsarbeitForschungPeer-Review

Schilling, T, Brandes, G, Tudorache, I, Cebotari, S, Hilfiker, A, Meyer, T, Biskup, C, Bauer, M, Waldmann, KH, Bach, FW, Haverich, A & Hassel, T 2013, 'In vivo degradation of magnesium alloy LA63 scaffolds for temporary stabilization of biological myocardial grafts in a swine model', Biomedizinische Technik, Jg. 58, Nr. 5, S. 407-416. https://doi.org/10.1515/bmt-2012-0047
Schilling, T., Brandes, G., Tudorache, I., Cebotari, S., Hilfiker, A., Meyer, T., Biskup, C., Bauer, M., Waldmann, K. H., Bach, F. W., Haverich, A., & Hassel, T. (2013). In vivo degradation of magnesium alloy LA63 scaffolds for temporary stabilization of biological myocardial grafts in a swine model. Biomedizinische Technik, 58(5), 407-416. https://doi.org/10.1515/bmt-2012-0047
Schilling T, Brandes G, Tudorache I, Cebotari S, Hilfiker A, Meyer T et al. In vivo degradation of magnesium alloy LA63 scaffolds for temporary stabilization of biological myocardial grafts in a swine model. Biomedizinische Technik. 2013 Okt 1;58(5):407-416. Epub 2013 Aug 29. doi: 10.1515/bmt-2012-0047
Schilling, Tobias ; Brandes, Gudrun ; Tudorache, Igor et al. / In vivo degradation of magnesium alloy LA63 scaffolds for temporary stabilization of biological myocardial grafts in a swine model. in: Biomedizinische Technik. 2013 ; Jahrgang 58, Nr. 5. S. 407-416.
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abstract = "Synthetic or biological patch materials used for surgical myocardial reconstruction are often fragile. Therefore, a transient support by degradable magnesium scaffolds can reduce the risk of dilation or rupture of the patch until physiological remodeling has led to a sufficient mechanical durability. However, there is evidence that magnesium implants can influence the growth and physiological behavior of the host's cells and tissue. Hence, we epicardially implanted scaffolds of the magnesium fluoride-coated magnesium alloy LA63 in a swine model to assess biocompatibility and degradation kinetics. Chemical analysis of the pigs' organs revealed no toxic accumulation of magnesium ions in the skeletal muscle, myocardium, liver, kidney, and bone of the pigs 1, 3, and 6 months postimplantation. The implants were surrounded by a fibrous granulation tissue, but no signs of necrosis were histologically evaluable. A sufficiently slow degradation rate of the magnesium alloy scaffold can be demonstrated via micro-computed tomography investigation. We conclude that stabilizing scaffolds of the magnesium fluoride-coated magnesium alloy LA63 can be used for epicardial application because no significant adverse effects to myocardial tissue were noted. Thus, degradable stabilizing scaffolds of this magnesium alloy with a slow degradation rate can extend the indication of innovative biological and synthetic patch materials.",
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T1 - In vivo degradation of magnesium alloy LA63 scaffolds for temporary stabilization of biological myocardial grafts in a swine model

AU - Schilling, Tobias

AU - Brandes, Gudrun

AU - Tudorache, Igor

AU - Cebotari, Serghei

AU - Hilfiker, Andres

AU - Meyer, Tanja

AU - Biskup, Christian

AU - Bauer, Michael

AU - Waldmann, Karl Heinz

AU - Bach, Friedrich Wilhelm

AU - Haverich, Axel

AU - Hassel, Thomas

N1 - Funding Information: Acknowledgments: The project is funded by the German Research Foundation (Collaborative Research Center (SFB) 599/ Project R7). The excellent technical assistance of Christian Klose (Institute of Material Science, Leibniz University Hannover, Hannover, Germany) and Elke Mallon (Institute of Cell Biology in the Center of Anatomy

PY - 2013/10/1

Y1 - 2013/10/1

N2 - Synthetic or biological patch materials used for surgical myocardial reconstruction are often fragile. Therefore, a transient support by degradable magnesium scaffolds can reduce the risk of dilation or rupture of the patch until physiological remodeling has led to a sufficient mechanical durability. However, there is evidence that magnesium implants can influence the growth and physiological behavior of the host's cells and tissue. Hence, we epicardially implanted scaffolds of the magnesium fluoride-coated magnesium alloy LA63 in a swine model to assess biocompatibility and degradation kinetics. Chemical analysis of the pigs' organs revealed no toxic accumulation of magnesium ions in the skeletal muscle, myocardium, liver, kidney, and bone of the pigs 1, 3, and 6 months postimplantation. The implants were surrounded by a fibrous granulation tissue, but no signs of necrosis were histologically evaluable. A sufficiently slow degradation rate of the magnesium alloy scaffold can be demonstrated via micro-computed tomography investigation. We conclude that stabilizing scaffolds of the magnesium fluoride-coated magnesium alloy LA63 can be used for epicardial application because no significant adverse effects to myocardial tissue were noted. Thus, degradable stabilizing scaffolds of this magnesium alloy with a slow degradation rate can extend the indication of innovative biological and synthetic patch materials.

AB - Synthetic or biological patch materials used for surgical myocardial reconstruction are often fragile. Therefore, a transient support by degradable magnesium scaffolds can reduce the risk of dilation or rupture of the patch until physiological remodeling has led to a sufficient mechanical durability. However, there is evidence that magnesium implants can influence the growth and physiological behavior of the host's cells and tissue. Hence, we epicardially implanted scaffolds of the magnesium fluoride-coated magnesium alloy LA63 in a swine model to assess biocompatibility and degradation kinetics. Chemical analysis of the pigs' organs revealed no toxic accumulation of magnesium ions in the skeletal muscle, myocardium, liver, kidney, and bone of the pigs 1, 3, and 6 months postimplantation. The implants were surrounded by a fibrous granulation tissue, but no signs of necrosis were histologically evaluable. A sufficiently slow degradation rate of the magnesium alloy scaffold can be demonstrated via micro-computed tomography investigation. We conclude that stabilizing scaffolds of the magnesium fluoride-coated magnesium alloy LA63 can be used for epicardial application because no significant adverse effects to myocardial tissue were noted. Thus, degradable stabilizing scaffolds of this magnesium alloy with a slow degradation rate can extend the indication of innovative biological and synthetic patch materials.

KW - Biocompatibility

KW - Corrosion

KW - Fluoride coating

KW - Patch

KW - Reconstruction

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