<resource xmlns:datacite="http://datacite.org/schema/kernel-4">
<creators>
<creator>
<creatorName nameType="Personal">Lukas Weber</creatorName>
<givenName>Lukas</givenName>
<familyName>Weber</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Jelena Horky</creatorName>
<givenName>Jelena</givenName>
<familyName>Horky</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Christopher Riedmüller</creatorName>
<givenName>Christopher</givenName>
<familyName>Riedmüller</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Carina Kampleitner</creatorName>
<givenName>Carina</givenName>
<familyName>Kampleitner</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Eylem Acar</creatorName>
<givenName>Eylem</givenName>
<familyName>Acar</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Mariangela Fedel</creatorName>
<givenName>Mariangela</givenName>
<familyName>Fedel</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Claudia Höchsmann (Centre of Pathobiology, Department of Biological Sciences and Pathobiology, Departments, University of Veterinary Medicine Vienna)</creatorName>
<givenName>Claudia</givenName>
<familyName>Höchsmann</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Magdalena Eskinja</creatorName>
<givenName>Magdalena</givenName>
<familyName>Eskinja</familyName>
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<creator>
<creatorName nameType="Personal">Stefan Mitsche</creatorName>
<givenName>Stefan</givenName>
<familyName>Mitsche</familyName>
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<creator>
<creatorName nameType="Personal">Bernhard Mingler</creatorName>
<givenName>Bernhard</givenName>
<familyName>Mingler</familyName>
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<creator>
<creatorName nameType="Personal">Laszlo Sajti</creatorName>
<givenName>Laszlo</givenName>
<familyName>Sajti</familyName>
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<creator>
<creatorName nameType="Personal">Gregor Mori</creatorName>
<givenName>Gregor</givenName>
<familyName>Mori</familyName>
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<creator>
<creatorName nameType="Personal">Manfred Bammer</creatorName>
<givenName>Manfred</givenName>
<familyName>Bammer</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Ingrid Walter (Centre of Pathobiology, Department of Biological Sciences and Pathobiology, Departments, University of Veterinary Medicine Vienna)</creatorName>
<givenName>Ingrid</givenName>
<familyName>Walter</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Stefan Tangl</creatorName>
<givenName>Stefan</givenName>
<familyName>Tangl</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Helga Bergmeister</creatorName>
<givenName>Helga</givenName>
<familyName>Bergmeister</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Bruno K. Podesser</creatorName>
<givenName>Bruno K.</givenName>
<familyName>Podesser</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Marjan Enayati</creatorName>
<givenName>Marjan</givenName>
<familyName>Enayati</familyName>
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</creators>
<titles>
<title>A high-toughness, rare-earth-free magnesium alloy with excellent biocompatibility profile: Integrated in vitro and in vivo characterization</title>
</titles>
<publisher>Elsevier</publisher>
<publicationYear>2026</publicationYear>
<descriptions>
<description descriptionType="Other">Bioresorbable magnesium (Mg) alloys are promising alternatives to permanent implants in cardiovascular and orthopedic applications. Alloying with rare earth elements (REEs) can enhance corrosion resistance and mechanical strength, though their long-term biological behavior and biosafety are still being clarified. Herein, we compared the widely used REE-containing alloy WE43 with a previously self-designed REE-free alloy, ZX00 (Mg–0.6Zn–0.5Ca), focusing on biocompatibility, toxicity, degradation, and mechanical performance in vitro and in vivo. ZX00 demonstrated significantly higher fibroblast viability than WE43 in vitro (100.00% ± 9.30% vs. 43.00% ± 6.88%; p &lt; 0.0001) and did not elicit inflammatory responses in primary human macrophages, while both alloys showed comparable hemocompatibility. After 5 months of subcutaneous implantation in rats, ZX00 and WE43 exhibited similar overall biocompatibility, with mild gas formation observed in X-ray imaging and histology. Although ZX00 degraded faster than WE43 according to micro-computed tomography and histological analyses, it retained markedly superior ductility after 5 months of implantation, due to uniform, non-localized corrosion. No systemic toxicity was detected for either alloy through histopathological assessment of multiple organs and hematological analyses. This study shows that the REE-free ZX00 alloy possesses the biological and mechanical requirements for demanding biomedical environments, positioning it as a promising candidate for cardiovascular applications and marking a first step toward a bioabsorbable material specifically designed for cardiac annuloplasty devices.</description>
</descriptions>
<resourceType resourceTypeGeneral="Text">PDFDocument</resourceType>
<language>eng</language>
<dates>
<date dateType="Created">2026-10-16T07:53:39.782302771Z</date>
<date dateType="Issued">2026</date>
</dates>
<subjects>
<subject>Magnesium alloy</subject>
<subject>Biocompatibility</subject>
<subject>Inflammatory response</subject>
<subject>Biodegradability</subject>
<subject>Mechanical performance</subject>
</subjects>
<sizes>
<size>17639909 b</size>
</sizes>
<formats>
<format>application/pdf</format>
</formats>
<rightsList>
<rights rightsURI="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</rights>
</rightsList>
</resource>
