In-Vitro Biocompatibility Study and Comparison of Magnesium AZ31 and PEEK 450G Biomaterials used as Cardiovascular Stent Implants

Jump To References Section

Authors

  • Department of Mechanical Engineering, Bearys Institute of Technology, Visvesvaraya Technological University, Mangalore, Karnataka ,IN
  • Department of Mechanical Engineering, MSRIT, Visvesvaraya Technological University, Bengaluru, Karnataka ,IN
  • Department of Mechanical Engineering (W&SM), Sri Jayachamarajendra (Govt.) Polytechnic, Bengaluru, Karnataka ,IN
  • Department of Mechanical Engineering, PES College of Engineering, Visvesvaraya Technological University, Mandya, Karnataka ,IN
  • Department of Zoology, St. Joseph’s University, Bengaluru, Karnataka ,IN

DOI:

https://doi.org/10.18311/jmmf/2023/33358

Keywords:

Cytotoxicity; Biomaterials; PEEK 450G; In-Vitro; Biocompatibility; Cardiovascular stent implant

Abstract

This research article intended to study and comparison of cytotoxicity effects of Magnesium AZ31 and PEEK 450G biomaterials. L-929 mouse fibroblast cell line was used to measure cytotoxicity effect of Magnesium AZ31 and PEEK 450G biomaterials by extraction method. Biocompatibility in-vitro cytotoxicity test was performed on L-929 mouse fibroblast cell line for Magnesium AZ31 and PEEK 450G samples. In extraction process, leachates take out from the test samples were used for measurements of cytotoxicity. Since there was reactivity and the reactivity grade was greater than ‘2’ in Magnesium AZ31 biomaterial, test sample was measured as non-toxic, where as in PEEK 450G biomaterial there was no reactivity, no reduction in cell growth and no cell lysis, the grade was zero, and test sample was measured as non-toxic. Hence PEEK 450G biomaterial reveals an outstanding cytotoxicity behaviour than Magnesium AZ31. This is an added advantage for cardiovascular stent implant applications.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Downloads

Published

2023-04-12

How to Cite

Kumar, V., C. M. Ramesha, V. Sharanraj, Sadashiva M., & Kavya K. (2023). In-Vitro Biocompatibility Study and Comparison of Magnesium AZ31 and PEEK 450G Biomaterials used as Cardiovascular Stent Implants. Journal of Mines, Metals and Fuels, 71(1), 67–72. https://doi.org/10.18311/jmmf/2023/33358

Issue

Section

Articles

 

References

Benjamin, et al. (2018): Heart disease and stroke statistics 2018 update: a report from the American Heart Association. Circulation, 137:67-492.

Kumar, et al. (2018): “Biomechanical Analysis on Stent Materials used as Cardiovascular Implants” AIP Proceedings, Vol 1943, Issue 1, pp 1-11.

Kumar V, et al. (2019): Finite element analysis of PEEK 450G biomaterial used as cardiovascular stent implant, Vessel plus, 3:35, pp 1-13.

Yoruc¸ & Sener¸ et al. (2012): Biomaterials. In: Prof. Kara S, editor. A roadmap of biomedical engineers and milestones; ISBN: 978-953-51-0609-8.

Williams DF. Review: tissue biomaterial interactions. J Mat Sci, Vol 22(10), 1987, pp 3421- 3445.

Sharanraj, et al. (2019). “Finite Element Analysis of Zirconia Ceramic Biomaterials Used in Medical Dental Implants”, Interceram 68, Issue 3, pp 24-31.

V. Sharanraj, & Ramesha; (2017): “Finite Element Analysis of Ti-6Al-4V ELI and Alumina Bioinert Material Used in Molar Tooth Dental Implant Applications”, Interceram 66 [03-04], pp 90-94.

J.Black, (1997): Biological performance of materials: Fundamentals of Biocompatibility, 3rd Edition, pp 137.

Lo¨nnroth & Dahl JE. (2001). Cytotoxicity of dental glass ionomers evaluated using dimethyl thiazoldiphenyl-tetrazolium and neutral red tests. Acta Odontol Scand Vol 59(1), pp 349.

Cory et al. (1991): Use of an aqueous soluble tetrazolium/ formazan assay for cell growth assays in culture. Cancer Commun Vol 3(7), pp 207- 212.

Jordi et al. (2017): Polyetheretherketone (PEEK) as a medical and dental material. A literature review, Medical Research Archives, vol.5, pp 1-16.

International Standard ISO 10993, Fourth Edition: 2012-07-01, “Biological Evaluation of Medical Devices - Part 12: Sample Preparation and Reference Materials”.

International Standard ISO 10993, Third Edition: 2009-06-01, “Biological Evaluation of Medical Devices - Part 5: Tests for In vitro Cytotoxicity”.