AI Article Synopsis

  • Magnesium pyrophosphate modified tetracalcium phosphate/monetite cement mixtures (MgTTCPM) were created using a simple ball milling method, chosen for their favorable setting properties compared to other additives.
  • These mixtures showed consistent dissolution of the MgPO phase and the formation of weakly bound HAP nanoparticles, leading to a compressive strength of 14 MPa and a setting time between 5-10 minutes, influenced by their composition.
  • The cements exhibited no cytotoxicity and promoted the growth of mesenchymal stem cells, with increased expression of bone-related genes, suggesting they could be effective biomaterials for treating bone defects.

Article Abstract

Magnesium pyrophosphate modified tetracalcium phosphate/monetite cement mixtures (MgTTCPM) were prepared by simple mechanical homogenization of compounds in a ball mill. The MgPO was chosen due to the suitable setting properties of the final cements, in contrast to cements with the addition of amorphous (Ca, Mg) CO or newberite, which significantly extended the setting time even in small amounts (corresponding ~to 1 wt% of Mg in final cements). The results showed the gradual dissolution of the same amount of MgPO phase, regardless of its content in the cement mixtures, and the refinement of formed HAP nanoparticles, which were joined into weakly and mutually bound spherical agglomerates. The compressive strength of composite cements was reduced to 14 MPa and the setting time was 5-10 min depending on the composition. Cytotoxicity of cements or their extracts was not detected and increased proliferative activity of mesenchymal stem cells with upregulation of osteopontin and osteonectin genes was verified in cells cultured for 7 and 15 days in cement extracts. The above facts, including insignificant changes in the pH of simulated body fluid solution and mechanical strength close to cancellous bone, indicate that MgTTCPM cement mixtures could be suitable biomaterials for use in the treatment of bone defects.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000233PMC
http://dx.doi.org/10.3390/ma15072586DOI Listing

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