Peer-Reviewed Journal Details
Mandatory Fields
Clements, J,Walker, G,Pentlavalli, S,Dunne, N
2014
October
Journal Of Materials Science-Materials In Medicine
Optimisation of a two-liquid component pre-filled acrylic bone cement system: a design of experiments approach to optimise cement final properties
Published
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Optional Fields
VERTEBRAL BODY AUGMENTATION CALCIUM-PHOSPHATE CEMENT RESIDUAL MONOMER CONTENT MECHANICAL-PROPERTIES FATIGUE-STRENGTH TEMPERATURE POROSITY POLYMERIZATION SHRINKAGE VARIABLES
25
2287
2296
The initial composition of acrylic bone cement along with the mixing and delivery technique used can influence its final properties and therefore its clinical success in vivo. The polymerisation of acrylic bone cement is complex with a number of processes happening simultaneously. Acrylic bone cement mixing and delivery systems have undergone several design changes in their advancement, although the cement constituents themselves have remained unchanged since they were first used. This study was conducted to determine the factors that had the greatest effect on the final properties of acrylic bone cement using a pre-filled bone cement mixing and delivery system. A design of experiments (DoE) approach was used to determine the impact of the factors associated with this mixing and delivery method on the final properties of the cement produced. The DoE illustrated that all factors present within this study had a significant impact on the final properties of the cement. An optimum cement composition was hypothesised and tested. This optimum recipe produced cement with final mechanical and thermal properties within the clinical guidelines and stated by ISO 5833 (International Standard Organisation (ISO), International standard 5833: implants for surgery-acrylic resin cements, 2002), however the low setting times observed would not be clinically viable and could result in complications during the surgical technique. As a result further development would be required to improve the setting time of the cement in order for it to be deemed suitable for use in total joint replacement surgery.
10.1007/s10856-014-5260-y
Grant Details