Mechanical and Bioactive Properties of PMMA Bone Cement: A Review

被引:6
|
作者
Seesala, Venkata Sundeep [1 ]
Sheikh, Lubna [1 ]
Basu, Bikramjit [2 ]
Mukherjee, Subrata [1 ]
机构
[1] Tata Steel Ltd, Res & Dev Div, Adv Mat & Characterizat Grp, Jamshedpur 831001, India
[2] Indian Inst Sci, Mat Res Ctr, Lab Biomat, Bengaluru 560012, India
来源
关键词
poly(methyl methacrylate); bioactive fillers; mechanical properties; antibacterial properties; viscosity; IN-VITRO BIOCOMPATIBILITY; POLY(METHYL METHACRYLATE); BIOLOGICAL-PROPERTIES; GRAPHENE OXIDE; ANTIBACTERIAL ACTIVITY; SURFACE MODIFICATION; SETTING PROPERTIES; DENTURE BASE; HYDROXYAPATITE; COMPOSITE;
D O I
10.1021/acsbiomaterials.4c00779
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Over the past few decades, poly(methyl methacrylate) (PMMA) based bone cement has been clinically used extensively in orthopedics for arthroplasty and kyphoplasty, due to its biocompatibility and excellent primary fixation to the host bone. In this focused review, we discuss the use of various fillers and secondary chemical moieties to improve the bioactivity and the physicochemical properties. The viscosity of the PMMA blend formulations and working time are crucial to achieving intimate contact with the osseous tissue, which is highly sensitive to organic or inorganic fillers. Hydroxyapatite as a reinforcement resulted in compromised mechanical properties of the modified cement. The possible mechanisms of the additive- or filler-dependent strengthening or weakening of the PMMA blend are critically reviewed. The addition of layered double hydroxides with surface functionalization appears to be a promising approach to enhance the bonding of filler with the PMMA matrix. Such an approach consequently improves the mechanical properties, owing to enhanced dispersion as well as contributions from crack bridging. Finally, the use of emerging alternatives, such as nanoparticles, and the use of natural biomolecules were highlighted to improve bioactivity and antibacterial properties.
引用
收藏
页码:5939 / 5959
页数:21
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