Nano-TiO2 Reinforced PEEK/PEI Blends as Biomaterials for Load-Bearing Implant Applications

被引:186
作者
Diez-Pascual, Ana M. [1 ]
Diez-Vicente, Angel L. [2 ]
机构
[1] Univ Alcala de Henares, Fac Biol Environm Sci & Chem, Analyt Chem Phys Chem & Chem Engn Dept, E-28871 Alcala De Henares, Madrid, Spain
[2] Airbus Operat SL, Madrid 28906, Spain
关键词
PEEK/PEI blends; biocomposites; TiO2; nanoparticles; antimicrobials; load-bearing implants; MECHANICAL-PROPERTIES; TIO2; NANOPARTICLES; PERFORMANCE; BEHAVIOR; NANOCOMPOSITES; TITANIUM; POLY(ETHERETHERKETONE); BIONANOCOMPOSITES; RELAXATION; KINETICS;
D O I
10.1021/acsami.5b00210
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
Biocompatible ternary nanocomposites based on poly(ether ether ketone) (PEEK)/poly(ether imide) (PEI) blends reinforced with bioactive titanium dioxide (TiO2) nanoparticles were fabricated via ultrasonication followed by melt-blending. The developed biomaterials were characterized using FT-IR, SEM, XRD, DSC, TGA, and DMA. Further, their water-absorption, tensile, tribological, dielectric, and antibacterial properties were evaluated. PEI acts as a coupling agent, since it can interact both with PEEK via pi-pi stacking and polar interactions as well as with the nanoparticles through hydrogen bonding, as corroborated by the FT-IR spectra, which resulted in a homogeneous titania dispersion within the biopolymer blend without applying any particle surface treatment or polymer functionalization. A change from promotion to retardation in the crystallization rate of the matrix was found with increasing TiO2 concentration, while its crystalline structure remained unaltered. The nanoparticles stiffened, strengthened, and toughened the matrix simultaneously, and the optimal properties were achieved at 4.0 wt % TiO2. More interesting, the tensile properties were retained after steam sterilization in an autoclave or exposure to a simulated body fluid (SBF). The nanocomposites also displayed reduced water absorption though higher thermal stability, storage modulus, glass transition temperature, dielectric constant, and dielectric loss compared to the control blend. Further, remarkable enhancements in the tribological properties under both SBF and dry environments were attained. The nanoparticles conferred antibacterial action versus Gram-positive and Gram-negative bacteria in the presence and the absence of UV light, and the highest inhibition was attained at 4.0 wt % nanoparticle concentration. These nanocomposites are expected to be used in long-term load-bearing implant applications.
引用
收藏
页码:5561 / 5573
页数:13
相关论文
共 57 条
[1]
Tensile properties, tension-tension fatigue and biological response of polyetheretherketone-hydroxyapatite composites for load-bearing orthopedic implants [J].
Abu Bakar, MS ;
Cheng, MHW ;
Tang, SM ;
Yu, SC ;
Liao, K ;
Tan, CT ;
Khor, KA ;
Cheang, P .
BIOMATERIALS, 2003, 24 (13) :2245-2250
[2]
Albertin K., 2007, J. Int. Cir. Syst, P89, DOI [10.29292/jics.v2i2.272, DOI 10.29292/JICS.V2I2.272]
[3]
Alexander LE., 1969, X-ray Diffraction Methods in Polymer Scienc
[4]
Amini Ami R, 2011, J Long Term Eff Med Implants, V21, P93
[5]
[Anonymous], 1998, Handbook of biomaterial properties, thermoplastic polymers in biomedical applications: Structures, Properties and Processing, DOI DOI 10.1007/978-1-4615-5801-9_19
[6]
[Anonymous], INFRARED SPECTRA INO
[7]
Fabrication and Properties of High Performance PEEK/Si3N4 Nanocomposites [J].
Balaji, V. ;
Tiwari, A. N. ;
Goyal, R. K. .
JOURNAL OF APPLIED POLYMER SCIENCE, 2011, 119 (01) :311-318
[8]
Tribological investigation of the effects of particle size, loading and crystallinity on poly(ethylene) terephthalate nanocomposites [J].
Bhimaraj, Praveen ;
Burris, David ;
Sawyer, W. Gregory ;
Toney, C. Gregory ;
Siegel, Richard W. ;
Schadler, Linda S. .
WEAR, 2008, 264 (7-8) :632-637
[9]
FRICTION AND WEAR STUDIES OF BULK POLYETHERIMIDE [J].
BIJWE, J ;
TEWARI, US ;
VASUDEVAN, P .
JOURNAL OF MATERIALS SCIENCE, 1990, 25 (1B) :548-556
[10]
Bacterial cell shape [J].
Cabeen, MT ;
Jacobs-Wagner, C .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (08) :601-610