Additively Manufactured and Surface Biofunctionalized Porous Nitinol

被引:85
作者
Karaji, Z. Gorgin [1 ,3 ]
Speirs, M. [4 ]
Dadbakhsh, S. [4 ]
Kruth, J. -P. [4 ]
Weinans, H. [1 ,2 ,5 ]
Zadpoor, A. A. [5 ]
Yavari, S. Amin [1 ,5 ]
机构
[1] Univ Med Ctr Utrecht, Dept Orthoped, NL-3584 CX Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Rheumatol, NL-3584 CX Utrecht, Netherlands
[3] Kermanshah Univ Technol, Dept Mech Engn, Kermanshah 6376667178, Iran
[4] Katholieke Univ Leuven, PMA Div, Dept Mech Engn, B-3001 Leuven, Belgium
[5] Delft Univ Technol, Dept Biomech Engn, NL-2628 CD Delft, Netherlands
关键词
shape memory alloys; additive manufacturing; biomimetic topology; osteogenic coatings; controlled release; BONE TISSUE REGENERATION; SHAPE-MEMORY ALLOYS; IMPLANT OSSEOINTEGRATION; SCAFFOLD DESIGN; EFFECTIVE IMMOBILIZATION; MORPHOGENETIC PROTEIN-2; TITANIUM BIOMATERIALS; BEHAVIOR; RECONSTRUCTION; POLYDOPAMINE;
D O I
10.1021/acsami.6b14026
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Enhanced bone tissue regeneration and improved osseointegration are among the most important goals in design of multifunctional orthopedic biomaterials. In this study, we used additive manufacturing (selective laser melting) to develop multifunctional porous nitinol that combines superelasticity with a rationally designed microarchitecture and biofunctionalized surface. The rational design based on triply periodic minimal surfaces aimed to properly adjust the pore size), increase the surface area (thereby amplifying-the effects of surface biofunctionalization), and resemble the curvature characteristics of trabecular bone. The surface of additively manufactured (AM) porous:nitinol was biofunctionalized using polydopamine-immobilized rhBMP2 for better control of the release kinetics. The actual morphological properties of porous nitinol measured by microcomputed tomography (e.g., open/close porosity, and surface area) closely matched the design values. The superelasticity originated from the austenite phase formed in, the nitinol porous structure at room temperature. Polydopamine and rhBMP2 signature-peaks were confirmed by X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy tests. The release,of rhBMP2 continued until 28 days. The early time and long-term release profiles were found to be adjustable independent of each other; In vitro cell culture showed improved cell attachment, cell proliferation) cell morphology (spreading, spindle-like shape), and cell coverage as well as elevated levels of ALP activity and increased calcium content for biofunctionalized surfaces as compared to as-manufactured specimens. The demonstrated functionalities of porous nitinol-could be used as a basis for deployable orthopedic implants with rationally, designed microarchitectures that maximize bone tissue regeneration performance by release of biomolecules with adjustable and well-Controlled release profiles.
引用
收藏
页码:1293 / 1304
页数:12
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