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The development of highly effective bio‐lubricant coatings for arthritis treatment is extremely demanded. Herein, inspired by the efficient lubrication of articular cartilage, acrylic acid (AA) with (3‐(methacryloylamino) propyl) dimethyl (3‐sulfopropyl) ammonium hydroxide (MPDSAH) hydrogel coatings containing nanoparticles on Ti6Al4V substrate were designed and fabricated via UV grafting technology. SiO2 and SiO2 grafted with PAA polymer brushes (SiO2‐g‐PAA) were separately doped into the PAA‐PMPDSAH hydrogel. The PAA‐PMPDSAH/SiO2‐g‐PAA exhibits good tensile and compressive properties compared with PAA‐PMPDSAH/SiO2 hydrogel, with an enhancement of 183.4% in tensile modulus and 60.8% in compressive modulus. The PAA‐PMPDSAH/SiO2‐g‐PAA hydrogel coatings exhibit a low wear volume, 2.9 ± 0.16 × 106 μm3, representing a decline of 32.1% and 61.3% compared with the PAA‐PMPDSAH and PAA‐PMPDSAH/SiO2 hydrogel coatings, respectively. The antiwear performance has obviously improved. The hydrophilic PAA polymer brushes prevent the agglomeration of nanoparticles and promote homogeneously dispersion within the hydrogel. The three‐dimensional crosslinked network structure of hydrogel effectively protects the structural integrity of the polymer brushes, thereby facilitating enduring lubrication properties. This work provides a strategy for promising artificial joint lubrication in biomedical fields. [ABSTRACT FROM AUTHOR]

The development of coatings with efficient lubrication and load-bearing capacity is an urgent need for artificial joints. Here, we successfully fabricated poly (acrylic acid-co-acrylamide)/polyethyleneimine (P(AA-co-AAm)/PEI) coating on titanium alloy (Ti6Al4V) surface via UV irradiation and thermal treatment technique. The dual crosslinked network structures were composed of a P(AA-co-AAm) network via free radical polymerization and a PAA-co-PEI network via thermal crosslinking of amine and carboxyl groups. The thermally crosslinked P(AA-co-AAm)/PEI coatings exhibit a stable low friction coefficient (approximately 0.022) and exceptionally low wear volume, with a 93.8% and 92.6% reduction, respectively, in comparison to the pristine Ti6Al4V. These thermally crosslinked P(AA-co-AAm)/PEI hydrogel coatings exhibit excellent lubrication and anti-wear properties, providing a strategy for developing novel lubricating coatings in the biomedical field. [ABSTRACT FROM AUTHOR]

Natural joints have the hierarchical structure of bone and cartilage, providing excellent lubrication and load-carrying capacity. In our research, the hierarchical structure artificial joints of Poly Acrylic Acid (PAA)- Poly Acrylamide (PAAm) hydrogel coating and Ti6Al4V substrate were formed using a simple yet versatile method by mimicking the hierarchical structure of natural joints. The efficient lubrication at friction interfaces was achieved. The composition and microstructure were confirmed by Fourier-transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), Scanning electron microscopy (SEM). The hydrogel coatings were successfully prepared on the surface of Ti6Al4V substrate through the adsorption of the charged group. This hierarchical structure material exhibits the lower dynamic friction, approximately 0.085, which is much lower than bare Ti6Al4V, about 0.429. The wear on the surfaces after the tribological experiment is super-shallow and has no significant fracture area around the scratch. The PAA-PAAm hydrogel has a more uniform and compact cross-linked network porous structure, and the porous size is much smaller than PAA hydrogel. The cross-linked network porous structure is the main factor accounting for the low dynamic friction. This hierarchical structure of soft and hard improve the load-carrying ability and has the potential uses in artificial joints. [ABSTRACT FROM AUTHOR]