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Cartilage-like mechanical properties of poly (ethylene glycol)-diacrylate hydrogels

机译:聚(乙二醇) - 二氧丙酯水凝胶的软骨状机械性能

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摘要

Hydrogels prepared from poly-(ethylene glycol) (PEG) have been used in a variety of studies of cartilage tissue engineering. Such hydrogels may also be useful as a tunable mechanical material for cartilage repair. Previous studies have characterized the chemical and mechanical properties of PEG-based hydrogels, as modulated by precursor molecular weight and concentration. Cartilage mechanical properties vary substantially, with maturation, with depth from the articular surface, in health and disease, and in compression and tension. We hypothesized that PEG hydrogels could mimic a broad range of the compressive and tensile mechanical properties of articular cartilage. The objective of this study was to characterize the mechanical properties of PEG hydrogels over a broad range and with reference to articular cartilage. In particular, we assessed the effects of PEG precursor molecular weight (508 Da, 3.4 kDa, 6 kDa, and 10 kDa) and concentration (10–40%) on swelling property, equilibrium confined compressive modulus (HA0), compressive dynamic stiffness, and hydraulic permeability (kp0) of PEG hydrogels in static/dynamic confined compression tests, and equilibrium tensile modulus (Eten) in tension tests. As molecular weight of PEG decreased and concentration increased, hydrogels exhibited a decrease in swelling ratio (31.5–2.2), an increase in HA0 (0.01–2.46 MPa) and Eten (0.02–3.5 MPa), an increase in dynamic compressive stiffness (0.055–42.9 MPa), and a decrease in kp0 (1.2 × 10−15 to 8.5 × 10−15 m2/(Pa s)). The frequency-dependence of dynamic compressive stiffness amplitude and phase, as well as the strain-dependence of permeability, were typical of the time- and strain-dependent mechanical behavior of articular cartilage. HA0 and Eten were positively correlated with the final PEG concentration, accounting for swelling. These results indicate that PEG hydrogels can be prepared to mimic many of the static and dynamic mechanical properties of articular cartilage.
机译:由聚 - (乙二醇)(PEG)制备的水凝胶已用于软骨组织工程的各种研究中。这种水凝胶也可用作用于软骨修复的可调谐机械材料。以前的研究表征了PEG的水凝胶的化学和力学性能,如前体分子量和浓度的调节。软骨机械性能随着效果而变化,深度从关节表面,健康和疾病,以及压缩和张力。我们假设PEG水凝胶可以模仿关节软骨的广泛的压缩和拉伸力学性能。本研究的目的是在宽范围内表征PEG水凝胶的机械性能,并参考关节软骨。特别地,我们评估了PEG前体分子量(508〜3.4kDa,6kDa和10kDa)和浓度(10-40%)对溶胀性的影响,平衡限制压缩模量(HA0),压缩动态刚度,静电/动态狭窄压缩试验中PEG水凝胶的液压渗透率(KP0),张力试验中的平衡拉伸模量(ETEN)。由于PEG的分子量降低和浓度增加,水凝胶表现出溶胀比(31.5-2.2)的降低,HA0(0.01-2.46MPa)和ETEN(0.02-3.5MPa)的增加,动态压缩刚度增加(0.055 -42.9MPa),KP0的减少(1.2×10 -15 至8.5×10 -15 m 2 /(pa s) )。动态压缩刚度幅度和相的频率依赖性以及渗透性的应变依赖性是典型的关节软骨的时间和应变依赖性机械行为的典型。 Ha0和Eten与最终PEG浓度呈正相关,核算肿胀。这些结果表明,可以制备PEG水凝胶以模仿关节软骨的许多静态和动态的机械性能。

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