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多功能可生物降解的聚(丙烯酸)基水凝胶渗透到多孔钛植入物中以改善其生物功能性能。

Versatile Biodegradable Poly(acrylic acid)-Based Hydrogels Infiltrated in Porous Titanium Implants to Improve the Biofunctional Performance.

机构信息

Departamento de Química Orgánica y Farmacéutica, Facultad de Farmacia, Universidad de Sevilla, Seville 41012, Spain.

Departamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad de Sevilla, Seville 41012, Spain.

出版信息

Biomacromolecules. 2023 Nov 13;24(11):4743-4758. doi: 10.1021/acs.biomac.3c00532. Epub 2023 Sep 7.

Abstract

This research work proposes a synergistic approach to improve implants' performance through the use of porous Ti substrates to reduce the mismatch between Young's modulus of Ti (around 110 GPa) and the cortical bone (20-25 GPa), and the application of a biodegradable, acrylic acid-based polymeric coating to reduce bacterial adhesion and proliferation, and to enhance osseointegration. First, porous commercially pure Ti substrates with different porosities and pore size distributions were fabricated by using space-holder techniques to obtain substrates with improved tribomechanical behavior. On the other hand, a new diacrylate cross-linker containing a reduction-sensitive disulfide bond was synthesized to prepare biodegradable poly(acrylic acid)-based hydrogels with 1, 2, and 4% cross-linker. Finally, after the required characterization, both strategies were implemented, and the combination of 4% cross-linked poly(acrylic acid)-based hydrogel infiltrated in 30 vol % porosity, 100-200 μm average pore size, was revealed as an outstanding choice for enhancing implant performance.

摘要

本研究工作提出了一种协同方法,通过使用多孔 Ti 基底来改善植入物的性能,以减少 Ti(约 110GPa)与皮质骨(20-25GPa)之间的杨氏模量不匹配,以及应用可生物降解的、基于丙烯酸的聚合涂层来减少细菌黏附和增殖,并增强骨整合。首先,使用空间占位技术制造了具有不同孔隙率和孔径分布的多孔商用纯 Ti 基底,以获得具有改善摩擦学性能的基底。另一方面,合成了一种含有还原敏感二硫键的新型二丙烯酸酯交联剂,以制备具有 1%、2%和 4%交联剂的可生物降解的聚(丙烯酸)基水凝胶。最后,在进行了所需的表征后,实施了这两种策略,结果表明,4%交联的聚(丙烯酸)基水凝胶在 30vol%孔隙率、100-200μm 平均孔径下的渗透是增强植入物性能的绝佳选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15d9/10646965/33fd2e27e06b/bm3c00532_0001.jpg

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