Vida Khalili, Sannakaisa Virtanen, Aldo R. Boccaccini
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引用次数: 0
Abstract
In contemporary orthopedics, the demand for temporary biodegradable bone implants has driven the development of materials capable of supporting bone regeneration while gradually resorbing in the body, thereby eliminating the need for secondary removal surgery. Magnesium (Mg) and its alloys have emerged as promising candidates due to their bioactivity, osteoconductivity, and mechanical properties that closely match those of natural bone. Furthermore, the release of Mg2+ ions during degradation has been shown to stimulate osteoblast activity and enhance bone remodeling. Despite the advantages associated with Mg as a bone implant, there are also constraints on its clinical application. The elevated pH values inherent to the Mg corrosion process may adversely affect biocompatibility, in addition to general concerns about the burst release of H2 gas that originates from the cathodic reaction of Mg corrosion. To address these challenges, biomimetic surface modifications have emerged as a promising strategy to modulate the degradation behavior of Mg and its alloys. In particular, Dulbecco's Modified Eagle Medium (DMEM) cell culture medium serves as an effective biomimetic environment for forming corrosion-resistant layers on Mg-based implants, maintaining physiological pH and mimicking in vivo degradation behavior by facilitating the formation of a carbonated Ca/Mg-phosphate layer with superior resistance to Cl− attack compared to Mg(OH)2. Immersion in DMEM has been shown to induce the formation of calcium phosphate rich protective layers that mimic the natural bone environment and mitigate the rapid biodegradation of Mg and its alloys. This paper provides a review of recent advancements in DMEM modification of Mg-based alloys, including ex situ and in situ formation of protective layers, and in vitro biocorrosion behavior in cell culture medium. Key findings emphasize that synthetic buffers like Tris/HCl and HEPES accelerate corrosion and hinder calcium phosphate formation, while protein-rich media risk contamination during prolonged use. Additionally, electrostatic interactions in DMEM promote hydroxyapatite crystallization, functionalized intermediate layers enhance calcium phosphate deposition, and fluid dynamics must be carefully controlled to stabilize the protective layer. Despite recent progress, key knowledge gaps remain, including limited understanding of the long-term performance and mechanical stability of biomimetic layers under dynamic physiological conditions, as well as the unclear impact of complex in vivo factors like immune responses and enzymatic activity on their degradation.
在当代骨科中,对临时可生物降解骨植入物的需求推动了能够支持骨再生同时在体内逐渐吸收的材料的发展,从而消除了对二次移除手术的需要。镁(Mg)及其合金因其生物活性、骨导电性和力学性能与天然骨非常接近而成为有希望的候选者。此外,降解过程中Mg2+离子的释放已被证明可以刺激成骨细胞活性并增强骨重塑。尽管镁作为骨植入物有其优点,但其临床应用也存在限制。Mg腐蚀过程中固有的pH值升高可能会对生物相容性产生不利影响,此外人们还担心Mg腐蚀的阴极反应会产生氢气的爆裂释放。为了解决这些挑战,仿生表面修饰已经成为一种有前途的策略来调节Mg及其合金的降解行为。特别是,Dulbecco的Modified Eagle Medium (DMEM)细胞培养基作为一种有效的仿生环境,可以在镁基植入物上形成耐腐蚀层,维持生理pH值,并通过促进碳酸化Ca/Mg-磷酸盐层的形成,模拟体内降解行为,与Mg(OH)2相比,该层具有更强的抗Cl -侵蚀能力。研究表明,浸泡在DMEM中可以诱导形成富含磷酸钙的保护层,模拟自然骨环境,减缓Mg及其合金的快速生物降解。本文综述了DMEM改性镁基合金的最新进展,包括非原位和原位保护层的形成,以及在细胞培养基中的体外生物腐蚀行为。主要研究结果强调,合成缓冲剂如Tris/HCl和HEPES加速腐蚀并阻碍磷酸钙的形成,而富含蛋白质的介质在长期使用过程中有污染风险。此外,DMEM中的静电相互作用促进羟基磷灰石结晶,功能化中间层促进磷酸钙沉积,必须仔细控制流体动力学以稳定保护层。尽管最近取得了进展,但关键的知识差距仍然存在,包括对动态生理条件下仿生层的长期性能和机械稳定性的了解有限,以及免疫反应和酶活性等复杂体内因素对其降解的影响尚不清楚。
期刊介绍:
Journal of Biomedical Materials Research – Part B: Applied Biomaterials is a highly interdisciplinary peer-reviewed journal serving the needs of biomaterials professionals who design, develop, produce and apply biomaterials and medical devices. It has the common focus of biomaterials applied to the human body and covers all disciplines where medical devices are used. Papers are published on biomaterials related to medical device development and manufacture, degradation in the body, nano- and biomimetic- biomaterials interactions, mechanics of biomaterials, implant retrieval and analysis, tissue-biomaterial surface interactions, wound healing, infection, drug delivery, standards and regulation of devices, animal and pre-clinical studies of biomaterials and medical devices, and tissue-biopolymer-material combination products. Manuscripts are published in one of six formats:
• original research reports
• short research and development reports
• scientific reviews
• current concepts articles
• special reports
• editorials
Journal of Biomedical Materials Research – Part B: Applied Biomaterials is an official journal of the Society for Biomaterials, Japanese Society for Biomaterials, the Australasian Society for Biomaterials, and the Korean Society for Biomaterials. Manuscripts from all countries are invited but must be in English. Authors are not required to be members of the affiliated Societies, but members of these societies are encouraged to submit their work to the journal for consideration.