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Specifications for Innovative, Enabling Biomaterials Based on the Principles of Biocompatibility Mechanisms

机译:基于生物相容性机制原理的创新性生物材料规范

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In any engineering discipline, whenever products are designed, manufactured and ultimately utilized for the benefits of society, a series of specifications for the product are defined, and maybe refined, in order that they perform as effectively as possible, with due attention being paid to the safety and economic aspects. These specifications are established with respect to all of the relevant properties, including those determined by mechanical, physical, chemical, manufacturing and environmental conditions, and the resulting design and materials selection reflects the optimal balance. In areas of medical technology, these specifications should be based on both functionality, which determines whether a device can actually perform as intended, and biocompatibility, which determines how the device interacts, both acutely and chronically, with the body. Unfortunately, whilst so much progress has been made with the development of superior functionality for the treatment and diagnosis of so many disease states, this is not the same for biocompatibility, where the single most-important currently adopted specification is that the device should do no harm, which falls far short of the ideal requirement. This paper addresses the profound need for biomaterials specifications to be based on the mechanisms of biocompatibility.
机译:在任何工程学科中,只要设计,制造并最终使用产品以造福社会,就应定义并完善产品的一系列规格,以使它们尽可能有效地发挥作用,并应引起足够的重视。安全和经济方面。这些规格是针对所有相关属性(包括由机械,物理,化学,制造和环境条件确定的那些属性)建立的,所得到的设计和材料选择反映了最佳的平衡。在医疗技术领域,这些规范应基于功能性和生物相容性,这两个功能性决定了设备是否可以按预期运行,生物相容性则决定了设备与人体的急性和慢性相互作用。不幸的是,尽管在开发和开发用于治疗和诊断许多疾病状态的高级功能方面已取得了很大进展,但对于生物相容性而言却是不一样的,在生物相容性方面,当前采用的最重要的单一规范是该设备不应伤害,远未达到理想要求。本文提出了基于生物相容性机理的对生物材料规格的深刻需求。

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