软骨组织与胶原生物材料的激光焊接(体外研究)。

Sovremennye tekhnologii v meditsine Pub Date : 2023-01-01 Epub Date: 2023-12-27 DOI:10.17691/stm2023.15.6.04
N Yu Ignatieva, O L Zakharkina, A P Sviridov
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引用次数: 0

摘要

本研究的目的是评估激光焊接生物组织和材料的有效性,白蛋白焊料在完整的和化学修饰的猪鼻中隔软骨关节上进行大量加热。材料和方法:焊接材料为猪鼻中隔软骨和完整软骨,经双胰蛋白酶和甘油醛处理的钢板。25%的白蛋白溶液作为焊料。用波长为1.56 μm和1.68 μm的激光通过光纤加热结。该过程使用数字USB显微镜进行监测。材料焊接后,对样品进行力学测试,并测定焊料附近区域完整胶原蛋白的比例。利用热成像仪记录了激光照射区域温度场的动态变化。结果:在波长为1.68 μm /1.56 μm的激光照射下,连续应用两层/三层焊料进行激光加热,可有效焊接软骨组织与胶原生物材料。当λ=1.68 μm时,焊接层的激光功率密度为0.7/0.8 W/mm2(平均表面温度~85℃);当λ=1.56 μm时,焊接层的激光功率密度为1.77/1.34/0.96 W/mm2(平均表面温度~100℃)。当λ=1.56 μm时,焊接试样的抗拉强度达到完整软骨抗拉强度的12%,当λ=1.68 μm时,焊接试样的抗拉强度达到15%。在靠近第一层白蛋白的组织区域,约300 μm厚度的胶原网络被破坏。在其他区域,胶原蛋白主要被保存下来。结论:在λ=1.56 μm和λ=1.68 μm的辐射下,激光焊接化学修饰完好的软骨,不仅被焊料吸收,而且被组织吸收。然而,为了使退化面积最小化,有必要使激光光斑的直径和结构与完整软骨之间的焊料填充腔的大小相匹配。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Laser Soldering of Cartilage Tissue to Collagenous Biomaterial (an <i>in vitro</i> Study).

Laser Soldering of Cartilage Tissue to Collagenous Biomaterial (an <i>in vitro</i> Study).

Laser Soldering of Cartilage Tissue to Collagenous Biomaterial (an <i>in vitro</i> Study).

Laser Soldering of Cartilage Tissue to Collagenous Biomaterial (an in vitro Study).

The aim of the study was to assess the effectiveness of laser soldering of biological tissues and materials for bulk heating of albumin solder on the joints of the intact and chemically modified cartilage of the porcine nasal septum.

Materials and methods: The materials for soldering were double-trypsinized and glyceraldehyde-treated plates made from cartilage of the porcine nasal septum, and intact cartilage. A 25% albumin solution was used as a solder. The junction was heated by laser radiation with the wavelengths of 1.56 and 1.68 μm through an optical fiber. The process was monitored using a digital USB microscope. After the materials were soldered, mechanical tests of the samples were conducted, and the fraction of intact collagen in the areas adjacent to the solder was determined. A thermal imager was used to record the dynamics of the temperature field in the area of laser exposure.

Results: The effective soldering of cartilage tissue with collagenous biomaterial occurs with sequential application and laser heating of two/three layers of solder for radiation with wavelengths of 1.68/1.56 μm, respectively. The laser power densities for the solder layers were 0.7/0.8 W/mm2 (the average surface temperature ~85°C) for λ=1.68 μm and 1.77/1.34/0.96 W/mm2 (the average surface temperature ~100°C) for λ=1.56 μm. The tensile strength of the soldered samples reached ~12% for λ=1.56 μm and ~15% for λ=1.68 μm of the tensile strength of intact cartilage. In the tissue areas adjacent to the first layer of albumin, at a thickness of ~300 μm, most of the collagen network was destroyed. In other areas, collagen was predominantly preserved.

Conclusion: Laser soldering of chemically modified and intact cartilages can be effectively conducted using radiation of λ=1.56 μm and λ=1.68 μm, absorbed not only by the solder, but also by the tissue. However, to minimize the area of degradation, it is necessary to match the diameter of the laser spot and the size of the solder-filled cavity between the construction and the intact cartilage.

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