Biocompatibility of an interspinous implant made of titanium alloys

V. Orlov, Y. Nashchekina, A. Nashchekin, O. N. Ozeryanskaya, S. D. Mirzametov, D. Svistov
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Abstract

BACKGROUND: At present, metal implants are widely used in neuro-orthopedics, of which titanium alloys are of particular interest. A team of authors developed an original combined implant for posterior spinal fusion as an import substitution, which can be used from one-way access during minimally invasive operations on the lumbar spine. The implant was manufactured at the Endocarbon Enterprise in Penza. For better osseointegration, it is made of VT6 alloy and titanium nickelide. The middle part of the implant is laser-treated to create an uneven surface in the hope of better integration in the tissues of the body. This study was conducted to assess the cytotoxicity and biocompatibility of this implant for its further application in clinical practice. AIM: To determine the cytotoxicity of an interspinous implant made of titanium alloys for its further introduction into spinal surgery. MATERIALS AND METHODS: To determine the cytotoxicity of titanium samples of interspinous implants, a methyltetrazolium test was conducted to assess the viability of stromal cells in the presence of a nutrient medium after incubation with the test material. The biocompatibility of the material was analyzed using scanning electron microscopy of samples 1 and 7 days after cell culture. RESULTS: The viability of cells cultured in the presence of a nutrient medium after incubation with samples of titanium VT6 was 105% and that of titanium nickelide was 98%, which were comparable to the viability of cells in a standard nutrient medium. With electron microscopy, after 1 day of cultivation, cells form a monolayer on a titanium surface, all cells were well spread out and formed intercellular contacts, and after 7 days of cultivation, the number of cells increased and they formed a dense monolayer. CONCLUSIONS: The interspinous implant, which includes alloys of titanium VT6 and titanium nickelide, is biocompatible with cultured cells and can be introduced into spinal surgery.
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钛合金棘间植入物的生物相容性
背景:目前,金属植入物在神经矫形术中应用广泛,其中钛合金尤其受到关注。一组作者开发了一种用于后路脊柱融合的原始联合植入物作为进口替代,可用于腰椎微创手术的单向通道。植入物是在奔萨岛的内碳企业制造的。为了更好的骨整合,它是由VT6合金和镍化钛制成的。植入物的中间部分经过激光处理,形成凹凸不平的表面,希望能更好地与身体组织融合。本研究旨在评估该植入物的细胞毒性和生物相容性,为其进一步的临床应用奠定基础。目的:确定钛合金棘间植入物的细胞毒性,为其在脊柱外科手术中的进一步应用奠定基础。材料和方法:为了确定棘间植入物钛样品的细胞毒性,采用甲基四氮唑试验来评估基质细胞在营养培养基存在下与试验材料孵育后的活力。细胞培养后第1天和第7天,用扫描电镜分析材料的生物相容性。结果:VT6钛样品与镍化钛样品孵育后,在营养培养基中培养的细胞存活率为105%,镍化钛样品的细胞存活率为98%,与标准营养培养基中的细胞存活率相当。电镜观察,培养1 d后,细胞在钛表面形成单层,所有细胞分布良好,形成细胞间接触,培养7 d后,细胞数量增加,形成致密的单层。结论:由VT6钛和镍化钛合金组成的棘间植入物与培养细胞具有生物相容性,可用于脊柱外科手术。
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来源期刊
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.50
自引率
0.00%
发文量
38
期刊介绍: The target audience of the journal is researches, physicians, orthopedic trauma, burn, and pediatric surgeons, anesthesiologists, pediatricians, neurologists, oral surgeons, and all specialists in related fields of medicine.
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