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不锈钢钉表面涂覆成纤维细胞生长因子-钙磷复合层是否具有抗感染作用?

Do Stainless-Steel Pins Coated with Fibroblast Growth Factor-Calcium Phosphatase Composite Layers Have Anti-Infective Effects?

机构信息

Department of Orthopaedic Surgery, University of Tsukuba, Tsukuba 305-8571, Ibaraki, Japan.

Center for Medical Science, Ibaraki Prefectural University of Health Sciences, Ami 300-0394, Ibaraki, Japan.

出版信息

Medicina (Kaunas). 2024 Aug 30;60(9):1419. doi: 10.3390/medicina60091419.

DOI:10.3390/medicina60091419
PMID:39336460
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11434512/
Abstract

The most problematic complication of external fixation is infection at the pin insertion site. Technology that improves the adhesion of the external fixation pin to the skin, subcutaneous tissue, and bone may prevent infection at the pin site. The purpose of this study is to formulate a calcium phosphate-fibroblast growth factor (Cp-FGF) coating on a stainless-steel external fixation pin and to verify its effectiveness in reducing infection at the pin site and its possible influence on bone fixation in animal experiments. We compared stainless-steel screws without coating (SS group; = 32), those with a calcium phosphate coating (Cp group; = 30), those with a Cp-FGF coating (FGF group; = 32), and those with a Cp-FGF coating having enhanced biological activity (FGF+ group; = 32) in male Japanese white domesticated rabbits. Screws were inserted percutaneously into the bilateral proximal tibial diaphysis of the rabbits and implanted for 4 weeks. Screws and periscrew tissue were observed postoperatively for qualitatively assessing infection. Infection assessment by gross findings after 4 weeks (at screw removal) showed no significant differences between the groups. Histopathological evaluation of soft tissue infection and bone tissue infection showed no significant differences between the groups for either soft tissue or bone tissue. Since neither the FGF+ group nor the FGF group showed anti-infective effects, the biological activity of FGF is not the only determining factor. We compared SEM, XRD, coating detaching test, sustained release test, and bioassay to examine physicochemical properties among the coatings but found no sufficient differences. It is suggested that improving the tissue adhesion to and/or biocompatibility of pins is also important to improve the in vivo performance of Cp-FGF-coated external fixation pins.

摘要

外固定最成问题的并发症是针插入部位的感染。提高外固定针与皮肤、皮下组织和骨骼附着力的技术可能会防止针部位感染。本研究的目的是在不锈钢外固定针上涂覆钙磷-成纤维细胞生长因子(Cp-FGF),并通过动物实验验证其在减少针部位感染方面的有效性及其对骨固定的可能影响。

我们比较了未涂层的不锈钢螺钉(SS 组,n = 32)、钙磷涂层的螺钉(Cp 组,n = 30)、Cp-FGF 涂层的螺钉(FGF 组,n = 32)和具有增强生物学活性的 Cp-FGF 涂层的螺钉(FGF+组,n = 32)在雄性日本白兔中的效果。将螺钉经皮插入双侧胫骨近端骨干,并植入 4 周。术后观察螺钉和螺钉周围组织,定性评估感染情况。

4 周后(螺钉取出时)的大体观察感染评估显示各组之间无显著差异。软组织感染和骨组织感染的组织病理学评估显示,各组软组织和骨组织的感染均无显著差异。由于 FGF+组和 FGF 组均未显示出抗感染作用,因此 FGF 的生物活性不是唯一的决定因素。我们比较了 SEM、XRD、涂层脱落试验、持续释放试验和生物测定,以检查涂层之间的理化性质,但未发现足够的差异。

提示提高钉的组织附着力和/或生物相容性对于改善 Cp-FGF 涂层外固定钉的体内性能也很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/402b1949b36e/medicina-60-01419-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/c5ef40f51b0d/medicina-60-01419-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/7de3bebc623d/medicina-60-01419-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/88760bb2ff35/medicina-60-01419-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/2dcc5c91e85b/medicina-60-01419-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/f06d68c2ef20/medicina-60-01419-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/bc477995ce51/medicina-60-01419-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/01548bb3eb56/medicina-60-01419-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/3522e75410ed/medicina-60-01419-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/402b1949b36e/medicina-60-01419-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/c5ef40f51b0d/medicina-60-01419-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/1f75a4ec439f/medicina-60-01419-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/4d41abb66a5d/medicina-60-01419-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/7de3bebc623d/medicina-60-01419-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/88760bb2ff35/medicina-60-01419-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/2dcc5c91e85b/medicina-60-01419-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/f06d68c2ef20/medicina-60-01419-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/bc477995ce51/medicina-60-01419-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/01548bb3eb56/medicina-60-01419-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/3522e75410ed/medicina-60-01419-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f60/11434512/402b1949b36e/medicina-60-01419-g011.jpg

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