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用于抗感染和无色素沉着骨组织工程的磷酸银改性碳酸磷灰石蜂窝支架

Silver phosphate-modified carbonate apatite honeycomb scaffolds for anti-infective and pigmentation-free bone tissue engineering.

作者信息

Hayashi Koichiro, Shimabukuro Masaya, Zhang Cheng, Taleb Alashkar Ahmad Nazir, Kishida Ryo, Tsuchiya Akira, Ishikawa Kunio

机构信息

Department of Biomaterials, Faculty of Dental Science, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 2-3-10, Kanda-Surugadai, Chiyoda-ku, Tokyo, 101-0062, Japan.

出版信息

Mater Today Bio. 2024 Jul 18;27:101161. doi: 10.1016/j.mtbio.2024.101161. eCollection 2024 Aug.

DOI:10.1016/j.mtbio.2024.101161
PMID:39155941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11326936/
Abstract

Bone regeneration using synthetic materials has a high rate of surgical site infection, resulting in severe pain for patients and often requiring revision surgery. We propose AgPO-based surface modification and structural control of scaffolds for preventing infections in bone regeneration. We demonstrated the differences in toxicity and antibacterial activity between in vitro and in vivo studies and determined the optimal silver content in terms of overall anti-infection effects, bone regeneration, toxicity, and pigmentation. A honeycomb structure comprising osteoconductive and resorbable carbonate apatite (CAp) was used as the base scaffold. CAp in the scaffold surface was partially replaced with different concentrations of AgPO via controlled dissolution-precipitation reactions in an AgNO solution. Both bone regeneration and infection prevention were achieved at 860-2300 ppm of silver. Despite the absence of AgPO, honeycomb scaffolds were less susceptible to infection, even under conditions where infection occurs in clinically used three-dimensional porous scaffolds. Regardless of in vitro cytotoxicity at >5200 ppm of silver, increasing the silver content to 21,000 ppm did not adversely affect in vivo bone formation and scaffold resorption or cause acute systemic toxicity. Rather, bone formation was enhanced with 5200 ppm of silver. However, pigmentation was observed at that concentration. Hence, we concluded that the optimal silver concentration range is 860-2300 ppm for anti-infective and pigmentation-free bone regeneration. Bone regeneration was achieved via surface modification, resulting in the rapid release of silver ions immediately after implantation, followed by gradual release over several months. The scaffold structure may also aid in preventing bacterial growth within the scaffolds.

摘要

使用合成材料进行骨再生时手术部位感染率很高,给患者带来剧痛,且常常需要进行翻修手术。我们提出基于AgPO的支架表面改性和结构控制以预防骨再生中的感染。我们展示了体外和体内研究在毒性和抗菌活性方面的差异,并根据总体抗感染效果、骨再生、毒性和色素沉着确定了最佳银含量。一种包含具有骨传导性和可吸收性的碳酸磷灰石(CAp)的蜂窝结构被用作基础支架。通过在AgNO溶液中进行受控的溶解 - 沉淀反应,支架表面的CAp被不同浓度的AgPO部分取代。在银含量为860 - 2300 ppm时实现了骨再生和感染预防。尽管不存在AgPO,但蜂窝支架即使在临床使用的三维多孔支架发生感染的条件下也较不易感染。无论银含量>5200 ppm时的体外细胞毒性如何,将银含量增加到21,000 ppm对体内骨形成和支架吸收没有不利影响,也不会引起急性全身毒性。相反,5200 ppm的银促进了骨形成。然而,在该浓度下观察到了色素沉着。因此,我们得出结论,对于抗感染且无色素沉着的骨再生,最佳银浓度范围是860 - 2300 ppm。通过表面改性实现了骨再生,植入后银离子立即快速释放,随后在几个月内逐渐释放。支架结构也可能有助于防止细菌在支架内生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/5ba965715709/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/c41923f45cd6/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/5080029c4133/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/e9ee365849f5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/e656f891080b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/ef3ec78754d1/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/eb9b078ba23c/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/11c1e2143994/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/0c16b3207999/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/0ce018e4f8ec/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/5ba965715709/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/c41923f45cd6/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/5080029c4133/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/e9ee365849f5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/e656f891080b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/ef3ec78754d1/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/eb9b078ba23c/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/11c1e2143994/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/0c16b3207999/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/0ce018e4f8ec/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d610/11326936/5ba965715709/gr9.jpg

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