磷灰石涂层聚l -丙交酯支架修复大鼠颅骨缺损的骨再生效果评价

Q4 Engineering
Kenichirou Yasui, Y. Hashimoto, S. Baba, S. Hontsu, N. Matsumoto
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引用次数: 0

摘要

唇腭裂是一种常见的先天性畸形,由遗传和环境因素共同引起[1,2]。唇裂导致的牙槽骨缺失会导致进食和语言等问题;因此,强烈建议手术闭合[3,4]。自体骨移植治疗唇腭裂已成为修复腭裂部位上颌弓功能和结构的一种广泛接受的治疗方式[5,6]。然而,该手术具有很大的侵入性,可采集的骨量有限。同种异体骨移植物可能传播疾病,并可引起免疫相关并发症。因此,有必要开发一种替代现有骨移植材料的人工合成材料。近年来,聚l -丙交酯(PLLA)因其令人印象深刻的生物相容性、可生物降解性、最小的炎症反应和优异的力学性能而被广泛评价为生物支架材料。然而,已知PLLA由于其疏水性和缺乏细胞识别信号[9]而表现出较差的细胞-物质相互作用。为了促进细胞粘附,人们经常尝试对聚乳酸进行表面改性。磷灰石涂层聚l -丙交酯支架修复大鼠颅骨缺损的骨再生效果评价
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Bone Regeneration of Apatite Coating Poly-L-lactide Scaffold in Rat Calvarial Defects
133 Introduction Cleft lip and palate is a frequently occurring congenital malformation that is caused by genetic and environmental factors [1, 2]. Loss of alveolar bone due to the cleft can lead to problems with feeding and speech, among other difficulties; therefore, surgical closure is strongly recommended [3, 4]. Autogenous bone grafting for patients with cleft lip and palate has become a well-accepted treatment modality to restore the function and structure of the maxillary arch at the cleft site [5, 6]. However, the procedure is very invasive and the amount of collectable bone is limited. Allogeneic bone grafts may transmit diseases and can cause immune-related complications. It is therefore necessary to develop a synthetic alternative to current graft materials for bone regeneration [7]. In recent years, poly(L-lactide) (PLLA) has been widely evaluated as a scaffold biomaterial because of its impressive biocompatibility, biodegradability, minimal inflammatory reaction, and excellent mechanical properties [8]. However, PLLA is known to show poor cell–material interaction because of its hydrophobic nature and lack of cell recognition signals [9]. In order to promote cell adhesion, surface modification of PLLA is often attempted [9]. Evaluation of Bone Regeneration of Apatite Coating Poly-L-lactide Scaffold in Rat Calvarial Defects
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来源期刊
Nano Biomedicine
Nano Biomedicine Engineering-Biomedical Engineering
CiteScore
0.30
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