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人成骨细胞在镁取代磷酸三钙致密片剂上的黏附与增殖

Human osteoblasts adhesion and proliferation on magnesium-substituted tricalcium phosphate dense tablets.

作者信息

Sader Marcia S, Legeros Racquel Z, Soares Gloria A

机构信息

Metallurgical and Materials Department, COPPE/UFRJ, Rio de Janeiro, RJ, Brazil.

出版信息

J Mater Sci Mater Med. 2009 Feb;20(2):521-7. doi: 10.1007/s10856-008-3610-3. Epub 2008 Nov 6.

Abstract

Tricalcium phosphate (TCP) is recognized as a promising bone replacement material due to its high bioactivity and resorbable properties. To mimic biological apatites, incorporation of magnesium (Mg) in TCP was proposed. Mg-substituted TCP (beta-TCMP) and beta-TCP dense tablets were obtained by pressing and sintering at 1,000 degrees C Mg-substituted calcium deficient apatite (Mg-CDA) and commercial TCP, respectively. The materials were characterized using X-ray diffraction, infrared spectroscopy and electron microscopy. Human osteoblast cells (SaOs2) were seeded onto the sintered tablets for 4 h, 24 h and 7 days. Results showed that Mg-CDA was completely transformed into beta-TCMP. Moreover, beta-TCMP stimulated adhesion and proliferation of human osteoblast cells. Consequently, the magnesium incorporation on calcium deficient apatites followed by sintering at 1,000 degrees C seems to be a useful path to obtain biocompatible and non cytotoxic dense tablets with TCP structure with potential application on bone engineering.

摘要

磷酸三钙(TCP)因其高生物活性和可吸收特性而被认为是一种很有前景的骨替代材料。为了模拟生物磷灰石,有人提出在TCP中引入镁(Mg)。分别通过在1000℃下压制和烧结Mg取代的缺钙磷灰石(Mg-CDA)和商业TCP,获得了Mg取代的TCP(β-TCMP)和β-TCP致密片。使用X射线衍射、红外光谱和电子显微镜对材料进行了表征。将人成骨细胞(SaOs2)接种到烧结片上4小时、24小时和7天。结果表明,Mg-CDA完全转化为β-TCMP。此外,β-TCMP刺激了人成骨细胞的粘附和增殖。因此,在缺钙磷灰石上引入镁并随后在1000℃下烧结似乎是获得具有TCP结构的生物相容性和无细胞毒性致密片的有用途径,有望应用于骨工程。

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