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通过聚合物诱导液相先驱体(PILP)工艺开发类骨复合材料。第 1 部分:聚合物分子量的影响。

Development of bone-like composites via the polymer-induced liquid-precursor (PILP) process. Part 1: influence of polymer molecular weight.

机构信息

Materials Science and Engineering Department, University of Florida, Gainesville, FL 32611-6400, USA.

出版信息

Acta Biomater. 2010 Sep;6(9):3676-86. doi: 10.1016/j.actbio.2010.03.036. Epub 2010 Mar 30.

Abstract

Bone is an organic-inorganic composite consisting primarily of collagen fibrils and hydroxyapatite crystals intricately interlocked to provide skeletal and metabolic functions. Non-collagenous proteins (NCPs) are also present, and although only a minor component, the NCPs are thought to play an important role in modulating the mineralization process. During secondary bone formation, an interpenetrating structure is created by intrafibrillar mineralization of the collagen matrix. Many researchers have tried to develop bone-like collagen-hydroxyapatite (HA) composites via the conventional crystallization process of nucleation and growth. While those methods have been successful in inducing heterogeneous nucleation of HA on the surface of collagen scaffolds, they have failed to produce a composite with the interpenetrating nanostructured architecture of bone. Our group has shown that intrafibrillar mineralization of type I collagen can be achieved using a polymer-induced liquid-precursor (PILP) process. In this process, acidic polypeptides are included in the mineralization solution to mimic the function of the acidic NCPs, and in vitro studies have found that acidic peptides such as polyaspartate induce a liquid-phase amorphous mineral precursor. Using this PILP process, we have been able to prepare collagen-HA composites with the fundamental nanostructure of bone, wherein HA nanocrystals are embedded within the collagen fibrils. This study shows that through further optimization a very high degree of mineralization can be achieved, with compositions matching that of bone. Synthetic collagen sponges were mineralized with calcium phosphate while analyzing various parameters of the reaction, with the focus of this report on the molecular weight of the polymeric process-directing agent. In order to determine whether intrafibrillar mineralization was achieved, an in-depth characterization of the mineralized composites was performed, including wide-angle X-ray diffraction, electron microscopy and thermogravimetric analyses. The results of this work lead us closer to the development of bone-like collagen-HA composites that could become the next generation of synthetic bone grafts.

摘要

骨是一种有机-无机复合材料,主要由胶原纤维和羟基磷灰石晶体交织而成,为骨骼和代谢功能提供支持。非胶原蛋白(NCPs)也存在,尽管它们只是次要成分,但被认为在调节矿化过程中起着重要作用。在二次骨形成过程中,通过胶原基质的纤维内矿化形成了一个互穿结构。许多研究人员试图通过传统的成核和生长结晶过程来开发类骨胶原-羟基磷灰石(HA)复合材料。虽然这些方法已经成功地在胶原支架表面诱导了 HA 的异质成核,但它们未能产生具有骨的互穿纳米结构的复合材料。我们的研究小组已经表明,使用聚合物诱导的液相前体(PILP)过程可以实现 I 型胶原的纤维内矿化。在该过程中,酸性多肽被包含在矿化溶液中以模拟酸性 NCPs 的功能,并且体外研究发现,多天冬氨酸等酸性肽诱导液相无定形矿物前体。使用这种 PILP 过程,我们已经能够制备具有骨基本纳米结构的胶原-HA 复合材料,其中 HA 纳米晶体嵌入在胶原纤维内。这项研究表明,通过进一步优化,可以达到非常高的矿化程度,其组成与骨相匹配。合成胶原海绵用磷酸钙进行矿化,同时分析反应的各种参数,本报告的重点是聚合过程导向剂的分子量。为了确定是否实现了纤维内矿化,对矿化复合材料进行了深入的表征,包括广角 X 射线衍射、电子显微镜和热重分析。这项工作的结果使我们更接近于开发类骨胶原-HA 复合材料,这种复合材料可能成为下一代合成骨移植物。

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