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功能化聚己内酯/羟基磷灰石纳米复合材料作为用于骨再生的微孔膜

Functionalized PCL/HA nanocomposites as microporous membranes for bone regeneration.

作者信息

Basile Maria Assunta, d'Ayala Giovanna Gomez, Malinconico Mario, Laurienzo Paola, Coudane Jean, Nottelet Benjamin, Ragione Fulvio Della, Oliva Adriana

机构信息

Institute for Polymers, Composites and Biomaterials, CNR, Via Campi Flegrei 34, Pozzuoli (Naples), Italy.

Institute for Polymers, Composites and Biomaterials, CNR, Via Campi Flegrei 34, Pozzuoli (Naples), Italy.

出版信息

Mater Sci Eng C Mater Biol Appl. 2015 Mar;48:457-68. doi: 10.1016/j.msec.2014.12.019. Epub 2014 Dec 9.

Abstract

In the present work, microporous membranes based on poly(ε-caprolactone) (PCL) and PCL functionalized with amine (PCL-DMAEA) or anhydride groups (PCL-MAGMA) were realized by solvent-non solvent phase inversion and proposed for use in Guided Tissue Regeneration (GTR). Nanowhiskers of hydroxyapatite (HA) were also incorporated in the polymer matrix to realize nanocomposite membranes. Scanning Electron Microscopy (SEM) showed improved interfacial adhesion with HA for functionalized polymers, and highlighted substantial differences in the porosity. A relationship between the developed porous structure of the membrane and the chemical nature of grafted groups was proposed. Compared to virgin PCL, hydrophilicity increases for functionalized PCL, while the addition of HA influences significantly the hydrophilic characteristics only in the case of virgin polymer. A significant increase of in vitro degradation rate was found for PCL-MAGMA based membranes, and at lower extent of PCL-DMAEA membranes. The novel materials were investigated regarding their potential as support for cell growth in bone repair using multipotent mesenchymal stromal cells (MSC) as a model. MSC plated onto the various membranes were analyzed in terms of adhesion, proliferation and osteogenic capacity that resulted to be related to chemical as well as porous structure. In particular, PCL-DMAEA and the relative nanocomposite membranes are the most promising in terms of cell-biomaterial interactions.

摘要

在本研究中,通过溶剂-非溶剂相转化法制备了基于聚(ε-己内酯)(PCL)以及用胺(PCL-DMAEA)或酸酐基团(PCL-MAGMA)功能化的PCL的微孔膜,并提出将其用于引导组织再生(GTR)。还将羟基磷灰石(HA)纳米晶须掺入聚合物基质中以制备纳米复合膜。扫描电子显微镜(SEM)显示功能化聚合物与HA之间的界面粘附性得到改善,并突出了孔隙率的显著差异。提出了膜的发达多孔结构与接枝基团化学性质之间的关系。与原始PCL相比,功能化PCL的亲水性增加,而仅在原始聚合物的情况下,HA的添加才会显著影响亲水特性。发现基于PCL-MAGMA的膜的体外降解速率显著增加,而PCL-DMAEA膜的降解速率增加程度较低。以多能间充质基质细胞(MSC)为模型,研究了这些新型材料作为骨修复中细胞生长支架的潜力。分析了接种在各种膜上的MSC的粘附、增殖和成骨能力,结果表明这些能力与化学结构以及多孔结构有关。特别是,PCL-DMAEA及其相关的纳米复合膜在细胞-生物材料相互作用方面最具前景。

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