Faculty of Science and Technology, College of Liberal Arts, University of Westminster, London W1W 6UW, U.K.
Institute of Biomaterials, Department of Materials Science and Engineering, University of Erlangen-Nuremberg, Erlangen 91058, Germany.
ACS Biomater Sci Eng. 2024 Aug 12;10(8):5136-5153. doi: 10.1021/acsbiomaterials.4c00624. Epub 2024 Jul 26.
In this work, we investigated, for the first time, the possibility of developing scaffolds for bone tissue engineering through three-dimensional (3D) melt-extrusion printing of medium chain length polyhydroxyalkanoate (mcl-PHA) (i.e., poly(3-hydroxyoctanoate--hydroxydecanoate--hydroxydodecanoate), P(3HO--3HD--3HDD)). The process parameters were successfully optimized to produce well-defined and reproducible 3D P(3HO--3HD--3HDD) scaffolds, showing high cell viability (100%) toward both undifferentiated and differentiated MC3T3-E1 cells. To introduce antibacterial features in the developed scaffolds, two strategies were investigated. For the first strategy, P(3HO--3HD--3HDD) was combined with PHAs containing thioester groups in their side chains (i.e., PHACOS), inherently antibacterial PHAs. The 3D blend scaffolds were able to induce a 70% reduction of 6538P cells by direct contact testing, confirming their antibacterial properties. Additionally, the scaffolds were able to support the growth of MC3T3-E1 cells, showing the potential for bone regeneration. For the second strategy, composite materials were produced by the combination of P(3HO--3HD--HDD) with a novel antibacterial hydroxyapatite doped with selenium and strontium ions (Se-Sr-HA). The composite material with 10 wt % Se-Sr-HA as a filler showed high antibacterial activity against both Gram-positive ( 6538P) and Gram-negative bacteria ( 8739), through a dual mechanism: by direct contact (inducing 80% reduction of both bacterial strains) and through the release of active ions (leading to a 54% bacterial cell count reduction for 6538P and 30% for 8739 after 24 h). Moreover, the composite scaffolds showed high viability of MC3T3-E1 cells through both indirect and direct testing, showing promising results for their application in bone tissue engineering.
在这项工作中,我们首次研究了通过中链长度聚羟基烷酸酯(mcl-PHA)(即聚(3-羟基辛酸-3-羟基癸酸-3-羟基十二酸),P(3HO-3HD-3HDD))的三维(3D)熔融挤出打印来开发骨组织工程支架的可能性。成功优化了工艺参数以生产具有良好定义和可重现性的 3D P(3HO-3HD-3HDD)支架,显示出对未分化和分化的 MC3T3-E1 细胞均具有 100%的高细胞活力。为了在开发的支架中引入抗菌特性,研究了两种策略。对于第一种策略,将 P(3HO-3HD-3HDD)与侧链中含有硫酯基团的 PHAs(即 PHACOS),即固有抗菌的 PHAs 结合。3D 共混支架通过直接接触测试能够将 6538P 细胞减少 70%,证实了其抗菌性能。此外,支架能够支持 MC3T3-E1 细胞的生长,显示出骨再生的潜力。对于第二种策略,通过 P(3HO-3HD-3HDD)与新型抗菌硒和锶掺杂的羟基磷灰石(Se-Sr-HA)的组合来生产复合材料。当复合材料中的 Se-Sr-HA 填充剂含量为 10wt%时,对革兰氏阳性菌(6538P)和革兰氏阴性菌(8739)均表现出高抗菌活性,这是通过两种机制实现的:直接接触(诱导两种细菌菌株减少 80%)和通过释放活性离子(在 24 小时后,对 6538P 导致减少 54%的细菌细胞计数,对 8739 导致减少 30%)。此外,复合支架通过间接和直接测试显示出对 MC3T3-E1 细胞的高存活率,为其在骨组织工程中的应用提供了有希望的结果。