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3D 熔融挤出打印中长链聚羟基烷酸酯及其作为抗生素免费抗菌骨再生支架的应用。

3D Melt-Extrusion Printing of Medium Chain Length Polyhydroxyalkanoates and Their Application as Antibiotic-Free Antibacterial Scaffolds for Bone Regeneration.

机构信息

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.

出版信息

ACS Biomater Sci Eng. 2024 Aug 12;10(8):5136-5153. doi: 10.1021/acsbiomaterials.4c00624. Epub 2024 Jul 26.

DOI:10.1021/acsbiomaterials.4c00624
PMID:39058405
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11322914/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/11322914/132d9c750dd7/ab4c00624_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/11322914/9ea08b087b58/ab4c00624_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/11322914/2c7a37ff43a2/ab4c00624_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/11322914/4faf4593154c/ab4c00624_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/11322914/bef2add8027c/ab4c00624_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/11322914/132d9c750dd7/ab4c00624_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/11322914/9ea08b087b58/ab4c00624_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/11322914/2c7a37ff43a2/ab4c00624_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/11322914/4faf4593154c/ab4c00624_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/11322914/bef2add8027c/ab4c00624_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d1e/11322914/132d9c750dd7/ab4c00624_0005.jpg

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