Physical Chemistry I, Department of Chemistry and Biology & Research Center of Micro and Nanochemistry and Engineering (Cμ) , University of Siegen , 57076 Siegen , Germany.
Biomaterials, Drug Delivery and Nanotechnology Unit, Centre for Biomedical and Biomaterials Research (CBBR) , MSIRI Building, University of Mauritius , 80837 Réduit , Mauritius.
ACS Appl Mater Interfaces. 2019 Feb 13;11(6):5834-5850. doi: 10.1021/acsami.8b19929. Epub 2019 Jan 30.
The potential of electrospun polydioxanone (PDX) mats as scaffolds for skeletal tissue regeneration was significantly enhanced through improvement of the cell-mediated biomimetic mineralization and multicellular response. This was achieved by blending PDX ( i) with poly(hydroxybutyrate- co-valerate) (PHBV) in the presence of hydroxyapatite (HA) and ( ii) with aloe vera (AV) extract containing a mixture of acemannan/glucomannan. In an exhaustive study, the behavior of the most relevant cell lines involved in the skeletal tissue healing cascade, i.e. fibroblasts, macrophages, endothelial cells and preosteoblasts, on the scaffolds was investigated. The scaffolds were shown to be nontoxic, to exhibit insignificant inflammatory responses in macrophages, and to be degradable by macrophage-secreted enzymes. As a result of different phase separation in PDX/PHBV/HA and PDX/AV blend mats, cells interacted differentially. Presumably due to varying tension states of cell-matrix interactions, thinner microtubules and significantly more cell adhesion sites and filopodia were formed on PDX/AV compared to PDX/PHBV/HA. While PDX/PHBV/HA supported micrometer-sized spherical particles, nanosized rod-like HA was observed to nucleate and grow on PDX/AV fibers, allowing the mineralized PDX/AV scaffold to retain its porosity over a longer time for cellular infiltration. Finally, PDX/AV exhibited better in vivo biocompatibility compared to PDX/PHBV/HA, as indicated by the reduced fibrous capsule thickness and enhanced blood vessel formation. Overall, PDX/AV blend mats showed a significantly enhanced potential for skeletal tissue regeneration compared to the already promising PDX/PHBV/HA blends.
静电纺丝聚二氧环己酮(PDX)垫作为骨骼组织再生支架的潜力通过改善细胞介导的仿生矿化和多细胞反应得到了显著增强。这是通过在 PDX 中(i)与聚(羟基丁酸酯-共-戊酸酯)(PHBV)共混,同时存在羟基磷灰石(HA)和(ii)与含有甘露聚糖/葡聚糖混合物的芦荟提取物共混来实现的。在一项详尽的研究中,研究了最相关的细胞系(即成纤维细胞、巨噬细胞、内皮细胞和成骨前体细胞)在支架上的行为。结果表明,支架无毒,巨噬细胞无明显炎症反应,且可被巨噬细胞分泌的酶降解。由于 PDX/PHBV/HA 和 PDX/AV 共混垫中的不同相分离,细胞的相互作用也不同。由于细胞-基质相互作用的张力状态不同,与 PDX/PHBV/HA 相比,PDX/AV 上形成了更薄的微管和更多的细胞黏附位点和丝状伪足。虽然 PDX/PHBV/HA 支持微米级的球形颗粒,但观察到纳米级的棒状 HA 在 PDX/AV 纤维上成核和生长,使矿化的 PDX/AV 支架在更长的时间内保持其多孔性,以利于细胞渗透。最后,与 PDX/PHBV/HA 相比,PDX/AV 表现出更好的体内生物相容性,这表现为纤维囊厚度降低和血管形成增强。总体而言,与已经很有前途的 PDX/PHBV/HA 共混物相比,PDX/AV 共混物显示出显著增强的骨骼组织再生潜力。