4.3 Article

Attapulgite-doped electrospun PCL scaffolds for enhanced bone regeneration in rat cranium defects

期刊

BIOMATERIALS ADVANCES
卷 133, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.msec.2022.112656

关键词

Attapulgite (ATP); Polyethylene glycol; Polycaprolactone; Electrospun scaffolds; Bone tissue engineering

资金

  1. Key Project of Science and Technology of Jiangsu Province [BE2018644]
  2. Science and Technology Support Plan of Changzhou City (Social Development) [CE20185047]

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Electrospun PCL scaffolds, widely used in tissue engineering, have the potential to mimic the natural extracellular matrix structure. However, their small pore size and low bioactivity hinder cell migration and tissue formation. In this study, different materials were used to fabricate porous scaffolds, and the removal of water-soluble fibers increased the porosity. Biocompatibility and osteogenesis were evaluated, and the results showed that washed PCL/PEG/ATP scaffolds promoted better cell infiltration and differentiation into osteoblasts compared to PCL scaffolds. In vivo studies also demonstrated enhanced bone regeneration in rat cranium defects using ATP-doped electrospun PCL scaffolds.
Electrospun PCL scaffolds have been widely used for tissue engineering as they have shown great potential to mimic the structure of the natural extracellular matrix (ECM). However, the small pore size and low bioactivity of the scaffolds limit cell migration and tissue formation. In this study, PCL (polycaprolactone), PCL/PFG (polyethylene glycol), and PCL/PEG/ATP (nano-attapulgite) scaffolds were fabricated via electrospinning. To increase the porosity of the scaffolds, they were washed to remove water-soluble PEG fibers. Then the porous structure was measured using scanning electron microscopy (SEM) and atomic force microscopy (AFM), which showed an increased porosity when PEG fibers were removed in PCL/PEG and PCL/PEG/ATP scaffolds. Moreover, the mechanical properties were also analyzed in dry and wet conditions. In vino mouse multipotent mesenchymal precursor cells were used to assess the biocompatibility of the scaffolds, and osteogenesis was analyzed using CCK-8 and real-time PCR (RT-PCR) methods. Moreover, in vivo mu CT, histological and immunohistochemical analyses were conducted to evaluate new bone formation in rat cranium defect models. Washed PCL/PEG/ATP scaffolds were implanted into the cranium defects in rats for 4 or 8 weeks, better cell infiltration was observed in these scaffolds than in unwashed ones. The result demonstrated that washed PCL/PEG/ATP scaffold facilitated the differentiation of MSCs into osteoblasts compared with PCL scaffold, as proved by the increased expression of osteogenic key genes as well as Smad1, Smad4, and Smad5. Furthermore, in vivo studies demonstrated that using the ATP-doped electrospun PCL scaffold can improve the bone regeneration of rat cranium defects. Particularly, the PCL/ATP-30% scaffold has the best effect compared to the other scaffolds. The enhanced osteogenesis and bone repair were related to the PCL/ATP activated BMP/Smad signaling pathway.

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