Szczegóły publikacji

Opis bibliograficzny

Layered PCL scaffolds modified with bioactive additives fabricated by electrospinning and 3D-printing for the nasal bone and cartilage defects / Anna Kurowska, Anna Nikodem, Adam Jabłoński, Jarosław Janusz, Piotr Szczygieł, Magdalena ZIĄBKA, Elżbieta Menaszek, Michał DZIADEK, Barbara ZAGRAJCZUK, Magdalena Kobielarz, Izabella Rajzer // Materials and Design ; ISSN 0264-1275. — Tytuł poprz.: Materials in Engineering ; ISSN: 0261-3069. — 2023 — vol. 233 art. no. 112255, s. 1–11. — Bibliogr. s. 10–11, Abstr. — Publikacja dostępna online od: 2023-08-16. — M. Dziadek - dod. afiliacja: Jagiellonian University


Autorzy (11)


Słowa kluczowe

bioglass3D printingelectrospinningfilamentdrugZn-doped bioglasspolycaprolactonebilayer scaffold

Dane bibliometryczne

ID BaDAP148218
Data dodania do BaDAP2023-09-28
Tekst źródłowyURL
DOI10.1016/j.matdes.2023.112255
Rok publikacji2023
Typ publikacjiartykuł w czasopiśmie
Otwarty dostęptak
Creative Commons
Czasopismo/seriaMaterials & Design

Abstract

This paper presents a method for fabricating layered materials supporting the reconstruction of nasal tissues by combining the 3D/fused deposition modeling (FDM) technology with electrospinning (ES). Polycaprolactone (PCL) scaffolds modified with bioglass (BG) and zinc (Zn)-doped BG were printed from the connectable filaments sticks. Then, using the ES, a nanofibrous membrane with particles of the pharmaceutical drug Osteogenon (OST), was applied directly on a spatial scaffold. The layered scaffolds were investigated by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and micro-computed tomography (µCT). The bioactivity and biocompatibility of the scaffolds were evaluated by in vitro studies. The results indicated that the presence of the OST drug in the top layer of scaffolds promoted bioactivity. The presence of a membrane had a positive effect on the production and secretion of aggrecan (Agg), and incorporation of BG particles significantly improved the production and secretion of collagen type II (Col2). Each of the introduced PCL modifications leads to articular cartilage cell (NHAC-kn) viability improvement and results in a decrease in the cytotoxicity of the material. Moreover, in the long-term culture, cell proliferation was positively affected by the introduction of the OST-modified membrane and also by the addition of Zn-doped BG particles.

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