Szczegóły publikacji

Opis bibliograficzny

Modulating surface properties and osteoblast responses in bone regeneration via positive and negative charges during electrospinning of poly(l-lactide-co-$\varepsilon$-caprolactone) (PLCL) scaffolds / Katarzyna MARSZALIK, Martyna POLAK, Krzysztof BERNIAK, Joanna KNAPCZYK-KORCZAK, Piotr K. SZEWCZYK, Mateusz M. MARZEC, Urszula STACHEWICZ // ACS Biomaterials Science & Engineering [Dokument elektroniczny]. — Czasopismo elektroniczne ; ISSN  2373-9878 . — 2026 — vol. 12 iss. 1, s. 543–558. — Wymagania systemowe: Adobe Reader. — Bibliogr. s. 556–558, Abstr. — Publikacja dostępna online od: 2025-11-27

Autorzy (7)

Słowa kluczowe

copolymerscollagen formationelectrospinningfiberscell-material interactionsvoltage polarityPLCL

Dane bibliometryczne

ID BaDAP165764
Data dodania do BaDAP2026-03-04
Tekst źródłowyURL
DOI10.1021/acsbiomaterials.5c01568
Rok publikacji2026
Typ publikacjiartykuł w czasopiśmie
Otwarty dostęptak
Creative Commons
Czasopismo/seriaACS Biomaterials Science & Engineering

Abstract

The global demand for faster and more effective bone regeneration calls for biomimetic scaffolds that actively guide cell behavior beyond providing structural support. Electrospinning offers unique opportunities to tailor scaffold properties, yet the influence of positive and negative voltage polarities during fabrication on cell–material interactions remains largely unexplored. Here, we investigate poly(l-lactide-co-ε-caprolactone) (PLCL) scaffolds, a statistical copolymer combining strength and elasticity, produced under positive (PLCL+) and negative (PLCL−) polarity. Both scaffold types display comparable morphologies and bulk chemistry. However, X-ray photoelectron spectroscopy reveals charge dependent surface chemistry, with PLCL– enriched in O═C and O–C groups. Zeta potential results highlight pronounced voltage polarity effects under aqueous conditions at pH 7.5, showing −29.19 mV for PLCL+ and −34.77 mV for PLCL–. Biologically, both scaffolds support rapid osteoblast attachment, with robust filopodia and collagen type I deposition by day 14. Strikingly, PLCL+ scaffolds promote deeper cellular infiltration and broader cytoskeletal distribution, whereas PLCL– scaffolds enhance proliferation, but with a flatter cell morphology. These findings reveal that subtle, charge-driven surface chemical differences in random copolymer scaffolds profoundly modulate osteoblast behavior. This work identifies electrospinning voltage polarity as a powerful yet underutilized design parameter for engineering next-generation scaffolds for bone tissue regeneration.

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#169908Data dodania: 10.9.2026
Modulating surface properties of electrospun PLCL scaffolds via voltage polarity for biomedical applications / Katarzyna MARSZALIK, Martyna POLAK, Joanna KNAPCZYK-KORCZAK, Krzysztof BERNIAK, Piotr SZEWCZYK, Mateusz MARZEC, Urszula STACHEWICZ // W: ICFPAM 2026 [Dokument elektroniczny] : 17th International Conference on Frontiers of Polymers and Advanced Materials : 6–9 September, Kraków, Poland : book of abstracts / editor-in-chief Jacek Nizioł. — Wersja do Windows. — Dane tekstowe. — Kraków : Faculty of Physics and Computer Science & Faculty of Materials Science and Ceramics. AGH University of Kraków, [2026]. — e-ISBN: 978-83-925779-8-0. — S. [193–194]. — Wymagania systemowe: Adobe Reader. — Tryb dostępu: https://drive.google.com/file/d/1YF2LK8qhnRZK_kK80ytXVkii5lLG... [2026-09-08]. — Bibliogr. s. [194]
artykuł
#120177Data dodania: 15.3.2019
Surface-potential-controlled cell proliferation and collagen mineralization on electrospun polyvinylidene fluoride (PVDF) fiber scaffolds for bone regeneration / Piotr K. SZEWCZYK, Sara METWALLY, Joanna E. KARBOWNICZEK, Mateusz M. MARZEC, Ewa STODOLAK-ZYCH, Adam GRUSZCZYŃSKI, Andrzej BERNASIK, Urszula STACHEWICZ // ACS Biomaterials Science & Engineering [Dokument elektroniczny]. - Czasopismo elektroniczne ; ISSN 2373-9878. — 2019 — vol. 5 iss. 2, s. 582–593. — Wymagania systemowe: Adobe Reader. — Bibliogr. s. 591–593, Abstr. — Publikacja dostępna online od: 2018-12-20. — A. Bernasik – dod. afiliacja: ACMiN