Biodegradable Nanofiber Membranes for Air-Liquid Interface Culture: Advancing Airway In Vitro Models

  • Sema Tuncer
  • , Secil Subasi Can
  • , Hayriye Akel Bilgic
  • , Busra Kilic
  • , Gulcin Gunal
  • , Halil Murat Aydin
  • , Cagatay Karaaslan*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Chronic airway diseases represent a significant global health challenge, and reliable in vitro model systems are essential for elucidating the molecular mechanisms underlying these conditions. Although air–liquid interface (ALI) culture systems are among the most effective models for studying airway epithelial cells under physiological conditions, the nonbiodegradable membranes commonly used in current systems present certain limitations. In the present study, biodegradable poly(l-lactic acid) (PLLA) and poly(ε-caprolactone) (PCL) nanofiber membranes were fabricated using the electrospinning technique, and novel transwell membrane systems were developed. Optimization studies revealed that the nanofiber diameters ranged between 50 and 275 nm, forming a structure closely resembling the native lung extracellular matrix. Degradation analyses indicated that PLLA and PCL membranes remained structurally stable for up to six months, making them suitable for long-term in vitro airway modeling applications. Attenuated total reflectance–Fourier transform infrared (ATR-FTIR) spectroscopy confirmed the chemical stability of the membranes. Additionally, cell culture assays demonstrated high cell viability and strong cellular adhesion. Immunocytochemical analysis revealed β-tubulin expression in bronchial epithelial cells differentiated on the membranes, indicating successful epithelial maturation. These findings suggest that biodegradable membranes provide a promising platform for in vitro airway modeling. Furthermore, the use of biodegradable membranes is expected to address a critical need by accurately mimicking the tracheal and bronchial architecture as submucosal tissue analogues, thereby advancing the development of preclinical airway tissue graft constructs.

Original languageEnglish
Pages (from-to)39693-39705
Number of pages13
JournalACS Omega
Volume10
Issue number35
Early online date21 Aug 2025
DOIs
Publication statusPublished - 9 Sept 2025

Bibliographical note

Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society

Funding

This work was supported by The Scientific and Technological Research Council of Türkiye [grant number 219S324] and the Hacettepe University Scientific Research Projects Coordination Unit [grant number FHD-2019-18044].

FundersFunder number
Türkiye Bilimsel ve Teknolojik Araştırma Kurumu219S324
Hacettepe ÜniversitesiFHD-2019-18044

    Keywords

    • Absence
    • Acid)
    • Cell-adhesion
    • Deficiency
    • Degradation
    • Disease
    • Fabrication
    • Poly-l-lactide
    • Proliferation
    • System

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