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April 3, 2026Materiale Plastice0 citationsOpen Access

AChitosan/Oxidized Pullulan Composite Film for LocalizedCisplatin Delivery and In Vitro Evaluation on NasopharyngealCells

BCBing CaoSGSHANSHAN GUYHYi Hu

Key Points

  • The aim is to evaluate a composite film made from chitosan and oxidized pullulan for localized drug delivery in nasopharyngeal carcinoma.
  • Composite film prepared using Schiff base crosslinking of chitosan and oxidized pullulan
  • Characterization through FTIR analysis
  • In vitro assays for drug release, cytocompatibility, and cell migration evaluation
  • Composite film showed distinct C=N peak in FTIR spectra
  • Enhanced wet adhesion of 55 kPa compared to individual components
  • Cisplatin-loaded films achieved 72-hour sustained release and reduced CNE-2 cell viability to 28%
  • Drug-free film was non-cytotoxic
  • Film extracts promoted nasopharyngeal epithelial cell migration shown by RTCA assay

Abstract

Background: Postoperative wound sealing and localized drug delivery are critical needs in nasopharyngeal carcinoma (NPC) management.Natural polysaccharide-based films offer a biocompatible platform for addressing these challenges.Methods: A composite film was prepared by Schiff base crosslinking of chitosan and oxidized pullulan.The film was characterized by FTIR, and its adhesion, drug release, cytocompatibility, and effects on cell migration were evaluated using in vitro assays. Results:The composite film exhibited a distinct C=N peak in FTIR spectra and significantly enhanced wet adhesion (55 kPa) compared to individual components.Cisplatin-loaded films showed sustained release over 72 h and reduced the viability of CNE-2 cells to 28%.The drug-free film was non-cytotoxic.Extracts from the composite film promoted nasopharyngeal epithelial cell migration, as shown by RTCA assay.Conclusion: This study explored the in vitro characteristics of a chitosan/oxidized pullulan film and evaluated its basic biological performance at the cellular level capable of localized drug release and supporting cell-level healing responses.Further validation in more complex models is warranted.

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Cite This Study

Cao et al. (2026) studied this question.

synapsesocial.com/papers/69cf59635a333a8214609f62https://doi.org/10.37358/mp.26.1.72501
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