ORIGINAL RESEARCH article

Front. Bioeng. Biotechnol.

Sec. Nanobiotechnology

Volume 13 - 2025 | doi: 10.3389/fbioe.2025.1535793

This article is part of the Research TopicNanodrug Delivery Strategies for Enhanced Cancer Chemo-ImmunotherapyView all 3 articles

Bleomycin-Loaded Folic Acid-Conjugated Nanoliposomes: A Novel Formulation for Targeted Treatment of Oral Cancer

Provisionally accepted
Elham  SaberianElham Saberian1Janka  JenčováJanka Jenčová1Andrej  JenčaAndrej Jenča1Andrej  JenčaAndrej Jenča1Fateme  SalehipoorFateme Salehipoor2Hadi  Zare-ZardiniHadi Zare-Zardini3*Adriána  PetrášováAdriána Petrášová1*Peter  DžupaPeter Džupa1Meysam  EbrahimifarMeysam Ebrahimifar4Mohammadreza  AllahyartorkamanMohammadreza Allahyartorkaman5Jozef  JenčaJozef Jenča1
  • 1University of Pavol Jozef Šafárik, Košice, Slovakia
  • 2Islamic Azad University Najafabad, Najafabad, Isfahan, Iran
  • 3Department of Biomedical Engineering, Meybod University, Meybod, Iran, Meybod, Yazd, Iran
  • 4Islamic Azad University of Shahreza, Shahreza, Iran
  • 5National Taiwan University, Taipei, Taiwan

The final, formatted version of the article will be published soon.

Introduction: Targeted delivery of anticancer drugs holds great promise for enhancing therapeutic efficacy while minimizing adverse effects. The folate receptor (FR)-mediated approach offers a selective strategy to target cancer cells overexpressing FR. Bleomycin, an established antitumor antibiotic, suffers from limited efficacy due to poor diffusion into tumor cells. This study examined the anti-cancer potential of folate-targeted liposomal Bleomycin (FL-BLEOMYCIN) in comparison to non-targeted L-BLEOMYCIN on oral cavity cancer (CAL27). The study also investigated FL-Bleomycin's capacity to halt the cell cycle in the G2/M phase using flow cytometry.Methods: FL-Bleomycin was produced using thin-layer hydration, followed by incorporation of folic acid into nanoliposomes. To evaluate the release profile, drug release tests were carried out. Cytotoxicity of FL-Bleomycin, L-Bleomycin, and traditional Bleomycin was evaluated using cell viability assays. The cell cycle arrest caused by FL-Bleomycin was examined using flow cytometry. Finally, FL-Bleomycin uptake studies were performed to assess the internalization of FL-Bleomycin by CAL27 cells.The findings suggest that FL-Bleomycin is a potential method for delivering drugs precisely in tumors expressing folic acid receptors. Its potential for successful cancer treatment is shown by its higher internalization, improved cytotoxicity, and cell cycle prevention in CAL 27 cells. To find out how effective FL-Bleomycin is in vivo and whether it may be used to treat other FR-expressing tumors, more research is necessary.

Keywords: Nanoliposomes, folate receptor, Targeted Drug Delivery, Bleomycin, cancer therapy

Received: 27 Nov 2024; Accepted: 03 Apr 2025.

Copyright: © 2025 Saberian, Jenčová, Jenča, Jenča, Salehipoor, Zare-Zardini, Petrášová, Džupa, Ebrahimifar, Allahyartorkaman and Jenča. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Hadi Zare-Zardini, Department of Biomedical Engineering, Meybod University, Meybod, Iran, Meybod, Yazd, Iran
Adriána Petrášová, University of Pavol Jozef Šafárik, Košice, 041 80, Slovakia

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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