Unlocking Novel Anticancer Strategies: Bioactive Hydrogels for Local Delivery of Plasma‐Derived Oxidants in an In Ovo Cancer Model

Author:

Espona‐Noguera Albert12ORCID,Živanić Milica123,Smits Evelien4,Bogaerts Annemie3,Privat‐Maldonado Angela3,Canal Cristina125ORCID

Affiliation:

1. Biomaterials Biomechanics and Tissue Engineering Group Department of Materials Science and Engineering and Research Centre for Biomedical Engineering Universitat Politècnica de Catalunya BarcelonaTech (UPC) Av. Eduard Maristany 10–14 Barcelona 08019 Spain

2. Barcelona Research Center in Multiscale Science and Engineering Universitat Politècnica de Catalunya BarcelonaTech (UPC) Barcelona 08019 Spain

3. Plasma Lab for Applications in Sustainability and Medicine‐Antwerp (PLASMANT) Department of Chemistry University of Antwerp Antwerp 2610 Belgium

4. Center for Oncological Research Integrated Personalized and Precision Oncology Network University of Antwerp Antwerp 2610 Belgium

5. Centro de Investigación Biomédica en Red de Bioingeniería Biomateriales y Nanomedicina Instituto de Salud Carlos II Barcelona 28029 Spain

Abstract

AbstractCold atmospheric plasma (CAP) is a tool with the ability to generate reactive oxygen and nitrogen species (RONS), which can induce therapeutic effects like disinfection, wound healing, and cancer treatment. In the plasma oncology field, CAP‐treated hydrogels (PTHs) are being explored for the local administration of CAP‐derived RONS as a novel anticancer approach. PTHs have shown anticancer effects in vitro, however, they have not yet been studied in more relevant cancer models. In this context, the present study explores for the first time the therapeutic potential of PTHs using an advanced in ovo cancer model. PTHs composed of alginate (Alg), gelatin (Gel), Alg/Gel combination, or Alg/hyaluronic acid (HA) combination are investigated. All embryos survived the PTHs treatment, suggesting that the in ovo model could become a time‐ and cost‐effective tool for developing hydrogel‐based anticancer approaches. Results revealed a notable reduction in CD44+ cell population and their proliferative state for the CAP‐treated Alg‐HA condition. Moreover, the CAP‐treated Alg‐HA formulation alters the extracellular matrix composition, which may help combat drug‐resistance. In conclusion, the present study validates the utility of in ovo cancer model for PTHs exploration and highlights the promising potential of Alg‐based PTHs containing HA and CAP‐derived RONS for cancer treatment.

Funder

Generalitat de Catalunya

European Cooperation in Science and Technology

Publisher

Wiley

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