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A Polyurethane Electrospun Membrane Loaded with Bismuth Lipophilic Nanoparticles (BisBAL NPs): Proliferation, Bactericidal, and Antitumor Properties, and Effects on MRSA and Human Breast Cancer Cells

  • Jesús Alejandro Torres-Betancourt
    ,
  • Rene Hernández-Delgadillo
    ,
  • Juan Valerio Cauich-Rodríguez
    ,
  • Diego Adrián Oliva-Rico
    ,
  • Juan Manuel Solis-Soto
    ,
  • Claudia María García-Cuellar
  • Universidad Autonoma de Nuevo Leon
    ,
  • Centro de Investigacion Cientifica de Yucatan
    ,
  • Instituto Nacional de Cancerologia - Mexico
    ,
  • Centro de Investigacion en Materiales Avanzados
    ,
Research Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Publication metrics

Metrics

SciVal
Citations
3
SciVal
FWCI
0.28
SciVal
Author count
14
SciVal
Paper percentile
40
Scopus
Citations

Abstract

Electrospun membranes (EMs) have a wide range of applications, including use as local delivery systems. In this study, we manufactured a polyurethane Tecoflex™ EM loaded with bismuth-based lipophilic nanoparticles (Tecoflex™ EMs-BisBAL NPs). The physicochemical and mechanical characteristics, along with the antitumor and bactericidal effects, were evaluated using a breast cancer cell line and methicillin-susceptible and resistant Staphylococcus aureus (MRSA). Drug-free Tecoflex™ EMs and Tecoflex™ EMs-BisBAL NPs had similar fiber diameters of 4.65 ± 1.42 µm and 3.95 ± 1.32 µm, respectively. Drug-free Tecoflex™ EMs did not negatively impact a human fibroblast culture, indicating that the vehicle is biocompatible. Tecoflex™ EMs-BisBAL NPs increased 94% more in size than drug-free Tecoflex™ EMs, indicating that the BisBAL NPs enhanced hydration capacity. Tecoflex™ EMs-BisBAL NPs were highly bactericidal against both methicillin-susceptible S. aureus and MRSA clinical isolates, inhibiting their growth by 93.11% and 61.70%, respectively. Additionally, Tecoflex™ EMs-BisBAL NPs decreased the viability of MCF-7 tumor cells by 86% after 24 h exposure and 70.1% within 15 min. Regarding the mechanism of action of Tecoflex™ EMs-BisBAL NPs, it appears to disrupt the tumor cell membrane. In conclusion, Tecoflex™ EMs-BisBAL NPs constitute an innovative low-cost drug delivery system for human breast cancer and postoperative wound infections.

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Article number

309

Journal (Volume, Issue Number)

Journal of Functional Biomaterials (Volume 15, Issue 10)

Publication milestones

  • Published - 10/2024

Publication status

Published - 10/2024

Publication IDs

  • Scopus: 85207311312

Funding Details

This study was supported by CONACHyT for the Sectorial Fund for Education Research CB 2017-2018-A1-S-20148.
FundersFunding numbers
CONACHyT for the Sectorial Fund for Education Research
CB 2017-2018-A1-S-20148