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February 16, 20260 citationsOpen Access

Hybrid Oxygen-Sensing Bio-Scaffolds for 3D Micro-Tissue Models

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LLLiang LiOllscoil na Gaillimhe – University of GalwayAZAlexander V. ZhdanovDPDmitri B. Papkovsky

Key Points

  • The aim is to develop hybrid bio-scaffolds that enhance O2-sensing capabilities in 3D tissue models.
  • The bio-scaffolds combine Matrigel and nanoparticulate probes for enhanced O2 detection.
  • HCT116 cells were cultured in Matrigel–NP hybrid scaffolds.
  • Oxygenation and O2 gradients were monitored using fluorescence plate reader and phosphorescence lifetime imaging microscopy.
  • Matrigel hybrids with NanO2 and Nano-IR showed superior characteristics.
  • Improved stability and lower cytotoxicity were observed in the new scaffolds.

Abstract

Culturing cells and micro-tissue samples in 3D bio-scaffolding structures is gaining popularity; however, precise control of tissue micro-environment in such systems remains challenging. We describe a family of new hybrid bio-scaffolds with 3D O2-sensing ability, produced by simple means from readily available bio-scaffolding and O2-sensing materials. Three different types of phosphorescent O2-sensing materials—polymeric microparticles (MPs), supramolecular probe MitoXpress and nanoparticulate probes NanO2 and Nano-IR (NPs)—were integrated in Matrigel and agarose scaffolding materials and evaluated. Key working characteristics of such hybrid scaffolds, including heterogeneity, stability, cytotoxicity, optical signals and O2-sensing properties, ease of fabrication and use, were compared. The results show superiority of the Matrigel hybrids with NanO2 and Nano-IR probes. Demonstration experiments were conducted with HCT116 cells and individual spheroids derived from these cells, culturing them in the Matrigel–NP hybrid scaffolds and monitoring oxygenation and local O2 gradients on a time-resolved fluorescence plate reader and by phosphorescence lifetime imaging microscopy (PLIM).

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Cite This Study

Li et al. (2026) studied this question.

synapsesocial.com/papers/69926503eb1f82dc367a0e7ahttps://doi.org/10.3390/bios16020122
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