# Nanobubble-Mediated Oxygen Delivery Mitigates Hypoxia-Induced ROS and HIF-1α Expression in UC-MSCs

**Authors:** Sergio M. Víafara-García, Gloria Torres, Carlos Chacón, Juan L. Palma, Javier Rojas-Nunez, Esteban Landaeta, Juan Pablo Acevedo Cox

PMC · DOI: 10.3390/nano16040225 · Nanomaterials · 2026-02-10

## TL;DR

This study shows that oxygen nanobubbles help protect stem cells from hypoxia by reducing harmful stress and improving cell survival.

## Contribution

The use of Tivida®-stabilized oxygen nanobubbles for mitigating hypoxia in UC-MSCs is a novel oxygen delivery strategy.

## Key findings

- TONBs increased dissolved oxygen levels in culture media up to ~18 ppm.
- TONB treatment reduced mitochondrial ROS levels by ~20% under hypoxia.
- HIF-1α expression was downregulated by ~8–9 fold in TONB-treated cells.

## Abstract

Hypoxia and nutrient-deprived microenvironments pose significant challenges to the survival of transplanted human umbilical cord mesenchymal stem cells (UC-MSCs), necessitating the development of controllable oxygen delivery strategies. In this study, we engineered fluorosurfactant-coated oxygen nanobubbles (Tivida®-stabilized; TONBs) and assessed their cytoprotective effects in a two-dimensional (2D) ischemia-mimetic model (1% O2 and 1% FBS). The TONBs were characterized by nanoparticle tracking analysis and zeta potential, while dissolved oxygen (DO) release was quantified in DMEM culture media. TONBs formed stable sub-200 nm populations with high colloidal stability (−58 mV) and demonstrated elevated DO levels up to ~18 ppm, compared to DMEM control (~ 8 ppm). Under hypoxic stress, TONB treatment preserved metabolic activity and viability, reduced mitochondrial ROS levels by ~20% and resulted in an ~8–9 fold downregulation of HIF-1α expression relative to untreated hypoxic controls. These results indicate that TONBs provide oxygen buffering to mitigate hypoxia-driven metabolic stress, supporting their potential as an oxygen delivery adjunct for regenerative medicine applications and tissue engineering applications.

## Linked entities

- **Genes:** HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091]
- **Chemicals:** doxorubicin (PubChem CID 31703)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891] {aka LEM6, PGC-1(alpha), PGC-1alpha, PGC-1v, PGC1, PGC1A}, POTEF (POTE ankyrin domain family member F) [NCBI Gene 728378] {aka A26C1B, POTE2alpha, POTEACTIN}, CTRL (chymotrypsin like) [NCBI Gene 1506] {aka CTRL1}, ANXA5 (annexin A5) [NCBI Gene 308] {aka ANX5, CPB-I, ENX2, HEL-S-7, PP4, RPRGL3}
- **Diseases:** Hypoxia (MESH:D000860), Necrosis (MESH:D009336), H (MESH:D000848), Ischemia (MESH:D007511), stroke (MESH:D020521), pulmonary fibrosis (MESH:D011658), Hypoxic (MESH:D002534), infarcted tissues (MESH:D007238), cytotoxicity (MESH:D064420), ischemic stroke (MESH:D002544), ischemic (MESH:D002545), ischemic heart disease (MESH:D017202), retinal ischemia (MESH:D012173), myocardial infarction (MESH:D009203), mitochondrial dysfunction (MESH:D028361), ALS (MESH:D000690), inflammation (MESH:D007249), injury to (MESH:D014947)
- **Chemicals:** MitoSOX (MESH:C521281), ROS (MESH:D017382), RNS60 (MESH:C000627108), oligomycin (MESH:D009840), DMSO (MESH:D004121), glucose (MESH:D005947), SO3 (MESH:C011118), SDS (MESH:D012967), PVDF (MESH:C024865), Tween-20 (MESH:D011136), PBS (MESH:D007854), PLGA (MESH:D000077182), TBS (MESH:D013725), lipid (MESH:D008055), L-glutamine (MESH:D005973), CO2 (MESH:D002245), MitoSOX  Red (MESH:C000597839), water (MESH:D014867), ATP (MESH:D000255), polyacrylamide (MESH:C016679), streptomycin (MESH:D013307), 2-DG (MESH:D003847), penicillin (MESH:D010406), O2 (MESH:D010100), PI (MESH:D010716), Menadione (MESH:D024483), sodium hydrogen carbonate (MESH:D017693), pyruvate (MESH:D019289), DMEM (-), superoxide (MESH:D013481)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** MG63 — Homo sapiens (Human), Osteosarcoma, Cancer cell line (CVCL_0426), -MSCs — Homo sapiens (Human), Somatic stem cell (CVCL_WG60), UC-MSCs — Homo sapiens (Human), Finite cell line (CVCL_B5ZH)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942944/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942944/full.md

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Source: https://tomesphere.com/paper/PMC12942944