Redox Buffering Capacity of Nanomaterials as an Index of ROS-Based Therapeutics and Toxicity: A Preclinical Animal Study
- PMID: 34060316
- DOI: 10.1021/acsbiomaterials.1c00402
Redox Buffering Capacity of Nanomaterials as an Index of ROS-Based Therapeutics and Toxicity: A Preclinical Animal Study
Abstract
Precise control of intracellular redox status, i.e., maintenance of the physiological level of reactive oxygen species (ROS) for mediating normal cellular functions (oxidative eustress) while evading the excess ROS stress (distress), is central to the concept of redox medicine. In this regard, engineered nanoparticles with unique ROS generation, transition, and depletion functions have the potential to be the choice of redox therapeutics. However, it is always challenging to estimate whether ROS-induced intracellular events are beneficial or deleterious to the cell. Here, we propose the concept of redox buffering capacity as a therapeutic index of engineered nanomaterials. As a steady redox state is maintained for normal functioning cells, we hypothesize that the ability of a nanomaterial to preserve this homeostatic condition will dictate its therapeutic efficacy. Additionally, the redox buffering capacity is expected to provide information about the nanoparticle toxicity. Here, using citrate-functionalized trimanganese tetroxide nanoparticles (C-Mn3O4 NPs) as a model nanosystem, we explored its redox buffering capacity in erythrocytes. Furthermore, we went on to study the chronic toxic effect (if any) of this nanomaterial in the animal model to co-relate with the experimentally estimated redox buffering capacity. This study could function as a framework for assessing the capability of a nanomaterial as redox medicine (whether maintains eustress or damages by creating distress), thus orienting its application and safety for clinical use.
Keywords: nanotherapy; nanotoxicity; redox buffering; redox homeostasis; redox therapeutics.
Similar articles
-
Redox nanomedicine ameliorates chronic kidney disease (CKD) by mitochondrial reconditioning in mice.Commun Biol. 2021 Aug 26;4(1):1013. doi: 10.1038/s42003-021-02546-8. Commun Biol. 2021. PMID: 34446827 Free PMC article.
-
Chitosan functionalized Mn3O4 nanoparticles counteracts ulcerative colitis in mice through modulation of cellular redox state.Commun Biol. 2023 Jun 16;6(1):647. doi: 10.1038/s42003-023-05023-6. Commun Biol. 2023. PMID: 37328528 Free PMC article.
-
Role of Nanomedicine in Redox Mediated Healing at Molecular Level.Biomol Concepts. 2019 Oct 29;10(1):160-174. doi: 10.1515/bmc-2019-0019. Biomol Concepts. 2019. PMID: 31661433 Review.
-
The role of intracellular redox imbalance in nanomaterial induced cellular damage and genotoxicity: a review.Environ Mol Mutagen. 2015 Mar;56(2):111-24. doi: 10.1002/em.21926. Epub 2014 Nov 26. Environ Mol Mutagen. 2015. PMID: 25427446 Review.
-
Chemical mechanisms of the toxicological properties of nanomaterials: generation of intracellular reactive oxygen species.Chem Asian J. 2013 Oct;8(10):2342-53. doi: 10.1002/asia.201300542. Epub 2013 Jul 23. Chem Asian J. 2013. PMID: 23881693
Cited by
-
Chemoprevention of bilirubin encephalopathy with a nanoceutical agent.Pediatr Res. 2023 Mar;93(4):827-837. doi: 10.1038/s41390-022-02179-5. Epub 2022 Jul 6. Pediatr Res. 2023. PMID: 35794251
-
Redox nanomedicine ameliorates chronic kidney disease (CKD) by mitochondrial reconditioning in mice.Commun Biol. 2021 Aug 26;4(1):1013. doi: 10.1038/s42003-021-02546-8. Commun Biol. 2021. PMID: 34446827 Free PMC article.
-
Chitosan functionalized Mn3O4 nanoparticles counteracts ulcerative colitis in mice through modulation of cellular redox state.Commun Biol. 2023 Jun 16;6(1):647. doi: 10.1038/s42003-023-05023-6. Commun Biol. 2023. PMID: 37328528 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Research Materials