TY - JOUR
T1 - Characterization of Oxygen Nanobubbles and In Vitro Evaluation of Retinal Cells in Hypoxia
AU - Messerschmidt, Victoria
AU - Ren, Wen
AU - Tsipursky, Michael
AU - Irudayaraj, Joseph
N1 - The authors thank Jonathan P. Samuelson DVM, MS, DACVP at the University of Illinois College of Veterinary Medicine for evaluation of the stained rabbit retinas. Rabbit toxicology study was conducted at the Toxicology Research Laboratory at the University of Illinois, Chicago. The authors also thank Steven Roth at UIC (University of Illinois, Chicago) for the insightful discussions. Partial funding for this work was provided by the NSF SBIR Phase I grant (Award# 2032323) to ReVive Biotechnology LLC, with subaward to UIUC, and the Mikashi Award from the Carl Woese Institute for Genomic Biology at UIUC.
Partial funding for this work was provided by the NSF SBIR Phase I grant (Award# 2032323) to ReVive Biotechnology LLC, with subaward to UIUC, and the Mikashi Award from the Carl Woese Institute for Genomic Biology at UIUC.
PY - 2023/2
Y1 - 2023/2
N2 - Purpose: Vein or artery occlusion causes a hypoxic environment by preventing oxygen delivery and diffusion to tissues. Diseases such as retinal vein occlusion, central retinal artery occlusion, or diabetic retinopathy create a stroke-type condition that leads to functional blindness in the effected eye. We aim to develop an oxygen delivery system consisting of oxygen nanobubbles (ONBs) that can mitigate retinal ischemia during a severe hypoxic event such as central retinal artery occlusion. Methods: ONBs were synthesized to encapsulate oxygen saturated molecular medical grade water. Stability, oxygen release, biocompatibility, reactive oxygen species, super-oxide, MTT, and terminal uridine nick-end labeling assays were performed. Cell viability was evaluated, and safety experiments were conducted in rabbits. Results: The ONBs were approximately 220 nm in diameter, with a zeta potential of −58.8 mV. Oxygen release studies indicated that 74.06 μg of O2 is released from the ONBs after 12 hours at 37°C. Cell studies indicated that ONBs are safe and cells are viable. There was no significant increase in reactive oxygen species, superoxide, or double-stranded DNA damage after ONB treatment. ONBs preserve mitochondrial function and viability. Histological sections from rabbit eyes indicated that ONBs were not toxic. Conclusions: The ONBs proposed have excellent oxygen holding and release properties to mitigate ischemic conditions in the retina. They are sterile, stable, and nontoxic. Translation Relevance: ONB technology was evaluated for its physical properties, oxygen release, sterility, stability, and safety. Our results indicate that ONBs could be a viable treatment approach to mitigate hypoxia during ischemic conditions in the eye upon timely administration.
AB - Purpose: Vein or artery occlusion causes a hypoxic environment by preventing oxygen delivery and diffusion to tissues. Diseases such as retinal vein occlusion, central retinal artery occlusion, or diabetic retinopathy create a stroke-type condition that leads to functional blindness in the effected eye. We aim to develop an oxygen delivery system consisting of oxygen nanobubbles (ONBs) that can mitigate retinal ischemia during a severe hypoxic event such as central retinal artery occlusion. Methods: ONBs were synthesized to encapsulate oxygen saturated molecular medical grade water. Stability, oxygen release, biocompatibility, reactive oxygen species, super-oxide, MTT, and terminal uridine nick-end labeling assays were performed. Cell viability was evaluated, and safety experiments were conducted in rabbits. Results: The ONBs were approximately 220 nm in diameter, with a zeta potential of −58.8 mV. Oxygen release studies indicated that 74.06 μg of O2 is released from the ONBs after 12 hours at 37°C. Cell studies indicated that ONBs are safe and cells are viable. There was no significant increase in reactive oxygen species, superoxide, or double-stranded DNA damage after ONB treatment. ONBs preserve mitochondrial function and viability. Histological sections from rabbit eyes indicated that ONBs were not toxic. Conclusions: The ONBs proposed have excellent oxygen holding and release properties to mitigate ischemic conditions in the retina. They are sterile, stable, and nontoxic. Translation Relevance: ONB technology was evaluated for its physical properties, oxygen release, sterility, stability, and safety. Our results indicate that ONBs could be a viable treatment approach to mitigate hypoxia during ischemic conditions in the eye upon timely administration.
KW - hypoxia
KW - oxygen nanobubbles
KW - retina
KW - safety and efficacy
KW - treatment
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U2 - 10.1167/tvst.12.2.16
DO - 10.1167/tvst.12.2.16
M3 - Article
C2 - 36763051
AN - SCOPUS:85147895674
SN - 2164-2591
VL - 12
JO - Translational Vision Science and Technology
JF - Translational Vision Science and Technology
IS - 2
M1 - 16
ER -