期刊
NANOMEDICINE
卷 18, 期 12, 页码 923-940出版社
FUTURE MEDICINE LTD
DOI: 10.2217/nnm-2023-0092
关键词
bile acid; encapsulation; free radicals; lithocholic acid; nanoparticle; oxidative stress; probucol; sensorineural hearing loss
Oxidative stress, associated with sensorineural hearing loss (SHL), can be prevented or treated using potent antioxidants like probucol. However, due to the isolated position of SHL, refining therapeutic methods is necessary, and nanoparticles could be a promising approach. In this study, nanoparticles formulated with polymers and excipients were found to be robust and stable, protecting auditory cells from cellular toxicity and oxidative stress. These PB-based nanoparticles could be a novel therapeutic agent for SHL.
Plain language summaryOxidative stress is an imbalance of cellular processes in which the production of free radicals outweighs the cellular defense mechanism. The association of oxidative stress with the pathophysiology of sensorineural hearing loss (SHL) is well established. SHL development is associated with chronic damage in the structure of the inner ear or auditory nerve. Therefore, potent antioxidants such as probucol could be one way to prevent or treat SHL. However, due to its isolated position, SHL is challenging to treat, imposing a desperate need for refining existing therapeutic methods; one way to do this is by optimizing the formulation using nanoparticles. We aimed to design a novel, stable formulation of PB using polymers and excipients to develop nanoparticles and examine the efficiency of these formulations on the HEI-OC1 stress cell line. We found that the prepared nanoparticle is robust and stable and protects HEI-OC1 from cellular toxicity and oxidative stress. It could be a novel therapeutic agent to treat or prevent SHL. Background: Sensorineural hearing loss has been associated with oxidative stress. However, an antioxidant that passes effectively through the ear remains elusive. Method: Probucol (PB)-based nanoparticles were formed using a spray-drying encapsulation technique, characterized and tested in vitro. Results: Uniform, spherical nanoparticles were produced. The addition of lithocholic acid to PB formulations did not affect drug content or production yield, but it did modify capsule size, surface tension, electrokinetic stability and drug release. Cell viability, bioenergetics and inflammatory profiles were improved when auditory cells were exposed to PB-based nanoparticles, which showed antioxidant properties (p < 0.05). Conclusion: PB-based nanoparticles can potentially protect the auditory cell line from oxidative stress and could be used in future in vivo studies as a potential new therapeutic agent for sensorineural hearing loss.
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