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Updated: Oct 24, 2025

Trans-Tympanic Drug Delivery for the Treatment of Ototoxicity
Published on: March 16, 2018
Preferential Cochleotoxicity of Cisplatin.
Pattarawadee Prayuenyong1,2, David M Baguley2,3,4, Corné J Kros5
1Department of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand.
Cisplatin causes more hearing loss (ototoxicity) than balance problems. This review suggests the inner ear’s cochlea may be more vulnerable due to its unique physiology and blood barrier, aiding cisplatin entry into hair cells.
Area of Science:
- Ototoxicity research
- Inner ear physiology
- Pharmacology
Background:
- Cisplatin chemotherapy is known to cause ototoxicity, primarily affecting the cochlea.
- Vestibular dysfunction is less consistently reported, suggesting differential susceptibility within the inner ear.
- Inner ear hair cells may possess inherent characteristics influencing cisplatin sensitivity.
Purpose of the Study:
- To explain the preferential cochleotoxicity of cisplatin.
- To explore the role of inner ear anatomy and physiology in cisplatin's ototoxic effects.
- To identify potential targets for otoprotective strategies.
Main Methods:
- Review of existing literature on cisplatin ototoxicity.
- Analysis of inner ear anatomy and physiology.
- Hypothesizing mechanisms of differential drug uptake and hair cell susceptibility.
Main Results:
- Cisplatin-induced ototoxicity predominantly impacts the cochlea over the vestibule.
- Differences in blood-labyrinth barrier drug trafficking or hair cell uptake may exist between cochlear and vestibular compartments.
- The endocochlear potential, driven by the stria vascularis, might enhance cisplatin entry into cochlear hair cells.
Conclusions:
- The stria vascularis and endocochlear potential may contribute to preferential cochlear damage.
- Understanding these mechanisms could lead to otoprotective interventions against cisplatin ototoxicity.
- Further research into the stria vascularis is crucial for developing such therapies.
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