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Solid Lipid Nanoparticles Loaded with Edaravone for Inner Ear Protection After Noise Exposure
BACKGROUND: Antioxidants and the duration of treatment after noise exposure on hearing recovery are important. We investigated the protective effects of an antioxidant substance, edaravone, and its slow-release dosage form, edaravone solid lipid nanoparticles (SLNs), in steady noise-exposed guinea p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837839/ https://www.ncbi.nlm.nih.gov/pubmed/25591563 http://dx.doi.org/10.4103/0366-6999.149202 |
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author | Gao, Gang Liu, Ya Zhou, Chang-Hua Jiang, Ping Sun, Jian-Jun |
author_facet | Gao, Gang Liu, Ya Zhou, Chang-Hua Jiang, Ping Sun, Jian-Jun |
author_sort | Gao, Gang |
collection | PubMed |
description | BACKGROUND: Antioxidants and the duration of treatment after noise exposure on hearing recovery are important. We investigated the protective effects of an antioxidant substance, edaravone, and its slow-release dosage form, edaravone solid lipid nanoparticles (SLNs), in steady noise-exposed guinea pigs. METHODS: SLNs loaded with edaravone were produced by an ultrasound technique. Edaravone solution or edaravone SLNs were administered by intratympanic or intravenous injection after the 1(st) day of noise exposure. Guinea pigs were exposed to 110 dB sound pressure level (SPL) noise, centered at 0.25–4.0 kHz, for 4 days at 2 h/d. After noise exposure, the guinea pigs underwent auditory brainstem response (ABR) threshold measurements, reactive oxygen species (ROS) were detected in their cochleas with electron spin resonance (ESR), and outer hair cells (OHCs) were counted with silvernitrate (AgNO(3)) staining at 1, 4, and 6 days. RESULTS: The ultrasound technique was able to prepare adequate edaravone SLNs with a mean particle size of 93.6 nm and entrapment efficiency of 76.7%. Acoustic stress-induced ROS formation and edaravone exerted a protective effect on the cochlea. Comparisons of hearing thresholds and ROS changes in different animal groups showed that the threshold shift and ROS generation were significantly lower in treated animals than in those without treatment, especially in the edaravone SLN intratympanic injection group. CONCLUSIONS: Edaravone SLNs show noticeable slow-release effects and have certain protective effects against noise-induced hearing loss (NIHL). |
format | Online Article Text |
id | pubmed-4837839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48378392016-05-02 Solid Lipid Nanoparticles Loaded with Edaravone for Inner Ear Protection After Noise Exposure Gao, Gang Liu, Ya Zhou, Chang-Hua Jiang, Ping Sun, Jian-Jun Chin Med J (Engl) Original Article BACKGROUND: Antioxidants and the duration of treatment after noise exposure on hearing recovery are important. We investigated the protective effects of an antioxidant substance, edaravone, and its slow-release dosage form, edaravone solid lipid nanoparticles (SLNs), in steady noise-exposed guinea pigs. METHODS: SLNs loaded with edaravone were produced by an ultrasound technique. Edaravone solution or edaravone SLNs were administered by intratympanic or intravenous injection after the 1(st) day of noise exposure. Guinea pigs were exposed to 110 dB sound pressure level (SPL) noise, centered at 0.25–4.0 kHz, for 4 days at 2 h/d. After noise exposure, the guinea pigs underwent auditory brainstem response (ABR) threshold measurements, reactive oxygen species (ROS) were detected in their cochleas with electron spin resonance (ESR), and outer hair cells (OHCs) were counted with silvernitrate (AgNO(3)) staining at 1, 4, and 6 days. RESULTS: The ultrasound technique was able to prepare adequate edaravone SLNs with a mean particle size of 93.6 nm and entrapment efficiency of 76.7%. Acoustic stress-induced ROS formation and edaravone exerted a protective effect on the cochlea. Comparisons of hearing thresholds and ROS changes in different animal groups showed that the threshold shift and ROS generation were significantly lower in treated animals than in those without treatment, especially in the edaravone SLN intratympanic injection group. CONCLUSIONS: Edaravone SLNs show noticeable slow-release effects and have certain protective effects against noise-induced hearing loss (NIHL). Medknow Publications & Media Pvt Ltd 2015-01-20 /pmc/articles/PMC4837839/ /pubmed/25591563 http://dx.doi.org/10.4103/0366-6999.149202 Text en Copyright: © 2015 Chinese Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Gao, Gang Liu, Ya Zhou, Chang-Hua Jiang, Ping Sun, Jian-Jun Solid Lipid Nanoparticles Loaded with Edaravone for Inner Ear Protection After Noise Exposure |
title | Solid Lipid Nanoparticles Loaded with Edaravone for Inner Ear Protection After Noise Exposure |
title_full | Solid Lipid Nanoparticles Loaded with Edaravone for Inner Ear Protection After Noise Exposure |
title_fullStr | Solid Lipid Nanoparticles Loaded with Edaravone for Inner Ear Protection After Noise Exposure |
title_full_unstemmed | Solid Lipid Nanoparticles Loaded with Edaravone for Inner Ear Protection After Noise Exposure |
title_short | Solid Lipid Nanoparticles Loaded with Edaravone for Inner Ear Protection After Noise Exposure |
title_sort | solid lipid nanoparticles loaded with edaravone for inner ear protection after noise exposure |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837839/ https://www.ncbi.nlm.nih.gov/pubmed/25591563 http://dx.doi.org/10.4103/0366-6999.149202 |
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