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Ultrasound-assisted gatifloxacin delivery in mouse cornea, in vivo
Gatifloxacin is a 4th generation fluoroquinolone antibiotic used in the clinic to treat ocular infection. One limitation of gatifloxacin is its relatively poor corneal penetration, and the increase of its trans-corneal delivery would be beneficial to reduce the amount or frequency of daily dose. In...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820539/ https://www.ncbi.nlm.nih.gov/pubmed/31664145 http://dx.doi.org/10.1038/s41598-019-52069-w |
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author | Jegal, Uk Lee, Jun Ho Lee, Jungbin Jeong, Hyerin Kim, Myoung Joon Kim, Ki Hean |
author_facet | Jegal, Uk Lee, Jun Ho Lee, Jungbin Jeong, Hyerin Kim, Myoung Joon Kim, Ki Hean |
author_sort | Jegal, Uk |
collection | PubMed |
description | Gatifloxacin is a 4th generation fluoroquinolone antibiotic used in the clinic to treat ocular infection. One limitation of gatifloxacin is its relatively poor corneal penetration, and the increase of its trans-corneal delivery would be beneficial to reduce the amount or frequency of daily dose. In this study, ultrasound treatment was applied to enhance the trans-corneal delivery of gatifloxacin without damage. Experiments were conducted on mouse eyes in ex vivo and in vivo conditions. Ultrasound waves with 1 MHz in frequency, 1.3 W/cm(2) in intensity were applied onto the mouse cornea for 5 minutes, and then gatifloxacin ophthalmic solution was instilled and left there for 10 minutes. 3D gatifloxacin distribution in the cornea was measured by two-photon microscopy (TPM) imaging based on its intrinsic fluorescence. Longitudinal TPM imaging of ultrasound treated mouse corneas showed the increase of initial gatifloxacin intensities on the corneal surface compared to untreated mouse corneas by 67%, and then the increased gatifloxacin delivery into the cornea from the surface at later time. The delivered gatifloxacin in the corneal epithelium stayed longer in the ultrasound treated corneas than in the untreated corneas. The enhanced trans-corneal delivery and extended stay of gatifloxacin in the mouse cornea by ultrasound treatment could be beneficial for therapeutic effects. This study demonstrated the detail process of enhanced trans-corneal gatifloxacin delivery by ultrasound treatment. |
format | Online Article Text |
id | pubmed-6820539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68205392019-11-04 Ultrasound-assisted gatifloxacin delivery in mouse cornea, in vivo Jegal, Uk Lee, Jun Ho Lee, Jungbin Jeong, Hyerin Kim, Myoung Joon Kim, Ki Hean Sci Rep Article Gatifloxacin is a 4th generation fluoroquinolone antibiotic used in the clinic to treat ocular infection. One limitation of gatifloxacin is its relatively poor corneal penetration, and the increase of its trans-corneal delivery would be beneficial to reduce the amount or frequency of daily dose. In this study, ultrasound treatment was applied to enhance the trans-corneal delivery of gatifloxacin without damage. Experiments were conducted on mouse eyes in ex vivo and in vivo conditions. Ultrasound waves with 1 MHz in frequency, 1.3 W/cm(2) in intensity were applied onto the mouse cornea for 5 minutes, and then gatifloxacin ophthalmic solution was instilled and left there for 10 minutes. 3D gatifloxacin distribution in the cornea was measured by two-photon microscopy (TPM) imaging based on its intrinsic fluorescence. Longitudinal TPM imaging of ultrasound treated mouse corneas showed the increase of initial gatifloxacin intensities on the corneal surface compared to untreated mouse corneas by 67%, and then the increased gatifloxacin delivery into the cornea from the surface at later time. The delivered gatifloxacin in the corneal epithelium stayed longer in the ultrasound treated corneas than in the untreated corneas. The enhanced trans-corneal delivery and extended stay of gatifloxacin in the mouse cornea by ultrasound treatment could be beneficial for therapeutic effects. This study demonstrated the detail process of enhanced trans-corneal gatifloxacin delivery by ultrasound treatment. Nature Publishing Group UK 2019-10-29 /pmc/articles/PMC6820539/ /pubmed/31664145 http://dx.doi.org/10.1038/s41598-019-52069-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jegal, Uk Lee, Jun Ho Lee, Jungbin Jeong, Hyerin Kim, Myoung Joon Kim, Ki Hean Ultrasound-assisted gatifloxacin delivery in mouse cornea, in vivo |
title | Ultrasound-assisted gatifloxacin delivery in mouse cornea, in vivo |
title_full | Ultrasound-assisted gatifloxacin delivery in mouse cornea, in vivo |
title_fullStr | Ultrasound-assisted gatifloxacin delivery in mouse cornea, in vivo |
title_full_unstemmed | Ultrasound-assisted gatifloxacin delivery in mouse cornea, in vivo |
title_short | Ultrasound-assisted gatifloxacin delivery in mouse cornea, in vivo |
title_sort | ultrasound-assisted gatifloxacin delivery in mouse cornea, in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820539/ https://www.ncbi.nlm.nih.gov/pubmed/31664145 http://dx.doi.org/10.1038/s41598-019-52069-w |
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