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Novel ophthalmic formulation of myriocin: implications in retinitis pigmentosa
Myriocin is an antibiotic derived from Mycelia sterilia, and is a potent inhibitor of serine palmitoyltransferase, the enzyme involved in the first step of sphingosine synthesis. Myriocin, inhibiting ceramide synthesis, has a great potential for treatment of diseases characterized by high ceramide l...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419690/ https://www.ncbi.nlm.nih.gov/pubmed/30883241 http://dx.doi.org/10.1080/10717544.2019.1574936 |
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author | Platania, Chiara Bianca Maria Dei Cas, Michele Cianciolo, Simona Fidilio, Annamaria Lazzara, Francesca Paroni, Rita Pignatello, Rosario Strettoi, Enrica Ghidoni, Riccardo Drago, Filippo Bucolo, Claudio |
author_facet | Platania, Chiara Bianca Maria Dei Cas, Michele Cianciolo, Simona Fidilio, Annamaria Lazzara, Francesca Paroni, Rita Pignatello, Rosario Strettoi, Enrica Ghidoni, Riccardo Drago, Filippo Bucolo, Claudio |
author_sort | Platania, Chiara Bianca Maria |
collection | PubMed |
description | Myriocin is an antibiotic derived from Mycelia sterilia, and is a potent inhibitor of serine palmitoyltransferase, the enzyme involved in the first step of sphingosine synthesis. Myriocin, inhibiting ceramide synthesis, has a great potential for treatment of diseases characterized by high ceramide levels in affected tissues, such as retinitis pigmentosa (RP). Drug delivery to the retina is a challenging task, which is generally by-passed through intravitreal injection, that represents a risky invasive procedure. We, therefore, developed and characterized an ophthalmic topical nanotechnological formulation based on a nanostructured lipid carrier (NLC) and containing myriocin. The ocular distribution of myriocin in the back of the eye was assessed both in rabbits and mice using LC-MS/MS. Moreover, rabbit retinal sphingolipid and ceramides levels, after myriocin-NLC (Myr-NLC) eye drops treatment, were assessed. The results demonstrated that Myr-NLC formulation is well tolerated and provided effective levels of myriocin in the back of the eye both in rabbits and mice. We found that Myr-NLC eye drops treatment was able to significantly decrease retinal sphingolipid levels. In conclusion, these data suggest that the Myr-NLC ophthalmic formulation is suitable for pharmaceutical development and warrants further clinical evaluation of this eye drops for the treatment of RP. |
format | Online Article Text |
id | pubmed-6419690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-64196902019-03-19 Novel ophthalmic formulation of myriocin: implications in retinitis pigmentosa Platania, Chiara Bianca Maria Dei Cas, Michele Cianciolo, Simona Fidilio, Annamaria Lazzara, Francesca Paroni, Rita Pignatello, Rosario Strettoi, Enrica Ghidoni, Riccardo Drago, Filippo Bucolo, Claudio Drug Deliv Research Article Myriocin is an antibiotic derived from Mycelia sterilia, and is a potent inhibitor of serine palmitoyltransferase, the enzyme involved in the first step of sphingosine synthesis. Myriocin, inhibiting ceramide synthesis, has a great potential for treatment of diseases characterized by high ceramide levels in affected tissues, such as retinitis pigmentosa (RP). Drug delivery to the retina is a challenging task, which is generally by-passed through intravitreal injection, that represents a risky invasive procedure. We, therefore, developed and characterized an ophthalmic topical nanotechnological formulation based on a nanostructured lipid carrier (NLC) and containing myriocin. The ocular distribution of myriocin in the back of the eye was assessed both in rabbits and mice using LC-MS/MS. Moreover, rabbit retinal sphingolipid and ceramides levels, after myriocin-NLC (Myr-NLC) eye drops treatment, were assessed. The results demonstrated that Myr-NLC formulation is well tolerated and provided effective levels of myriocin in the back of the eye both in rabbits and mice. We found that Myr-NLC eye drops treatment was able to significantly decrease retinal sphingolipid levels. In conclusion, these data suggest that the Myr-NLC ophthalmic formulation is suitable for pharmaceutical development and warrants further clinical evaluation of this eye drops for the treatment of RP. Taylor & Francis 2019-03-11 /pmc/articles/PMC6419690/ /pubmed/30883241 http://dx.doi.org/10.1080/10717544.2019.1574936 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Platania, Chiara Bianca Maria Dei Cas, Michele Cianciolo, Simona Fidilio, Annamaria Lazzara, Francesca Paroni, Rita Pignatello, Rosario Strettoi, Enrica Ghidoni, Riccardo Drago, Filippo Bucolo, Claudio Novel ophthalmic formulation of myriocin: implications in retinitis pigmentosa |
title | Novel ophthalmic formulation of myriocin: implications in retinitis pigmentosa |
title_full | Novel ophthalmic formulation of myriocin: implications in retinitis pigmentosa |
title_fullStr | Novel ophthalmic formulation of myriocin: implications in retinitis pigmentosa |
title_full_unstemmed | Novel ophthalmic formulation of myriocin: implications in retinitis pigmentosa |
title_short | Novel ophthalmic formulation of myriocin: implications in retinitis pigmentosa |
title_sort | novel ophthalmic formulation of myriocin: implications in retinitis pigmentosa |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419690/ https://www.ncbi.nlm.nih.gov/pubmed/30883241 http://dx.doi.org/10.1080/10717544.2019.1574936 |
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