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Topical ocular delivery of nanoparticles with epoetin beta in Wistar Hannover rats
Topical instillation of drugs targeting the posterior ocular segment is an expanding area of research. Chitosan and hyaluronic acid have remarkable mucoadhesive properties and potentially enhance pre-corneal retention time after topical instillation. Bearing this in mind, we explored the possibility...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883504/ https://www.ncbi.nlm.nih.gov/pubmed/36707615 http://dx.doi.org/10.1038/s41598-023-28845-0 |
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author | Silva, Beatriz Gonçalves, Lídia M. São Braz, Berta Delgado, Esmeralda |
author_facet | Silva, Beatriz Gonçalves, Lídia M. São Braz, Berta Delgado, Esmeralda |
author_sort | Silva, Beatriz |
collection | PubMed |
description | Topical instillation of drugs targeting the posterior ocular segment is an expanding area of research. Chitosan and hyaluronic acid have remarkable mucoadhesive properties and potentially enhance pre-corneal retention time after topical instillation. Bearing this in mind, we explored the possibility of delivering epoetin beta (EPOβ) to the posterior segment of the eye in a chitosan-hyaluronic acid (CS/HA-EPOβ) nanoparticulate system using the topical route of administration. Complete ophthalmological examinations, electroretinography and microhematocrit evaluations were performed in Wistar Hannover (WH) rats, before and after topical administration of nanoparticles. The right eye received CS/HA-EPOβ and the left eye received only empty nanocarriers (control). Animals were split into 6 groups and at designated timepoints, all animals from each group (n = 3) were euthanized and both eyes enucleated. Retinal morphology and EPOβ ocular distribution were assessed, respectively, through hematoxylin and eosin (HE) and immunofluorescence staining. After topical administration, no adverse ocular signs were noted and no significant changes either in microhematocrits nor in electroretinographies were detected. During the study, intraocular pressure (IOP) was always kept within physiological range bilaterally. No histological changes were detected in any of the ocular globes. Immunofluorescence enabled the identification of EPOβ in the retina 12 h after the administration, its presence still being detectable at day 21. In conclusion, CS/HA nanoparticles could efficiently deliver EPOβ to the retina of WH rats after topical instillation, being considered biologically safe. Topical administration of this nanoformulation could be a valuable tool for retinal neuroprotection, decreasing risks associated with more invasive routes of administration, being cost effective and also increasing long-term patients’ compliance. |
format | Online Article Text |
id | pubmed-9883504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98835042023-01-29 Topical ocular delivery of nanoparticles with epoetin beta in Wistar Hannover rats Silva, Beatriz Gonçalves, Lídia M. São Braz, Berta Delgado, Esmeralda Sci Rep Article Topical instillation of drugs targeting the posterior ocular segment is an expanding area of research. Chitosan and hyaluronic acid have remarkable mucoadhesive properties and potentially enhance pre-corneal retention time after topical instillation. Bearing this in mind, we explored the possibility of delivering epoetin beta (EPOβ) to the posterior segment of the eye in a chitosan-hyaluronic acid (CS/HA-EPOβ) nanoparticulate system using the topical route of administration. Complete ophthalmological examinations, electroretinography and microhematocrit evaluations were performed in Wistar Hannover (WH) rats, before and after topical administration of nanoparticles. The right eye received CS/HA-EPOβ and the left eye received only empty nanocarriers (control). Animals were split into 6 groups and at designated timepoints, all animals from each group (n = 3) were euthanized and both eyes enucleated. Retinal morphology and EPOβ ocular distribution were assessed, respectively, through hematoxylin and eosin (HE) and immunofluorescence staining. After topical administration, no adverse ocular signs were noted and no significant changes either in microhematocrits nor in electroretinographies were detected. During the study, intraocular pressure (IOP) was always kept within physiological range bilaterally. No histological changes were detected in any of the ocular globes. Immunofluorescence enabled the identification of EPOβ in the retina 12 h after the administration, its presence still being detectable at day 21. In conclusion, CS/HA nanoparticles could efficiently deliver EPOβ to the retina of WH rats after topical instillation, being considered biologically safe. Topical administration of this nanoformulation could be a valuable tool for retinal neuroprotection, decreasing risks associated with more invasive routes of administration, being cost effective and also increasing long-term patients’ compliance. Nature Publishing Group UK 2023-01-27 /pmc/articles/PMC9883504/ /pubmed/36707615 http://dx.doi.org/10.1038/s41598-023-28845-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Silva, Beatriz Gonçalves, Lídia M. São Braz, Berta Delgado, Esmeralda Topical ocular delivery of nanoparticles with epoetin beta in Wistar Hannover rats |
title | Topical ocular delivery of nanoparticles with epoetin beta in Wistar Hannover rats |
title_full | Topical ocular delivery of nanoparticles with epoetin beta in Wistar Hannover rats |
title_fullStr | Topical ocular delivery of nanoparticles with epoetin beta in Wistar Hannover rats |
title_full_unstemmed | Topical ocular delivery of nanoparticles with epoetin beta in Wistar Hannover rats |
title_short | Topical ocular delivery of nanoparticles with epoetin beta in Wistar Hannover rats |
title_sort | topical ocular delivery of nanoparticles with epoetin beta in wistar hannover rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883504/ https://www.ncbi.nlm.nih.gov/pubmed/36707615 http://dx.doi.org/10.1038/s41598-023-28845-0 |
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