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Eyedrop-based macromolecular ophthalmic drug delivery for ocular fundus disease treatment
Therapeutic antibodies are extensively used to treat fundus diseases by intravitreal injection, as eyedrop formulation has been rather challenging due to the presence of ocular barriers. Here, an innovative penetrating carrier was developed for antibody delivery in eyedrop formulations. We found tha...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9882978/ https://www.ncbi.nlm.nih.gov/pubmed/36706184 http://dx.doi.org/10.1126/sciadv.abq3104 |
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author | Shen, Jingjing Gao, Huiqin Chen, Linfu Jiang, Yutong Li, Shu Chao, Yu Liu, Nanhui Wang, Yufei Wei, Ting Liu, Yan Li, Jipeng Chen, Muchao Zhu, Jiafei Liang, Juan Zhou, Xiaoyu Zhang, Xiaofeng Gu, Ping Chen, Qian Liu, Zhuang |
author_facet | Shen, Jingjing Gao, Huiqin Chen, Linfu Jiang, Yutong Li, Shu Chao, Yu Liu, Nanhui Wang, Yufei Wei, Ting Liu, Yan Li, Jipeng Chen, Muchao Zhu, Jiafei Liang, Juan Zhou, Xiaoyu Zhang, Xiaofeng Gu, Ping Chen, Qian Liu, Zhuang |
author_sort | Shen, Jingjing |
collection | PubMed |
description | Therapeutic antibodies are extensively used to treat fundus diseases by intravitreal injection, as eyedrop formulation has been rather challenging due to the presence of ocular barriers. Here, an innovative penetrating carrier was developed for antibody delivery in eyedrop formulations. We found that fluorocarbon-modified chitosan (FCS) would self-assemble with proteins to form nanocomplexes, which could effectively pass across the complicated ocular structure to reach the posterior eye segments in both mice and rabbits. In a choroidal melanoma–bearing mouse model, eyedrops containing FCS/anti-PDL1 could induce stronger antitumor immune responses than those triggered by intravenous injection of anti-PDL1. Moreover, in choroidal neovascularization–bearing mouse and rabbit models, FCS/anti-VEGFA eyedrops effectively inhibited vascular proliferation, achieving comparable therapeutic responses to those observed with intravitreal injection of anti-VEGFA. Our work presents an effective delivery carrier to treat fundus diseases using eyedrop of therapeutic proteins, which may enable at-home treatment of many eye diseases with great patient compliance. |
format | Online Article Text |
id | pubmed-9882978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-98829782023-02-08 Eyedrop-based macromolecular ophthalmic drug delivery for ocular fundus disease treatment Shen, Jingjing Gao, Huiqin Chen, Linfu Jiang, Yutong Li, Shu Chao, Yu Liu, Nanhui Wang, Yufei Wei, Ting Liu, Yan Li, Jipeng Chen, Muchao Zhu, Jiafei Liang, Juan Zhou, Xiaoyu Zhang, Xiaofeng Gu, Ping Chen, Qian Liu, Zhuang Sci Adv Biomedicine and Life Sciences Therapeutic antibodies are extensively used to treat fundus diseases by intravitreal injection, as eyedrop formulation has been rather challenging due to the presence of ocular barriers. Here, an innovative penetrating carrier was developed for antibody delivery in eyedrop formulations. We found that fluorocarbon-modified chitosan (FCS) would self-assemble with proteins to form nanocomplexes, which could effectively pass across the complicated ocular structure to reach the posterior eye segments in both mice and rabbits. In a choroidal melanoma–bearing mouse model, eyedrops containing FCS/anti-PDL1 could induce stronger antitumor immune responses than those triggered by intravenous injection of anti-PDL1. Moreover, in choroidal neovascularization–bearing mouse and rabbit models, FCS/anti-VEGFA eyedrops effectively inhibited vascular proliferation, achieving comparable therapeutic responses to those observed with intravitreal injection of anti-VEGFA. Our work presents an effective delivery carrier to treat fundus diseases using eyedrop of therapeutic proteins, which may enable at-home treatment of many eye diseases with great patient compliance. American Association for the Advancement of Science 2023-01-27 /pmc/articles/PMC9882978/ /pubmed/36706184 http://dx.doi.org/10.1126/sciadv.abq3104 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Shen, Jingjing Gao, Huiqin Chen, Linfu Jiang, Yutong Li, Shu Chao, Yu Liu, Nanhui Wang, Yufei Wei, Ting Liu, Yan Li, Jipeng Chen, Muchao Zhu, Jiafei Liang, Juan Zhou, Xiaoyu Zhang, Xiaofeng Gu, Ping Chen, Qian Liu, Zhuang Eyedrop-based macromolecular ophthalmic drug delivery for ocular fundus disease treatment |
title | Eyedrop-based macromolecular ophthalmic drug delivery for ocular fundus disease treatment |
title_full | Eyedrop-based macromolecular ophthalmic drug delivery for ocular fundus disease treatment |
title_fullStr | Eyedrop-based macromolecular ophthalmic drug delivery for ocular fundus disease treatment |
title_full_unstemmed | Eyedrop-based macromolecular ophthalmic drug delivery for ocular fundus disease treatment |
title_short | Eyedrop-based macromolecular ophthalmic drug delivery for ocular fundus disease treatment |
title_sort | eyedrop-based macromolecular ophthalmic drug delivery for ocular fundus disease treatment |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9882978/ https://www.ncbi.nlm.nih.gov/pubmed/36706184 http://dx.doi.org/10.1126/sciadv.abq3104 |
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