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A Novel Device for Suprachoroidal Drug Delivery to Retina: Evaluation in Nonhuman Primates

PURPOSE: Evaluation of distribution and tolerance of suprachoroidal injection of indocyanine green (ICG) in nonhuman primates (NHPs) using a novel suprachoroidal (SC) delivery technology. METHODS: Three live and three euthanized African green monkeys were injected with 150 or 200 µL ICG/eye into the...

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Autores principales: Rotenstreich, Ygal, Sher, Ifat, Lawrence, Matthew, Mangelus, Miriam, Ingerman, Avner, Barak, Yoreh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257339/
https://www.ncbi.nlm.nih.gov/pubmed/37289173
http://dx.doi.org/10.1167/tvst.12.6.3
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author Rotenstreich, Ygal
Sher, Ifat
Lawrence, Matthew
Mangelus, Miriam
Ingerman, Avner
Barak, Yoreh
author_facet Rotenstreich, Ygal
Sher, Ifat
Lawrence, Matthew
Mangelus, Miriam
Ingerman, Avner
Barak, Yoreh
author_sort Rotenstreich, Ygal
collection PubMed
description PURPOSE: Evaluation of distribution and tolerance of suprachoroidal injection of indocyanine green (ICG) in nonhuman primates (NHPs) using a novel suprachoroidal (SC) delivery technology. METHODS: Three live and three euthanized African green monkeys were injected with 150 or 200 µL ICG/eye into the SC space of both eyes, 2.5 mm posterior to the limbus in the inferior quadrant, utilizing a novel SC injector. Eyes were analyzed by imaging of scleral flatmounts. Live animals were observed for 24 hours for general health. Ophthalmic evaluation included slit-lamp biomicroscopy, tonometry, fundus imaging, confocal laser ophthalmoscopy, and spectral-domain optical coherence tomography (SD-OCT) before and at 10 minutes and 1, 3, and 24 hours post-injection. RESULTS: SC dosing was successfully performed in all eyes. Infrared fundus imaging demonstrated ICG distribution throughout the posterior segment, reaching the macula within 24 hours post-injection. No inflammation, intravitreal penetration, SC blebs, retinal detachment, or hemorrhages were detected. No significant changes were observed in retinal thickness by SD-OCT (P = 0.267, ANOVA). A mild, statistically insignificant elevation in intraocular pressure was observed within 10 minutes post-injection (mean ± standard error: 7.28 ± 5.09 mmHg; P = 0.061) and was spontaneously resolved within the first hour after dosing. CONCLUSIONS: Suprachoroidal injection of 150 to 200 µL ICG dye was successfully performed and well tolerated in NHP eyes, with rapid distribution into the macular region and throughout the posterior pole. TRANSLATIONAL RELEVANCE: This novel SC drug delivery system may potentially provide safe and effective delivery of therapeutics to the posterior pole region in humans.
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spelling pubmed-102573392023-06-11 A Novel Device for Suprachoroidal Drug Delivery to Retina: Evaluation in Nonhuman Primates Rotenstreich, Ygal Sher, Ifat Lawrence, Matthew Mangelus, Miriam Ingerman, Avner Barak, Yoreh Transl Vis Sci Technol Retina PURPOSE: Evaluation of distribution and tolerance of suprachoroidal injection of indocyanine green (ICG) in nonhuman primates (NHPs) using a novel suprachoroidal (SC) delivery technology. METHODS: Three live and three euthanized African green monkeys were injected with 150 or 200 µL ICG/eye into the SC space of both eyes, 2.5 mm posterior to the limbus in the inferior quadrant, utilizing a novel SC injector. Eyes were analyzed by imaging of scleral flatmounts. Live animals were observed for 24 hours for general health. Ophthalmic evaluation included slit-lamp biomicroscopy, tonometry, fundus imaging, confocal laser ophthalmoscopy, and spectral-domain optical coherence tomography (SD-OCT) before and at 10 minutes and 1, 3, and 24 hours post-injection. RESULTS: SC dosing was successfully performed in all eyes. Infrared fundus imaging demonstrated ICG distribution throughout the posterior segment, reaching the macula within 24 hours post-injection. No inflammation, intravitreal penetration, SC blebs, retinal detachment, or hemorrhages were detected. No significant changes were observed in retinal thickness by SD-OCT (P = 0.267, ANOVA). A mild, statistically insignificant elevation in intraocular pressure was observed within 10 minutes post-injection (mean ± standard error: 7.28 ± 5.09 mmHg; P = 0.061) and was spontaneously resolved within the first hour after dosing. CONCLUSIONS: Suprachoroidal injection of 150 to 200 µL ICG dye was successfully performed and well tolerated in NHP eyes, with rapid distribution into the macular region and throughout the posterior pole. TRANSLATIONAL RELEVANCE: This novel SC drug delivery system may potentially provide safe and effective delivery of therapeutics to the posterior pole region in humans. The Association for Research in Vision and Ophthalmology 2023-06-08 /pmc/articles/PMC10257339/ /pubmed/37289173 http://dx.doi.org/10.1167/tvst.12.6.3 Text en Copyright 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Retina
Rotenstreich, Ygal
Sher, Ifat
Lawrence, Matthew
Mangelus, Miriam
Ingerman, Avner
Barak, Yoreh
A Novel Device for Suprachoroidal Drug Delivery to Retina: Evaluation in Nonhuman Primates
title A Novel Device for Suprachoroidal Drug Delivery to Retina: Evaluation in Nonhuman Primates
title_full A Novel Device for Suprachoroidal Drug Delivery to Retina: Evaluation in Nonhuman Primates
title_fullStr A Novel Device for Suprachoroidal Drug Delivery to Retina: Evaluation in Nonhuman Primates
title_full_unstemmed A Novel Device for Suprachoroidal Drug Delivery to Retina: Evaluation in Nonhuman Primates
title_short A Novel Device for Suprachoroidal Drug Delivery to Retina: Evaluation in Nonhuman Primates
title_sort novel device for suprachoroidal drug delivery to retina: evaluation in nonhuman primates
topic Retina
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257339/
https://www.ncbi.nlm.nih.gov/pubmed/37289173
http://dx.doi.org/10.1167/tvst.12.6.3
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