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Thickness and Closure Kinetics of the Suprachoroidal Space Following Microneedle Injection of Liquid Formulations

PURPOSE: To determine the effect of injection volume and formulation of a microneedle injection into the suprachoroidal space (SCS) on SCS thickness and closure kinetics. METHODS: Microneedle injections containing 25 to 150 μL Hanks' balanced salt solution (HBSS) were performed in the rabbit SC...

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Autores principales: Chiang, Bryce, Venugopal, Nitin, Grossniklaus, Hans E., Jung, Jae Hwan, Edelhauser, Henry F., Prausnitz, Mark R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5283084/
https://www.ncbi.nlm.nih.gov/pubmed/28125842
http://dx.doi.org/10.1167/iovs.16-20377
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author Chiang, Bryce
Venugopal, Nitin
Grossniklaus, Hans E.
Jung, Jae Hwan
Edelhauser, Henry F.
Prausnitz, Mark R.
author_facet Chiang, Bryce
Venugopal, Nitin
Grossniklaus, Hans E.
Jung, Jae Hwan
Edelhauser, Henry F.
Prausnitz, Mark R.
author_sort Chiang, Bryce
collection PubMed
description PURPOSE: To determine the effect of injection volume and formulation of a microneedle injection into the suprachoroidal space (SCS) on SCS thickness and closure kinetics. METHODS: Microneedle injections containing 25 to 150 μL Hanks' balanced salt solution (HBSS) were performed in the rabbit SCS ex vivo. Distribution of SCS thickness was measured by ultrasonography and three-dimensional (3D) cryo-reconstruction. Microneedle injections were performed in the rabbit SCS in vivo using HBSS, Discovisc, and 1% to 5% carboxymethyl cellulose (CMC) in HBSS. Ultrasonography was used to track SCS thickness over time. RESULTS: Increasing HBSS injection volume increased the area of expanded SCS, but did not increase SCS thickness ex vivo. With SCS injections in vivo, the SCS initially expanded to thicknesses of 0.43 ± 0.06 mm with HBSS, 1.5 ± 0.4 mm with Discovisc, and 0.69 to 2.1 mm with 1% to 5% CMC. After injection with HBSS, Discovisc, and 1% CMC solution, the SCS collapsed to baseline with time constants of 19 minutes, 6 hours, and 2.4 days, respectively. In contrast, injections with 3% to 5% CMC solution resulted in SCS expansion to 2.3 to 2.8 mm over the course of 2.8 to 9.1 hours, after which the SCS collapsed to baseline with time constants of 4.5 to 9.2 days. CONCLUSIONS: With low-viscosity formulations, SCS expands to a thickness that remains roughly constant, independent of the volume of fluid injected. Increasing injection fluid viscosity significantly increased SCS thickness. Expansion of the SCS is hypothesized to be controlled by a balance between the viscous forces of the liquid formulation and the resistive biomechanical forces of the tissue.
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spelling pubmed-52830842017-02-01 Thickness and Closure Kinetics of the Suprachoroidal Space Following Microneedle Injection of Liquid Formulations Chiang, Bryce Venugopal, Nitin Grossniklaus, Hans E. Jung, Jae Hwan Edelhauser, Henry F. Prausnitz, Mark R. Invest Ophthalmol Vis Sci Physiology and Pharmacology PURPOSE: To determine the effect of injection volume and formulation of a microneedle injection into the suprachoroidal space (SCS) on SCS thickness and closure kinetics. METHODS: Microneedle injections containing 25 to 150 μL Hanks' balanced salt solution (HBSS) were performed in the rabbit SCS ex vivo. Distribution of SCS thickness was measured by ultrasonography and three-dimensional (3D) cryo-reconstruction. Microneedle injections were performed in the rabbit SCS in vivo using HBSS, Discovisc, and 1% to 5% carboxymethyl cellulose (CMC) in HBSS. Ultrasonography was used to track SCS thickness over time. RESULTS: Increasing HBSS injection volume increased the area of expanded SCS, but did not increase SCS thickness ex vivo. With SCS injections in vivo, the SCS initially expanded to thicknesses of 0.43 ± 0.06 mm with HBSS, 1.5 ± 0.4 mm with Discovisc, and 0.69 to 2.1 mm with 1% to 5% CMC. After injection with HBSS, Discovisc, and 1% CMC solution, the SCS collapsed to baseline with time constants of 19 minutes, 6 hours, and 2.4 days, respectively. In contrast, injections with 3% to 5% CMC solution resulted in SCS expansion to 2.3 to 2.8 mm over the course of 2.8 to 9.1 hours, after which the SCS collapsed to baseline with time constants of 4.5 to 9.2 days. CONCLUSIONS: With low-viscosity formulations, SCS expands to a thickness that remains roughly constant, independent of the volume of fluid injected. Increasing injection fluid viscosity significantly increased SCS thickness. Expansion of the SCS is hypothesized to be controlled by a balance between the viscous forces of the liquid formulation and the resistive biomechanical forces of the tissue. The Association for Research in Vision and Ophthalmology 2017-01 /pmc/articles/PMC5283084/ /pubmed/28125842 http://dx.doi.org/10.1167/iovs.16-20377 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Physiology and Pharmacology
Chiang, Bryce
Venugopal, Nitin
Grossniklaus, Hans E.
Jung, Jae Hwan
Edelhauser, Henry F.
Prausnitz, Mark R.
Thickness and Closure Kinetics of the Suprachoroidal Space Following Microneedle Injection of Liquid Formulations
title Thickness and Closure Kinetics of the Suprachoroidal Space Following Microneedle Injection of Liquid Formulations
title_full Thickness and Closure Kinetics of the Suprachoroidal Space Following Microneedle Injection of Liquid Formulations
title_fullStr Thickness and Closure Kinetics of the Suprachoroidal Space Following Microneedle Injection of Liquid Formulations
title_full_unstemmed Thickness and Closure Kinetics of the Suprachoroidal Space Following Microneedle Injection of Liquid Formulations
title_short Thickness and Closure Kinetics of the Suprachoroidal Space Following Microneedle Injection of Liquid Formulations
title_sort thickness and closure kinetics of the suprachoroidal space following microneedle injection of liquid formulations
topic Physiology and Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5283084/
https://www.ncbi.nlm.nih.gov/pubmed/28125842
http://dx.doi.org/10.1167/iovs.16-20377
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