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Optisol gs medium

Manufactured by Bausch & Lomb
Sourced in United States

Optisol-GS medium is a storage solution used for preserving corneal tissue prior to transplantation. It is designed to maintain the viability and integrity of the cornea during storage and transportation.

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3 protocols using optisol gs medium

1

Corneal Endothelium Imaging and Pressure Control

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The donor corneas were received from Lions Eye Bank at Albany and Rochester, New York. Corneas were preserved upon recovery in Optisol-GS medium (Bausch and Lomb, Rochester) inside a storage container for corneas and were delivered to the University of Rochester inside a polystyrene box filled with packs of ice. The donor age ranged from 32 to 66 years. Time from death to tissue preservation was about 5 to 22 h. Donor tissue details are summarized in Table 1. Prior to imaging, corneas were stored at room temperature for 1 h to improve the image quality.37 (link) As a reference, a conventional noncontact specular microscope, Kerato Analyzer (EKA-98, Konan Medical Inc., Japan) was first employed to image the central location of the corneal endothelium through the storage container. A USAF calibration target (R1L1S1P, THORLABS) was used to convert the number of pixels into the physical dimension of endothelial cells area. Corneas were then removed from the storage container and mounted onto a corneal artificial chamber (Moria, Inc., France) equipped with a microfluidic system that was used to control the physiological pressure inside the anterior chamber. The latter was perfused using Optisol to avoid air bubbles inside the anterior chamber.
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2

Corneal Stromal Ablation for DMEK

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A total of 23 human corneal buttons were obtained from the Philipps University of Marburg after removal of the Descemet membrane for DMEK (Descemet Membrane Endothelial Keratoplasty) in specimens with a consent for both transplantation and research. Corneal buttons were preserved in Optisol GS medium (Bausch & Lomb, Rochester, NY, USA) and kept refrigerated for a maximum of 14 days before measurement. Prior to measurements, corneal buttons were mounted on an artificial anterior chamber (Schwind eye-tech-solutions, Kleinostheim, Germany) and the partially degraded epithelial layer was removed to ensure a smooth surface and facilitate later surface detection. Subsequently, one group of corneal buttons (n = 11) underwent 20 µm excimer laser ablation (AMARIS 750; Schwind eye-tech solutions) within an optical zone of 10 mm diameter from the anterior stroma to remove Bowman's layer. In the other group (n = 12) Bowman's layer was left intact.
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3

Corneal Endothelial Cell Density Evaluation

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The corneoscleral buttons were stored in Optisol -GS medium (Bausch & Lomb, Irvine, CA, USA) at 4 °C. The endothelial cell density (ECD) was quantified using EB-3000 XYZ Eyebank specular microscope (HAI Laboratories Inc., Lexington, MA, USA). All corneas with ECD ≥ 2800 cells/mm2 were utilized for surgery.
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