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Micron oct

Manufactured by Phoenix Pharmaceuticals

The Micron OCT is a high-resolution optical coherence tomography (OCT) imaging system designed for research and clinical applications. It provides detailed, cross-sectional images of biological samples, enabling visualization of tissue microstructure. The core function of the Micron OCT is to capture and display these high-resolution images without interpretation or extrapolation.

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2 protocols using micron oct

1

Retinal Thickness Monitoring via OCT Imaging in Mouse Laser Injury Model

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OCT images were taken 1, 3, 7, 14, 30, 90, and 180 days after laser photocoagulation, as were corresponding OCT scans using a Micron IV fundus camera and an OCT Scan Head equipped with a mouse objective lens (Phoenix Research Labs, Pleasanton, CA, USA). The OCT device featured a broadband superluminescent diode at 830 nm, customized for retinal imaging of mice. The scan region on the mouse retina was 1.8 mm in the X and Y directions. Linear OCT scans consisted of a series of 1024 single point A-Scans. Right eyes had previously been dilated with 0.5% tropicamide (Santen Pharmaceutical Co. Ltd., Osaka, Japan) and hydroxyl ethyl cellulose (Senju Pharmaceutical Co. Ltd., Osaka, Japan), used as coupling gel. Images were captured from 20 positions for each eye using StreamPix 6 and Micron OCT commercial software (Phoenix Research Labs). Captured images were quantitatively analysed using “In Sight” software, which can automatically detect and measure each retinal layer. Using this software, the retinal thickness was measured at 20 recorded positions for each eye, and the average of all positions represented the overall retinal thickness.
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2

Quantitative Retinal GFP Imaging

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Fundus photographs were taken 3 to 4 months post injections with a Micron III (Phoenix Research Labs, Pleasanton, CA, USA) system equipped with an excitation filter at 482 nm and an emission filter at 536 nm. In addition, OCT scans and corresponding retinal fundus images were taken using the Phoenix Image-Guided OCT (Phoenix Research Labs) and Micron IV, respectively. Images were captured post injection at indicated time points using Micron OCT and StreamPix 5 commercial software (Phoenix Research Labs). Animals were anesthetized with an intraperitoneal injection of ketamine (85 mg/kg) and xylazine (5 mg/kg) 20 minutes prior to fundus imaging. The distribution of the GFP signals of the central retina was measured utilizing ImageJ (http://rsb.info.nih.gov/ij/ index.html; in the public domain). Briefly, photographs centered on the optic disc were used; the photographs were converted into grayscale 8-bit images, and an intensity threshold was applied to select GFP-positive areas from background signals. The number of GFP-positive pixels was counted and the percentage of positive pixels in the image was calculated. Statistical analyses were performed using Prism 7 (GraphPad Software, La Jolla, CA, USA).
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