Evidence map›Paper›PMID 26551329›Full record

ArticleInvestigative ophthalmology & visual science2015

A Novel, Real-Time, In Vivo Mouse Retinal Imaging System.

Mark C Butler, Jack M Sullivan

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Relieving bottlenecks in RNA drug discovery for retinal diseases.Advances in experimental medicine and biology · 2012
    Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Mark C ButlerResearch Service, VA Western New York Healthcare System, Buffalo, New York, United States 2Department of Ophthalmology, Ross Eye Institute, University at Buffalo-SUNY, Buffalo, New York, United States.
Jack M SullivanResearch Service, VA Western New York Healthcare System, Buffalo, New York, United States 2Department of Ophthalmology, Ross Eye Institute, University at Buffalo-SUNY, Buffalo, New York, United States 3Department of Pharmacology/Toxicology, University at.

Funding

A Ribozyme Rescue Strategy for Autosomal Dominant RPR01EY013433 · NEI · UPSTATE MEDICAL UNIVERSITY · PI SULLIVAN, JOHN M. · 2003 to 2019
$4.0M
UB VISION INFRASTRUCTURE CENTERR24EY016662 · NEI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI GONZALEZ-FERNANDEZ, FEDERICO · 2005 to 2009
$989k
A RIBOZYME RESCUE STRATEGY FOR DRY AGE-RELATED MACULAR DEGENERATIONI01BX000669 · VA · VA WESTERN NEW YORK HEALTHCARE SYSTEM · PI SULLIVAN, JOHN M. · 2009 to 2025
–
BLRD VA I01 BX000669NEI NIH HHS R01 EY013433NEI NIH HHS R24 EY016662
6 · The paper itself

Abstract

purposeTo develop an efficient, low-cost instrument for robust real-time imaging of the mouse retina in vivo, and assess system capabilities by evaluating various animal models.

methodsFollowing multiple disappointing attempts to visualize the mouse retina during a subretinal injection using commercially available systems, we identified the key limitation to be inadequate illumination due to off axis illumination and poor optical train optimization. Therefore, we designed a paraxial illumination system for Greenough-type stereo dissecting microscope incorporating an optimized optical launch and an efficiently coupled fiber optic delivery system. Excitation and emission filters control spectral bandwidth. A color coupled-charged device (CCD) camera is coupled to the microscope for image capture. Although, field of view (FOV) is constrained by the small pupil aperture, the high optical power of the mouse eye, and the long working distance (needed for surgical manipulations), these limitations can be compensated by eye positioning in order to observe the entire retina.

resultsThe retinal imaging system delivers an adjustable narrow beam to the dilated pupil with minimal vignetting. The optic nerve, vasculature, and posterior pole are crisply visualized and the entire retina can be observed through eye positioning. Normal and degenerative retinal phenotypes can be followed over time. Subretinal or intraocular injection procedures are followed in real time. Real-time, intravenous fluorescein angiography for the live mouse has been achieved.

conclusionsA novel device is established for real-time viewing and image capture of the small animal retina during subretinal injections for preclinical gene therapy studies.

Indexed as

AnimalsDisease Models, AnimalEquipment DesignFluorescein AngiographyFundus OculiMiceMice, Inbred C57BLMicroscopyRetinaRetinal Degeneration

Identifiers

PMID26551329
PMCPMC4642603

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.