IOVS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by McLaren, J. W.
Right arrow Articles by Brubaker, R. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McLaren, J. W.
Right arrow Articles by Brubaker, R. F.

Investigative Ophthalmology & Visual Science, Vol 29, 1285-1293, Copyright © 1988 by Association for Research in Vision and Ophthalmology


ARTICLES AND REPORTS

A scanning ocular spectrofluorophotometer

JW McLaren and RF Brubaker
Department of Ophthalmology, Mayo Clinic, Rochester, MN 55905.

We describe an instrument called a scanning ocular spectrofluorophotometer (SOSF) that measures fluorescence in a two- dimensional cross-section through the anterior chamber and cornea and provides the ability to change excitation and emission wavelengths rapidly. The output of a xenon arc lamp is filtered by a diffraction grating monochromator which has a bandpass of 4 nm and a range of 400 to 800 nm. Light emitted from the fluorophore is filtered by a variable wavelength interference filter which has a bandpass of approximately 11 nm and a range of 400 to 700 nm. To demonstrate the versatility of the instrument, we measured the spectra of fluorescein, fluorescein glucuronide and rhodamine B in the anterior chambers and corneas of pigmented rabbits after topical administration. We also measured simultaneously and independently the redistribution and disappearance of a mixture of fluorescein-labeled dextran and rhodamine B after intracameral injection. Rhodamine B was very rapidly absorbed by the cornea and lens while fluorescein-dextran was not measurable in the cornea before 4 hr. The SOSF provides a means of carrying out spectrofluorophotometry in the living eye and carrying out kinetic experiments which would otherwise be awkward or impossible.


This article has been cited by other articles:


Home page
Br J OphthalmolHome page
J Miller, W S Wilson, C G Wilson, and D Uttamchandani
Minimally invasive, direct, real time measurement of drug concentration in the anterior eye
Br J Ophthalmol, September 1, 2005; 89(9): 1147 - 1151.
[Abstract] [Full Text] [PDF]


Home page
Arch OphthalmolHome page
N. Ziai, J. W. Dolan, R. D. Kacere, and R. F. Brubaker
The Effects on Aqueous Dynamics of PhXA41, a New Prostaglandin F2{alpha} Analogue, After Topical Application in Normal and Ocular Hypertensive Human Eyes
Arch Ophthalmol, October 1, 1993; 111(10): 1351 - 1358.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1988 by the Association for Research in Vision and Ophthalmology