1995PubMedRequires access

[Differential value of various vital stains of corneal endothelium].

Frank Wilhelm, Matthias F. Melzig, T Görscher, G Franke

Open publisher page 6 citations

Abstract

Specular microscopy shows the integrity of the endothelial cell pattern, and vital staining methods allow the evaluation of endothelial viability. Dyes commonly used such as trypan blue enter the cells passively through the disturbed membrane. The uptake of fluorescein diacetate (FDA) is an active process. To compare the efficiency of the two methods we performed double stainings and examined the results. Pig cornea endothelium was stained by both trypan blue and FDA and vital and non-vital cells were compared. More non-vital cells were stained by FDA than by trypan blue, indicating that cells with membranes that are not permeable by trypan blue cannot metabolize FDA. This fact is important where estimating the endothelial viability of donor corneas.

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What this paper is about

Specular microscopy shows the integrity of the endothelial cell pattern, and vital staining methods allow the evaluation of endothelial viability. Dyes commonly used such as trypan blue enter the cells passively through the disturbed membrane. The uptake of fluorescein diacetate (FDA) is an active process. To compare the efficiency of the two methods we performed double stainings and examined the results. Pig cornea endothelium was stained by both trypan blue and FDA and vital and non-vital cells were compared. More non-vital cells were stained by FDA than by trypan blue, indicating that cells with membranes that are not permeable by trypan blue cannot metabolize FDA. This fact is important where estimating the endothelial viability of donor corneas.

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OpenAlex reports 6 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Specular microscopy shows the integrity of the endothelial cell pattern, and vital staining methods allow the evaluation of endothelial viability. Dyes commonly used such as trypan blue enter the cells passively through the disturbed membrane. The uptake of fluorescein diacetate (FDA) is an active process. To compare the efficiency of the two methods we performed double stainings and examined the results. Pig cornea endothelium was stained by both trypan blue and FDA and vital and non-vital cells were compared. More non-vital cells were stained by FDA than by trypan blue, indicating that cells with membranes that are not permeable by trypan blue cannot metabolize FDA. This fact is important where estimating the endothelial viability of donor corneas.

Key concepts: Trypan blue, Vital stain, Corneal endothelium, Endothelium, Cornea, Fluorescein, Staining, Viability assay

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