Proflavine Hemisulfate as a Fluorescent Contrast Agent for Point-of-Care Cytology.
Proflavine hemisulfate, an acridine-derived fluorescent dye, can be used as a rapid stain for cytologic examination of biological specimens. Proflavine fluorescently stains cell nuclei and cytoplasmic structures, owing to its small amphipathic structure and ability to intercalate DNA. In this manusc...
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2015-01-01
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Series: | PLoS ONE |
Online Access: | https://doi.org/10.1371/journal.pone.0125598 |
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doaj-60fa1c11acbd4a84853b438f43e96d672021-03-03T20:04:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01105e012559810.1371/journal.pone.0125598Proflavine Hemisulfate as a Fluorescent Contrast Agent for Point-of-Care Cytology.Sandra P PrietoAmy J PowlessJackson W BoiceShree G SharmaTimothy J MuldoonProflavine hemisulfate, an acridine-derived fluorescent dye, can be used as a rapid stain for cytologic examination of biological specimens. Proflavine fluorescently stains cell nuclei and cytoplasmic structures, owing to its small amphipathic structure and ability to intercalate DNA. In this manuscript, we demonstrated the use of proflavine as a rapid cytologic dye on a number of specimens, including normal exfoliated oral squamous cells, cultured human oral squamous carcinoma cells, and leukocytes derived from whole blood specimens using a custom-built, portable, LED-illuminated fluorescence microscope. No incubation time was needed after suspending cells in 0.01% (w/v) proflavine diluted in saline. Images of proflavine stained oral cells had clearly visible nuclei as well as granular cytoplasm, while stained leukocytes exhibited bright nuclei, and highlighted the multilobar nature of nuclei in neutrophils. We also demonstrated the utility of quantitative analysis of digital images of proflavine stained cells, which can be used to detect significant morphological differences between different cell types. Proflavine stained oral cells have well-defined nuclei and cell membranes which allowed for quantitative analysis of nuclear to cytoplasmic ratios, as well as image texture analysis to extract quantitative image features.https://doi.org/10.1371/journal.pone.0125598 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sandra P Prieto Amy J Powless Jackson W Boice Shree G Sharma Timothy J Muldoon |
spellingShingle |
Sandra P Prieto Amy J Powless Jackson W Boice Shree G Sharma Timothy J Muldoon Proflavine Hemisulfate as a Fluorescent Contrast Agent for Point-of-Care Cytology. PLoS ONE |
author_facet |
Sandra P Prieto Amy J Powless Jackson W Boice Shree G Sharma Timothy J Muldoon |
author_sort |
Sandra P Prieto |
title |
Proflavine Hemisulfate as a Fluorescent Contrast Agent for Point-of-Care Cytology. |
title_short |
Proflavine Hemisulfate as a Fluorescent Contrast Agent for Point-of-Care Cytology. |
title_full |
Proflavine Hemisulfate as a Fluorescent Contrast Agent for Point-of-Care Cytology. |
title_fullStr |
Proflavine Hemisulfate as a Fluorescent Contrast Agent for Point-of-Care Cytology. |
title_full_unstemmed |
Proflavine Hemisulfate as a Fluorescent Contrast Agent for Point-of-Care Cytology. |
title_sort |
proflavine hemisulfate as a fluorescent contrast agent for point-of-care cytology. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2015-01-01 |
description |
Proflavine hemisulfate, an acridine-derived fluorescent dye, can be used as a rapid stain for cytologic examination of biological specimens. Proflavine fluorescently stains cell nuclei and cytoplasmic structures, owing to its small amphipathic structure and ability to intercalate DNA. In this manuscript, we demonstrated the use of proflavine as a rapid cytologic dye on a number of specimens, including normal exfoliated oral squamous cells, cultured human oral squamous carcinoma cells, and leukocytes derived from whole blood specimens using a custom-built, portable, LED-illuminated fluorescence microscope. No incubation time was needed after suspending cells in 0.01% (w/v) proflavine diluted in saline. Images of proflavine stained oral cells had clearly visible nuclei as well as granular cytoplasm, while stained leukocytes exhibited bright nuclei, and highlighted the multilobar nature of nuclei in neutrophils. We also demonstrated the utility of quantitative analysis of digital images of proflavine stained cells, which can be used to detect significant morphological differences between different cell types. Proflavine stained oral cells have well-defined nuclei and cell membranes which allowed for quantitative analysis of nuclear to cytoplasmic ratios, as well as image texture analysis to extract quantitative image features. |
url |
https://doi.org/10.1371/journal.pone.0125598 |
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