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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Main Authors: Sandra P Prieto, Amy J Powless, Jackson W Boice, Shree G Sharma, Timothy J Muldoon
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0125598
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spelling 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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