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Monitoring Dehydration and Clearing in Tissue Processing for High-Quality Clinical Pathology

The development of precision testing for disease diagnosis has advanced medicine by specifically matching patients with drugs to treat specific diseases. High-quality diagnostics start with high-quality tissue specimens. The development and optimization of tissue handling and processing have lagged...

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Autores principales: Lerch, Melissa L., Bauer, Daniel R., Theiss, Abbey, Chafin, David, Otter, Michael, Baird, Geoffrey S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6703239/
https://www.ncbi.nlm.nih.gov/pubmed/31107113
http://dx.doi.org/10.1089/bio.2018.0122
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author Lerch, Melissa L.
Bauer, Daniel R.
Theiss, Abbey
Chafin, David
Otter, Michael
Baird, Geoffrey S.
author_facet Lerch, Melissa L.
Bauer, Daniel R.
Theiss, Abbey
Chafin, David
Otter, Michael
Baird, Geoffrey S.
author_sort Lerch, Melissa L.
collection PubMed
description The development of precision testing for disease diagnosis has advanced medicine by specifically matching patients with drugs to treat specific diseases. High-quality diagnostics start with high-quality tissue specimens. The development and optimization of tissue handling and processing have lagged behind bioassay development. Ultrasound time-of-flight (TOF) technology has been successfully used to monitor the critical processing step of tissue fixation with formalin. In this study, we expand the use of this technology to monitor tissue dehydration and clearing by analyzing TOF signals from 270 different specimens, representing 13 different tissue types obtained through surgical resections. We determined the time constant τ(90) for each tissue type for the following tissue processing solvents: 70% ethanol, 90% ethanol, 100% ethanol, and xylene. The TOF signals were correlated with tissue morphology to ensure that high-quality tissue was produced. Tissues can be grouped into those exhibiting fast and slow reagent diffusion. We monitored incomplete dehydration of tissue by skipping a key processing step, dehydration in absolute ethanol, and then correlated the τ(90) with poor histomorphology, demonstrating that the technique can detect significant processing errors. Ultrasound TOF technology can therefore be used to monitor all phases of tissue processing cycle and yields an important preanalytical quality metric.
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spelling pubmed-67032392019-08-22 Monitoring Dehydration and Clearing in Tissue Processing for High-Quality Clinical Pathology Lerch, Melissa L. Bauer, Daniel R. Theiss, Abbey Chafin, David Otter, Michael Baird, Geoffrey S. Biopreserv Biobank Original Articles The development of precision testing for disease diagnosis has advanced medicine by specifically matching patients with drugs to treat specific diseases. High-quality diagnostics start with high-quality tissue specimens. The development and optimization of tissue handling and processing have lagged behind bioassay development. Ultrasound time-of-flight (TOF) technology has been successfully used to monitor the critical processing step of tissue fixation with formalin. In this study, we expand the use of this technology to monitor tissue dehydration and clearing by analyzing TOF signals from 270 different specimens, representing 13 different tissue types obtained through surgical resections. We determined the time constant τ(90) for each tissue type for the following tissue processing solvents: 70% ethanol, 90% ethanol, 100% ethanol, and xylene. The TOF signals were correlated with tissue morphology to ensure that high-quality tissue was produced. Tissues can be grouped into those exhibiting fast and slow reagent diffusion. We monitored incomplete dehydration of tissue by skipping a key processing step, dehydration in absolute ethanol, and then correlated the τ(90) with poor histomorphology, demonstrating that the technique can detect significant processing errors. Ultrasound TOF technology can therefore be used to monitor all phases of tissue processing cycle and yields an important preanalytical quality metric. Mary Ann Liebert, Inc., publishers 2019-08-01 2019-08-12 /pmc/articles/PMC6703239/ /pubmed/31107113 http://dx.doi.org/10.1089/bio.2018.0122 Text en © Melissa L. Lerch, et al., 2019; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are cited.
spellingShingle Original Articles
Lerch, Melissa L.
Bauer, Daniel R.
Theiss, Abbey
Chafin, David
Otter, Michael
Baird, Geoffrey S.
Monitoring Dehydration and Clearing in Tissue Processing for High-Quality Clinical Pathology
title Monitoring Dehydration and Clearing in Tissue Processing for High-Quality Clinical Pathology
title_full Monitoring Dehydration and Clearing in Tissue Processing for High-Quality Clinical Pathology
title_fullStr Monitoring Dehydration and Clearing in Tissue Processing for High-Quality Clinical Pathology
title_full_unstemmed Monitoring Dehydration and Clearing in Tissue Processing for High-Quality Clinical Pathology
title_short Monitoring Dehydration and Clearing in Tissue Processing for High-Quality Clinical Pathology
title_sort monitoring dehydration and clearing in tissue processing for high-quality clinical pathology
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6703239/
https://www.ncbi.nlm.nih.gov/pubmed/31107113
http://dx.doi.org/10.1089/bio.2018.0122
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