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Detection of glycosaminoglycan loss in articular cartilage by fluorescence lifetime imaging
Glycosaminoglycan (GAG) loss is an early marker of osteoarthritis, which is a clinical late stage disease that affects millions of people worldwide. The goal of our study was to evaluate the ability of a fiber-based fluorescence lifetime imaging (FLIm) technique to detect GAG loss in articular carti...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Photo-Optical Instrumentation Engineers
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357192/ https://www.ncbi.nlm.nih.gov/pubmed/30578627 http://dx.doi.org/10.1117/1.JBO.23.12.126002 |
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author | Zhou, Xiangnan Haudenschild, Anne K. Sherlock, Benjamin E. Hu, Jerry C. Leach, J. Kent Athanasiou, Kyriacos A. Marcu, Laura |
author_facet | Zhou, Xiangnan Haudenschild, Anne K. Sherlock, Benjamin E. Hu, Jerry C. Leach, J. Kent Athanasiou, Kyriacos A. Marcu, Laura |
author_sort | Zhou, Xiangnan |
collection | PubMed |
description | Glycosaminoglycan (GAG) loss is an early marker of osteoarthritis, which is a clinical late stage disease that affects millions of people worldwide. The goal of our study was to evaluate the ability of a fiber-based fluorescence lifetime imaging (FLIm) technique to detect GAG loss in articular cartilage. Native bovine cartilage explants ([Formula: see text]) were exposed to 0 (control), 0.5 (low), or [Formula: see text] (high) concentrations of chondroitinase ABC (cABC) to create samples with different levels of GAG loss. FLIm assessment (excitation: 355 nm; detection: channel 1: 375 to 410 nm, channel 2: 450 to 485 nm, channel 3: 530 to 565 nm) was conducted on depth-resolved cross-sections of the cartilage sample. FLIm images, validated with histology, revealed that loss of GAG resulted in a decrease of fluorescence lifetime values in channel 2 ([Formula: see text] , [Formula: see text]) and channel 3 ([Formula: see text] , [Formula: see text]) compared to control samples (channel 2: 6.34 ns; channel 3: 5.22 ns). Fluorescence intensity ratio values were lower in channel 1 (37%, [Formula: see text]) and channel 2 (31% decrease, [Formula: see text]) and higher in channel 3 (23%, [Formula: see text]) relative to control samples. These results show that FLIm can detect the loss of GAG in articular cartilage and support further investigation into the feasibility of in vivo FLIm arthroscopy. |
format | Online Article Text |
id | pubmed-8357192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Society of Photo-Optical Instrumentation Engineers |
record_format | MEDLINE/PubMed |
spelling | pubmed-83571922021-08-12 Detection of glycosaminoglycan loss in articular cartilage by fluorescence lifetime imaging Zhou, Xiangnan Haudenschild, Anne K. Sherlock, Benjamin E. Hu, Jerry C. Leach, J. Kent Athanasiou, Kyriacos A. Marcu, Laura J Biomed Opt Imaging Glycosaminoglycan (GAG) loss is an early marker of osteoarthritis, which is a clinical late stage disease that affects millions of people worldwide. The goal of our study was to evaluate the ability of a fiber-based fluorescence lifetime imaging (FLIm) technique to detect GAG loss in articular cartilage. Native bovine cartilage explants ([Formula: see text]) were exposed to 0 (control), 0.5 (low), or [Formula: see text] (high) concentrations of chondroitinase ABC (cABC) to create samples with different levels of GAG loss. FLIm assessment (excitation: 355 nm; detection: channel 1: 375 to 410 nm, channel 2: 450 to 485 nm, channel 3: 530 to 565 nm) was conducted on depth-resolved cross-sections of the cartilage sample. FLIm images, validated with histology, revealed that loss of GAG resulted in a decrease of fluorescence lifetime values in channel 2 ([Formula: see text] , [Formula: see text]) and channel 3 ([Formula: see text] , [Formula: see text]) compared to control samples (channel 2: 6.34 ns; channel 3: 5.22 ns). Fluorescence intensity ratio values were lower in channel 1 (37%, [Formula: see text]) and channel 2 (31% decrease, [Formula: see text]) and higher in channel 3 (23%, [Formula: see text]) relative to control samples. These results show that FLIm can detect the loss of GAG in articular cartilage and support further investigation into the feasibility of in vivo FLIm arthroscopy. Society of Photo-Optical Instrumentation Engineers 2018-12-21 2018-12 /pmc/articles/PMC8357192/ /pubmed/30578627 http://dx.doi.org/10.1117/1.JBO.23.12.126002 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI. |
spellingShingle | Imaging Zhou, Xiangnan Haudenschild, Anne K. Sherlock, Benjamin E. Hu, Jerry C. Leach, J. Kent Athanasiou, Kyriacos A. Marcu, Laura Detection of glycosaminoglycan loss in articular cartilage by fluorescence lifetime imaging |
title | Detection of glycosaminoglycan loss in articular cartilage by fluorescence lifetime imaging |
title_full | Detection of glycosaminoglycan loss in articular cartilage by fluorescence lifetime imaging |
title_fullStr | Detection of glycosaminoglycan loss in articular cartilage by fluorescence lifetime imaging |
title_full_unstemmed | Detection of glycosaminoglycan loss in articular cartilage by fluorescence lifetime imaging |
title_short | Detection of glycosaminoglycan loss in articular cartilage by fluorescence lifetime imaging |
title_sort | detection of glycosaminoglycan loss in articular cartilage by fluorescence lifetime imaging |
topic | Imaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357192/ https://www.ncbi.nlm.nih.gov/pubmed/30578627 http://dx.doi.org/10.1117/1.JBO.23.12.126002 |
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