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Liver segment imaging using monocyte sequestration: a potential tool for fluorescence-guided liver surgery

Background: The accurate determination of liver segment anatomy is essential to perform liver resection without complications and to ensure long-term outcomes after this operation. There are several perioperative methods for segment identification and surgical navigation, such as intraoperative ultr...

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Autores principales: Qian, Baifeng, Kyuno, Daisuke, Schäfer, Michael, Gross, Wolfgang, Mehrabi, Arianeb, Ryschich, Eduard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299692/
https://www.ncbi.nlm.nih.gov/pubmed/30613285
http://dx.doi.org/10.7150/thno.29223
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author Qian, Baifeng
Kyuno, Daisuke
Schäfer, Michael
Gross, Wolfgang
Mehrabi, Arianeb
Ryschich, Eduard
author_facet Qian, Baifeng
Kyuno, Daisuke
Schäfer, Michael
Gross, Wolfgang
Mehrabi, Arianeb
Ryschich, Eduard
author_sort Qian, Baifeng
collection PubMed
description Background: The accurate determination of liver segment anatomy is essential to perform liver resection without complications and to ensure long-term outcomes after this operation. There are several perioperative methods for segment identification and surgical navigation, such as intraoperative ultrasound, indigo carmine and near-infrared imaging with indocyanine green. The present study experimentally analyzed the usefulness of monocyte sequestration for liver segment labeling and imaging. Methods: Human monocytes were isolated from peripheral blood and directly or indirectly labeled with calcein or IRDye 800CW. Potential toxicity, labeling stability, and adhesion to ICAM-1 were analyzed in vitro. Monocyte sequestration in the liver microvasculature and liver segment labeling and boundary demarcation were studied using isolated mouse and pig liver perfusion and via intraportal injection in mouse liver tumor models. Results: The highest monocyte labeling efficiency was achieved using direct labeling with IRDye 800CW. Labeling was stable and did not influence cell viability. The labeled monocytes were highly sequestrated in the liver microvasculature, both after ex vivo perfusion and after injection in vivo , resulting in excellent labeling of selected liver segments and strong segment boundary demarcation. In contrast to results to a normal liver, monocyte sequestration was very low in tumor-associated blood vessels. Conclusions: The present experimental study shows that sequestration of labeled monocytes after superselective application demarcates the selected liver segment. These results illustrate potential of this technique for surgical navigation during liver surgery.
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spelling pubmed-62996922019-01-04 Liver segment imaging using monocyte sequestration: a potential tool for fluorescence-guided liver surgery Qian, Baifeng Kyuno, Daisuke Schäfer, Michael Gross, Wolfgang Mehrabi, Arianeb Ryschich, Eduard Theranostics Research Paper Background: The accurate determination of liver segment anatomy is essential to perform liver resection without complications and to ensure long-term outcomes after this operation. There are several perioperative methods for segment identification and surgical navigation, such as intraoperative ultrasound, indigo carmine and near-infrared imaging with indocyanine green. The present study experimentally analyzed the usefulness of monocyte sequestration for liver segment labeling and imaging. Methods: Human monocytes were isolated from peripheral blood and directly or indirectly labeled with calcein or IRDye 800CW. Potential toxicity, labeling stability, and adhesion to ICAM-1 were analyzed in vitro. Monocyte sequestration in the liver microvasculature and liver segment labeling and boundary demarcation were studied using isolated mouse and pig liver perfusion and via intraportal injection in mouse liver tumor models. Results: The highest monocyte labeling efficiency was achieved using direct labeling with IRDye 800CW. Labeling was stable and did not influence cell viability. The labeled monocytes were highly sequestrated in the liver microvasculature, both after ex vivo perfusion and after injection in vivo , resulting in excellent labeling of selected liver segments and strong segment boundary demarcation. In contrast to results to a normal liver, monocyte sequestration was very low in tumor-associated blood vessels. Conclusions: The present experimental study shows that sequestration of labeled monocytes after superselective application demarcates the selected liver segment. These results illustrate potential of this technique for surgical navigation during liver surgery. Ivyspring International Publisher 2018-11-29 /pmc/articles/PMC6299692/ /pubmed/30613285 http://dx.doi.org/10.7150/thno.29223 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Qian, Baifeng
Kyuno, Daisuke
Schäfer, Michael
Gross, Wolfgang
Mehrabi, Arianeb
Ryschich, Eduard
Liver segment imaging using monocyte sequestration: a potential tool for fluorescence-guided liver surgery
title Liver segment imaging using monocyte sequestration: a potential tool for fluorescence-guided liver surgery
title_full Liver segment imaging using monocyte sequestration: a potential tool for fluorescence-guided liver surgery
title_fullStr Liver segment imaging using monocyte sequestration: a potential tool for fluorescence-guided liver surgery
title_full_unstemmed Liver segment imaging using monocyte sequestration: a potential tool for fluorescence-guided liver surgery
title_short Liver segment imaging using monocyte sequestration: a potential tool for fluorescence-guided liver surgery
title_sort liver segment imaging using monocyte sequestration: a potential tool for fluorescence-guided liver surgery
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299692/
https://www.ncbi.nlm.nih.gov/pubmed/30613285
http://dx.doi.org/10.7150/thno.29223
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