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A clinical trial of super-stable homogeneous lipiodol-nanoICG formulation-guided precise fluorescent laparoscopic hepatocellular carcinoma resection

BACKGROUND: Applying traditional fluorescence navigation technologies in hepatocellular carcinoma is severely restricted by high false-positive rates, variable tumor differentiation, and unstable fluorescence performance. RESULTS: In this study, a green, economical and safe nanomedicine formulation...

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Autores principales: He, Pan, Xiong, Yongfu, Ye, Jinfa, Chen, Biaoqi, Cheng, Hongwei, Liu, Hao, Zheng, Yating, Chu, Chengchao, Mao, Jingsong, Chen, Aizheng, Zhang, Yang, Li, Jingdong, Tian, Jie, Liu, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164554/
https://www.ncbi.nlm.nih.gov/pubmed/35658966
http://dx.doi.org/10.1186/s12951-022-01467-w
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author He, Pan
Xiong, Yongfu
Ye, Jinfa
Chen, Biaoqi
Cheng, Hongwei
Liu, Hao
Zheng, Yating
Chu, Chengchao
Mao, Jingsong
Chen, Aizheng
Zhang, Yang
Li, Jingdong
Tian, Jie
Liu, Gang
author_facet He, Pan
Xiong, Yongfu
Ye, Jinfa
Chen, Biaoqi
Cheng, Hongwei
Liu, Hao
Zheng, Yating
Chu, Chengchao
Mao, Jingsong
Chen, Aizheng
Zhang, Yang
Li, Jingdong
Tian, Jie
Liu, Gang
author_sort He, Pan
collection PubMed
description BACKGROUND: Applying traditional fluorescence navigation technologies in hepatocellular carcinoma is severely restricted by high false-positive rates, variable tumor differentiation, and unstable fluorescence performance. RESULTS: In this study, a green, economical and safe nanomedicine formulation technology was developed to construct carrier-free indocyanine green nanoparticles (nanoICG) with a small uniform size and better fluorescent properties without any molecular structure changes compared to the ICG molecule. Subsequently, nanoICG dispersed into lipiodol via a super-stable homogeneous intermixed formulation technology (SHIFT&nanoICG) for transhepatic arterial embolization combined with fluorescent laparoscopic hepatectomy to eliminate the existing shortcomings. A 52-year-old liver cancer patient was recruited for the clinical trial of SHIFT&nanoICG. We demonstrate that SHIFT&nanoICG could accurately identify and mark the lesion with excellent stability, embolism, optical imaging performance, and higher tumor-to-normal tissue ratio, especially in the detection of the microsatellite lesions (0.4 × 0.3 cm), which could not be detected by preoperative imaging, to realize a complete resection of hepatocellular carcinoma under fluorescence laparoscopy in a shorter period (within 2 h) and with less intraoperative blood loss (50 mL). CONCLUSIONS: This simple and effective strategy integrates the diagnosis and treatment of hepatocellular carcinoma, and thus, it has great potential in various clinical applications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01467-w.
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spelling pubmed-91645542022-06-05 A clinical trial of super-stable homogeneous lipiodol-nanoICG formulation-guided precise fluorescent laparoscopic hepatocellular carcinoma resection He, Pan Xiong, Yongfu Ye, Jinfa Chen, Biaoqi Cheng, Hongwei Liu, Hao Zheng, Yating Chu, Chengchao Mao, Jingsong Chen, Aizheng Zhang, Yang Li, Jingdong Tian, Jie Liu, Gang J Nanobiotechnology Research BACKGROUND: Applying traditional fluorescence navigation technologies in hepatocellular carcinoma is severely restricted by high false-positive rates, variable tumor differentiation, and unstable fluorescence performance. RESULTS: In this study, a green, economical and safe nanomedicine formulation technology was developed to construct carrier-free indocyanine green nanoparticles (nanoICG) with a small uniform size and better fluorescent properties without any molecular structure changes compared to the ICG molecule. Subsequently, nanoICG dispersed into lipiodol via a super-stable homogeneous intermixed formulation technology (SHIFT&nanoICG) for transhepatic arterial embolization combined with fluorescent laparoscopic hepatectomy to eliminate the existing shortcomings. A 52-year-old liver cancer patient was recruited for the clinical trial of SHIFT&nanoICG. We demonstrate that SHIFT&nanoICG could accurately identify and mark the lesion with excellent stability, embolism, optical imaging performance, and higher tumor-to-normal tissue ratio, especially in the detection of the microsatellite lesions (0.4 × 0.3 cm), which could not be detected by preoperative imaging, to realize a complete resection of hepatocellular carcinoma under fluorescence laparoscopy in a shorter period (within 2 h) and with less intraoperative blood loss (50 mL). CONCLUSIONS: This simple and effective strategy integrates the diagnosis and treatment of hepatocellular carcinoma, and thus, it has great potential in various clinical applications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01467-w. BioMed Central 2022-06-03 /pmc/articles/PMC9164554/ /pubmed/35658966 http://dx.doi.org/10.1186/s12951-022-01467-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
He, Pan
Xiong, Yongfu
Ye, Jinfa
Chen, Biaoqi
Cheng, Hongwei
Liu, Hao
Zheng, Yating
Chu, Chengchao
Mao, Jingsong
Chen, Aizheng
Zhang, Yang
Li, Jingdong
Tian, Jie
Liu, Gang
A clinical trial of super-stable homogeneous lipiodol-nanoICG formulation-guided precise fluorescent laparoscopic hepatocellular carcinoma resection
title A clinical trial of super-stable homogeneous lipiodol-nanoICG formulation-guided precise fluorescent laparoscopic hepatocellular carcinoma resection
title_full A clinical trial of super-stable homogeneous lipiodol-nanoICG formulation-guided precise fluorescent laparoscopic hepatocellular carcinoma resection
title_fullStr A clinical trial of super-stable homogeneous lipiodol-nanoICG formulation-guided precise fluorescent laparoscopic hepatocellular carcinoma resection
title_full_unstemmed A clinical trial of super-stable homogeneous lipiodol-nanoICG formulation-guided precise fluorescent laparoscopic hepatocellular carcinoma resection
title_short A clinical trial of super-stable homogeneous lipiodol-nanoICG formulation-guided precise fluorescent laparoscopic hepatocellular carcinoma resection
title_sort clinical trial of super-stable homogeneous lipiodol-nanoicg formulation-guided precise fluorescent laparoscopic hepatocellular carcinoma resection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164554/
https://www.ncbi.nlm.nih.gov/pubmed/35658966
http://dx.doi.org/10.1186/s12951-022-01467-w
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