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Validation of Ultrasonic Harmonic Scalpel for Real-Time Tissue Identification Using Rapid Evaporative Ionization Mass Spectrometry

[Image: see text] In this study, we integrate rapid evaporative ionization mass spectrometry (REIMS) with the Harmonic scalpel, an advanced laparoscopic surgical instrument that utilizes ultrasound energy to dissect and coagulate tissues. It provides unparalleled manipulation capability to surgeons...

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Autores principales: Manoli, Eftychios, Mason, Sam, Ford, Lauren, Adebesin, Afeez, Bodai, Zsolt, Darzi, Ara, Kinross, James, Takats, Zoltan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153397/
https://www.ncbi.nlm.nih.gov/pubmed/33787247
http://dx.doi.org/10.1021/acs.analchem.1c00270
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author Manoli, Eftychios
Mason, Sam
Ford, Lauren
Adebesin, Afeez
Bodai, Zsolt
Darzi, Ara
Kinross, James
Takats, Zoltan
author_facet Manoli, Eftychios
Mason, Sam
Ford, Lauren
Adebesin, Afeez
Bodai, Zsolt
Darzi, Ara
Kinross, James
Takats, Zoltan
author_sort Manoli, Eftychios
collection PubMed
description [Image: see text] In this study, we integrate rapid evaporative ionization mass spectrometry (REIMS) with the Harmonic scalpel, an advanced laparoscopic surgical instrument that utilizes ultrasound energy to dissect and coagulate tissues. It provides unparalleled manipulation capability to surgeons and has superseded traditional electrosurgical tools particularly in abdominal surgery, but is yet to be validated with REIMS. The REIMS platform coupled with the Harmonic device was shown to produce tissue-specific lipid profiles through the analysis of porcine tissues in both negative and positive ionization modes. Comparison with other methods of electrosurgical dissection, such as monopolar electrosurgery and CO(2) laser, showed spectral differences in the profile dependent on the energy device used. The Harmonic device demonstrated major spectral differences in the phospholipid region of m/z 600–1000 compared with the monopolar electrosurgical and CO(2) laser-generated spectra. Within the Harmonic REIMS spectra, high intensities of diglycerides and triglycerides were observed. In contrast, monopolar electrosurgical and laser spectra demonstrated high abundances of glycerophospholipids. The Harmonic scalpel was able to differentiate between the liver, muscle, colon, and small intestine, demonstrating 100% diagnostic accuracy. The validation of the Harmonic device–mass spectrometry combination will allow the platform to be used safely and robustly for real-time in vivo surgical tissue identification in a variety of clinical applications.
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spelling pubmed-81533972021-05-27 Validation of Ultrasonic Harmonic Scalpel for Real-Time Tissue Identification Using Rapid Evaporative Ionization Mass Spectrometry Manoli, Eftychios Mason, Sam Ford, Lauren Adebesin, Afeez Bodai, Zsolt Darzi, Ara Kinross, James Takats, Zoltan Anal Chem [Image: see text] In this study, we integrate rapid evaporative ionization mass spectrometry (REIMS) with the Harmonic scalpel, an advanced laparoscopic surgical instrument that utilizes ultrasound energy to dissect and coagulate tissues. It provides unparalleled manipulation capability to surgeons and has superseded traditional electrosurgical tools particularly in abdominal surgery, but is yet to be validated with REIMS. The REIMS platform coupled with the Harmonic device was shown to produce tissue-specific lipid profiles through the analysis of porcine tissues in both negative and positive ionization modes. Comparison with other methods of electrosurgical dissection, such as monopolar electrosurgery and CO(2) laser, showed spectral differences in the profile dependent on the energy device used. The Harmonic device demonstrated major spectral differences in the phospholipid region of m/z 600–1000 compared with the monopolar electrosurgical and CO(2) laser-generated spectra. Within the Harmonic REIMS spectra, high intensities of diglycerides and triglycerides were observed. In contrast, monopolar electrosurgical and laser spectra demonstrated high abundances of glycerophospholipids. The Harmonic scalpel was able to differentiate between the liver, muscle, colon, and small intestine, demonstrating 100% diagnostic accuracy. The validation of the Harmonic device–mass spectrometry combination will allow the platform to be used safely and robustly for real-time in vivo surgical tissue identification in a variety of clinical applications. American Chemical Society 2021-03-31 2021-04-13 /pmc/articles/PMC8153397/ /pubmed/33787247 http://dx.doi.org/10.1021/acs.analchem.1c00270 Text en © 2021 American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Manoli, Eftychios
Mason, Sam
Ford, Lauren
Adebesin, Afeez
Bodai, Zsolt
Darzi, Ara
Kinross, James
Takats, Zoltan
Validation of Ultrasonic Harmonic Scalpel for Real-Time Tissue Identification Using Rapid Evaporative Ionization Mass Spectrometry
title Validation of Ultrasonic Harmonic Scalpel for Real-Time Tissue Identification Using Rapid Evaporative Ionization Mass Spectrometry
title_full Validation of Ultrasonic Harmonic Scalpel for Real-Time Tissue Identification Using Rapid Evaporative Ionization Mass Spectrometry
title_fullStr Validation of Ultrasonic Harmonic Scalpel for Real-Time Tissue Identification Using Rapid Evaporative Ionization Mass Spectrometry
title_full_unstemmed Validation of Ultrasonic Harmonic Scalpel for Real-Time Tissue Identification Using Rapid Evaporative Ionization Mass Spectrometry
title_short Validation of Ultrasonic Harmonic Scalpel for Real-Time Tissue Identification Using Rapid Evaporative Ionization Mass Spectrometry
title_sort validation of ultrasonic harmonic scalpel for real-time tissue identification using rapid evaporative ionization mass spectrometry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153397/
https://www.ncbi.nlm.nih.gov/pubmed/33787247
http://dx.doi.org/10.1021/acs.analchem.1c00270
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