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Molecular Ultrasound Imaging

In the last decade, molecular ultrasound imaging has been rapidly progressing. It has proven promising to diagnose angiogenesis, inflammation, and thrombosis, and many intravascular targets, such as VEGFR2, integrins, and selectins, have been successfully visualized in vivo. Furthermore, pre-clinica...

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Autores principales: Köse, Gurbet, Darguzyte, Milita, Kiessling, Fabian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601169/
https://www.ncbi.nlm.nih.gov/pubmed/32998422
http://dx.doi.org/10.3390/nano10101935
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author Köse, Gurbet
Darguzyte, Milita
Kiessling, Fabian
author_facet Köse, Gurbet
Darguzyte, Milita
Kiessling, Fabian
author_sort Köse, Gurbet
collection PubMed
description In the last decade, molecular ultrasound imaging has been rapidly progressing. It has proven promising to diagnose angiogenesis, inflammation, and thrombosis, and many intravascular targets, such as VEGFR2, integrins, and selectins, have been successfully visualized in vivo. Furthermore, pre-clinical studies demonstrated that molecular ultrasound increased sensitivity and specificity in disease detection, classification, and therapy response monitoring compared to current clinically applied ultrasound technologies. Several techniques were developed to detect target-bound microbubbles comprising sensitive particle acoustic quantification (SPAQ), destruction-replenishment analysis, and dwelling time assessment. Moreover, some groups tried to assess microbubble binding by a change in their echogenicity after target binding. These techniques can be complemented by radiation force ultrasound improving target binding by pushing microbubbles to vessel walls. Two targeted microbubble formulations are already in clinical trials for tumor detection and liver lesion characterization, and further clinical scale targeted microbubbles are prepared for clinical translation. The recent enormous progress in the field of molecular ultrasound imaging is summarized in this review article by introducing the most relevant detection technologies, concepts for targeted nano- and micro-bubbles, as well as their applications to characterize various diseases. Finally, progress in clinical translation is highlighted, and roadblocks are discussed that currently slow the clinical translation.
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spelling pubmed-76011692020-11-01 Molecular Ultrasound Imaging Köse, Gurbet Darguzyte, Milita Kiessling, Fabian Nanomaterials (Basel) Review In the last decade, molecular ultrasound imaging has been rapidly progressing. It has proven promising to diagnose angiogenesis, inflammation, and thrombosis, and many intravascular targets, such as VEGFR2, integrins, and selectins, have been successfully visualized in vivo. Furthermore, pre-clinical studies demonstrated that molecular ultrasound increased sensitivity and specificity in disease detection, classification, and therapy response monitoring compared to current clinically applied ultrasound technologies. Several techniques were developed to detect target-bound microbubbles comprising sensitive particle acoustic quantification (SPAQ), destruction-replenishment analysis, and dwelling time assessment. Moreover, some groups tried to assess microbubble binding by a change in their echogenicity after target binding. These techniques can be complemented by radiation force ultrasound improving target binding by pushing microbubbles to vessel walls. Two targeted microbubble formulations are already in clinical trials for tumor detection and liver lesion characterization, and further clinical scale targeted microbubbles are prepared for clinical translation. The recent enormous progress in the field of molecular ultrasound imaging is summarized in this review article by introducing the most relevant detection technologies, concepts for targeted nano- and micro-bubbles, as well as their applications to characterize various diseases. Finally, progress in clinical translation is highlighted, and roadblocks are discussed that currently slow the clinical translation. MDPI 2020-09-28 /pmc/articles/PMC7601169/ /pubmed/32998422 http://dx.doi.org/10.3390/nano10101935 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Köse, Gurbet
Darguzyte, Milita
Kiessling, Fabian
Molecular Ultrasound Imaging
title Molecular Ultrasound Imaging
title_full Molecular Ultrasound Imaging
title_fullStr Molecular Ultrasound Imaging
title_full_unstemmed Molecular Ultrasound Imaging
title_short Molecular Ultrasound Imaging
title_sort molecular ultrasound imaging
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601169/
https://www.ncbi.nlm.nih.gov/pubmed/32998422
http://dx.doi.org/10.3390/nano10101935
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