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The characterization of an economic and portable LED-based photoacoustic imaging system to facilitate molecular imaging
Photoacoustic imaging (PAI) is a non-invasive, high-resolution hybrid imaging modality that combines optical excitation and ultrasound detection. PAI can image endogenous chromophores (melanin, hemoglobin, etc.) and exogenous contrast agents in different medical applications. However, most current e...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723278/ https://www.ncbi.nlm.nih.gov/pubmed/29234601 http://dx.doi.org/10.1016/j.pacs.2017.11.001 |
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author | Hariri, Ali Lemaster, Jeanne Wang, Junxin Jeevarathinam, AnanthaKrishnan S. Chao, Daniel L. Jokerst, Jesse V. |
author_facet | Hariri, Ali Lemaster, Jeanne Wang, Junxin Jeevarathinam, AnanthaKrishnan S. Chao, Daniel L. Jokerst, Jesse V. |
author_sort | Hariri, Ali |
collection | PubMed |
description | Photoacoustic imaging (PAI) is a non-invasive, high-resolution hybrid imaging modality that combines optical excitation and ultrasound detection. PAI can image endogenous chromophores (melanin, hemoglobin, etc.) and exogenous contrast agents in different medical applications. However, most current equipment uses sophisticated and complicated OPO lasers with tuning and stability features inconsistent with broad clinical deployment. As the number of applications of PAI in medicine increases, there is an urgent need to make the imaging equipment more compact, portable, and affordable. Here, portable light emitting diode – based photoacoustic imaging (PLED-PAI) was introduced and characterized in terms of system specifications, light source characterizations, photoacoustic spatial/temporal resolution, and penetration. The system uses two LED arrays attached to the sides of a conventional ultrasound transducer. The LED pulse repetition rate is tunable between 1 K Hz, 2 K Hz, 3 K Hz, and 4 K Hz. The axial resolution was 0.268 mm, and the lateral resolution was between 0.55 and 0.59 mm. The system could detect optical absorber (pencil lead) at a depth of 3.2 cm and the detection limits of indocyanine green (ICG) and methylene blue (MB) were 9 μM and 0.78 mM. In vivo imaging of labeled human mesenchymal stem cells was achieved to confirm compatibility with small animal imaging. The characterization we report here may have value to other groups evaluating commercially available photoacoustic imaging equipment. |
format | Online Article Text |
id | pubmed-5723278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-57232782017-12-11 The characterization of an economic and portable LED-based photoacoustic imaging system to facilitate molecular imaging Hariri, Ali Lemaster, Jeanne Wang, Junxin Jeevarathinam, AnanthaKrishnan S. Chao, Daniel L. Jokerst, Jesse V. Photoacoustics Research Article Photoacoustic imaging (PAI) is a non-invasive, high-resolution hybrid imaging modality that combines optical excitation and ultrasound detection. PAI can image endogenous chromophores (melanin, hemoglobin, etc.) and exogenous contrast agents in different medical applications. However, most current equipment uses sophisticated and complicated OPO lasers with tuning and stability features inconsistent with broad clinical deployment. As the number of applications of PAI in medicine increases, there is an urgent need to make the imaging equipment more compact, portable, and affordable. Here, portable light emitting diode – based photoacoustic imaging (PLED-PAI) was introduced and characterized in terms of system specifications, light source characterizations, photoacoustic spatial/temporal resolution, and penetration. The system uses two LED arrays attached to the sides of a conventional ultrasound transducer. The LED pulse repetition rate is tunable between 1 K Hz, 2 K Hz, 3 K Hz, and 4 K Hz. The axial resolution was 0.268 mm, and the lateral resolution was between 0.55 and 0.59 mm. The system could detect optical absorber (pencil lead) at a depth of 3.2 cm and the detection limits of indocyanine green (ICG) and methylene blue (MB) were 9 μM and 0.78 mM. In vivo imaging of labeled human mesenchymal stem cells was achieved to confirm compatibility with small animal imaging. The characterization we report here may have value to other groups evaluating commercially available photoacoustic imaging equipment. Elsevier 2017-11-26 /pmc/articles/PMC5723278/ /pubmed/29234601 http://dx.doi.org/10.1016/j.pacs.2017.11.001 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Hariri, Ali Lemaster, Jeanne Wang, Junxin Jeevarathinam, AnanthaKrishnan S. Chao, Daniel L. Jokerst, Jesse V. The characterization of an economic and portable LED-based photoacoustic imaging system to facilitate molecular imaging |
title | The characterization of an economic and portable LED-based photoacoustic imaging system to facilitate molecular imaging |
title_full | The characterization of an economic and portable LED-based photoacoustic imaging system to facilitate molecular imaging |
title_fullStr | The characterization of an economic and portable LED-based photoacoustic imaging system to facilitate molecular imaging |
title_full_unstemmed | The characterization of an economic and portable LED-based photoacoustic imaging system to facilitate molecular imaging |
title_short | The characterization of an economic and portable LED-based photoacoustic imaging system to facilitate molecular imaging |
title_sort | characterization of an economic and portable led-based photoacoustic imaging system to facilitate molecular imaging |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723278/ https://www.ncbi.nlm.nih.gov/pubmed/29234601 http://dx.doi.org/10.1016/j.pacs.2017.11.001 |
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