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Interstitial diffuse radiance spectroscopy of gold nanocages and nanorods in bulk muscle tissues

Radiance spectroscopy was applied to the interstitial detection of localized inclusions containing Au nanocages or nanorods with various concentrations embedded in porcine muscle phantoms. The radiance was quantified using a perturbation approach, which enabled the separation of contributions from t...

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Autores principales: Grabtchak, Serge, Montgomery, Logan G, Pang, Bo, Wang, Yi, Zhang, Chao, Li, Zhiyuan, Xia, Younan, Whelan, William M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335609/
https://www.ncbi.nlm.nih.gov/pubmed/25709450
http://dx.doi.org/10.2147/IJN.S79246
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author Grabtchak, Serge
Montgomery, Logan G
Pang, Bo
Wang, Yi
Zhang, Chao
Li, Zhiyuan
Xia, Younan
Whelan, William M
author_facet Grabtchak, Serge
Montgomery, Logan G
Pang, Bo
Wang, Yi
Zhang, Chao
Li, Zhiyuan
Xia, Younan
Whelan, William M
author_sort Grabtchak, Serge
collection PubMed
description Radiance spectroscopy was applied to the interstitial detection of localized inclusions containing Au nanocages or nanorods with various concentrations embedded in porcine muscle phantoms. The radiance was quantified using a perturbation approach, which enabled the separation of contributions from the porcine phantom and the localized inclusion, with the inclusion serving as a perturbation probe of photon distributions in the turbid medium. Positioning the inclusion at various places in the phantom allowed for tracking of photons that originated from a light source, passed through the inclusion’s location, and reached a detector. The inclusions with high extinction coefficients were able to absorb nearly all photons in the range of 650–900 nm, leading to a spectrally flat radiance signal. This signal could be converted to the relative density of photons incident on the inclusion. Finally, the experimentally measured quantities were expressed via the relative perturbation and arranged into the classical Beer–Lambert law that allowed one to extract the extinction coefficients of various types of Au nanoparticles in both the transmission and back reflection geometries. It was shown that the spatial variation of perturbation could be described as 1/r dependence, where r is the distance between the inclusion and the detector. Due to a larger absorption cross section, Au nanocages produced greater perturbations than Au nanorods of equal particle concentration, indicating a better suitability of Au nanocages as contrast agents for optical measurements in turbid media. Individual measurements from different inclusions were combined into detectability maps.
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spelling pubmed-43356092015-02-23 Interstitial diffuse radiance spectroscopy of gold nanocages and nanorods in bulk muscle tissues Grabtchak, Serge Montgomery, Logan G Pang, Bo Wang, Yi Zhang, Chao Li, Zhiyuan Xia, Younan Whelan, William M Int J Nanomedicine Original Research Radiance spectroscopy was applied to the interstitial detection of localized inclusions containing Au nanocages or nanorods with various concentrations embedded in porcine muscle phantoms. The radiance was quantified using a perturbation approach, which enabled the separation of contributions from the porcine phantom and the localized inclusion, with the inclusion serving as a perturbation probe of photon distributions in the turbid medium. Positioning the inclusion at various places in the phantom allowed for tracking of photons that originated from a light source, passed through the inclusion’s location, and reached a detector. The inclusions with high extinction coefficients were able to absorb nearly all photons in the range of 650–900 nm, leading to a spectrally flat radiance signal. This signal could be converted to the relative density of photons incident on the inclusion. Finally, the experimentally measured quantities were expressed via the relative perturbation and arranged into the classical Beer–Lambert law that allowed one to extract the extinction coefficients of various types of Au nanoparticles in both the transmission and back reflection geometries. It was shown that the spatial variation of perturbation could be described as 1/r dependence, where r is the distance between the inclusion and the detector. Due to a larger absorption cross section, Au nanocages produced greater perturbations than Au nanorods of equal particle concentration, indicating a better suitability of Au nanocages as contrast agents for optical measurements in turbid media. Individual measurements from different inclusions were combined into detectability maps. Dove Medical Press 2015-02-13 /pmc/articles/PMC4335609/ /pubmed/25709450 http://dx.doi.org/10.2147/IJN.S79246 Text en © 2015 Grabtchak et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Grabtchak, Serge
Montgomery, Logan G
Pang, Bo
Wang, Yi
Zhang, Chao
Li, Zhiyuan
Xia, Younan
Whelan, William M
Interstitial diffuse radiance spectroscopy of gold nanocages and nanorods in bulk muscle tissues
title Interstitial diffuse radiance spectroscopy of gold nanocages and nanorods in bulk muscle tissues
title_full Interstitial diffuse radiance spectroscopy of gold nanocages and nanorods in bulk muscle tissues
title_fullStr Interstitial diffuse radiance spectroscopy of gold nanocages and nanorods in bulk muscle tissues
title_full_unstemmed Interstitial diffuse radiance spectroscopy of gold nanocages and nanorods in bulk muscle tissues
title_short Interstitial diffuse radiance spectroscopy of gold nanocages and nanorods in bulk muscle tissues
title_sort interstitial diffuse radiance spectroscopy of gold nanocages and nanorods in bulk muscle tissues
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335609/
https://www.ncbi.nlm.nih.gov/pubmed/25709450
http://dx.doi.org/10.2147/IJN.S79246
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