Non-invasive and quantitative in vivo monitoring of gold nanoparticle concentration and tissue hemodynamics by hybrid optical spectroscopies
Non-invasive and quantitative in vivo monitoring of gold nanoparticle concentration and tissue hemodynamics by hybrid optical spectroscopies
Owing to their unique combination of chemical and physical properties, inorganic nanoparticles show a great deal of potential as suitable agents for early diagnostics and less invasive therapies. Yet, their translation to the clinic has been hindered, in part, by the lack of non-invasive methods to quantify their concentration in vivo while also assessing their effect on the tissue physiology. In this work, we demonstrate that diffuse optical techniques, employing near-infrared light, have the potential to address this need in the case of gold nanoparticles which support localized surface plasmons. An orthoxenograft mouse model of clear cell renal cell carcinoma was non-invasively assessed by diffuse reflectance and correlation spectroscopies before and over several days following a single intravenous tail vein injection of polyethylene glycol-coated gold nanorods (AuNRs-PEG). Our platform enables to resolve the kinetics of the AuNR-PEG uptake by the tumor in quantitative agreement with ex vivo inductively coupled plasma mass spectroscopy. Furthermore, it allows for the simultaneous monitoring of local tissue hemodynamics, enabling us to conclude that AuNRs-PEG do not significantly alter the animal physiology. We note that the penetration depth of this current probe was a few millimeters but can readily be extended to centimeters, hence gaining clinical relevance. This study and the methodology presented here complement the nanomedicine toolbox by providing a flexible platform, extendable to other absorbing agents that can potentially be translated to human trials.
5595-5606
Mireles, Miguel
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Morales-Dalmau, Jordi
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Johansson, Johannes D.
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Vidal-Rosas, Ernesto E.
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Vilches, Clara
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Martínez-Lozano, Mar
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Sanz, Vanesa
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De Miguel, Ignacio
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Casanovas, Oriol
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Quidant, Romain
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Durduran, Turgut
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Mireles, Miguel
9b26978e-08a2-44cf-be2d-c0b50533c0d1
Morales-Dalmau, Jordi
d3849b49-e72f-48cf-8346-c0961ecf34aa
Johansson, Johannes D.
f11bb57e-fcdb-4b2f-9df9-141cce32ead1
Vidal-Rosas, Ernesto E.
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Vilches, Clara
39ce14c9-6e83-42bf-9a3d-5f7461728ab6
Martínez-Lozano, Mar
25d2f76d-06cd-45f4-aba4-7a44a4ba233e
Sanz, Vanesa
26c8810b-10a5-422e-bd02-ae99b5595b2f
De Miguel, Ignacio
2ceeedd7-b51c-47e5-a2aa-664d44e47f5b
Casanovas, Oriol
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Quidant, Romain
12cf3db7-237e-4abb-8f64-11693e4cb896
Durduran, Turgut
c6f37f76-48e3-495a-87b4-45e8f40068c9
Mireles, Miguel, Morales-Dalmau, Jordi, Johansson, Johannes D., Vidal-Rosas, Ernesto E., Vilches, Clara, Martínez-Lozano, Mar, Sanz, Vanesa, De Miguel, Ignacio, Casanovas, Oriol, Quidant, Romain and Durduran, Turgut
(2019)
Non-invasive and quantitative in vivo monitoring of gold nanoparticle concentration and tissue hemodynamics by hybrid optical spectroscopies.
Nanoscale, 11 (12), .
(doi:10.1039/c8nr08790c).
Abstract
Owing to their unique combination of chemical and physical properties, inorganic nanoparticles show a great deal of potential as suitable agents for early diagnostics and less invasive therapies. Yet, their translation to the clinic has been hindered, in part, by the lack of non-invasive methods to quantify their concentration in vivo while also assessing their effect on the tissue physiology. In this work, we demonstrate that diffuse optical techniques, employing near-infrared light, have the potential to address this need in the case of gold nanoparticles which support localized surface plasmons. An orthoxenograft mouse model of clear cell renal cell carcinoma was non-invasively assessed by diffuse reflectance and correlation spectroscopies before and over several days following a single intravenous tail vein injection of polyethylene glycol-coated gold nanorods (AuNRs-PEG). Our platform enables to resolve the kinetics of the AuNR-PEG uptake by the tumor in quantitative agreement with ex vivo inductively coupled plasma mass spectroscopy. Furthermore, it allows for the simultaneous monitoring of local tissue hemodynamics, enabling us to conclude that AuNRs-PEG do not significantly alter the animal physiology. We note that the penetration depth of this current probe was a few millimeters but can readily be extended to centimeters, hence gaining clinical relevance. This study and the methodology presented here complement the nanomedicine toolbox by providing a flexible platform, extendable to other absorbing agents that can potentially be translated to human trials.
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Accepted/In Press date: 17 February 2019
e-pub ahead of print date: 21 February 2019
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Local EPrints ID: 489085
URI: http://eprints.soton.ac.uk/id/eprint/489085
ISSN: 2040-3364
PURE UUID: 012bdb98-9372-42c2-83c2-43dbfec495c8
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Date deposited: 12 Apr 2024 17:00
Last modified: 06 Jun 2024 02:18
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Contributors
Author:
Miguel Mireles
Author:
Jordi Morales-Dalmau
Author:
Johannes D. Johansson
Author:
Ernesto E. Vidal-Rosas
Author:
Clara Vilches
Author:
Mar Martínez-Lozano
Author:
Vanesa Sanz
Author:
Ignacio De Miguel
Author:
Oriol Casanovas
Author:
Romain Quidant
Author:
Turgut Durduran
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