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Assessment and Modeling of Plasmonic Photothermal Therapy Delivered via a Fiberoptic Microneedle Device Ex Vivo

Plasmonic photothermal therapy (PPTT) has potential as a superior treatment method for pancreatic cancer, a disease with high mortality partially attributable to the currently non-selective treatment options. PPTT utilizes gold nanoparticles infused into a targeted tissue volume and exposed to a spe...

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Autores principales: Akhter, Forhad, Manrique-Bedoya, Santiago, Moreau, Chris, Smith, Andrea Lynn, Feng, Yusheng, Mayer, Kathryn M., Hood, R. Lyle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8703536/
https://www.ncbi.nlm.nih.gov/pubmed/34959414
http://dx.doi.org/10.3390/pharmaceutics13122133
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author Akhter, Forhad
Manrique-Bedoya, Santiago
Moreau, Chris
Smith, Andrea Lynn
Feng, Yusheng
Mayer, Kathryn M.
Hood, R. Lyle
author_facet Akhter, Forhad
Manrique-Bedoya, Santiago
Moreau, Chris
Smith, Andrea Lynn
Feng, Yusheng
Mayer, Kathryn M.
Hood, R. Lyle
author_sort Akhter, Forhad
collection PubMed
description Plasmonic photothermal therapy (PPTT) has potential as a superior treatment method for pancreatic cancer, a disease with high mortality partially attributable to the currently non-selective treatment options. PPTT utilizes gold nanoparticles infused into a targeted tissue volume and exposed to a specific light wavelength to induce selective hyperthermia. The current study focuses on developing this approach within an ex vivo porcine pancreas model via an innovative fiberoptic microneedle device (FMD) for co-delivering light and gold nanoparticles. The effects of laser wavelengths (808 vs. 1064 nm), irradiances (20–50 mW·mm(−2)), and gold nanorod (GNR) concentrations (0.1–3 nM) on tissue temperature profiles were evaluated to assess and control hyperthermic generation. The GNRs had a peak absorbance at ~800 nm. Results showed that, at 808 nm, photon absorption and subsequent heat generation within tissue without GNRs was 65% less than 1064 nm. The combination of GNRs and 808 nm resulted in a 200% higher temperature rise than the 1064 nm under similar conditions. A computational model was developed to predict the temperature shift and was validated against experimental results with a deviation of <5%. These results show promise for both a predictive model and spatially selective, tunable treatment modality for pancreatic cancer.
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spelling pubmed-87035362021-12-25 Assessment and Modeling of Plasmonic Photothermal Therapy Delivered via a Fiberoptic Microneedle Device Ex Vivo Akhter, Forhad Manrique-Bedoya, Santiago Moreau, Chris Smith, Andrea Lynn Feng, Yusheng Mayer, Kathryn M. Hood, R. Lyle Pharmaceutics Article Plasmonic photothermal therapy (PPTT) has potential as a superior treatment method for pancreatic cancer, a disease with high mortality partially attributable to the currently non-selective treatment options. PPTT utilizes gold nanoparticles infused into a targeted tissue volume and exposed to a specific light wavelength to induce selective hyperthermia. The current study focuses on developing this approach within an ex vivo porcine pancreas model via an innovative fiberoptic microneedle device (FMD) for co-delivering light and gold nanoparticles. The effects of laser wavelengths (808 vs. 1064 nm), irradiances (20–50 mW·mm(−2)), and gold nanorod (GNR) concentrations (0.1–3 nM) on tissue temperature profiles were evaluated to assess and control hyperthermic generation. The GNRs had a peak absorbance at ~800 nm. Results showed that, at 808 nm, photon absorption and subsequent heat generation within tissue without GNRs was 65% less than 1064 nm. The combination of GNRs and 808 nm resulted in a 200% higher temperature rise than the 1064 nm under similar conditions. A computational model was developed to predict the temperature shift and was validated against experimental results with a deviation of <5%. These results show promise for both a predictive model and spatially selective, tunable treatment modality for pancreatic cancer. MDPI 2021-12-10 /pmc/articles/PMC8703536/ /pubmed/34959414 http://dx.doi.org/10.3390/pharmaceutics13122133 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Akhter, Forhad
Manrique-Bedoya, Santiago
Moreau, Chris
Smith, Andrea Lynn
Feng, Yusheng
Mayer, Kathryn M.
Hood, R. Lyle
Assessment and Modeling of Plasmonic Photothermal Therapy Delivered via a Fiberoptic Microneedle Device Ex Vivo
title Assessment and Modeling of Plasmonic Photothermal Therapy Delivered via a Fiberoptic Microneedle Device Ex Vivo
title_full Assessment and Modeling of Plasmonic Photothermal Therapy Delivered via a Fiberoptic Microneedle Device Ex Vivo
title_fullStr Assessment and Modeling of Plasmonic Photothermal Therapy Delivered via a Fiberoptic Microneedle Device Ex Vivo
title_full_unstemmed Assessment and Modeling of Plasmonic Photothermal Therapy Delivered via a Fiberoptic Microneedle Device Ex Vivo
title_short Assessment and Modeling of Plasmonic Photothermal Therapy Delivered via a Fiberoptic Microneedle Device Ex Vivo
title_sort assessment and modeling of plasmonic photothermal therapy delivered via a fiberoptic microneedle device ex vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8703536/
https://www.ncbi.nlm.nih.gov/pubmed/34959414
http://dx.doi.org/10.3390/pharmaceutics13122133
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