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Theranostic Nanoseeds for Efficacious Internal Radiation Therapy of Unresectable Solid Tumors
Malignant tumors are considered “unresectable” if they are adhere to vital structures or the surgery would cause irreversible damages to the patients. Though a variety of cytotoxic drugs and radiation therapies are currently available in clinical practice to treat such tumor masses, these therapeuti...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745015/ https://www.ncbi.nlm.nih.gov/pubmed/26852805 http://dx.doi.org/10.1038/srep20614 |
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author | Moeendarbari, Sina Tekade, Rakesh Mulgaonkar, Aditi Christensen, Preston Ramezani, Saleh Hassan, Gedaa Jiang, Ruiqian Öz, Orhan K. Hao, Yaowu Sun, Xiankai |
author_facet | Moeendarbari, Sina Tekade, Rakesh Mulgaonkar, Aditi Christensen, Preston Ramezani, Saleh Hassan, Gedaa Jiang, Ruiqian Öz, Orhan K. Hao, Yaowu Sun, Xiankai |
author_sort | Moeendarbari, Sina |
collection | PubMed |
description | Malignant tumors are considered “unresectable” if they are adhere to vital structures or the surgery would cause irreversible damages to the patients. Though a variety of cytotoxic drugs and radiation therapies are currently available in clinical practice to treat such tumor masses, these therapeutic modalities are always associated with substantial side effects. Here, we report an injectable nanoparticle-based internal radiation source that potentially offers more efficacious treatment of unresectable solid tumors without significant adverse side effects. Using a highly efficient incorporation procedure, palladium-103, a brachytherapy radioisotope in clinical practice, was coated to monodispersed hollow gold nanoparticles with a diameter about 120 nm, to form (103)Pd@Au nanoseeds. The therapeutic efficacy of (103)Pd@Au nanoseeds were assessed when intratumorally injected into a prostate cancer xenograft model. Five weeks after a single-dose treatment, a significant tumor burden reduction (>80%) was observed without noticeable side effects on the liver, spleen and other organs. Impressively, >95% nanoseeds were retained inside the tumors as monitored by Single Photon Emission Computed Tomography (SPECT) with the gamma emissions of (103)Pd. These findings show that this nanoseed-based brachytherapy has the potential to provide a theranostic solution to unresectable solid tumors. |
format | Online Article Text |
id | pubmed-4745015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47450152016-02-16 Theranostic Nanoseeds for Efficacious Internal Radiation Therapy of Unresectable Solid Tumors Moeendarbari, Sina Tekade, Rakesh Mulgaonkar, Aditi Christensen, Preston Ramezani, Saleh Hassan, Gedaa Jiang, Ruiqian Öz, Orhan K. Hao, Yaowu Sun, Xiankai Sci Rep Article Malignant tumors are considered “unresectable” if they are adhere to vital structures or the surgery would cause irreversible damages to the patients. Though a variety of cytotoxic drugs and radiation therapies are currently available in clinical practice to treat such tumor masses, these therapeutic modalities are always associated with substantial side effects. Here, we report an injectable nanoparticle-based internal radiation source that potentially offers more efficacious treatment of unresectable solid tumors without significant adverse side effects. Using a highly efficient incorporation procedure, palladium-103, a brachytherapy radioisotope in clinical practice, was coated to monodispersed hollow gold nanoparticles with a diameter about 120 nm, to form (103)Pd@Au nanoseeds. The therapeutic efficacy of (103)Pd@Au nanoseeds were assessed when intratumorally injected into a prostate cancer xenograft model. Five weeks after a single-dose treatment, a significant tumor burden reduction (>80%) was observed without noticeable side effects on the liver, spleen and other organs. Impressively, >95% nanoseeds were retained inside the tumors as monitored by Single Photon Emission Computed Tomography (SPECT) with the gamma emissions of (103)Pd. These findings show that this nanoseed-based brachytherapy has the potential to provide a theranostic solution to unresectable solid tumors. Nature Publishing Group 2016-02-08 /pmc/articles/PMC4745015/ /pubmed/26852805 http://dx.doi.org/10.1038/srep20614 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Moeendarbari, Sina Tekade, Rakesh Mulgaonkar, Aditi Christensen, Preston Ramezani, Saleh Hassan, Gedaa Jiang, Ruiqian Öz, Orhan K. Hao, Yaowu Sun, Xiankai Theranostic Nanoseeds for Efficacious Internal Radiation Therapy of Unresectable Solid Tumors |
title | Theranostic Nanoseeds for Efficacious Internal Radiation Therapy of Unresectable Solid Tumors |
title_full | Theranostic Nanoseeds for Efficacious Internal Radiation Therapy of Unresectable Solid Tumors |
title_fullStr | Theranostic Nanoseeds for Efficacious Internal Radiation Therapy of Unresectable Solid Tumors |
title_full_unstemmed | Theranostic Nanoseeds for Efficacious Internal Radiation Therapy of Unresectable Solid Tumors |
title_short | Theranostic Nanoseeds for Efficacious Internal Radiation Therapy of Unresectable Solid Tumors |
title_sort | theranostic nanoseeds for efficacious internal radiation therapy of unresectable solid tumors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745015/ https://www.ncbi.nlm.nih.gov/pubmed/26852805 http://dx.doi.org/10.1038/srep20614 |
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