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Gold-Loaded Polymeric Micelles for Computed Tomography-Guided Radiation Therapy Treatment and Radiosensitization

[Image: see text] Gold nanoparticles (AuNPs) have generated interest as both imaging and therapeutic agents. AuNPs are attractive for imaging applications since they are nontoxic and provide nearly three times greater X-ray attenuation per unit weight than iodine. As therapeutic agents, AuNPs can se...

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Autores principales: Al Zaki, Ajlan, Joh, Daniel, Cheng, Zhiliang, De Barros, André Luís Branco, Kao, Gary, Dorsey, Jay, Tsourkas, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2013
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906892/
https://www.ncbi.nlm.nih.gov/pubmed/24377302
http://dx.doi.org/10.1021/nn405701q
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author Al Zaki, Ajlan
Joh, Daniel
Cheng, Zhiliang
De Barros, André Luís Branco
Kao, Gary
Dorsey, Jay
Tsourkas, Andrew
author_facet Al Zaki, Ajlan
Joh, Daniel
Cheng, Zhiliang
De Barros, André Luís Branco
Kao, Gary
Dorsey, Jay
Tsourkas, Andrew
author_sort Al Zaki, Ajlan
collection PubMed
description [Image: see text] Gold nanoparticles (AuNPs) have generated interest as both imaging and therapeutic agents. AuNPs are attractive for imaging applications since they are nontoxic and provide nearly three times greater X-ray attenuation per unit weight than iodine. As therapeutic agents, AuNPs can sensitize tumor cells to ionizing radiation. To create a nanoplatform that could simultaneously exhibit long circulation times, achieve appreciable tumor accumulation, generate computed tomography (CT) image contrast, and serve as a radiosensitizer, gold-loaded polymeric micelles (GPMs) were prepared. Specifically, 1.9 nm AuNPs were encapsulated within the hydrophobic core of micelles formed with the amphiphilic diblock copolymer poly(ethylene glycol)-b-poly(ε-capralactone). GPMs were produced with low polydispersity and mean hydrodynamic diameters ranging from 25 to 150 nm. Following intravenous injection, GPMs provided blood pool contrast for up to 24 h and improved the delineation of tumor margins via CT. Thus, GPM-enhanced CT imaging was used to guide radiation therapy delivered via a small animal radiation research platform. In combination with the radiosensitizing capabilities of gold, tumor-bearing mice exhibited a 1.7-fold improvement in the median survival time, compared with mice receiving radiation alone. It is envisioned that translation of these capabilities to human cancer patients could guide and enhance the efficacy of radiation therapy.
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spelling pubmed-39068922014-01-31 Gold-Loaded Polymeric Micelles for Computed Tomography-Guided Radiation Therapy Treatment and Radiosensitization Al Zaki, Ajlan Joh, Daniel Cheng, Zhiliang De Barros, André Luís Branco Kao, Gary Dorsey, Jay Tsourkas, Andrew ACS Nano [Image: see text] Gold nanoparticles (AuNPs) have generated interest as both imaging and therapeutic agents. AuNPs are attractive for imaging applications since they are nontoxic and provide nearly three times greater X-ray attenuation per unit weight than iodine. As therapeutic agents, AuNPs can sensitize tumor cells to ionizing radiation. To create a nanoplatform that could simultaneously exhibit long circulation times, achieve appreciable tumor accumulation, generate computed tomography (CT) image contrast, and serve as a radiosensitizer, gold-loaded polymeric micelles (GPMs) were prepared. Specifically, 1.9 nm AuNPs were encapsulated within the hydrophobic core of micelles formed with the amphiphilic diblock copolymer poly(ethylene glycol)-b-poly(ε-capralactone). GPMs were produced with low polydispersity and mean hydrodynamic diameters ranging from 25 to 150 nm. Following intravenous injection, GPMs provided blood pool contrast for up to 24 h and improved the delineation of tumor margins via CT. Thus, GPM-enhanced CT imaging was used to guide radiation therapy delivered via a small animal radiation research platform. In combination with the radiosensitizing capabilities of gold, tumor-bearing mice exhibited a 1.7-fold improvement in the median survival time, compared with mice receiving radiation alone. It is envisioned that translation of these capabilities to human cancer patients could guide and enhance the efficacy of radiation therapy. American Chemical Society 2013-12-30 2014-01-28 /pmc/articles/PMC3906892/ /pubmed/24377302 http://dx.doi.org/10.1021/nn405701q Text en Copyright © 2013 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Al Zaki, Ajlan
Joh, Daniel
Cheng, Zhiliang
De Barros, André Luís Branco
Kao, Gary
Dorsey, Jay
Tsourkas, Andrew
Gold-Loaded Polymeric Micelles for Computed Tomography-Guided Radiation Therapy Treatment and Radiosensitization
title Gold-Loaded Polymeric Micelles for Computed Tomography-Guided Radiation Therapy Treatment and Radiosensitization
title_full Gold-Loaded Polymeric Micelles for Computed Tomography-Guided Radiation Therapy Treatment and Radiosensitization
title_fullStr Gold-Loaded Polymeric Micelles for Computed Tomography-Guided Radiation Therapy Treatment and Radiosensitization
title_full_unstemmed Gold-Loaded Polymeric Micelles for Computed Tomography-Guided Radiation Therapy Treatment and Radiosensitization
title_short Gold-Loaded Polymeric Micelles for Computed Tomography-Guided Radiation Therapy Treatment and Radiosensitization
title_sort gold-loaded polymeric micelles for computed tomography-guided radiation therapy treatment and radiosensitization
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906892/
https://www.ncbi.nlm.nih.gov/pubmed/24377302
http://dx.doi.org/10.1021/nn405701q
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