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Anti-CD24 bio Modified PEGylated Gold Nanoparticles as Targeted Computed Tomography Contrast Agent

Purpose: Molecular imaging is one of the import methods for recognition of cancer at the early stage in order to enhance the capacity of remedy. This study was aimed to introduce a new contrast agent that was targeted with CD24 so as to improve the CT scan detection of cancer cells with higher CD24...

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Autores principales: Ghaziyani, Mona Fazel, Pourhassan Moghaddam, Mohammad, Shahbazi-Gahrouei, Daryoush, Ghavami, Mostafa, Mohammadi, Ali, Abbasi, Mehran Mesgari, Baradaran, Behzad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6311644/
https://www.ncbi.nlm.nih.gov/pubmed/30607332
http://dx.doi.org/10.15171/apb.2018.068
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author Ghaziyani, Mona Fazel
Pourhassan Moghaddam, Mohammad
Shahbazi-Gahrouei, Daryoush
Ghavami, Mostafa
Mohammadi, Ali
Abbasi, Mehran Mesgari
Baradaran, Behzad
author_facet Ghaziyani, Mona Fazel
Pourhassan Moghaddam, Mohammad
Shahbazi-Gahrouei, Daryoush
Ghavami, Mostafa
Mohammadi, Ali
Abbasi, Mehran Mesgari
Baradaran, Behzad
author_sort Ghaziyani, Mona Fazel
collection PubMed
description Purpose: Molecular imaging is one of the import methods for recognition of cancer at the early stage in order to enhance the capacity of remedy. This study was aimed to introduce a new contrast agent that was targeted with CD24 so as to improve the CT scan detection of cancer cells with higher CD24 expression. Methods: The surface modifications of gold nanoparticles (Au-NPs) were done with long PEG (HS-PEG-CH3O) and short PEG (HS-PEG-COOH) chains to enhance their stability and capacity for immobilization of different antibodies. MTT assay was carried out to assess the biocompatibility of the NPs. The obtained contrast agent was implemented in the targeted CT imaging based on in vitro and in vivo studies of breast cancer. Results: The results revealed that the attached CD24 to the cell surface of PEGylated Au-NPs could enhance significantly the cells CT number (40.45 HU in 4T1, while it was 16.61 HU in CT26) It was shown that the attenuation coefficient of the molecularly targeted cells was more than 2 times excessive than the control groups. Further, the tumor region in model of xenograft tumor has higher density compare to the omnipaque groups, 60 min after injection (45 Hu vs.81 Hu). These results showed that the nanoparticles stayed in tumor region for longer time. Conclusion: It is predicted that the synthesized nanoparticle can be used as computed tomography contrast agent. Also, it can be used to identify the tumor cells with higher expression of CD24 at the early stages more efficiently compare to the other routine methods.
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spelling pubmed-63116442019-01-03 Anti-CD24 bio Modified PEGylated Gold Nanoparticles as Targeted Computed Tomography Contrast Agent Ghaziyani, Mona Fazel Pourhassan Moghaddam, Mohammad Shahbazi-Gahrouei, Daryoush Ghavami, Mostafa Mohammadi, Ali Abbasi, Mehran Mesgari Baradaran, Behzad Adv Pharm Bull Research Article Purpose: Molecular imaging is one of the import methods for recognition of cancer at the early stage in order to enhance the capacity of remedy. This study was aimed to introduce a new contrast agent that was targeted with CD24 so as to improve the CT scan detection of cancer cells with higher CD24 expression. Methods: The surface modifications of gold nanoparticles (Au-NPs) were done with long PEG (HS-PEG-CH3O) and short PEG (HS-PEG-COOH) chains to enhance their stability and capacity for immobilization of different antibodies. MTT assay was carried out to assess the biocompatibility of the NPs. The obtained contrast agent was implemented in the targeted CT imaging based on in vitro and in vivo studies of breast cancer. Results: The results revealed that the attached CD24 to the cell surface of PEGylated Au-NPs could enhance significantly the cells CT number (40.45 HU in 4T1, while it was 16.61 HU in CT26) It was shown that the attenuation coefficient of the molecularly targeted cells was more than 2 times excessive than the control groups. Further, the tumor region in model of xenograft tumor has higher density compare to the omnipaque groups, 60 min after injection (45 Hu vs.81 Hu). These results showed that the nanoparticles stayed in tumor region for longer time. Conclusion: It is predicted that the synthesized nanoparticle can be used as computed tomography contrast agent. Also, it can be used to identify the tumor cells with higher expression of CD24 at the early stages more efficiently compare to the other routine methods. Tabriz University of Medical Sciences 2018-11 2018-11-29 /pmc/articles/PMC6311644/ /pubmed/30607332 http://dx.doi.org/10.15171/apb.2018.068 Text en ©2018 The Authors. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, as long as the original authors and source are cited. No permission is required from the authors or the publishers.
spellingShingle Research Article
Ghaziyani, Mona Fazel
Pourhassan Moghaddam, Mohammad
Shahbazi-Gahrouei, Daryoush
Ghavami, Mostafa
Mohammadi, Ali
Abbasi, Mehran Mesgari
Baradaran, Behzad
Anti-CD24 bio Modified PEGylated Gold Nanoparticles as Targeted Computed Tomography Contrast Agent
title Anti-CD24 bio Modified PEGylated Gold Nanoparticles as Targeted Computed Tomography Contrast Agent
title_full Anti-CD24 bio Modified PEGylated Gold Nanoparticles as Targeted Computed Tomography Contrast Agent
title_fullStr Anti-CD24 bio Modified PEGylated Gold Nanoparticles as Targeted Computed Tomography Contrast Agent
title_full_unstemmed Anti-CD24 bio Modified PEGylated Gold Nanoparticles as Targeted Computed Tomography Contrast Agent
title_short Anti-CD24 bio Modified PEGylated Gold Nanoparticles as Targeted Computed Tomography Contrast Agent
title_sort anti-cd24 bio modified pegylated gold nanoparticles as targeted computed tomography contrast agent
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6311644/
https://www.ncbi.nlm.nih.gov/pubmed/30607332
http://dx.doi.org/10.15171/apb.2018.068
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