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Gd(3+)-Asparagine-Anionic Linear Globular Dendrimer Second-Generation G2 Complexes: Novel Nanobiohybrid Theranostics

Designing a unique theranostic biocompatible, biodegradable, and cost-effective agent which is easy to be synthesized as a biohybrid material was the aim of this study. In this matter, asparagine attached to anionic linear globular dendrimer G2 (as a biocompatible, biodegradable, and cost-effective...

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Autores principales: Hashempour Alamdari, Nasim, Alaei-Beirami, Mahmood, Sadat Shandiz, Seyed Ataollah, Hejazinia, Hadi, Rasouli, Rahimeh, Saffari, Mostafa, Sadat Ebrahimi, Seyed Esmaeil, Assadi, Artin, Shafiee Ardestani, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5635473/
https://www.ncbi.nlm.nih.gov/pubmed/29097918
http://dx.doi.org/10.1155/2017/3625729
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author Hashempour Alamdari, Nasim
Alaei-Beirami, Mahmood
Sadat Shandiz, Seyed Ataollah
Hejazinia, Hadi
Rasouli, Rahimeh
Saffari, Mostafa
Sadat Ebrahimi, Seyed Esmaeil
Assadi, Artin
Shafiee Ardestani, Mehdi
author_facet Hashempour Alamdari, Nasim
Alaei-Beirami, Mahmood
Sadat Shandiz, Seyed Ataollah
Hejazinia, Hadi
Rasouli, Rahimeh
Saffari, Mostafa
Sadat Ebrahimi, Seyed Esmaeil
Assadi, Artin
Shafiee Ardestani, Mehdi
author_sort Hashempour Alamdari, Nasim
collection PubMed
description Designing a unique theranostic biocompatible, biodegradable, and cost-effective agent which is easy to be synthesized as a biohybrid material was the aim of this study. In this matter, asparagine attached to anionic linear globular dendrimer G2 (as a biocompatible, biodegradable, and cost-effective agent which is negatively charged nanosized and water soluble polymer that outweighs other traditionally used dendrimers) and finally contrast agent (Gd(3+)) was loaded (which made complexes) in synthesized asparagine-dendrimer. Observations revealed that, in addition to successful colon cancer and brain targeting, Gd(3+)-dendrimer-asparagine, the proposed theranostic agent, could increase T1 MR relaxation times, decrease T2 MR relaxation times significantly, and improve contrast of image as well as illustrating good cellular uptake based on florescent microscopy/flow cytometry and ICP-mass data. In addition to that, it increased tumor growth inhibition percentage (TGI%) significantly compared to FDA approved contrast agent, Magnevist. Totally, Gd3+-anionic linear globular dendrimer G2-asparagine could be introduced to the cancer imaging/therapy (theranostics) protocols after in vivo MR and fluorescent analysis and passing clinical trials. Hence, this nanotheranostic agent would be a promising candidate for brain drug delivery and imaging in the future.
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spelling pubmed-56354732017-10-31 Gd(3+)-Asparagine-Anionic Linear Globular Dendrimer Second-Generation G2 Complexes: Novel Nanobiohybrid Theranostics Hashempour Alamdari, Nasim Alaei-Beirami, Mahmood Sadat Shandiz, Seyed Ataollah Hejazinia, Hadi Rasouli, Rahimeh Saffari, Mostafa Sadat Ebrahimi, Seyed Esmaeil Assadi, Artin Shafiee Ardestani, Mehdi Contrast Media Mol Imaging Research Article Designing a unique theranostic biocompatible, biodegradable, and cost-effective agent which is easy to be synthesized as a biohybrid material was the aim of this study. In this matter, asparagine attached to anionic linear globular dendrimer G2 (as a biocompatible, biodegradable, and cost-effective agent which is negatively charged nanosized and water soluble polymer that outweighs other traditionally used dendrimers) and finally contrast agent (Gd(3+)) was loaded (which made complexes) in synthesized asparagine-dendrimer. Observations revealed that, in addition to successful colon cancer and brain targeting, Gd(3+)-dendrimer-asparagine, the proposed theranostic agent, could increase T1 MR relaxation times, decrease T2 MR relaxation times significantly, and improve contrast of image as well as illustrating good cellular uptake based on florescent microscopy/flow cytometry and ICP-mass data. In addition to that, it increased tumor growth inhibition percentage (TGI%) significantly compared to FDA approved contrast agent, Magnevist. Totally, Gd3+-anionic linear globular dendrimer G2-asparagine could be introduced to the cancer imaging/therapy (theranostics) protocols after in vivo MR and fluorescent analysis and passing clinical trials. Hence, this nanotheranostic agent would be a promising candidate for brain drug delivery and imaging in the future. Hindawi 2017-09-26 /pmc/articles/PMC5635473/ /pubmed/29097918 http://dx.doi.org/10.1155/2017/3625729 Text en Copyright © 2017 Nasim Hashempour Alamdari et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hashempour Alamdari, Nasim
Alaei-Beirami, Mahmood
Sadat Shandiz, Seyed Ataollah
Hejazinia, Hadi
Rasouli, Rahimeh
Saffari, Mostafa
Sadat Ebrahimi, Seyed Esmaeil
Assadi, Artin
Shafiee Ardestani, Mehdi
Gd(3+)-Asparagine-Anionic Linear Globular Dendrimer Second-Generation G2 Complexes: Novel Nanobiohybrid Theranostics
title Gd(3+)-Asparagine-Anionic Linear Globular Dendrimer Second-Generation G2 Complexes: Novel Nanobiohybrid Theranostics
title_full Gd(3+)-Asparagine-Anionic Linear Globular Dendrimer Second-Generation G2 Complexes: Novel Nanobiohybrid Theranostics
title_fullStr Gd(3+)-Asparagine-Anionic Linear Globular Dendrimer Second-Generation G2 Complexes: Novel Nanobiohybrid Theranostics
title_full_unstemmed Gd(3+)-Asparagine-Anionic Linear Globular Dendrimer Second-Generation G2 Complexes: Novel Nanobiohybrid Theranostics
title_short Gd(3+)-Asparagine-Anionic Linear Globular Dendrimer Second-Generation G2 Complexes: Novel Nanobiohybrid Theranostics
title_sort gd(3+)-asparagine-anionic linear globular dendrimer second-generation g2 complexes: novel nanobiohybrid theranostics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5635473/
https://www.ncbi.nlm.nih.gov/pubmed/29097918
http://dx.doi.org/10.1155/2017/3625729
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