Treatment of tumour tissue with radio‐frequency hyperthermia (using antibody‐carrying nanoparticles)

Abstract Intelligent inorganic nanoparticles were designed and produced for use in imaging and annihilating tumour cells by radio‐frequency (RF) hyperthermia. Nanoparticles synthesised to provide RF hyperthermia must have magnetite properties. For this purpose, magnetite nanoparticles were first syn...

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Main Authors: Reza Didarian, Ibrahim Vargel
Format: Article
Language:English
Published: Wiley 2021-10-01
Series:IET Nanobiotechnology
Online Access:https://doi.org/10.1049/nbt2.12061
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spelling doaj-0a7aa150f18e437899818716b23e4c4a2021-09-14T08:09:21ZengWileyIET Nanobiotechnology1751-87411751-875X2021-10-0115863965310.1049/nbt2.12061Treatment of tumour tissue with radio‐frequency hyperthermia (using antibody‐carrying nanoparticles)Reza Didarian0Ibrahim Vargel1Department of Nanotechnology and Nanomedicine Hacettepe University Beytepe Campus Ankara TurkeyDepartment of Plastic Reconstructive and Aesthetic Surgery Hacettepe University, Sıhhiye Ankara TurkeyAbstract Intelligent inorganic nanoparticles were designed and produced for use in imaging and annihilating tumour cells by radio‐frequency (RF) hyperthermia. Nanoparticles synthesised to provide RF hyperthermia must have magnetite properties. For this purpose, magnetite nanoparticles were first synthesised by the coprecipitation method (10–15 NM). These superparamagnetic nanoparticles were then covered with gold ions without losing their magnetic properties. In this step, gold ions are reduced around the magnetite nanoparticles. Surface modification of the gold‐coated magnetic nanoparticles was performed in the next step. A self‐assembled monolayer was created using cysteamine (2‐aminoethanethiol) molecules, which have two different end groups (SH and NH2). These molecules react with the gold surface by SH groups. The NH2 groups give a positive charge to the nanoparticles. After that, a monoclonal antibody (Monoclonal Anti‐N‐CAM Clone NCAM‐OB11) was immobilised by the 1‐ethyl‐3‐(3‐dimethylaminopropyl)carbodiimide/N‐hydroxysuccinimide method. Then, the antenna RF system (144.00015 MHz) was created for RF hyperthermia. The antibody‐nanoparticle binding rate and cytotoxicity tests were followed by in vitro and in vivo experiments. As the main result, antibody‐bound gold‐coated magnetic nanoparticles were successfully connected to tumour cells. After RF hyperthermia, the tumour size decreased owing to apoptosis and necrosis of tumour cells.https://doi.org/10.1049/nbt2.12061
collection DOAJ
language English
format Article
sources DOAJ
author Reza Didarian
Ibrahim Vargel
spellingShingle Reza Didarian
Ibrahim Vargel
Treatment of tumour tissue with radio‐frequency hyperthermia (using antibody‐carrying nanoparticles)
IET Nanobiotechnology
author_facet Reza Didarian
Ibrahim Vargel
author_sort Reza Didarian
title Treatment of tumour tissue with radio‐frequency hyperthermia (using antibody‐carrying nanoparticles)
title_short Treatment of tumour tissue with radio‐frequency hyperthermia (using antibody‐carrying nanoparticles)
title_full Treatment of tumour tissue with radio‐frequency hyperthermia (using antibody‐carrying nanoparticles)
title_fullStr Treatment of tumour tissue with radio‐frequency hyperthermia (using antibody‐carrying nanoparticles)
title_full_unstemmed Treatment of tumour tissue with radio‐frequency hyperthermia (using antibody‐carrying nanoparticles)
title_sort treatment of tumour tissue with radio‐frequency hyperthermia (using antibody‐carrying nanoparticles)
publisher Wiley
series IET Nanobiotechnology
issn 1751-8741
1751-875X
publishDate 2021-10-01
description Abstract Intelligent inorganic nanoparticles were designed and produced for use in imaging and annihilating tumour cells by radio‐frequency (RF) hyperthermia. Nanoparticles synthesised to provide RF hyperthermia must have magnetite properties. For this purpose, magnetite nanoparticles were first synthesised by the coprecipitation method (10–15 NM). These superparamagnetic nanoparticles were then covered with gold ions without losing their magnetic properties. In this step, gold ions are reduced around the magnetite nanoparticles. Surface modification of the gold‐coated magnetic nanoparticles was performed in the next step. A self‐assembled monolayer was created using cysteamine (2‐aminoethanethiol) molecules, which have two different end groups (SH and NH2). These molecules react with the gold surface by SH groups. The NH2 groups give a positive charge to the nanoparticles. After that, a monoclonal antibody (Monoclonal Anti‐N‐CAM Clone NCAM‐OB11) was immobilised by the 1‐ethyl‐3‐(3‐dimethylaminopropyl)carbodiimide/N‐hydroxysuccinimide method. Then, the antenna RF system (144.00015 MHz) was created for RF hyperthermia. The antibody‐nanoparticle binding rate and cytotoxicity tests were followed by in vitro and in vivo experiments. As the main result, antibody‐bound gold‐coated magnetic nanoparticles were successfully connected to tumour cells. After RF hyperthermia, the tumour size decreased owing to apoptosis and necrosis of tumour cells.
url https://doi.org/10.1049/nbt2.12061
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