In vitro evaluation of actively targetable superparamagnetic nanoparticles to the folate receptor positive cancer cells

Engineering of a physiologically compatible, stable and targetable SPIONs-CA-FA formulation was reported. Initially fabricated superparamagnetic iron oxide nanoparticles (SPIONs) were coated with citric acid (CA) to hamper agglomeration as well as to ameliorate biocompatibility. Folic acid (FA) as a...

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Main Authors: Nasiri, R., Hamzehalipour Almaki, J., Idris, A. B., Abdul Majid, F. A., Nasiri, M., Salouti, M., Irfan, M., Amini, N., Marvibaigi, M.
Format: Article
Published: Elsevier Ltd 2016
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Online Access:http://eprints.utm.my/id/eprint/71867/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84981727581&doi=10.1016%2fj.msec.2016.07.076&partnerID=40&md5=4a3c86abd1ec0365bb99d45a2108fca7
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spelling my.utm.718672017-11-21T08:17:11Z http://eprints.utm.my/id/eprint/71867/ In vitro evaluation of actively targetable superparamagnetic nanoparticles to the folate receptor positive cancer cells Nasiri, R. Hamzehalipour Almaki, J. Idris, A. B. Abdul Majid, F. A. Nasiri, M. Salouti, M. Irfan, M. Amini, N. Marvibaigi, M. TP Chemical technology Engineering of a physiologically compatible, stable and targetable SPIONs-CA-FA formulation was reported. Initially fabricated superparamagnetic iron oxide nanoparticles (SPIONs) were coated with citric acid (CA) to hamper agglomeration as well as to ameliorate biocompatibility. Folic acid (FA) as a targeting agent was then conjugated to the citric acid coated SPIONs (SPIONs-CA) for targeting the specific receptors expressed on the FAR + cancer cells. Physiochemical characterizations were then performed to assure required properties like stability, size, phase purity, surface morphology, chemical integrity and magnetic properties. In vitro evaluations (MTT assay) were performed on HeLa, HSF 1184, MDA-MB-468 and MDA-MB-231cell lines to ensure the biocompatibility of SPIONs-CA-FA. There were no morphological changes and lysis in contact with erythrocytes recorded for SPIONs-CA-FA and SPIONs-CA. High level of SPIONs-CA-FA binding to FAR + cell lines was assured via qualitative and quantitative in vitro binding studies. Hence, SPIONs-CA-FA was introduced as a promising tool for biomedical applications like magnetic hyperthermia and drug delivery. The in vitro findings presented in this study need to be compared with those of in vivo studies. Elsevier Ltd 2016 Article PeerReviewed Nasiri, R. and Hamzehalipour Almaki, J. and Idris, A. B. and Abdul Majid, F. A. and Nasiri, M. and Salouti, M. and Irfan, M. and Amini, N. and Marvibaigi, M. (2016) In vitro evaluation of actively targetable superparamagnetic nanoparticles to the folate receptor positive cancer cells. Materials Science and Engineering C, 69 . pp. 1147-1158. ISSN 0928-4931 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84981727581&doi=10.1016%2fj.msec.2016.07.076&partnerID=40&md5=4a3c86abd1ec0365bb99d45a2108fca7
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
topic TP Chemical technology
spellingShingle TP Chemical technology
Nasiri, R.
Hamzehalipour Almaki, J.
Idris, A. B.
Abdul Majid, F. A.
Nasiri, M.
Salouti, M.
Irfan, M.
Amini, N.
Marvibaigi, M.
In vitro evaluation of actively targetable superparamagnetic nanoparticles to the folate receptor positive cancer cells
description Engineering of a physiologically compatible, stable and targetable SPIONs-CA-FA formulation was reported. Initially fabricated superparamagnetic iron oxide nanoparticles (SPIONs) were coated with citric acid (CA) to hamper agglomeration as well as to ameliorate biocompatibility. Folic acid (FA) as a targeting agent was then conjugated to the citric acid coated SPIONs (SPIONs-CA) for targeting the specific receptors expressed on the FAR + cancer cells. Physiochemical characterizations were then performed to assure required properties like stability, size, phase purity, surface morphology, chemical integrity and magnetic properties. In vitro evaluations (MTT assay) were performed on HeLa, HSF 1184, MDA-MB-468 and MDA-MB-231cell lines to ensure the biocompatibility of SPIONs-CA-FA. There were no morphological changes and lysis in contact with erythrocytes recorded for SPIONs-CA-FA and SPIONs-CA. High level of SPIONs-CA-FA binding to FAR + cell lines was assured via qualitative and quantitative in vitro binding studies. Hence, SPIONs-CA-FA was introduced as a promising tool for biomedical applications like magnetic hyperthermia and drug delivery. The in vitro findings presented in this study need to be compared with those of in vivo studies.
format Article
author Nasiri, R.
Hamzehalipour Almaki, J.
Idris, A. B.
Abdul Majid, F. A.
Nasiri, M.
Salouti, M.
Irfan, M.
Amini, N.
Marvibaigi, M.
author_facet Nasiri, R.
Hamzehalipour Almaki, J.
Idris, A. B.
Abdul Majid, F. A.
Nasiri, M.
Salouti, M.
Irfan, M.
Amini, N.
Marvibaigi, M.
author_sort Nasiri, R.
title In vitro evaluation of actively targetable superparamagnetic nanoparticles to the folate receptor positive cancer cells
title_short In vitro evaluation of actively targetable superparamagnetic nanoparticles to the folate receptor positive cancer cells
title_full In vitro evaluation of actively targetable superparamagnetic nanoparticles to the folate receptor positive cancer cells
title_fullStr In vitro evaluation of actively targetable superparamagnetic nanoparticles to the folate receptor positive cancer cells
title_full_unstemmed In vitro evaluation of actively targetable superparamagnetic nanoparticles to the folate receptor positive cancer cells
title_sort in vitro evaluation of actively targetable superparamagnetic nanoparticles to the folate receptor positive cancer cells
publisher Elsevier Ltd
publishDate 2016
url http://eprints.utm.my/id/eprint/71867/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84981727581&doi=10.1016%2fj.msec.2016.07.076&partnerID=40&md5=4a3c86abd1ec0365bb99d45a2108fca7
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