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Gold-silver alloy nanoshells: a new candidate for nanotherapeutics and diagnostics

We have developed novel gold-silver alloy nanoshells as magnetic resonance imaging (MRI) dual T(1 )(positive) and T(2 )(negative) contrast agents as an alternative to typical gadolinium (Gd)-based contrast agents. Specifically, we have doped iron oxide nanoparticles with Gd ions and sequestered the...

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Autores principales: Gheorghe, Dana E, Cui, Lili, Karmonik, Christof, Brazdeikis, Audrius, Penaloza, Jose M, Young, Joseph K, Drezek, Rebekah A, Bikram, Malavosklish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212091/
https://www.ncbi.nlm.nih.gov/pubmed/21995302
http://dx.doi.org/10.1186/1556-276X-6-554
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author Gheorghe, Dana E
Cui, Lili
Karmonik, Christof
Brazdeikis, Audrius
Penaloza, Jose M
Young, Joseph K
Drezek, Rebekah A
Bikram, Malavosklish
author_facet Gheorghe, Dana E
Cui, Lili
Karmonik, Christof
Brazdeikis, Audrius
Penaloza, Jose M
Young, Joseph K
Drezek, Rebekah A
Bikram, Malavosklish
author_sort Gheorghe, Dana E
collection PubMed
description We have developed novel gold-silver alloy nanoshells as magnetic resonance imaging (MRI) dual T(1 )(positive) and T(2 )(negative) contrast agents as an alternative to typical gadolinium (Gd)-based contrast agents. Specifically, we have doped iron oxide nanoparticles with Gd ions and sequestered the ions within the core by coating the nanoparticles with an alloy of gold and silver. Thus, these nanoparticles are very innovative and have the potential to overcome toxicities related to renal clearance of contrast agents such as nephrogenic systemic fibrosis. The morphology of the attained nanoparticles was characterized by XRD which demonstrated the successful incorporation of Gd(III) ions into the structure of the magnetite, with no major alterations of the spinel structure, as well as the growth of the gold-silver alloy shells. This was supported by TEM, ICP-AES, and SEM/EDS data. The nanoshells showed a saturation magnetization of 38 emu/g because of the presence of Gd ions within the crystalline structure with r(1 )and r(2 )values of 0.0119 and 0.9229 mL mg(-1 )s(-1), respectively (Au:Ag alloy = 1:1). T(1)- and T(2)-weighted images of the nanoshells showed that these agents can both increase the surrounding water proton signals in the T(1)-weighted image and reduce the signal in T(2)-weighted images. The as-synthesized nanoparticles exhibited strong absorption in the range of 600-800 nm, their optical properties being strongly dependent upon the thickness of the gold-silver alloy shell. Thus, these nanoshells have the potential to be utilized for tumor cell ablation because of their absorption as well as an imaging agent.
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spelling pubmed-32120912011-11-09 Gold-silver alloy nanoshells: a new candidate for nanotherapeutics and diagnostics Gheorghe, Dana E Cui, Lili Karmonik, Christof Brazdeikis, Audrius Penaloza, Jose M Young, Joseph K Drezek, Rebekah A Bikram, Malavosklish Nanoscale Res Lett Nano Express We have developed novel gold-silver alloy nanoshells as magnetic resonance imaging (MRI) dual T(1 )(positive) and T(2 )(negative) contrast agents as an alternative to typical gadolinium (Gd)-based contrast agents. Specifically, we have doped iron oxide nanoparticles with Gd ions and sequestered the ions within the core by coating the nanoparticles with an alloy of gold and silver. Thus, these nanoparticles are very innovative and have the potential to overcome toxicities related to renal clearance of contrast agents such as nephrogenic systemic fibrosis. The morphology of the attained nanoparticles was characterized by XRD which demonstrated the successful incorporation of Gd(III) ions into the structure of the magnetite, with no major alterations of the spinel structure, as well as the growth of the gold-silver alloy shells. This was supported by TEM, ICP-AES, and SEM/EDS data. The nanoshells showed a saturation magnetization of 38 emu/g because of the presence of Gd ions within the crystalline structure with r(1 )and r(2 )values of 0.0119 and 0.9229 mL mg(-1 )s(-1), respectively (Au:Ag alloy = 1:1). T(1)- and T(2)-weighted images of the nanoshells showed that these agents can both increase the surrounding water proton signals in the T(1)-weighted image and reduce the signal in T(2)-weighted images. The as-synthesized nanoparticles exhibited strong absorption in the range of 600-800 nm, their optical properties being strongly dependent upon the thickness of the gold-silver alloy shell. Thus, these nanoshells have the potential to be utilized for tumor cell ablation because of their absorption as well as an imaging agent. Springer 2011-10-13 /pmc/articles/PMC3212091/ /pubmed/21995302 http://dx.doi.org/10.1186/1556-276X-6-554 Text en Copyright ©2011 Gheorghe et al; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Nano Express
Gheorghe, Dana E
Cui, Lili
Karmonik, Christof
Brazdeikis, Audrius
Penaloza, Jose M
Young, Joseph K
Drezek, Rebekah A
Bikram, Malavosklish
Gold-silver alloy nanoshells: a new candidate for nanotherapeutics and diagnostics
title Gold-silver alloy nanoshells: a new candidate for nanotherapeutics and diagnostics
title_full Gold-silver alloy nanoshells: a new candidate for nanotherapeutics and diagnostics
title_fullStr Gold-silver alloy nanoshells: a new candidate for nanotherapeutics and diagnostics
title_full_unstemmed Gold-silver alloy nanoshells: a new candidate for nanotherapeutics and diagnostics
title_short Gold-silver alloy nanoshells: a new candidate for nanotherapeutics and diagnostics
title_sort gold-silver alloy nanoshells: a new candidate for nanotherapeutics and diagnostics
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212091/
https://www.ncbi.nlm.nih.gov/pubmed/21995302
http://dx.doi.org/10.1186/1556-276X-6-554
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