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PET Imaging of Soluble Yttrium-86-Labeled Carbon Nanotubes in Mice

BACKGROUND: The potential medical applications of nanomaterials are shaping the landscape of the nanobiotechnology field and driving it forward. A key factor in determining the suitability of these nanomaterials must be how they interface with biological systems. Single walled carbon nanotubes (CNT)...

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Autores principales: McDevitt, Michael R., Chattopadhyay, Debjit, Jaggi, Jaspreet S., Finn, Ronald D., Zanzonico, Pat B., Villa, Carlos, Rey, Diego, Mendenhall, Juana, Batt, Carl A., Njardarson, Jon T., Scheinberg, David A.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1975469/
https://www.ncbi.nlm.nih.gov/pubmed/17878942
http://dx.doi.org/10.1371/journal.pone.0000907
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author McDevitt, Michael R.
Chattopadhyay, Debjit
Jaggi, Jaspreet S.
Finn, Ronald D.
Zanzonico, Pat B.
Villa, Carlos
Rey, Diego
Mendenhall, Juana
Batt, Carl A.
Njardarson, Jon T.
Scheinberg, David A.
author_facet McDevitt, Michael R.
Chattopadhyay, Debjit
Jaggi, Jaspreet S.
Finn, Ronald D.
Zanzonico, Pat B.
Villa, Carlos
Rey, Diego
Mendenhall, Juana
Batt, Carl A.
Njardarson, Jon T.
Scheinberg, David A.
author_sort McDevitt, Michael R.
collection PubMed
description BACKGROUND: The potential medical applications of nanomaterials are shaping the landscape of the nanobiotechnology field and driving it forward. A key factor in determining the suitability of these nanomaterials must be how they interface with biological systems. Single walled carbon nanotubes (CNT) are being investigated as platforms for the delivery of biological, radiological, and chemical payloads to target tissues. CNT are mechanically robust graphene cylinders comprised of sp(2)-bonded carbon atoms and possessing highly regular structures with defined periodicity. CNT exhibit unique mechanochemical properties that can be exploited for the development of novel drug delivery platforms. In order to evaluate the potential usefulness of this CNT scaffold, we undertook an imaging study to determine the tissue biodistribution and pharmacokinetics of prototypical DOTA-functionalized CNT labeled with yttrium-86 and indium-111 ((86)Y-CNT and (111)In-CNT, respectively) in a mouse model. METHODOLOGY AND PRINCIPAL FINDINGS: The (86)Y-CNT construct was synthesized from amine-functionalized, water-soluble CNT by covalently attaching multiple copies of DOTA chelates and then radiolabeling with the positron-emitting metal-ion, yttrium-86. A gamma-emitting (111)In-CNT construct was similarly prepared and purified. The constructs were characterized spectroscopically, microscopically, and chromatographically. The whole-body distribution and clearance of yttrium-86 was characterized at 3 and 24 hours post-injection using positron emission tomography (PET). The yttrium-86 cleared the blood within 3 hours and distributed predominantly to the kidneys, liver, spleen and bone. Although the activity that accumulated in the kidney cleared with time, the whole-body clearance was slow. Differential uptake in these target tissues was observed following intraveneous or intraperitoneal injection. CONCLUSIONS: The whole-body PET images indicated that the major sites of accumulation of activity resulting from the administration of (86)Y-CNT were the kidney, liver, spleen, and to a much less extent the bone. Blood clearance was rapid and could be beneficial in the use of short-lived radionuclides in diagnostic applications.
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spelling pubmed-19754692007-09-19 PET Imaging of Soluble Yttrium-86-Labeled Carbon Nanotubes in Mice McDevitt, Michael R. Chattopadhyay, Debjit Jaggi, Jaspreet S. Finn, Ronald D. Zanzonico, Pat B. Villa, Carlos Rey, Diego Mendenhall, Juana Batt, Carl A. Njardarson, Jon T. Scheinberg, David A. PLoS One Research Article BACKGROUND: The potential medical applications of nanomaterials are shaping the landscape of the nanobiotechnology field and driving it forward. A key factor in determining the suitability of these nanomaterials must be how they interface with biological systems. Single walled carbon nanotubes (CNT) are being investigated as platforms for the delivery of biological, radiological, and chemical payloads to target tissues. CNT are mechanically robust graphene cylinders comprised of sp(2)-bonded carbon atoms and possessing highly regular structures with defined periodicity. CNT exhibit unique mechanochemical properties that can be exploited for the development of novel drug delivery platforms. In order to evaluate the potential usefulness of this CNT scaffold, we undertook an imaging study to determine the tissue biodistribution and pharmacokinetics of prototypical DOTA-functionalized CNT labeled with yttrium-86 and indium-111 ((86)Y-CNT and (111)In-CNT, respectively) in a mouse model. METHODOLOGY AND PRINCIPAL FINDINGS: The (86)Y-CNT construct was synthesized from amine-functionalized, water-soluble CNT by covalently attaching multiple copies of DOTA chelates and then radiolabeling with the positron-emitting metal-ion, yttrium-86. A gamma-emitting (111)In-CNT construct was similarly prepared and purified. The constructs were characterized spectroscopically, microscopically, and chromatographically. The whole-body distribution and clearance of yttrium-86 was characterized at 3 and 24 hours post-injection using positron emission tomography (PET). The yttrium-86 cleared the blood within 3 hours and distributed predominantly to the kidneys, liver, spleen and bone. Although the activity that accumulated in the kidney cleared with time, the whole-body clearance was slow. Differential uptake in these target tissues was observed following intraveneous or intraperitoneal injection. CONCLUSIONS: The whole-body PET images indicated that the major sites of accumulation of activity resulting from the administration of (86)Y-CNT were the kidney, liver, spleen, and to a much less extent the bone. Blood clearance was rapid and could be beneficial in the use of short-lived radionuclides in diagnostic applications. Public Library of Science 2007-09-19 /pmc/articles/PMC1975469/ /pubmed/17878942 http://dx.doi.org/10.1371/journal.pone.0000907 Text en McDevitt et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
McDevitt, Michael R.
Chattopadhyay, Debjit
Jaggi, Jaspreet S.
Finn, Ronald D.
Zanzonico, Pat B.
Villa, Carlos
Rey, Diego
Mendenhall, Juana
Batt, Carl A.
Njardarson, Jon T.
Scheinberg, David A.
PET Imaging of Soluble Yttrium-86-Labeled Carbon Nanotubes in Mice
title PET Imaging of Soluble Yttrium-86-Labeled Carbon Nanotubes in Mice
title_full PET Imaging of Soluble Yttrium-86-Labeled Carbon Nanotubes in Mice
title_fullStr PET Imaging of Soluble Yttrium-86-Labeled Carbon Nanotubes in Mice
title_full_unstemmed PET Imaging of Soluble Yttrium-86-Labeled Carbon Nanotubes in Mice
title_short PET Imaging of Soluble Yttrium-86-Labeled Carbon Nanotubes in Mice
title_sort pet imaging of soluble yttrium-86-labeled carbon nanotubes in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1975469/
https://www.ncbi.nlm.nih.gov/pubmed/17878942
http://dx.doi.org/10.1371/journal.pone.0000907
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