Cargando…
Quantitative Comparison of Tumor Delivery for Multiple Targeted Nanoparticles Simultaneously by Multiplex ICP-MS
Given the rapidly expanding library of disease biomarkers and targeting agents, the number of unique targeted nanoparticles is growing exponentially. The high variability and expense of animal testing often makes it unfeasible to examine this large number of nanoparticles in vivo. This often leads t...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894420/ https://www.ncbi.nlm.nih.gov/pubmed/25068300 http://dx.doi.org/10.1038/srep05840 |
_version_ | 1782435673815384064 |
---|---|
author | Elias, Andrew Crayton, Samuel H. Warden-Rothman, Robert Tsourkas, Andrew |
author_facet | Elias, Andrew Crayton, Samuel H. Warden-Rothman, Robert Tsourkas, Andrew |
author_sort | Elias, Andrew |
collection | PubMed |
description | Given the rapidly expanding library of disease biomarkers and targeting agents, the number of unique targeted nanoparticles is growing exponentially. The high variability and expense of animal testing often makes it unfeasible to examine this large number of nanoparticles in vivo. This often leads to the investigation of a single formulation that performed best in vitro. However, nanoparticle performance in vivo depends on many variables, many of which cannot be adequately assessed with cell-based assays. To address this issue, we developed a lanthanide-doped nanoparticle method that allows quantitative comparison of multiple targeted nanoparticles simultaneously. Specifically, superparamagnetic iron oxide (SPIO) nanoparticles with different targeting ligands were created, each with a unique lanthanide dopant. Following the simultaneous injection of the various SPIO compositions into tumor-bearing mice, inductively coupled plasma mass spectroscopy was used to quantitatively and orthogonally assess the concentration of each SPIO composition in serial blood and resected tumor samples. |
format | Online Article Text |
id | pubmed-4894420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48944202016-06-10 Quantitative Comparison of Tumor Delivery for Multiple Targeted Nanoparticles Simultaneously by Multiplex ICP-MS Elias, Andrew Crayton, Samuel H. Warden-Rothman, Robert Tsourkas, Andrew Sci Rep Article Given the rapidly expanding library of disease biomarkers and targeting agents, the number of unique targeted nanoparticles is growing exponentially. The high variability and expense of animal testing often makes it unfeasible to examine this large number of nanoparticles in vivo. This often leads to the investigation of a single formulation that performed best in vitro. However, nanoparticle performance in vivo depends on many variables, many of which cannot be adequately assessed with cell-based assays. To address this issue, we developed a lanthanide-doped nanoparticle method that allows quantitative comparison of multiple targeted nanoparticles simultaneously. Specifically, superparamagnetic iron oxide (SPIO) nanoparticles with different targeting ligands were created, each with a unique lanthanide dopant. Following the simultaneous injection of the various SPIO compositions into tumor-bearing mice, inductively coupled plasma mass spectroscopy was used to quantitatively and orthogonally assess the concentration of each SPIO composition in serial blood and resected tumor samples. Nature Publishing Group 2014-07-28 /pmc/articles/PMC4894420/ /pubmed/25068300 http://dx.doi.org/10.1038/srep05840 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Elias, Andrew Crayton, Samuel H. Warden-Rothman, Robert Tsourkas, Andrew Quantitative Comparison of Tumor Delivery for Multiple Targeted Nanoparticles Simultaneously by Multiplex ICP-MS |
title | Quantitative Comparison of Tumor Delivery for Multiple Targeted Nanoparticles Simultaneously by Multiplex ICP-MS |
title_full | Quantitative Comparison of Tumor Delivery for Multiple Targeted Nanoparticles Simultaneously by Multiplex ICP-MS |
title_fullStr | Quantitative Comparison of Tumor Delivery for Multiple Targeted Nanoparticles Simultaneously by Multiplex ICP-MS |
title_full_unstemmed | Quantitative Comparison of Tumor Delivery for Multiple Targeted Nanoparticles Simultaneously by Multiplex ICP-MS |
title_short | Quantitative Comparison of Tumor Delivery for Multiple Targeted Nanoparticles Simultaneously by Multiplex ICP-MS |
title_sort | quantitative comparison of tumor delivery for multiple targeted nanoparticles simultaneously by multiplex icp-ms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894420/ https://www.ncbi.nlm.nih.gov/pubmed/25068300 http://dx.doi.org/10.1038/srep05840 |
work_keys_str_mv | AT eliasandrew quantitativecomparisonoftumordeliveryformultipletargetednanoparticlessimultaneouslybymultiplexicpms AT craytonsamuelh quantitativecomparisonoftumordeliveryformultipletargetednanoparticlessimultaneouslybymultiplexicpms AT wardenrothmanrobert quantitativecomparisonoftumordeliveryformultipletargetednanoparticlessimultaneouslybymultiplexicpms AT tsourkasandrew quantitativecomparisonoftumordeliveryformultipletargetednanoparticlessimultaneouslybymultiplexicpms |