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Visualization of the distribution of nanoparticle-formulated AZD2811 in mouse tumor model using matrix-assisted laser desorption ionization mass spectrometry imaging

Penetration of nanoparticles into viable tumor regions is essential for an effective response. Mass spectrometry imaging (MSI) is a novel method for evaluating the intratumoral pharmacokinetics (PK) of a drug in terms of spatial distribution. The application of MSI for analysis of nanomedicine PK re...

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Autores principales: Ryu, Shoraku, Ohuchi, Mayu, Yagishita, Shigehiro, Shimoi, Tatsunori, Yonemori, Kan, Tamura, Kenji, Fujiwara, Yasuhiro, Hamada, Akinobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511311/
https://www.ncbi.nlm.nih.gov/pubmed/32968211
http://dx.doi.org/10.1038/s41598-020-72665-5
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author Ryu, Shoraku
Ohuchi, Mayu
Yagishita, Shigehiro
Shimoi, Tatsunori
Yonemori, Kan
Tamura, Kenji
Fujiwara, Yasuhiro
Hamada, Akinobu
author_facet Ryu, Shoraku
Ohuchi, Mayu
Yagishita, Shigehiro
Shimoi, Tatsunori
Yonemori, Kan
Tamura, Kenji
Fujiwara, Yasuhiro
Hamada, Akinobu
author_sort Ryu, Shoraku
collection PubMed
description Penetration of nanoparticles into viable tumor regions is essential for an effective response. Mass spectrometry imaging (MSI) is a novel method for evaluating the intratumoral pharmacokinetics (PK) of a drug in terms of spatial distribution. The application of MSI for analysis of nanomedicine PK remains in its infancy. In this study, we evaluated the applicability of MALDI-MSI for nanoparticle-formulated drug visualization in tumors and biopsies, with an aim toward future application in clinical nanomedicine research. We established an analytic method for the free drug (AZD2811) and then applied it to visualize nanoparticle-formulated AZD2811. MSI analysis demonstrated heterogeneous intratumoral drug distribution in three xenograft tumors. The intensity of MSI signals correlated well with total drug concentration in tumors, indicating that drug distribution can be monitored quantitatively. Analysis of tumor biopsies indicated that MSI is applicable for analyzing the distribution of nanoparticle-formulated drugs in tumor biopsies, suggesting clinical applicability.
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spelling pubmed-75113112020-09-24 Visualization of the distribution of nanoparticle-formulated AZD2811 in mouse tumor model using matrix-assisted laser desorption ionization mass spectrometry imaging Ryu, Shoraku Ohuchi, Mayu Yagishita, Shigehiro Shimoi, Tatsunori Yonemori, Kan Tamura, Kenji Fujiwara, Yasuhiro Hamada, Akinobu Sci Rep Article Penetration of nanoparticles into viable tumor regions is essential for an effective response. Mass spectrometry imaging (MSI) is a novel method for evaluating the intratumoral pharmacokinetics (PK) of a drug in terms of spatial distribution. The application of MSI for analysis of nanomedicine PK remains in its infancy. In this study, we evaluated the applicability of MALDI-MSI for nanoparticle-formulated drug visualization in tumors and biopsies, with an aim toward future application in clinical nanomedicine research. We established an analytic method for the free drug (AZD2811) and then applied it to visualize nanoparticle-formulated AZD2811. MSI analysis demonstrated heterogeneous intratumoral drug distribution in three xenograft tumors. The intensity of MSI signals correlated well with total drug concentration in tumors, indicating that drug distribution can be monitored quantitatively. Analysis of tumor biopsies indicated that MSI is applicable for analyzing the distribution of nanoparticle-formulated drugs in tumor biopsies, suggesting clinical applicability. Nature Publishing Group UK 2020-09-23 /pmc/articles/PMC7511311/ /pubmed/32968211 http://dx.doi.org/10.1038/s41598-020-72665-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ryu, Shoraku
Ohuchi, Mayu
Yagishita, Shigehiro
Shimoi, Tatsunori
Yonemori, Kan
Tamura, Kenji
Fujiwara, Yasuhiro
Hamada, Akinobu
Visualization of the distribution of nanoparticle-formulated AZD2811 in mouse tumor model using matrix-assisted laser desorption ionization mass spectrometry imaging
title Visualization of the distribution of nanoparticle-formulated AZD2811 in mouse tumor model using matrix-assisted laser desorption ionization mass spectrometry imaging
title_full Visualization of the distribution of nanoparticle-formulated AZD2811 in mouse tumor model using matrix-assisted laser desorption ionization mass spectrometry imaging
title_fullStr Visualization of the distribution of nanoparticle-formulated AZD2811 in mouse tumor model using matrix-assisted laser desorption ionization mass spectrometry imaging
title_full_unstemmed Visualization of the distribution of nanoparticle-formulated AZD2811 in mouse tumor model using matrix-assisted laser desorption ionization mass spectrometry imaging
title_short Visualization of the distribution of nanoparticle-formulated AZD2811 in mouse tumor model using matrix-assisted laser desorption ionization mass spectrometry imaging
title_sort visualization of the distribution of nanoparticle-formulated azd2811 in mouse tumor model using matrix-assisted laser desorption ionization mass spectrometry imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511311/
https://www.ncbi.nlm.nih.gov/pubmed/32968211
http://dx.doi.org/10.1038/s41598-020-72665-5
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