Ultrasound-triggered phase transition sensitive magnetic fluorescent nanodroplets as a multimodal imaging contrast agent in rat and mouse model

Ultrasound-triggered phase transition sensitive nanodroplets with multimodal imaging functionality were prepared via premix Shirasu porous glass (SPG) membrane emulsification method. The nanodroplets with fluorescence dye DiR and SPIO nanoparticles (DiR-SPIO-NDs) had a polymer shell and a liquid per...

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Veröffentlicht in:PloS one 2013-12, Vol.8 (12), p.e85003
Hauptverfasser: Cheng, Xin, Li, Huan, Chen, Yunchao, Luo, Binhua, Liu, Xuhan, Liu, Wei, Xu, Haibo, Yang, Xiangliang
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container_issue 12
container_start_page e85003
container_title PloS one
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creator Cheng, Xin
Li, Huan
Chen, Yunchao
Luo, Binhua
Liu, Xuhan
Liu, Wei
Xu, Haibo
Yang, Xiangliang
description Ultrasound-triggered phase transition sensitive nanodroplets with multimodal imaging functionality were prepared via premix Shirasu porous glass (SPG) membrane emulsification method. The nanodroplets with fluorescence dye DiR and SPIO nanoparticles (DiR-SPIO-NDs) had a polymer shell and a liquid perfluoropentane (PFP) core. The as-formed DiR-SPIO-NDs have a uniform size of 385 ± 5.0 nm with PDI of 0.169 ± 0.011. The TEM and microscopy imaging showed that the DiR-SPIO-NDs existed as core-shell spheres, and DiR and SPIO nanoparticles dispersed in the shell or core. The MTT and hemolysis studies demonstrated that the nanodroplets were biocompatible and safe. Moreover, the proposed nanodroplets exhibited significant ultrasound-triggered phase transition property under clinical diagnostic ultrasound irradiation due to the vaporization of PFP inside. Meanwhile, the high stability and R2 relaxivity of the DiR-SPIO-NDs suggested its applicability in MRI. The in vivo T2-weighted images of MRI and fluorescence images both showed that the image contrast in liver and spleen of rats and mice model were enhanced after the intravenous injection of DiR-SPIO-NDs. Furthermore, the ultrasound imaging (US) in mice tumor as well as MRI and fluorescence imaging in liver of rats and mice showed that the DiR-SPIO-NDs had long-lasting contrast ability in vivo. These in vitro and in vivo findings suggested that DiR-SPIO-NDs could potentially be a great MRI/US/fluorescence multimodal imaging contrast agent in the diagnosis of liver tissue diseases.
doi_str_mv 10.1371/journal.pone.0085003
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The nanodroplets with fluorescence dye DiR and SPIO nanoparticles (DiR-SPIO-NDs) had a polymer shell and a liquid perfluoropentane (PFP) core. The as-formed DiR-SPIO-NDs have a uniform size of 385 ± 5.0 nm with PDI of 0.169 ± 0.011. The TEM and microscopy imaging showed that the DiR-SPIO-NDs existed as core-shell spheres, and DiR and SPIO nanoparticles dispersed in the shell or core. The MTT and hemolysis studies demonstrated that the nanodroplets were biocompatible and safe. Moreover, the proposed nanodroplets exhibited significant ultrasound-triggered phase transition property under clinical diagnostic ultrasound irradiation due to the vaporization of PFP inside. Meanwhile, the high stability and R2 relaxivity of the DiR-SPIO-NDs suggested its applicability in MRI. The in vivo T2-weighted images of MRI and fluorescence images both showed that the image contrast in liver and spleen of rats and mice model were enhanced after the intravenous injection of DiR-SPIO-NDs. Furthermore, the ultrasound imaging (US) in mice tumor as well as MRI and fluorescence imaging in liver of rats and mice showed that the DiR-SPIO-NDs had long-lasting contrast ability in vivo. These in vitro and in vivo findings suggested that DiR-SPIO-NDs could potentially be a great MRI/US/fluorescence multimodal imaging contrast agent in the diagnosis of liver tissue diseases.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0085003</identifier><identifier>PMID: 24391983</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Biocompatibility ; Biology ; Biomedical materials ; Contrast agents ; Contrast media ; Contrast Media - chemistry ; Diagnostic systems ; Emulsification ; Engineering ; Engineering research ; Fluorescence ; Fluorocarbons - chemistry ; Hemolysis ; Hospitals ; Image contrast ; Intravenous administration ; Irradiation ; Life sciences ; Liver ; Liver diseases ; Magnetic resonance imaging ; Materials Science ; Medicine ; Methods ; Mice ; Microscopy ; Microscopy, Electron, Transmission ; Multimodal Imaging - methods ; Nanoparticles ; Nanoparticles - chemistry ; NMR ; Nuclear magnetic resonance ; Phase Transition ; Phase transitions ; Physiology ; Quantum dots ; Radiation ; Rats ; Spleen ; Surfactants ; Tetrazolium Salts ; Thiazoles ; Ultrasonic imaging ; Ultrasonography ; Ultrasound ; Ultrasound imaging ; Vaporization</subject><ispartof>PloS one, 2013-12, Vol.8 (12), p.e85003</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Cheng et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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The nanodroplets with fluorescence dye DiR and SPIO nanoparticles (DiR-SPIO-NDs) had a polymer shell and a liquid perfluoropentane (PFP) core. The as-formed DiR-SPIO-NDs have a uniform size of 385 ± 5.0 nm with PDI of 0.169 ± 0.011. The TEM and microscopy imaging showed that the DiR-SPIO-NDs existed as core-shell spheres, and DiR and SPIO nanoparticles dispersed in the shell or core. The MTT and hemolysis studies demonstrated that the nanodroplets were biocompatible and safe. Moreover, the proposed nanodroplets exhibited significant ultrasound-triggered phase transition property under clinical diagnostic ultrasound irradiation due to the vaporization of PFP inside. Meanwhile, the high stability and R2 relaxivity of the DiR-SPIO-NDs suggested its applicability in MRI. The in vivo T2-weighted images of MRI and fluorescence images both showed that the image contrast in liver and spleen of rats and mice model were enhanced after the intravenous injection of DiR-SPIO-NDs. Furthermore, the ultrasound imaging (US) in mice tumor as well as MRI and fluorescence imaging in liver of rats and mice showed that the DiR-SPIO-NDs had long-lasting contrast ability in vivo. These in vitro and in vivo findings suggested that DiR-SPIO-NDs could potentially be a great MRI/US/fluorescence multimodal imaging contrast agent in the diagnosis of liver tissue diseases.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24391983</pmid><doi>10.1371/journal.pone.0085003</doi><oa>free_for_read</oa></addata></record>
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subjects Animals
Biocompatibility
Biology
Biomedical materials
Contrast agents
Contrast media
Contrast Media - chemistry
Diagnostic systems
Emulsification
Engineering
Engineering research
Fluorescence
Fluorocarbons - chemistry
Hemolysis
Hospitals
Image contrast
Intravenous administration
Irradiation
Life sciences
Liver
Liver diseases
Magnetic resonance imaging
Materials Science
Medicine
Methods
Mice
Microscopy
Microscopy, Electron, Transmission
Multimodal Imaging - methods
Nanoparticles
Nanoparticles - chemistry
NMR
Nuclear magnetic resonance
Phase Transition
Phase transitions
Physiology
Quantum dots
Radiation
Rats
Spleen
Surfactants
Tetrazolium Salts
Thiazoles
Ultrasonic imaging
Ultrasonography
Ultrasound
Ultrasound imaging
Vaporization
title Ultrasound-triggered phase transition sensitive magnetic fluorescent nanodroplets as a multimodal imaging contrast agent in rat and mouse model
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