An x-ray fluorescence imaging system for gold nanoparticle detection
Gold nanoparticles (GNPs) may be used as a contrast agent to identify tumour location and can be modified to target and image specific tumour biological parameters. There are currently no imaging systems in the literature that have sufficient sensitivity to GNP concentration and distribution measure...
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Veröffentlicht in: | Physics in medicine & biology 2013-11, Vol.58 (21), p.7841-7855 |
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creator | Ricketts, K Guazzoni, C Castoldi, A Gibson, A P Royle, G J |
description | Gold nanoparticles (GNPs) may be used as a contrast agent to identify tumour location and can be modified to target and image specific tumour biological parameters. There are currently no imaging systems in the literature that have sufficient sensitivity to GNP concentration and distribution measurement at sufficient tissue depth for use in in vivo and in vitro studies. We have demonstrated that high detecting sensitivity of GNPs can be achieved using x-ray fluorescence; furthermore this technique enables greater depth imaging in comparison to optical modalities. Two x-ray fluorescence systems were developed and used to image a range of GNP imaging phantoms. The first system consisted of a 10 mm2 silicon drift detector coupled to a slightly focusing polycapillary optic which allowed 2D energy resolved imaging in step and scan mode. The system has sensitivity to GNP concentrations as low as 1 ppm. GNP concentrations different by a factor of 5 could be resolved, offering potential to distinguish tumour from non-tumour. The second system was designed to avoid slow step and scan image acquisition; the feasibility of excitation of the whole specimen with a wide beam and detection of the fluorescent x-rays with a pixellated controlled drift energy resolving detector without scanning was investigated. A parallel polycapillary optic coupled to the detector was successfully used to ascertain the position where fluorescence was emitted. The tissue penetration of the technique was demonstrated to be sufficient for near-surface small-animal studies, and for imaging 3D in vitro cellular constructs. Previous work demonstrates strong potential for both imaging systems to form quantitative images of GNP concentration. |
doi_str_mv | 10.1088/0031-9155/58/21/7841 |
format | Article |
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The second system was designed to avoid slow step and scan image acquisition; the feasibility of excitation of the whole specimen with a wide beam and detection of the fluorescent x-rays with a pixellated controlled drift energy resolving detector without scanning was investigated. A parallel polycapillary optic coupled to the detector was successfully used to ascertain the position where fluorescence was emitted. The tissue penetration of the technique was demonstrated to be sufficient for near-surface small-animal studies, and for imaging 3D in vitro cellular constructs. 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Med. Biol</addtitle><description>Gold nanoparticles (GNPs) may be used as a contrast agent to identify tumour location and can be modified to target and image specific tumour biological parameters. There are currently no imaging systems in the literature that have sufficient sensitivity to GNP concentration and distribution measurement at sufficient tissue depth for use in in vivo and in vitro studies. We have demonstrated that high detecting sensitivity of GNPs can be achieved using x-ray fluorescence; furthermore this technique enables greater depth imaging in comparison to optical modalities. Two x-ray fluorescence systems were developed and used to image a range of GNP imaging phantoms. The first system consisted of a 10 mm2 silicon drift detector coupled to a slightly focusing polycapillary optic which allowed 2D energy resolved imaging in step and scan mode. The system has sensitivity to GNP concentrations as low as 1 ppm. GNP concentrations different by a factor of 5 could be resolved, offering potential to distinguish tumour from non-tumour. The second system was designed to avoid slow step and scan image acquisition; the feasibility of excitation of the whole specimen with a wide beam and detection of the fluorescent x-rays with a pixellated controlled drift energy resolving detector without scanning was investigated. A parallel polycapillary optic coupled to the detector was successfully used to ascertain the position where fluorescence was emitted. The tissue penetration of the technique was demonstrated to be sufficient for near-surface small-animal studies, and for imaging 3D in vitro cellular constructs. Previous work demonstrates strong potential for both imaging systems to form quantitative images of GNP concentration.</description><subject>biomarkers</subject><subject>Gold - analysis</subject><subject>Gold - chemistry</subject><subject>gold nanoparticles</subject><subject>Metal Nanoparticles</subject><subject>Optical Imaging - instrumentation</subject><subject>Optical Imaging - methods</subject><subject>x-ray fluorescence</subject><subject>X-Rays</subject><issn>0031-9155</issn><issn>1361-6560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kLtOwzAUhi0EoqXwBghlZAnxcezEGatylSqxwGzZjlOlSuxgJxJ9exy1MOLlDP7-c_kQugX8AJjzDOMc0goYyxjPCGQlp3CGlpAXkBaswOdo-Ycs0FUIe4wBOKGXaEEoUEaALtHj2ibfqZeHpOkm503QxmqTtL3ctXaXhEMYTZ80zic719WJldYN0o-t7kxSm9HosXX2Gl00sgvm5lRX6PP56WPzmm7fX942622q84qOqdIFqAaXeaMUyDo-xZoKNwoqqkCVpGJGaiNzVtdaS8a5IVVeQvxmmpgiX6H7Y9_Bu6_JhFH0bVy466Q1bgoCKC0B0xiMKD2i2rsQvGnE4ONR_iAAi9mfmOWIWY5gXBAQs78YuztNmFRv6r_Qr7AI4CPQukHs3eRtPPj_nj8OonpC</recordid><startdate>20131107</startdate><enddate>20131107</enddate><creator>Ricketts, K</creator><creator>Guazzoni, C</creator><creator>Castoldi, A</creator><creator>Gibson, A P</creator><creator>Royle, G J</creator><general>IOP Publishing</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20131107</creationdate><title>An x-ray fluorescence imaging system for gold nanoparticle detection</title><author>Ricketts, K ; Guazzoni, C ; Castoldi, A ; Gibson, A P ; Royle, G J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-bc61bf073fbb1addddb5f90fb194b1b7295eacea35ddcca588e293711945c2e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>biomarkers</topic><topic>Gold - analysis</topic><topic>Gold - chemistry</topic><topic>gold nanoparticles</topic><topic>Metal Nanoparticles</topic><topic>Optical Imaging - instrumentation</topic><topic>Optical Imaging - methods</topic><topic>x-ray fluorescence</topic><topic>X-Rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ricketts, K</creatorcontrib><creatorcontrib>Guazzoni, C</creatorcontrib><creatorcontrib>Castoldi, A</creatorcontrib><creatorcontrib>Gibson, A P</creatorcontrib><creatorcontrib>Royle, G J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Physics in medicine & biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ricketts, K</au><au>Guazzoni, C</au><au>Castoldi, A</au><au>Gibson, A P</au><au>Royle, G J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An x-ray fluorescence imaging system for gold nanoparticle detection</atitle><jtitle>Physics in medicine & biology</jtitle><stitle>PMB</stitle><addtitle>Phys. Med. Biol</addtitle><date>2013-11-07</date><risdate>2013</risdate><volume>58</volume><issue>21</issue><spage>7841</spage><epage>7855</epage><pages>7841-7855</pages><issn>0031-9155</issn><eissn>1361-6560</eissn><coden>PHMBA7</coden><abstract>Gold nanoparticles (GNPs) may be used as a contrast agent to identify tumour location and can be modified to target and image specific tumour biological parameters. There are currently no imaging systems in the literature that have sufficient sensitivity to GNP concentration and distribution measurement at sufficient tissue depth for use in in vivo and in vitro studies. We have demonstrated that high detecting sensitivity of GNPs can be achieved using x-ray fluorescence; furthermore this technique enables greater depth imaging in comparison to optical modalities. Two x-ray fluorescence systems were developed and used to image a range of GNP imaging phantoms. The first system consisted of a 10 mm2 silicon drift detector coupled to a slightly focusing polycapillary optic which allowed 2D energy resolved imaging in step and scan mode. The system has sensitivity to GNP concentrations as low as 1 ppm. GNP concentrations different by a factor of 5 could be resolved, offering potential to distinguish tumour from non-tumour. The second system was designed to avoid slow step and scan image acquisition; the feasibility of excitation of the whole specimen with a wide beam and detection of the fluorescent x-rays with a pixellated controlled drift energy resolving detector without scanning was investigated. A parallel polycapillary optic coupled to the detector was successfully used to ascertain the position where fluorescence was emitted. The tissue penetration of the technique was demonstrated to be sufficient for near-surface small-animal studies, and for imaging 3D in vitro cellular constructs. 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subjects | biomarkers Gold - analysis Gold - chemistry gold nanoparticles Metal Nanoparticles Optical Imaging - instrumentation Optical Imaging - methods x-ray fluorescence X-Rays |
title | An x-ray fluorescence imaging system for gold nanoparticle detection |
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