Loading…

Targeted nanoparticles for detecting and treating cancer

Enabled by their size and supramolecular structures, nanoparticles (that is, particles of approximately 10 to 100 nanometers) promise to be particularly capable agents in the detection, diagnosis, and treatment of cancer. When loaded with chemotherapeutic agents, nanoparticle delivery to cancerous t...

Full description

Saved in:
Bibliographic Details
Published in:Drug development research 2006-01, Vol.67 (1), p.70-93
Main Authors: Sunderland, Christopher J., Steiert, Matthias, Talmadge, James E., Derfus, Austin M., Barry, Stephen E.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c4399-dd5145c585a84e6664a12914e586002f554eb1f4c3473d74d7ce65cd226ee3e03
cites cdi_FETCH-LOGICAL-c4399-dd5145c585a84e6664a12914e586002f554eb1f4c3473d74d7ce65cd226ee3e03
container_end_page 93
container_issue 1
container_start_page 70
container_title Drug development research
container_volume 67
creator Sunderland, Christopher J.
Steiert, Matthias
Talmadge, James E.
Derfus, Austin M.
Barry, Stephen E.
description Enabled by their size and supramolecular structures, nanoparticles (that is, particles of approximately 10 to 100 nanometers) promise to be particularly capable agents in the detection, diagnosis, and treatment of cancer. When loaded with chemotherapeutic agents, nanoparticle delivery to cancerous tissues relative to healthy tissues may be favorably biased by size and through the attachment of targeting ligands to the surface of the particle. Nanoparticles may be made from a variety of materials, and in addition to chemotherapeutic payloads, nanoparticles can incorporate non‐bioactive elements useful as diagnostic and device agents. For example, the inclusion of iron oxide colloids enables nanoparticle use as magnetic resonance imaging (MRI) contrast agents, and also, through the application of an alternating magnetic field (AMF), enables the particle to generate enough heat to be used for hyperthermic therapeutic applications. In this report, we also introduce novel Magnetic Nanoparticle Hydro‐Gel (MagNaGelTM) materials comprised of chemotherapeutic agents, iron oxide colloids, and targeting ligands. MagNaGel particles were fabricated in the 20‐ to 40‐nm size range with very narrow size dispersion. These particles demonstrate high (>10 wt %) chemotherapeutic loading, tumor‐associated biomolecular binding, good magnetic susceptibility, and attractive toxicity and circulation profiles in mouse models. Looking forward, the convergence of drug and device on the nano‐scale promises treatment modalities that cannot be practiced through traditionally distinct drug and device combinations. MagNaGel nanoparticles are drug‐device hybrids that, when used in conjunction with diagnostic MRI and inductive heating, may play a key role in new and powerful cancer treatment regimens. Drug Dev. Res. 67:70–93, 2006. © 2006 Wiley‐Liss, Inc.
doi_str_mv 10.1002/ddr.20069
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_19443571</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>19443571</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4399-dd5145c585a84e6664a12914e586002f554eb1f4c3473d74d7ce65cd226ee3e03</originalsourceid><addsrcrecordid>eNp1kE1Lw0AQhhdRsFYP_oOcBA9p93uzR2ltFIpfVHpc1t1JiaZJ3U3R_ntjo948DTM878zwIHRO8IhgTMfehxHFWOoDNCBYZymlWh-iAaaKppxpcoxOYnzFmBCeZQOULWxYQQs-qW3dbGxoS1dBTIomJL6bu7asV4mtfdIGsPvG2dpBOEVHha0inP3UIXqeXS8mN-n8Pr-dXM1T113TqfeCcOFEJmzGQUrJLaGacBCZ7P4thODwQgruGFfMK-6VAymcp1QCMMBsiC76vZvQvG8htmZdRgdVZWtottEQzTkTinTgZQ-60MQYoDCbUK5t2BmCzbcb07kxezcdO-7Zj7KC3f-gmU6ffhNpnyhjC59_CRvejFRMCbO8yw1-fMgZZjOzZF8-u3OQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19443571</pqid></control><display><type>article</type><title>Targeted nanoparticles for detecting and treating cancer</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Sunderland, Christopher J. ; Steiert, Matthias ; Talmadge, James E. ; Derfus, Austin M. ; Barry, Stephen E.</creator><creatorcontrib>Sunderland, Christopher J. ; Steiert, Matthias ; Talmadge, James E. ; Derfus, Austin M. ; Barry, Stephen E.</creatorcontrib><description>Enabled by their size and supramolecular structures, nanoparticles (that is, particles of approximately 10 to 100 nanometers) promise to be particularly capable agents in the detection, diagnosis, and treatment of cancer. When loaded with chemotherapeutic agents, nanoparticle delivery to cancerous tissues relative to healthy tissues may be favorably biased by size and through the attachment of targeting ligands to the surface of the particle. Nanoparticles may be made from a variety of materials, and in addition to chemotherapeutic payloads, nanoparticles can incorporate non‐bioactive elements useful as diagnostic and device agents. For example, the inclusion of iron oxide colloids enables nanoparticle use as magnetic resonance imaging (MRI) contrast agents, and also, through the application of an alternating magnetic field (AMF), enables the particle to generate enough heat to be used for hyperthermic therapeutic applications. In this report, we also introduce novel Magnetic Nanoparticle Hydro‐Gel (MagNaGelTM) materials comprised of chemotherapeutic agents, iron oxide colloids, and targeting ligands. MagNaGel particles were fabricated in the 20‐ to 40‐nm size range with very narrow size dispersion. These particles demonstrate high (&gt;10 wt %) chemotherapeutic loading, tumor‐associated biomolecular binding, good magnetic susceptibility, and attractive toxicity and circulation profiles in mouse models. Looking forward, the convergence of drug and device on the nano‐scale promises treatment modalities that cannot be practiced through traditionally distinct drug and device combinations. MagNaGel nanoparticles are drug‐device hybrids that, when used in conjunction with diagnostic MRI and inductive heating, may play a key role in new and powerful cancer treatment regimens. Drug Dev. Res. 67:70–93, 2006. © 2006 Wiley‐Liss, Inc.</description><identifier>ISSN: 0272-4391</identifier><identifier>EISSN: 1098-2299</identifier><identifier>DOI: 10.1002/ddr.20069</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>cancer ; drug delivery ; magnetic ; nanoparticles ; targeting</subject><ispartof>Drug development research, 2006-01, Vol.67 (1), p.70-93</ispartof><rights>2006 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4399-dd5145c585a84e6664a12914e586002f554eb1f4c3473d74d7ce65cd226ee3e03</citedby><cites>FETCH-LOGICAL-c4399-dd5145c585a84e6664a12914e586002f554eb1f4c3473d74d7ce65cd226ee3e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Sunderland, Christopher J.</creatorcontrib><creatorcontrib>Steiert, Matthias</creatorcontrib><creatorcontrib>Talmadge, James E.</creatorcontrib><creatorcontrib>Derfus, Austin M.</creatorcontrib><creatorcontrib>Barry, Stephen E.</creatorcontrib><title>Targeted nanoparticles for detecting and treating cancer</title><title>Drug development research</title><addtitle>Drug Dev. Res</addtitle><description>Enabled by their size and supramolecular structures, nanoparticles (that is, particles of approximately 10 to 100 nanometers) promise to be particularly capable agents in the detection, diagnosis, and treatment of cancer. When loaded with chemotherapeutic agents, nanoparticle delivery to cancerous tissues relative to healthy tissues may be favorably biased by size and through the attachment of targeting ligands to the surface of the particle. Nanoparticles may be made from a variety of materials, and in addition to chemotherapeutic payloads, nanoparticles can incorporate non‐bioactive elements useful as diagnostic and device agents. For example, the inclusion of iron oxide colloids enables nanoparticle use as magnetic resonance imaging (MRI) contrast agents, and also, through the application of an alternating magnetic field (AMF), enables the particle to generate enough heat to be used for hyperthermic therapeutic applications. In this report, we also introduce novel Magnetic Nanoparticle Hydro‐Gel (MagNaGelTM) materials comprised of chemotherapeutic agents, iron oxide colloids, and targeting ligands. MagNaGel particles were fabricated in the 20‐ to 40‐nm size range with very narrow size dispersion. These particles demonstrate high (&gt;10 wt %) chemotherapeutic loading, tumor‐associated biomolecular binding, good magnetic susceptibility, and attractive toxicity and circulation profiles in mouse models. Looking forward, the convergence of drug and device on the nano‐scale promises treatment modalities that cannot be practiced through traditionally distinct drug and device combinations. MagNaGel nanoparticles are drug‐device hybrids that, when used in conjunction with diagnostic MRI and inductive heating, may play a key role in new and powerful cancer treatment regimens. Drug Dev. Res. 67:70–93, 2006. © 2006 Wiley‐Liss, Inc.</description><subject>cancer</subject><subject>drug delivery</subject><subject>magnetic</subject><subject>nanoparticles</subject><subject>targeting</subject><issn>0272-4391</issn><issn>1098-2299</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp1kE1Lw0AQhhdRsFYP_oOcBA9p93uzR2ltFIpfVHpc1t1JiaZJ3U3R_ntjo948DTM878zwIHRO8IhgTMfehxHFWOoDNCBYZymlWh-iAaaKppxpcoxOYnzFmBCeZQOULWxYQQs-qW3dbGxoS1dBTIomJL6bu7asV4mtfdIGsPvG2dpBOEVHha0inP3UIXqeXS8mN-n8Pr-dXM1T113TqfeCcOFEJmzGQUrJLaGacBCZ7P4thODwQgruGFfMK-6VAymcp1QCMMBsiC76vZvQvG8htmZdRgdVZWtottEQzTkTinTgZQ-60MQYoDCbUK5t2BmCzbcb07kxezcdO-7Zj7KC3f-gmU6ffhNpnyhjC59_CRvejFRMCbO8yw1-fMgZZjOzZF8-u3OQ</recordid><startdate>200601</startdate><enddate>200601</enddate><creator>Sunderland, Christopher J.</creator><creator>Steiert, Matthias</creator><creator>Talmadge, James E.</creator><creator>Derfus, Austin M.</creator><creator>Barry, Stephen E.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>200601</creationdate><title>Targeted nanoparticles for detecting and treating cancer</title><author>Sunderland, Christopher J. ; Steiert, Matthias ; Talmadge, James E. ; Derfus, Austin M. ; Barry, Stephen E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4399-dd5145c585a84e6664a12914e586002f554eb1f4c3473d74d7ce65cd226ee3e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>cancer</topic><topic>drug delivery</topic><topic>magnetic</topic><topic>nanoparticles</topic><topic>targeting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sunderland, Christopher J.</creatorcontrib><creatorcontrib>Steiert, Matthias</creatorcontrib><creatorcontrib>Talmadge, James E.</creatorcontrib><creatorcontrib>Derfus, Austin M.</creatorcontrib><creatorcontrib>Barry, Stephen E.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Drug development research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sunderland, Christopher J.</au><au>Steiert, Matthias</au><au>Talmadge, James E.</au><au>Derfus, Austin M.</au><au>Barry, Stephen E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeted nanoparticles for detecting and treating cancer</atitle><jtitle>Drug development research</jtitle><addtitle>Drug Dev. Res</addtitle><date>2006-01</date><risdate>2006</risdate><volume>67</volume><issue>1</issue><spage>70</spage><epage>93</epage><pages>70-93</pages><issn>0272-4391</issn><eissn>1098-2299</eissn><abstract>Enabled by their size and supramolecular structures, nanoparticles (that is, particles of approximately 10 to 100 nanometers) promise to be particularly capable agents in the detection, diagnosis, and treatment of cancer. When loaded with chemotherapeutic agents, nanoparticle delivery to cancerous tissues relative to healthy tissues may be favorably biased by size and through the attachment of targeting ligands to the surface of the particle. Nanoparticles may be made from a variety of materials, and in addition to chemotherapeutic payloads, nanoparticles can incorporate non‐bioactive elements useful as diagnostic and device agents. For example, the inclusion of iron oxide colloids enables nanoparticle use as magnetic resonance imaging (MRI) contrast agents, and also, through the application of an alternating magnetic field (AMF), enables the particle to generate enough heat to be used for hyperthermic therapeutic applications. In this report, we also introduce novel Magnetic Nanoparticle Hydro‐Gel (MagNaGelTM) materials comprised of chemotherapeutic agents, iron oxide colloids, and targeting ligands. MagNaGel particles were fabricated in the 20‐ to 40‐nm size range with very narrow size dispersion. These particles demonstrate high (&gt;10 wt %) chemotherapeutic loading, tumor‐associated biomolecular binding, good magnetic susceptibility, and attractive toxicity and circulation profiles in mouse models. Looking forward, the convergence of drug and device on the nano‐scale promises treatment modalities that cannot be practiced through traditionally distinct drug and device combinations. MagNaGel nanoparticles are drug‐device hybrids that, when used in conjunction with diagnostic MRI and inductive heating, may play a key role in new and powerful cancer treatment regimens. Drug Dev. Res. 67:70–93, 2006. © 2006 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/ddr.20069</doi><tpages>24</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0272-4391
ispartof Drug development research, 2006-01, Vol.67 (1), p.70-93
issn 0272-4391
1098-2299
language eng
recordid cdi_proquest_miscellaneous_19443571
source Wiley-Blackwell Read & Publish Collection
subjects cancer
drug delivery
magnetic
nanoparticles
targeting
title Targeted nanoparticles for detecting and treating cancer
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T07%3A25%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Targeted%20nanoparticles%20for%20detecting%20and%20treating%20cancer&rft.jtitle=Drug%20development%20research&rft.au=Sunderland,%20Christopher%20J.&rft.date=2006-01&rft.volume=67&rft.issue=1&rft.spage=70&rft.epage=93&rft.pages=70-93&rft.issn=0272-4391&rft.eissn=1098-2299&rft_id=info:doi/10.1002/ddr.20069&rft_dat=%3Cproquest_cross%3E19443571%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4399-dd5145c585a84e6664a12914e586002f554eb1f4c3473d74d7ce65cd226ee3e03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=19443571&rft_id=info:pmid/&rfr_iscdi=true