Magnetic chitosan nanoparticles as a drug delivery system for targeting photodynamic therapy
Photodynamic therapy (PDT) has become an increasingly recognized alternative to cancer treatment in clinic. However, PDT therapy agents, namely photosensitizer (PS), are limited in application as a result of prolonged cutaneous photosensitivity, poor water solubility and inadequate selectivity, whic...
Gespeichert in:
Veröffentlicht in: | Nanotechnology 2009-04, Vol.20 (13), p.135102 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 13 |
container_start_page | 135102 |
container_title | Nanotechnology |
container_volume | 20 |
creator | Sun, Yun Chen, Zhi-long Yang, Xiao-xia Huang, Peng Zhou, Xin-ping Du, Xiao-xia |
description | Photodynamic therapy (PDT) has become an increasingly recognized alternative to cancer treatment in clinic. However, PDT therapy agents, namely photosensitizer (PS), are limited in application as a result of prolonged cutaneous photosensitivity, poor water solubility and inadequate selectivity, which are encountered by numerous chemical therapies. Magnetic chitosan nanoparticles provide excellent biocompatibility, biodegradability, non-toxicity and water solubility without compromising their magnetic targeting. Nevertheless, no previous attempt has been reported to develop an in vivo magnetic drug delivery system with chitosan nanoparticles for magnetic resonance imaging (MRI) monitored targeting photodynamic therapy. In this study, magnetic targeting chitosan nanoparticles (MTCNPs) were prepared and tailored as a drug delivery system and imaging agents for PS, designated as PHPP. Results showed that PHPP-MTCNPs could be used in MRI monitored targeting PDT with excellent targeting and imaging ability. Non-toxicity and high photodynamic efficacy on SW480 carcinoma cells both in vitro and in vivo were achieved with this method at the level of 0-100 microM. Notably, localization of nanoparticles in skin and hepatic tissue was significantly less than in tumor tissue, therefore photosensitivity and hepatotoxicity can be attenuated. |
doi_str_mv | 10.1088/0957-4484/20/13/135102 |
format | Article |
fullrecord | <record><control><sourceid>proquest_iop_p</sourceid><recordid>TN_cdi_proquest_miscellaneous_903624270</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20581120</sourcerecordid><originalsourceid>FETCH-LOGICAL-c549t-459c49312f0b0f2ebd033139669ca1d2c89f09ff1c10cddc872c648e26b6d5f93</originalsourceid><addsrcrecordid>eNqNkU2LFDEQhoMo7uzqX1hy0lPvVCXpTHKURd2Flb3oTQiZfMy0dHfapEfof2-GGfSg6EJBQfG8bx0eQq4RbhCUWoNuN40QSqwZrJHXaRHYM7JCLrGRLVPPyeoXdEEuS_kGgKgYviQXqAUDoeSKfP1kd2OYO0fdvptTsSMd7Zgmm-utD4XaOtTnw4760Hc_Ql5oWcocBhpTprPNu5oed3Tapzn5ZbRD7Zr3IdtpeUVeRNuX8Pq8r8iXD-8_3941D48f72_fPTSuFXpuRKud0BxZhC1EFrYeOEeupdTOomdO6Qg6RnQIznunNsxJoQKTW-nbqPkVeXvqnXL6fghlNkNXXOh7O4Z0KEYDl0ywDVTyzT9JLgRvldD_BRm0CpEdG-UJdDmVkkM0U-4GmxeDYI6qzNGCOVqoIYPcnFTV4PX5w2E7BP87dnZTATwBXZqeXtr8mfk7ayYf-U8HOauq</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20581120</pqid></control><display><type>article</type><title>Magnetic chitosan nanoparticles as a drug delivery system for targeting photodynamic therapy</title><source>MEDLINE</source><source>IOP Publishing Journals</source><source>Institute of Physics (IOP) Journals - HEAL-Link</source><creator>Sun, Yun ; Chen, Zhi-long ; Yang, Xiao-xia ; Huang, Peng ; Zhou, Xin-ping ; Du, Xiao-xia</creator><creatorcontrib>Sun, Yun ; Chen, Zhi-long ; Yang, Xiao-xia ; Huang, Peng ; Zhou, Xin-ping ; Du, Xiao-xia</creatorcontrib><description>Photodynamic therapy (PDT) has become an increasingly recognized alternative to cancer treatment in clinic. However, PDT therapy agents, namely photosensitizer (PS), are limited in application as a result of prolonged cutaneous photosensitivity, poor water solubility and inadequate selectivity, which are encountered by numerous chemical therapies. Magnetic chitosan nanoparticles provide excellent biocompatibility, biodegradability, non-toxicity and water solubility without compromising their magnetic targeting. Nevertheless, no previous attempt has been reported to develop an in vivo magnetic drug delivery system with chitosan nanoparticles for magnetic resonance imaging (MRI) monitored targeting photodynamic therapy. In this study, magnetic targeting chitosan nanoparticles (MTCNPs) were prepared and tailored as a drug delivery system and imaging agents for PS, designated as PHPP. Results showed that PHPP-MTCNPs could be used in MRI monitored targeting PDT with excellent targeting and imaging ability. Non-toxicity and high photodynamic efficacy on SW480 carcinoma cells both in vitro and in vivo were achieved with this method at the level of 0-100 microM. Notably, localization of nanoparticles in skin and hepatic tissue was significantly less than in tumor tissue, therefore photosensitivity and hepatotoxicity can be attenuated.</description><identifier>ISSN: 0957-4484</identifier><identifier>EISSN: 1361-6528</identifier><identifier>DOI: 10.1088/0957-4484/20/13/135102</identifier><identifier>PMID: 19420486</identifier><language>eng</language><publisher>England: IOP Publishing</publisher><subject>Animals ; Cell Line, Tumor ; Chitosan ; Drug Delivery Systems - methods ; Electromagnetic Fields ; Humans ; Magnetic Resonance Imaging - methods ; Mice ; Mice, Nude ; Microscopy, Electron, Transmission ; Nanoparticles - therapeutic use ; Nanoparticles - ultrastructure ; Photochemotherapy - methods ; Porphyrins ; Xenograft Model Antitumor Assays</subject><ispartof>Nanotechnology, 2009-04, Vol.20 (13), p.135102</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c549t-459c49312f0b0f2ebd033139669ca1d2c89f09ff1c10cddc872c648e26b6d5f93</citedby><cites>FETCH-LOGICAL-c549t-459c49312f0b0f2ebd033139669ca1d2c89f09ff1c10cddc872c648e26b6d5f93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://iopscience.iop.org/article/10.1088/0957-4484/20/13/135102/pdf$$EPDF$$P50$$Giop$$H</linktopdf><link.rule.ids>314,776,780,27901,27902,53805,53885</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19420486$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sun, Yun</creatorcontrib><creatorcontrib>Chen, Zhi-long</creatorcontrib><creatorcontrib>Yang, Xiao-xia</creatorcontrib><creatorcontrib>Huang, Peng</creatorcontrib><creatorcontrib>Zhou, Xin-ping</creatorcontrib><creatorcontrib>Du, Xiao-xia</creatorcontrib><title>Magnetic chitosan nanoparticles as a drug delivery system for targeting photodynamic therapy</title><title>Nanotechnology</title><addtitle>Nanotechnology</addtitle><description>Photodynamic therapy (PDT) has become an increasingly recognized alternative to cancer treatment in clinic. However, PDT therapy agents, namely photosensitizer (PS), are limited in application as a result of prolonged cutaneous photosensitivity, poor water solubility and inadequate selectivity, which are encountered by numerous chemical therapies. Magnetic chitosan nanoparticles provide excellent biocompatibility, biodegradability, non-toxicity and water solubility without compromising their magnetic targeting. Nevertheless, no previous attempt has been reported to develop an in vivo magnetic drug delivery system with chitosan nanoparticles for magnetic resonance imaging (MRI) monitored targeting photodynamic therapy. In this study, magnetic targeting chitosan nanoparticles (MTCNPs) were prepared and tailored as a drug delivery system and imaging agents for PS, designated as PHPP. Results showed that PHPP-MTCNPs could be used in MRI monitored targeting PDT with excellent targeting and imaging ability. Non-toxicity and high photodynamic efficacy on SW480 carcinoma cells both in vitro and in vivo were achieved with this method at the level of 0-100 microM. Notably, localization of nanoparticles in skin and hepatic tissue was significantly less than in tumor tissue, therefore photosensitivity and hepatotoxicity can be attenuated.</description><subject>Animals</subject><subject>Cell Line, Tumor</subject><subject>Chitosan</subject><subject>Drug Delivery Systems - methods</subject><subject>Electromagnetic Fields</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Microscopy, Electron, Transmission</subject><subject>Nanoparticles - therapeutic use</subject><subject>Nanoparticles - ultrastructure</subject><subject>Photochemotherapy - methods</subject><subject>Porphyrins</subject><subject>Xenograft Model Antitumor Assays</subject><issn>0957-4484</issn><issn>1361-6528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU2LFDEQhoMo7uzqX1hy0lPvVCXpTHKURd2Flb3oTQiZfMy0dHfapEfof2-GGfSg6EJBQfG8bx0eQq4RbhCUWoNuN40QSqwZrJHXaRHYM7JCLrGRLVPPyeoXdEEuS_kGgKgYviQXqAUDoeSKfP1kd2OYO0fdvptTsSMd7Zgmm-utD4XaOtTnw4760Hc_Ql5oWcocBhpTprPNu5oed3Tapzn5ZbRD7Zr3IdtpeUVeRNuX8Pq8r8iXD-8_3941D48f72_fPTSuFXpuRKud0BxZhC1EFrYeOEeupdTOomdO6Qg6RnQIznunNsxJoQKTW-nbqPkVeXvqnXL6fghlNkNXXOh7O4Z0KEYDl0ywDVTyzT9JLgRvldD_BRm0CpEdG-UJdDmVkkM0U-4GmxeDYI6qzNGCOVqoIYPcnFTV4PX5w2E7BP87dnZTATwBXZqeXtr8mfk7ayYf-U8HOauq</recordid><startdate>20090401</startdate><enddate>20090401</enddate><creator>Sun, Yun</creator><creator>Chen, Zhi-long</creator><creator>Yang, Xiao-xia</creator><creator>Huang, Peng</creator><creator>Zhou, Xin-ping</creator><creator>Du, Xiao-xia</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>F28</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20090401</creationdate><title>Magnetic chitosan nanoparticles as a drug delivery system for targeting photodynamic therapy</title><author>Sun, Yun ; Chen, Zhi-long ; Yang, Xiao-xia ; Huang, Peng ; Zhou, Xin-ping ; Du, Xiao-xia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c549t-459c49312f0b0f2ebd033139669ca1d2c89f09ff1c10cddc872c648e26b6d5f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Cell Line, Tumor</topic><topic>Chitosan</topic><topic>Drug Delivery Systems - methods</topic><topic>Electromagnetic Fields</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Microscopy, Electron, Transmission</topic><topic>Nanoparticles - therapeutic use</topic><topic>Nanoparticles - ultrastructure</topic><topic>Photochemotherapy - methods</topic><topic>Porphyrins</topic><topic>Xenograft Model Antitumor Assays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sun, Yun</creatorcontrib><creatorcontrib>Chen, Zhi-long</creatorcontrib><creatorcontrib>Yang, Xiao-xia</creatorcontrib><creatorcontrib>Huang, Peng</creatorcontrib><creatorcontrib>Zhou, Xin-ping</creatorcontrib><creatorcontrib>Du, Xiao-xia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</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><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Nanotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, Yun</au><au>Chen, Zhi-long</au><au>Yang, Xiao-xia</au><au>Huang, Peng</au><au>Zhou, Xin-ping</au><au>Du, Xiao-xia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Magnetic chitosan nanoparticles as a drug delivery system for targeting photodynamic therapy</atitle><jtitle>Nanotechnology</jtitle><addtitle>Nanotechnology</addtitle><date>2009-04-01</date><risdate>2009</risdate><volume>20</volume><issue>13</issue><spage>135102</spage><pages>135102-</pages><issn>0957-4484</issn><eissn>1361-6528</eissn><abstract>Photodynamic therapy (PDT) has become an increasingly recognized alternative to cancer treatment in clinic. However, PDT therapy agents, namely photosensitizer (PS), are limited in application as a result of prolonged cutaneous photosensitivity, poor water solubility and inadequate selectivity, which are encountered by numerous chemical therapies. Magnetic chitosan nanoparticles provide excellent biocompatibility, biodegradability, non-toxicity and water solubility without compromising their magnetic targeting. Nevertheless, no previous attempt has been reported to develop an in vivo magnetic drug delivery system with chitosan nanoparticles for magnetic resonance imaging (MRI) monitored targeting photodynamic therapy. In this study, magnetic targeting chitosan nanoparticles (MTCNPs) were prepared and tailored as a drug delivery system and imaging agents for PS, designated as PHPP. Results showed that PHPP-MTCNPs could be used in MRI monitored targeting PDT with excellent targeting and imaging ability. Non-toxicity and high photodynamic efficacy on SW480 carcinoma cells both in vitro and in vivo were achieved with this method at the level of 0-100 microM. Notably, localization of nanoparticles in skin and hepatic tissue was significantly less than in tumor tissue, therefore photosensitivity and hepatotoxicity can be attenuated.</abstract><cop>England</cop><pub>IOP Publishing</pub><pmid>19420486</pmid><doi>10.1088/0957-4484/20/13/135102</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0957-4484 |
ispartof | Nanotechnology, 2009-04, Vol.20 (13), p.135102 |
issn | 0957-4484 1361-6528 |
language | eng |
recordid | cdi_proquest_miscellaneous_903624270 |
source | MEDLINE; IOP Publishing Journals; Institute of Physics (IOP) Journals - HEAL-Link |
subjects | Animals Cell Line, Tumor Chitosan Drug Delivery Systems - methods Electromagnetic Fields Humans Magnetic Resonance Imaging - methods Mice Mice, Nude Microscopy, Electron, Transmission Nanoparticles - therapeutic use Nanoparticles - ultrastructure Photochemotherapy - methods Porphyrins Xenograft Model Antitumor Assays |
title | Magnetic chitosan nanoparticles as a drug delivery system for targeting photodynamic therapy |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T20%3A35%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_iop_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Magnetic%20chitosan%20nanoparticles%20as%20a%20drug%20delivery%20system%20for%20targeting%20photodynamic%20therapy&rft.jtitle=Nanotechnology&rft.au=Sun,%20Yun&rft.date=2009-04-01&rft.volume=20&rft.issue=13&rft.spage=135102&rft.pages=135102-&rft.issn=0957-4484&rft.eissn=1361-6528&rft_id=info:doi/10.1088/0957-4484/20/13/135102&rft_dat=%3Cproquest_iop_p%3E20581120%3C/proquest_iop_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=20581120&rft_id=info:pmid/19420486&rfr_iscdi=true |