Proton-Sponge Coated Quantum Dots for siRNA Delivery and Intracellular Imaging
We report the rational design of multifunctional nanoparticles for short-interfering RNA (siRNA) delivery and imaging based on the use of semiconductor quantum dots (QDs) and proton-absorbing polymeric coatings (proton sponges). With a balanced composition of tertiary amine and carboxylic acid group...
Gespeichert in:
Veröffentlicht in: | Journal of the American Chemical Society 2008-07, Vol.130 (28), p.9006-9012 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 9012 |
---|---|
container_issue | 28 |
container_start_page | 9006 |
container_title | Journal of the American Chemical Society |
container_volume | 130 |
creator | Yezhelyev, Maksym V Qi, Lifeng O’Regan, Ruth M Nie, Shuming Gao, Xiaohu |
description | We report the rational design of multifunctional nanoparticles for short-interfering RNA (siRNA) delivery and imaging based on the use of semiconductor quantum dots (QDs) and proton-absorbing polymeric coatings (proton sponges). With a balanced composition of tertiary amine and carboxylic acid groups, these nanoparticles are specifically designed to address longstanding barriers in siRNA delivery such as cellular penetration, endosomal release, carrier unpacking, and intracellular transport. The results demonstrate dramatic improvement in gene silencing efficiency by 10−20-fold and simultaneous reduction in cellular toxicity by 5−6-fold, when compared directly with existing transfection agents for MDA-MB-231 cells. The QD−siRNA nanoparticles are also dual-modality optical and electron-microscopy probes, allowing real-time tracking and ultrastructural localization of QDs during delivery and transfection. These new insights and capabilities represent a major step toward nanoparticle engineering for imaging and therapeutic applications. |
doi_str_mv | 10.1021/ja800086u |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2621273</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20909259</sourcerecordid><originalsourceid>FETCH-LOGICAL-a538t-e4fe64a8601c5be177cf89ec35788991217770235c88d46d132c90f85f2a41ff3</originalsourceid><addsrcrecordid>eNptkE1PGzEQhq2qqIS0B_4A8qVIHLa1veuPvSBF4aORIpqWtOVmGa8dNuzawd5F8O9xlCiA1NNoZh69884LwCFG3zAi-PtSCYSQYP0HMMCUoIxiwj6CQRqSjAuW74ODGJepLYjAn8A-FpSjAtMBuJoF33mXXa-8Wxg49qozFfzVK9f1LTzzXYTWBxjr31cjeGaa-tGEZ6hcBSeuC0qbpukbFeCkVYvaLT6DPauaaL5s6xD8uTifj39k05-Xk_Fomimaiy4zhTWsUIIhrOmtwZxrK0qjc8qFKEtM0oQjklMtRFWwCudEl8gKaokqsLX5EJxudFf9bWsqbdZmGrkKdavCs_Sqlu83rr6TC_8oCSOY8DwJHG8Fgn_oTexkW8f1N8oZ30dJUIlKQssEnmxAHXyMwdjdEYzkOn25Sz-xR29dvZLbuBOQbYA6duZpt1fhXjKecyrns2vJbub0X_G3lLPEf93wSke59H1wKdT_HH4BBOWa8A</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20909259</pqid></control><display><type>article</type><title>Proton-Sponge Coated Quantum Dots for siRNA Delivery and Intracellular Imaging</title><source>MEDLINE</source><source>ACS Publications</source><creator>Yezhelyev, Maksym V ; Qi, Lifeng ; O’Regan, Ruth M ; Nie, Shuming ; Gao, Xiaohu</creator><creatorcontrib>Yezhelyev, Maksym V ; Qi, Lifeng ; O’Regan, Ruth M ; Nie, Shuming ; Gao, Xiaohu</creatorcontrib><description>We report the rational design of multifunctional nanoparticles for short-interfering RNA (siRNA) delivery and imaging based on the use of semiconductor quantum dots (QDs) and proton-absorbing polymeric coatings (proton sponges). With a balanced composition of tertiary amine and carboxylic acid groups, these nanoparticles are specifically designed to address longstanding barriers in siRNA delivery such as cellular penetration, endosomal release, carrier unpacking, and intracellular transport. The results demonstrate dramatic improvement in gene silencing efficiency by 10−20-fold and simultaneous reduction in cellular toxicity by 5−6-fold, when compared directly with existing transfection agents for MDA-MB-231 cells. The QD−siRNA nanoparticles are also dual-modality optical and electron-microscopy probes, allowing real-time tracking and ultrastructural localization of QDs during delivery and transfection. These new insights and capabilities represent a major step toward nanoparticle engineering for imaging and therapeutic applications.</description><identifier>ISSN: 0002-7863</identifier><identifier>ISSN: 1272-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/ja800086u</identifier><identifier>PMID: 18570415</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Animals ; Cell Line, Tumor ; Cyclophilins - antagonists & inhibitors ; Cyclophilins - genetics ; Humans ; Mice ; Models, Molecular ; Nanoparticles - chemistry ; NIH 3T3 Cells ; Peptidylprolyl Isomerase - antagonists & inhibitors ; Peptidylprolyl Isomerase - genetics ; Protons ; Quantum Dots ; RNA, Small Interfering - administration & dosage ; RNA, Small Interfering - chemistry ; RNA, Small Interfering - genetics ; Transfection - methods</subject><ispartof>Journal of the American Chemical Society, 2008-07, Vol.130 (28), p.9006-9012</ispartof><rights>Copyright © 2008 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a538t-e4fe64a8601c5be177cf89ec35788991217770235c88d46d132c90f85f2a41ff3</citedby><cites>FETCH-LOGICAL-a538t-e4fe64a8601c5be177cf89ec35788991217770235c88d46d132c90f85f2a41ff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ja800086u$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ja800086u$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,777,781,882,2752,27057,27905,27906,56719,56769</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18570415$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yezhelyev, Maksym V</creatorcontrib><creatorcontrib>Qi, Lifeng</creatorcontrib><creatorcontrib>O’Regan, Ruth M</creatorcontrib><creatorcontrib>Nie, Shuming</creatorcontrib><creatorcontrib>Gao, Xiaohu</creatorcontrib><title>Proton-Sponge Coated Quantum Dots for siRNA Delivery and Intracellular Imaging</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>We report the rational design of multifunctional nanoparticles for short-interfering RNA (siRNA) delivery and imaging based on the use of semiconductor quantum dots (QDs) and proton-absorbing polymeric coatings (proton sponges). With a balanced composition of tertiary amine and carboxylic acid groups, these nanoparticles are specifically designed to address longstanding barriers in siRNA delivery such as cellular penetration, endosomal release, carrier unpacking, and intracellular transport. The results demonstrate dramatic improvement in gene silencing efficiency by 10−20-fold and simultaneous reduction in cellular toxicity by 5−6-fold, when compared directly with existing transfection agents for MDA-MB-231 cells. The QD−siRNA nanoparticles are also dual-modality optical and electron-microscopy probes, allowing real-time tracking and ultrastructural localization of QDs during delivery and transfection. These new insights and capabilities represent a major step toward nanoparticle engineering for imaging and therapeutic applications.</description><subject>Animals</subject><subject>Cell Line, Tumor</subject><subject>Cyclophilins - antagonists & inhibitors</subject><subject>Cyclophilins - genetics</subject><subject>Humans</subject><subject>Mice</subject><subject>Models, Molecular</subject><subject>Nanoparticles - chemistry</subject><subject>NIH 3T3 Cells</subject><subject>Peptidylprolyl Isomerase - antagonists & inhibitors</subject><subject>Peptidylprolyl Isomerase - genetics</subject><subject>Protons</subject><subject>Quantum Dots</subject><subject>RNA, Small Interfering - administration & dosage</subject><subject>RNA, Small Interfering - chemistry</subject><subject>RNA, Small Interfering - genetics</subject><subject>Transfection - methods</subject><issn>0002-7863</issn><issn>1272-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkE1PGzEQhq2qqIS0B_4A8qVIHLa1veuPvSBF4aORIpqWtOVmGa8dNuzawd5F8O9xlCiA1NNoZh69884LwCFG3zAi-PtSCYSQYP0HMMCUoIxiwj6CQRqSjAuW74ODGJepLYjAn8A-FpSjAtMBuJoF33mXXa-8Wxg49qozFfzVK9f1LTzzXYTWBxjr31cjeGaa-tGEZ6hcBSeuC0qbpukbFeCkVYvaLT6DPauaaL5s6xD8uTifj39k05-Xk_Fomimaiy4zhTWsUIIhrOmtwZxrK0qjc8qFKEtM0oQjklMtRFWwCudEl8gKaokqsLX5EJxudFf9bWsqbdZmGrkKdavCs_Sqlu83rr6TC_8oCSOY8DwJHG8Fgn_oTexkW8f1N8oZ30dJUIlKQssEnmxAHXyMwdjdEYzkOn25Sz-xR29dvZLbuBOQbYA6duZpt1fhXjKecyrns2vJbub0X_G3lLPEf93wSke59H1wKdT_HH4BBOWa8A</recordid><startdate>20080716</startdate><enddate>20080716</enddate><creator>Yezhelyev, Maksym V</creator><creator>Qi, Lifeng</creator><creator>O’Regan, Ruth M</creator><creator>Nie, Shuming</creator><creator>Gao, Xiaohu</creator><general>American Chemical Society</general><scope>BSCLL</scope><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>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20080716</creationdate><title>Proton-Sponge Coated Quantum Dots for siRNA Delivery and Intracellular Imaging</title><author>Yezhelyev, Maksym V ; Qi, Lifeng ; O’Regan, Ruth M ; Nie, Shuming ; Gao, Xiaohu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a538t-e4fe64a8601c5be177cf89ec35788991217770235c88d46d132c90f85f2a41ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Cell Line, Tumor</topic><topic>Cyclophilins - antagonists & inhibitors</topic><topic>Cyclophilins - genetics</topic><topic>Humans</topic><topic>Mice</topic><topic>Models, Molecular</topic><topic>Nanoparticles - chemistry</topic><topic>NIH 3T3 Cells</topic><topic>Peptidylprolyl Isomerase - antagonists & inhibitors</topic><topic>Peptidylprolyl Isomerase - genetics</topic><topic>Protons</topic><topic>Quantum Dots</topic><topic>RNA, Small Interfering - administration & dosage</topic><topic>RNA, Small Interfering - chemistry</topic><topic>RNA, Small Interfering - genetics</topic><topic>Transfection - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yezhelyev, Maksym V</creatorcontrib><creatorcontrib>Qi, Lifeng</creatorcontrib><creatorcontrib>O’Regan, Ruth M</creatorcontrib><creatorcontrib>Nie, Shuming</creatorcontrib><creatorcontrib>Gao, Xiaohu</creatorcontrib><collection>Istex</collection><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>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yezhelyev, Maksym V</au><au>Qi, Lifeng</au><au>O’Regan, Ruth M</au><au>Nie, Shuming</au><au>Gao, Xiaohu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proton-Sponge Coated Quantum Dots for siRNA Delivery and Intracellular Imaging</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2008-07-16</date><risdate>2008</risdate><volume>130</volume><issue>28</issue><spage>9006</spage><epage>9012</epage><pages>9006-9012</pages><issn>0002-7863</issn><issn>1272-7863</issn><eissn>1520-5126</eissn><abstract>We report the rational design of multifunctional nanoparticles for short-interfering RNA (siRNA) delivery and imaging based on the use of semiconductor quantum dots (QDs) and proton-absorbing polymeric coatings (proton sponges). With a balanced composition of tertiary amine and carboxylic acid groups, these nanoparticles are specifically designed to address longstanding barriers in siRNA delivery such as cellular penetration, endosomal release, carrier unpacking, and intracellular transport. The results demonstrate dramatic improvement in gene silencing efficiency by 10−20-fold and simultaneous reduction in cellular toxicity by 5−6-fold, when compared directly with existing transfection agents for MDA-MB-231 cells. The QD−siRNA nanoparticles are also dual-modality optical and electron-microscopy probes, allowing real-time tracking and ultrastructural localization of QDs during delivery and transfection. These new insights and capabilities represent a major step toward nanoparticle engineering for imaging and therapeutic applications.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>18570415</pmid><doi>10.1021/ja800086u</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0002-7863 |
ispartof | Journal of the American Chemical Society, 2008-07, Vol.130 (28), p.9006-9012 |
issn | 0002-7863 1272-7863 1520-5126 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2621273 |
source | MEDLINE; ACS Publications |
subjects | Animals Cell Line, Tumor Cyclophilins - antagonists & inhibitors Cyclophilins - genetics Humans Mice Models, Molecular Nanoparticles - chemistry NIH 3T3 Cells Peptidylprolyl Isomerase - antagonists & inhibitors Peptidylprolyl Isomerase - genetics Protons Quantum Dots RNA, Small Interfering - administration & dosage RNA, Small Interfering - chemistry RNA, Small Interfering - genetics Transfection - methods |
title | Proton-Sponge Coated Quantum Dots for siRNA Delivery and Intracellular Imaging |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T15%3A10%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Proton-Sponge%20Coated%20Quantum%20Dots%20for%20siRNA%20Delivery%20and%20Intracellular%20Imaging&rft.jtitle=Journal%20of%20the%20American%20Chemical%20Society&rft.au=Yezhelyev,%20Maksym%20V&rft.date=2008-07-16&rft.volume=130&rft.issue=28&rft.spage=9006&rft.epage=9012&rft.pages=9006-9012&rft.issn=0002-7863&rft.eissn=1520-5126&rft_id=info:doi/10.1021/ja800086u&rft_dat=%3Cproquest_pubme%3E20909259%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=20909259&rft_id=info:pmid/18570415&rfr_iscdi=true |