Polymer-Coated NaYF4:Yb3+, Er3+ Upconversion Nanoparticles for Charge-Dependent Cellular Imaging
Lanthanide-doped upconversion nanoparticles (UCNPs) are considered promising novel near-infrared (NIR) bioimaging agents with the characteristics of high contrast and high penetration depth. However, the interactions between charged UCNPs and mammalian cells have not been thoroughly studied, and the...
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Veröffentlicht in: | ACS nano 2011-10, Vol.5 (10), p.7838-7847 |
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description | Lanthanide-doped upconversion nanoparticles (UCNPs) are considered promising novel near-infrared (NIR) bioimaging agents with the characteristics of high contrast and high penetration depth. However, the interactions between charged UCNPs and mammalian cells have not been thoroughly studied, and the corresponding intracellular uptake pathways remain unclear. Herein, our research work involved the use of a hydrothermal method to synthesize polyvinylpyrrolidone-coated UCNPs (UCNP-PVP), and then a ligand exchange reaction was performed on UCNP-PVP, with the help of polyethylenimine (PEI) and poly(acrylic acid) (PAA), to generate UCNP-PEI and UCNP-PAA. These polymer-coated UCNPs demonstrated good dispersibility in aqueous medium, had the same elemental composition and crystal phase, shared similar TEM and dynamic light scattering (DLS) size distribution, and exhibited similar upconversion luminescence efficiency. However, the positively charged UCNP-PEI evinced greatly enhanced cellular uptake in comparison with its neutral or negative counterparts, as shown by multiphoton confocal microscopy and inductively coupled plasma mass spectrometry (ICP-MS) measurements. Meanwhile, we found that cationic UCNP-PEI can be effectively internalized mainly through the clathrin endocytic mechanism, as revealed by colocalization, chemical, and genetic inhibitor studies. This study elucidates the role of the surface polymer coatings in governing UCNP–cell interactions, and it is the first report on the endocytic mechanism of positively charged lanthanide-doped UCNPs. Furthermore, this study provides important guidance for the development of UCNPs as specific intracellular nanoprobes, allowing us to control the UCNP–cell interactions by tuning surface properties. |
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However, the interactions between charged UCNPs and mammalian cells have not been thoroughly studied, and the corresponding intracellular uptake pathways remain unclear. Herein, our research work involved the use of a hydrothermal method to synthesize polyvinylpyrrolidone-coated UCNPs (UCNP-PVP), and then a ligand exchange reaction was performed on UCNP-PVP, with the help of polyethylenimine (PEI) and poly(acrylic acid) (PAA), to generate UCNP-PEI and UCNP-PAA. These polymer-coated UCNPs demonstrated good dispersibility in aqueous medium, had the same elemental composition and crystal phase, shared similar TEM and dynamic light scattering (DLS) size distribution, and exhibited similar upconversion luminescence efficiency. However, the positively charged UCNP-PEI evinced greatly enhanced cellular uptake in comparison with its neutral or negative counterparts, as shown by multiphoton confocal microscopy and inductively coupled plasma mass spectrometry (ICP-MS) measurements. Meanwhile, we found that cationic UCNP-PEI can be effectively internalized mainly through the clathrin endocytic mechanism, as revealed by colocalization, chemical, and genetic inhibitor studies. This study elucidates the role of the surface polymer coatings in governing UCNP–cell interactions, and it is the first report on the endocytic mechanism of positively charged lanthanide-doped UCNPs. Furthermore, this study provides important guidance for the development of UCNPs as specific intracellular nanoprobes, allowing us to control the UCNP–cell interactions by tuning surface properties.</description><identifier>ISSN: 1936-0851</identifier><identifier>EISSN: 1936-086X</identifier><identifier>DOI: 10.1021/nn201896m</identifier><identifier>PMID: 21905691</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Chlorpromazine - pharmacology ; Clathrin - antagonists & inhibitors ; Clathrin - deficiency ; Clathrin - genetics ; Coated Vesicles - drug effects ; Coated Vesicles - metabolism ; Endocytosis - drug effects ; Endocytosis - genetics ; Erbium - chemistry ; Fluorides - chemistry ; Gene Knockdown Techniques ; HeLa Cells ; Humans ; Ligands ; Luminescent Measurements ; Molecular Imaging - methods ; Nanoparticles - chemistry ; Nanoparticles - toxicity ; Polymers - chemistry ; Polymers - metabolism ; Polymers - toxicity ; Surface Properties ; Ytterbium - chemistry ; Yttrium - chemistry</subject><ispartof>ACS nano, 2011-10, Vol.5 (10), p.7838-7847</ispartof><rights>Copyright © 2011 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/nn201896m$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/nn201896m$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>315,781,785,27078,27926,27927,56740,56790</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21905691$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jin, Jiefu</creatorcontrib><creatorcontrib>Gu, Yan-Juan</creatorcontrib><creatorcontrib>Man, Cornelia Wing-Yin</creatorcontrib><creatorcontrib>Cheng, Jinping</creatorcontrib><creatorcontrib>Xu, Zhenhua</creatorcontrib><creatorcontrib>Zhang, Yue</creatorcontrib><creatorcontrib>Wang, Huaishan</creatorcontrib><creatorcontrib>Lee, Vien Hoi-Yi</creatorcontrib><creatorcontrib>Cheng, Shuk Han</creatorcontrib><creatorcontrib>Wong, Wing-Tak</creatorcontrib><title>Polymer-Coated NaYF4:Yb3+, Er3+ Upconversion Nanoparticles for Charge-Dependent Cellular Imaging</title><title>ACS nano</title><addtitle>ACS Nano</addtitle><description>Lanthanide-doped upconversion nanoparticles (UCNPs) are considered promising novel near-infrared (NIR) bioimaging agents with the characteristics of high contrast and high penetration depth. However, the interactions between charged UCNPs and mammalian cells have not been thoroughly studied, and the corresponding intracellular uptake pathways remain unclear. Herein, our research work involved the use of a hydrothermal method to synthesize polyvinylpyrrolidone-coated UCNPs (UCNP-PVP), and then a ligand exchange reaction was performed on UCNP-PVP, with the help of polyethylenimine (PEI) and poly(acrylic acid) (PAA), to generate UCNP-PEI and UCNP-PAA. These polymer-coated UCNPs demonstrated good dispersibility in aqueous medium, had the same elemental composition and crystal phase, shared similar TEM and dynamic light scattering (DLS) size distribution, and exhibited similar upconversion luminescence efficiency. However, the positively charged UCNP-PEI evinced greatly enhanced cellular uptake in comparison with its neutral or negative counterparts, as shown by multiphoton confocal microscopy and inductively coupled plasma mass spectrometry (ICP-MS) measurements. Meanwhile, we found that cationic UCNP-PEI can be effectively internalized mainly through the clathrin endocytic mechanism, as revealed by colocalization, chemical, and genetic inhibitor studies. This study elucidates the role of the surface polymer coatings in governing UCNP–cell interactions, and it is the first report on the endocytic mechanism of positively charged lanthanide-doped UCNPs. Furthermore, this study provides important guidance for the development of UCNPs as specific intracellular nanoprobes, allowing us to control the UCNP–cell interactions by tuning surface properties.</description><subject>Chlorpromazine - pharmacology</subject><subject>Clathrin - antagonists & inhibitors</subject><subject>Clathrin - deficiency</subject><subject>Clathrin - genetics</subject><subject>Coated Vesicles - drug effects</subject><subject>Coated Vesicles - metabolism</subject><subject>Endocytosis - drug effects</subject><subject>Endocytosis - genetics</subject><subject>Erbium - chemistry</subject><subject>Fluorides - chemistry</subject><subject>Gene Knockdown Techniques</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Ligands</subject><subject>Luminescent Measurements</subject><subject>Molecular Imaging - methods</subject><subject>Nanoparticles - chemistry</subject><subject>Nanoparticles - toxicity</subject><subject>Polymers - chemistry</subject><subject>Polymers - metabolism</subject><subject>Polymers - toxicity</subject><subject>Surface Properties</subject><subject>Ytterbium - chemistry</subject><subject>Yttrium - chemistry</subject><issn>1936-0851</issn><issn>1936-086X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1Lw0AURQdRbK0u_AOSjbio0flIJhl3ElstFHVhwa7iZPJSU5KZOJMI_femtHb1HtzD5XIQuiT4jmBK7rWmmMSC10doSATjPo755_HhD8kAnTm3xjiM4oifogElAodckCH6ejfVpgbrJ0a2kHuvcjkNHpYZG996E8vG3qJRRv-CdaXRfapNI21bqgqcVxjrJd_SrsB_ggZ0Drr1EqiqrpLWm9VyVerVOTopZOXgYn9HaDGdfCQv_vzteZY8zn1JGW99KkiWYQjDOGA4UlxBIQgjSvGogFwEkDEaYir7VGY4yxnlWHGRYymB5ixiI3Sz622s-enAtWldOtWPkRpM51KBMQ8o4Vvyak92WQ152tiylnaT_kvpgesdIJVL16azuh-eEpxuZacH2ewPRO5t1A</recordid><startdate>20111025</startdate><enddate>20111025</enddate><creator>Jin, Jiefu</creator><creator>Gu, Yan-Juan</creator><creator>Man, Cornelia Wing-Yin</creator><creator>Cheng, Jinping</creator><creator>Xu, Zhenhua</creator><creator>Zhang, Yue</creator><creator>Wang, Huaishan</creator><creator>Lee, Vien Hoi-Yi</creator><creator>Cheng, Shuk Han</creator><creator>Wong, Wing-Tak</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20111025</creationdate><title>Polymer-Coated NaYF4:Yb3+, Er3+ Upconversion Nanoparticles for Charge-Dependent Cellular Imaging</title><author>Jin, Jiefu ; Gu, Yan-Juan ; Man, Cornelia Wing-Yin ; Cheng, Jinping ; Xu, Zhenhua ; Zhang, Yue ; Wang, Huaishan ; Lee, Vien Hoi-Yi ; Cheng, Shuk Han ; Wong, Wing-Tak</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a236t-291bb0e5584307c6cef9131cc67fed94eb32502a430ab0bd3260c69d0aae2d373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Chlorpromazine - pharmacology</topic><topic>Clathrin - antagonists & inhibitors</topic><topic>Clathrin - deficiency</topic><topic>Clathrin - genetics</topic><topic>Coated Vesicles - drug effects</topic><topic>Coated Vesicles - metabolism</topic><topic>Endocytosis - drug effects</topic><topic>Endocytosis - genetics</topic><topic>Erbium - chemistry</topic><topic>Fluorides - chemistry</topic><topic>Gene Knockdown Techniques</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Ligands</topic><topic>Luminescent Measurements</topic><topic>Molecular Imaging - methods</topic><topic>Nanoparticles - chemistry</topic><topic>Nanoparticles - toxicity</topic><topic>Polymers - chemistry</topic><topic>Polymers - metabolism</topic><topic>Polymers - toxicity</topic><topic>Surface Properties</topic><topic>Ytterbium - chemistry</topic><topic>Yttrium - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jin, Jiefu</creatorcontrib><creatorcontrib>Gu, Yan-Juan</creatorcontrib><creatorcontrib>Man, Cornelia Wing-Yin</creatorcontrib><creatorcontrib>Cheng, Jinping</creatorcontrib><creatorcontrib>Xu, Zhenhua</creatorcontrib><creatorcontrib>Zhang, Yue</creatorcontrib><creatorcontrib>Wang, Huaishan</creatorcontrib><creatorcontrib>Lee, Vien Hoi-Yi</creatorcontrib><creatorcontrib>Cheng, Shuk Han</creatorcontrib><creatorcontrib>Wong, Wing-Tak</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>ACS nano</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jin, Jiefu</au><au>Gu, Yan-Juan</au><au>Man, Cornelia Wing-Yin</au><au>Cheng, Jinping</au><au>Xu, Zhenhua</au><au>Zhang, Yue</au><au>Wang, Huaishan</au><au>Lee, Vien Hoi-Yi</au><au>Cheng, Shuk Han</au><au>Wong, Wing-Tak</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymer-Coated NaYF4:Yb3+, Er3+ Upconversion Nanoparticles for Charge-Dependent Cellular Imaging</atitle><jtitle>ACS nano</jtitle><addtitle>ACS Nano</addtitle><date>2011-10-25</date><risdate>2011</risdate><volume>5</volume><issue>10</issue><spage>7838</spage><epage>7847</epage><pages>7838-7847</pages><issn>1936-0851</issn><eissn>1936-086X</eissn><abstract>Lanthanide-doped upconversion nanoparticles (UCNPs) are considered promising novel near-infrared (NIR) bioimaging agents with the characteristics of high contrast and high penetration depth. However, the interactions between charged UCNPs and mammalian cells have not been thoroughly studied, and the corresponding intracellular uptake pathways remain unclear. Herein, our research work involved the use of a hydrothermal method to synthesize polyvinylpyrrolidone-coated UCNPs (UCNP-PVP), and then a ligand exchange reaction was performed on UCNP-PVP, with the help of polyethylenimine (PEI) and poly(acrylic acid) (PAA), to generate UCNP-PEI and UCNP-PAA. These polymer-coated UCNPs demonstrated good dispersibility in aqueous medium, had the same elemental composition and crystal phase, shared similar TEM and dynamic light scattering (DLS) size distribution, and exhibited similar upconversion luminescence efficiency. However, the positively charged UCNP-PEI evinced greatly enhanced cellular uptake in comparison with its neutral or negative counterparts, as shown by multiphoton confocal microscopy and inductively coupled plasma mass spectrometry (ICP-MS) measurements. Meanwhile, we found that cationic UCNP-PEI can be effectively internalized mainly through the clathrin endocytic mechanism, as revealed by colocalization, chemical, and genetic inhibitor studies. This study elucidates the role of the surface polymer coatings in governing UCNP–cell interactions, and it is the first report on the endocytic mechanism of positively charged lanthanide-doped UCNPs. Furthermore, this study provides important guidance for the development of UCNPs as specific intracellular nanoprobes, allowing us to control the UCNP–cell interactions by tuning surface properties.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>21905691</pmid><doi>10.1021/nn201896m</doi><tpages>10</tpages></addata></record> |
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subjects | Chlorpromazine - pharmacology Clathrin - antagonists & inhibitors Clathrin - deficiency Clathrin - genetics Coated Vesicles - drug effects Coated Vesicles - metabolism Endocytosis - drug effects Endocytosis - genetics Erbium - chemistry Fluorides - chemistry Gene Knockdown Techniques HeLa Cells Humans Ligands Luminescent Measurements Molecular Imaging - methods Nanoparticles - chemistry Nanoparticles - toxicity Polymers - chemistry Polymers - metabolism Polymers - toxicity Surface Properties Ytterbium - chemistry Yttrium - chemistry |
title | Polymer-Coated NaYF4:Yb3+, Er3+ Upconversion Nanoparticles for Charge-Dependent Cellular Imaging |
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