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Polydopamine-coated Au nanorods for targeted fluorescent cell imaging and photothermal therapy
Au nanorods (AuNRs) have attracted a great interest as a platform for constructing various composite core/shell nanoparticles for theranostics applications. However, the development of robust methods for coating AuNRs with a biocompatible shell of high loading capacity and with functional groups sti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466791/ https://www.ncbi.nlm.nih.gov/pubmed/31019866 http://dx.doi.org/10.3762/bjnano.10.79 |
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author | Khlebtsov, Boris Nikolayevich Burov, Andrey Mikhailovich Pylaev, Timofey Evgenevich Khlebtsov, Nikolai G |
author_facet | Khlebtsov, Boris Nikolayevich Burov, Andrey Mikhailovich Pylaev, Timofey Evgenevich Khlebtsov, Nikolai G |
author_sort | Khlebtsov, Boris Nikolayevich |
collection | PubMed |
description | Au nanorods (AuNRs) have attracted a great interest as a platform for constructing various composite core/shell nanoparticles for theranostics applications. However, the development of robust methods for coating AuNRs with a biocompatible shell of high loading capacity and with functional groups still remains challenging. Here, we coated AuNRs with a polydopamine (PDA) shell and functionalized AuNR-PDA particles with folic acid and rhodamine 123 (R123) to fabricate AuNR-PDA-R123-folate nanocomposites. To the best of our knowledge, such AuNR-PDA-based composites combining fluorescent imaging and plasmonic phothothermal abilities have not been reported previously. The multifunctional nanoparticles were stable in cell buffer, nontoxic and suitable for targeted fluorescent imaging and photothermal therapy of cancer cells. We demonstrate the enhanced accumulation of folate-functionalized nanoparticles in folate-positive HeLa cells in contrast to the folate-negative HEK 293 cells using fluorescent microscopy. The replacement of folic acid with polyethylene glycol (PEG) leads to a decrease in nanoparticle uptake by both folate-positive and folate-negative cells. We performed NIR light-mediated targeted phototherapy using AuNR-PDA-R123-folate and obtained a remarkable cancer cell killing efficiency in vitro in comparison with only weak-efficient nontargeted PEGylated nanoparticles. Our work illustrates that AuNR-PDA could be a promising nanoplatform for multifunctional tumor theranostics in the future. |
format | Online Article Text |
id | pubmed-6466791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-64667912019-04-24 Polydopamine-coated Au nanorods for targeted fluorescent cell imaging and photothermal therapy Khlebtsov, Boris Nikolayevich Burov, Andrey Mikhailovich Pylaev, Timofey Evgenevich Khlebtsov, Nikolai G Beilstein J Nanotechnol Full Research Paper Au nanorods (AuNRs) have attracted a great interest as a platform for constructing various composite core/shell nanoparticles for theranostics applications. However, the development of robust methods for coating AuNRs with a biocompatible shell of high loading capacity and with functional groups still remains challenging. Here, we coated AuNRs with a polydopamine (PDA) shell and functionalized AuNR-PDA particles with folic acid and rhodamine 123 (R123) to fabricate AuNR-PDA-R123-folate nanocomposites. To the best of our knowledge, such AuNR-PDA-based composites combining fluorescent imaging and plasmonic phothothermal abilities have not been reported previously. The multifunctional nanoparticles were stable in cell buffer, nontoxic and suitable for targeted fluorescent imaging and photothermal therapy of cancer cells. We demonstrate the enhanced accumulation of folate-functionalized nanoparticles in folate-positive HeLa cells in contrast to the folate-negative HEK 293 cells using fluorescent microscopy. The replacement of folic acid with polyethylene glycol (PEG) leads to a decrease in nanoparticle uptake by both folate-positive and folate-negative cells. We performed NIR light-mediated targeted phototherapy using AuNR-PDA-R123-folate and obtained a remarkable cancer cell killing efficiency in vitro in comparison with only weak-efficient nontargeted PEGylated nanoparticles. Our work illustrates that AuNR-PDA could be a promising nanoplatform for multifunctional tumor theranostics in the future. Beilstein-Institut 2019-04-01 /pmc/articles/PMC6466791/ /pubmed/31019866 http://dx.doi.org/10.3762/bjnano.10.79 Text en Copyright © 2019, Khlebtsov et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjnano/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Nanotechnology terms and conditions: (https://www.beilstein-journals.org/bjnano/terms) |
spellingShingle | Full Research Paper Khlebtsov, Boris Nikolayevich Burov, Andrey Mikhailovich Pylaev, Timofey Evgenevich Khlebtsov, Nikolai G Polydopamine-coated Au nanorods for targeted fluorescent cell imaging and photothermal therapy |
title | Polydopamine-coated Au nanorods for targeted fluorescent cell imaging and photothermal therapy |
title_full | Polydopamine-coated Au nanorods for targeted fluorescent cell imaging and photothermal therapy |
title_fullStr | Polydopamine-coated Au nanorods for targeted fluorescent cell imaging and photothermal therapy |
title_full_unstemmed | Polydopamine-coated Au nanorods for targeted fluorescent cell imaging and photothermal therapy |
title_short | Polydopamine-coated Au nanorods for targeted fluorescent cell imaging and photothermal therapy |
title_sort | polydopamine-coated au nanorods for targeted fluorescent cell imaging and photothermal therapy |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466791/ https://www.ncbi.nlm.nih.gov/pubmed/31019866 http://dx.doi.org/10.3762/bjnano.10.79 |
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