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Porphyrin-magnetite nanoconjugates for biological imaging
BACKGROUND: The use of silica coated magnetic nanoparticles as contrast agents has resulted in the production of highly stable, non-toxic solutions that can be manipulated via an external magnetic field. As a result, the interaction of these nanocomposites with cells is of vital importance in unders...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090322/ https://www.ncbi.nlm.nih.gov/pubmed/21477294 http://dx.doi.org/10.1186/1477-3155-9-13 |
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author | Nowostawska, Małgorzata Corr, Serena A Byrne, Stephen J Conroy, Jennifer Volkov, Yuri Gun'ko, Yurii K |
author_facet | Nowostawska, Małgorzata Corr, Serena A Byrne, Stephen J Conroy, Jennifer Volkov, Yuri Gun'ko, Yurii K |
author_sort | Nowostawska, Małgorzata |
collection | PubMed |
description | BACKGROUND: The use of silica coated magnetic nanoparticles as contrast agents has resulted in the production of highly stable, non-toxic solutions that can be manipulated via an external magnetic field. As a result, the interaction of these nanocomposites with cells is of vital importance in understanding their behaviour and biocompatibility. Here we report the preparation, characterisation and potential application of new "two-in-one" magnetic fluorescent nanocomposites composed of silica-coated magnetite nanoparticles covalently linked to a porphyrin moiety. METHOD: The experiments were performed by administering porphyrin functionalised silica-coated magnetite nanoparticles to THP-1 cells, a human acute monocytic leukaemia cell line. Cells were cultured in RPMI 1640 medium with 25 mM HEPES supplemented with heat-inactivated foetal bovine serum (FBS). RESULTS: We have synthesised, characterised and analysed in vitro, a new multimodal (magnetic and fluorescent) porphyrin magnetic nanoparticle composite (PMNC). Initial co-incubation experiments performed with THP-1 macrophage cells were promising; however the PMNC photobleached under confocal microscopy study. β-mercaptoethanol (β-ME) was employed to counteract this problem and resulted not only in enhanced fluorescence emission, but also allowed for elongated imaging and increased exposure times of the PMNC in a cellular environment. CONCLUSION: Our experiments have demonstrated that β-ME visibly enhances the emission intensity. No deleterious effects to the cells were witnessed upon co-incubation with β-ME alone and no increases in background fluorescence were recorded. These results should present an interest for further development of in vitro biological imaging techniques. |
format | Text |
id | pubmed-3090322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30903222011-05-10 Porphyrin-magnetite nanoconjugates for biological imaging Nowostawska, Małgorzata Corr, Serena A Byrne, Stephen J Conroy, Jennifer Volkov, Yuri Gun'ko, Yurii K J Nanobiotechnology Research BACKGROUND: The use of silica coated magnetic nanoparticles as contrast agents has resulted in the production of highly stable, non-toxic solutions that can be manipulated via an external magnetic field. As a result, the interaction of these nanocomposites with cells is of vital importance in understanding their behaviour and biocompatibility. Here we report the preparation, characterisation and potential application of new "two-in-one" magnetic fluorescent nanocomposites composed of silica-coated magnetite nanoparticles covalently linked to a porphyrin moiety. METHOD: The experiments were performed by administering porphyrin functionalised silica-coated magnetite nanoparticles to THP-1 cells, a human acute monocytic leukaemia cell line. Cells were cultured in RPMI 1640 medium with 25 mM HEPES supplemented with heat-inactivated foetal bovine serum (FBS). RESULTS: We have synthesised, characterised and analysed in vitro, a new multimodal (magnetic and fluorescent) porphyrin magnetic nanoparticle composite (PMNC). Initial co-incubation experiments performed with THP-1 macrophage cells were promising; however the PMNC photobleached under confocal microscopy study. β-mercaptoethanol (β-ME) was employed to counteract this problem and resulted not only in enhanced fluorescence emission, but also allowed for elongated imaging and increased exposure times of the PMNC in a cellular environment. CONCLUSION: Our experiments have demonstrated that β-ME visibly enhances the emission intensity. No deleterious effects to the cells were witnessed upon co-incubation with β-ME alone and no increases in background fluorescence were recorded. These results should present an interest for further development of in vitro biological imaging techniques. BioMed Central 2011-04-08 /pmc/articles/PMC3090322/ /pubmed/21477294 http://dx.doi.org/10.1186/1477-3155-9-13 Text en Copyright ©2011 Nowostawska et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Nowostawska, Małgorzata Corr, Serena A Byrne, Stephen J Conroy, Jennifer Volkov, Yuri Gun'ko, Yurii K Porphyrin-magnetite nanoconjugates for biological imaging |
title | Porphyrin-magnetite nanoconjugates for biological imaging |
title_full | Porphyrin-magnetite nanoconjugates for biological imaging |
title_fullStr | Porphyrin-magnetite nanoconjugates for biological imaging |
title_full_unstemmed | Porphyrin-magnetite nanoconjugates for biological imaging |
title_short | Porphyrin-magnetite nanoconjugates for biological imaging |
title_sort | porphyrin-magnetite nanoconjugates for biological imaging |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090322/ https://www.ncbi.nlm.nih.gov/pubmed/21477294 http://dx.doi.org/10.1186/1477-3155-9-13 |
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