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Self-illuminating quantum dots for highly sensitive in vivo real-time luminescent mapping of sentinel lymph nodes
Quantum dots (QDs) show promise as novel nanomaterials for sentinel lymph node (SLN) mapping through their use in noninvasive in vivo fluorescence imaging, and they have provided remarkable results. However, in vivo fluorescence imaging has limitations mainly reflected in the strong autofluorescence...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405894/ https://www.ncbi.nlm.nih.gov/pubmed/22848169 http://dx.doi.org/10.2147/IJN.S30709 |
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author | Wu, Qiang Chu, Maoquan |
author_facet | Wu, Qiang Chu, Maoquan |
author_sort | Wu, Qiang |
collection | PubMed |
description | Quantum dots (QDs) show promise as novel nanomaterials for sentinel lymph node (SLN) mapping through their use in noninvasive in vivo fluorescence imaging, and they have provided remarkable results. However, in vivo fluorescence imaging has limitations mainly reflected in the strong autofluorescence and low deepness of tissue penetration associated with this technique. Here, we report on the first use of self-illuminating QDs for mouse axillary SLN mapping by bioluminescence resonance energy transfer, which was found to overcome these limitations. We used CdTe/CdS QDs synthesized in aqueous solution to conjugate a mutant of the bioluminescent protein, Renilla reniformis luciferase. The nanobioconjugates obtained had an average hydrodynamic diameter of 19 nm, and their luminescence catalyzed by the substrate (coelenterazine) could penetrate into at least 20 mm of hairless pigskin, which could be observed using an in vivo imaging system equipped with a 700 nm emission filter. Conversely, the fluorescence of the nanobioconjugates penetrated no more than 10 mm of pigskin and was observed with a strong background. When 80 μL of the nanobioconjugates (containing about 0.5 μmol/L of QDs) and 5 μL of coelenterazine (1 μg/μL) were intradermally injected into a mouse paw, the axillary SLN could be imaged in real time without external excitation, and little background interference was detected. Furthermore, the decayed luminescence of QD-Luc8 in SLNs could be recovered after being intradermally reinjected with the coelenterazine. Our data showed that using self-illuminating QDs, as opposed to fluorescence QDs, has greatly enhanced sensitivity in SLN mapping, and that the SLN could be identified synchronously by the luminescence and fluorescence of the self-illuminating QDs. |
format | Online Article Text |
id | pubmed-3405894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34058942012-07-30 Self-illuminating quantum dots for highly sensitive in vivo real-time luminescent mapping of sentinel lymph nodes Wu, Qiang Chu, Maoquan Int J Nanomedicine Original Research Quantum dots (QDs) show promise as novel nanomaterials for sentinel lymph node (SLN) mapping through their use in noninvasive in vivo fluorescence imaging, and they have provided remarkable results. However, in vivo fluorescence imaging has limitations mainly reflected in the strong autofluorescence and low deepness of tissue penetration associated with this technique. Here, we report on the first use of self-illuminating QDs for mouse axillary SLN mapping by bioluminescence resonance energy transfer, which was found to overcome these limitations. We used CdTe/CdS QDs synthesized in aqueous solution to conjugate a mutant of the bioluminescent protein, Renilla reniformis luciferase. The nanobioconjugates obtained had an average hydrodynamic diameter of 19 nm, and their luminescence catalyzed by the substrate (coelenterazine) could penetrate into at least 20 mm of hairless pigskin, which could be observed using an in vivo imaging system equipped with a 700 nm emission filter. Conversely, the fluorescence of the nanobioconjugates penetrated no more than 10 mm of pigskin and was observed with a strong background. When 80 μL of the nanobioconjugates (containing about 0.5 μmol/L of QDs) and 5 μL of coelenterazine (1 μg/μL) were intradermally injected into a mouse paw, the axillary SLN could be imaged in real time without external excitation, and little background interference was detected. Furthermore, the decayed luminescence of QD-Luc8 in SLNs could be recovered after being intradermally reinjected with the coelenterazine. Our data showed that using self-illuminating QDs, as opposed to fluorescence QDs, has greatly enhanced sensitivity in SLN mapping, and that the SLN could be identified synchronously by the luminescence and fluorescence of the self-illuminating QDs. Dove Medical Press 2012 2012-07-05 /pmc/articles/PMC3405894/ /pubmed/22848169 http://dx.doi.org/10.2147/IJN.S30709 Text en © 2012 Wu and Chu publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Wu, Qiang Chu, Maoquan Self-illuminating quantum dots for highly sensitive in vivo real-time luminescent mapping of sentinel lymph nodes |
title | Self-illuminating quantum dots for highly sensitive in vivo real-time luminescent mapping of sentinel lymph nodes |
title_full | Self-illuminating quantum dots for highly sensitive in vivo real-time luminescent mapping of sentinel lymph nodes |
title_fullStr | Self-illuminating quantum dots for highly sensitive in vivo real-time luminescent mapping of sentinel lymph nodes |
title_full_unstemmed | Self-illuminating quantum dots for highly sensitive in vivo real-time luminescent mapping of sentinel lymph nodes |
title_short | Self-illuminating quantum dots for highly sensitive in vivo real-time luminescent mapping of sentinel lymph nodes |
title_sort | self-illuminating quantum dots for highly sensitive in vivo real-time luminescent mapping of sentinel lymph nodes |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405894/ https://www.ncbi.nlm.nih.gov/pubmed/22848169 http://dx.doi.org/10.2147/IJN.S30709 |
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