High-Resolution Shortwave Infrared Imaging of Vascular Disorders Using Gold Nanoclusters
We synthesized a generation of water-soluble, atomically precise gold nanoclusters (Au NCs) with anisotropic surface containing a short dithiol pegylated chain (AuMHA/TDT). The AuMHA/TDT exhibit a high brightness (QY ∼ 6%) in the shortwave infrared (SWIR) spectrum with a detection above 1250 nm. Fur...
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| Vydané v: | ACS nano Ročník 14; číslo 4; s. 4973 - 4981 |
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| Hlavní autori: | , , , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | English |
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United States
American Chemical Society
28.04.2020
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| ISSN: | 1936-0851, 1936-086X, 1936-086X |
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| Abstract | We synthesized a generation of water-soluble, atomically precise gold nanoclusters (Au NCs) with anisotropic surface containing a short dithiol pegylated chain (AuMHA/TDT). The AuMHA/TDT exhibit a high brightness (QY ∼ 6%) in the shortwave infrared (SWIR) spectrum with a detection above 1250 nm. Furthermore, they show an extended half-life in blood (t 1/2ß = 19.54 ± 0.05 h) and a very weak accumulation in organs. We also developed a non-invasive, whole-body vascular imaging system in the SWIR window with high-resolution, benefiting from a series of Monte Carlo image processing. The imaging process enabled to improve contrast by 1 order of magnitude and enhance the spatial resolution by 59%. After systemic administration of these nanoprobes in mice, we can quantify vessel complexity in depth (>4 mm), allowing to detect very subtle vascular disorders non-invasively in bone morphogenetic protein 9 (Bmp9)-deficient mice. The combination of these anisotropic surface charged Au NCs plus an improved SWIR imaging device allows a precise mapping at high-resolution and an in depth understanding of the organization of the vascular network in live animals. |
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| AbstractList | We synthesized a generation of water-soluble, atomically precise gold nanoclusters (Au NCs) with anisotropic surface containing a short dithiol pegylated chain (AuMHA/TDT). The AuMHA/TDT exhibit a high brightness (QY ∼ 6%) in the shortwave infrared (SWIR) spectrum with a detection above 1250 nm. Furthermore, they show an extended half-life in blood (
= 19.54 ± 0.05 h) and a very weak accumulation in organs. We also developed a non-invasive, whole-body vascular imaging system in the SWIR window with high-resolution, benefiting from a series of Monte Carlo image processing. The imaging process enabled to improve contrast by 1 order of magnitude and enhance the spatial resolution by 59%. After systemic administration of these nanoprobes in mice, we can quantify vessel complexity in depth (>4 mm), allowing to detect very subtle vascular disorders non-invasively in bone morphogenetic protein 9 (
)-deficient mice. The combination of these anisotropic surface charged Au NCs plus an improved SWIR imaging device allows a precise mapping at high-resolution and an in depth understanding of the organization of the vascular network in live animals. We synthesized a generation of water-soluble, atomically precise gold nanoclusters (Au NCs) with anisotropic surface containing a short dithiol pegylated chain (AuMHA/TDT). The AuMHA/TDT exhibit a high brightness (QY ∼ 6%) in the shortwave infrared (SWIR) spectrum with a detection above 1250 nm. Furthermore, they show an extended half-life in blood (t1/2ß = 19.54 ± 0.05 h) and a very weak accumulation in organs. We also developed a non-invasive, whole-body vascular imaging system in the SWIR window with high-resolution, benefiting from a series of Monte Carlo image processing. The imaging process enabled to improve contrast by 1 order of magnitude and enhance the spatial resolution by 59%. After systemic administration of these nanoprobes in mice, we can quantify vessel complexity in depth (>4 mm), allowing to detect very subtle vascular disorders non-invasively in bone morphogenetic protein 9 (Bmp9)-deficient mice. The combination of these anisotropic surface charged Au NCs plus an improved SWIR imaging device allows a precise mapping at high-resolution and an in depth understanding of the organization of the vascular network in live animals.We synthesized a generation of water-soluble, atomically precise gold nanoclusters (Au NCs) with anisotropic surface containing a short dithiol pegylated chain (AuMHA/TDT). The AuMHA/TDT exhibit a high brightness (QY ∼ 6%) in the shortwave infrared (SWIR) spectrum with a detection above 1250 nm. Furthermore, they show an extended half-life in blood (t1/2ß = 19.54 ± 0.05 h) and a very weak accumulation in organs. We also developed a non-invasive, whole-body vascular imaging system in the SWIR window with high-resolution, benefiting from a series of Monte Carlo image processing. The imaging process enabled to improve contrast by 1 order of magnitude and enhance the spatial resolution by 59%. After systemic administration of these nanoprobes in mice, we can quantify vessel complexity in depth (>4 mm), allowing to detect very subtle vascular disorders non-invasively in bone morphogenetic protein 9 (Bmp9)-deficient mice. The combination of these anisotropic surface charged Au NCs plus an improved SWIR imaging device allows a precise mapping at high-resolution and an in depth understanding of the organization of the vascular network in live animals. We synthesized a generation of water-soluble, atomically precise gold nanoclusters (Au NCs) with anisotropic surface containing a short dithiol pegylated chain (AuMHA/TDT). The AuMHA/TDT exhibit a high brightness (QY ∼ 6%) in the shortwave infrared (SWIR) spectrum with a detection above 1250 nm. Furthermore, they show an extended half-life in blood (t 1/2ß = 19.54 ± 0.05 h) and a very weak accumulation in organs. We also developed a non-invasive, whole-body vascular imaging system in the SWIR window with high-resolution, benefiting from a series of Monte Carlo image processing. The imaging process enabled to improve contrast by 1 order of magnitude and enhance the spatial resolution by 59%. After systemic administration of these nanoprobes in mice, we can quantify vessel complexity in depth (>4 mm), allowing to detect very subtle vascular disorders non-invasively in bone morphogenetic protein 9 (Bmp9)-deficient mice. The combination of these anisotropic surface charged Au NCs plus an improved SWIR imaging device allows a precise mapping at high-resolution and an in depth understanding of the organization of the vascular network in live animals. KEYWORDS: shortwave infrared fluorescence, gold nanoclusters, vascular disorder, Monte Carlo restoration imaging processing, bone morphogenetic protein 9 (Bmp9) We synthesized a generation of water-soluble, atomically precise gold nanoclusters (Au NCs) with anisotropic surface containing a short dithiol pegylated chain (AuMHA/TDT). The AuMHA/TDT exhibit a high brightness (QY ∼ 6%) in the shortwave infrared (SWIR) spectrum with a detection above 1250 nm. Furthermore, they show an extended half-life in blood (t 1/2ß = 19.54 ± 0.05 h) and a very weak accumulation in organs. We also developed a non-invasive, whole-body vascular imaging system in the SWIR window with high-resolution, benefiting from a series of Monte Carlo image processing. The imaging process enabled to improve contrast by 1 order of magnitude and enhance the spatial resolution by 59%. After systemic administration of these nanoprobes in mice, we can quantify vessel complexity in depth (>4 mm), allowing to detect very subtle vascular disorders non-invasively in bone morphogenetic protein 9 (Bmp9)-deficient mice. The combination of these anisotropic surface charged Au NCs plus an improved SWIR imaging device allows a precise mapping at high-resolution and an in depth understanding of the organization of the vascular network in live animals. |
| Author | Musnier, Benjamin Desroches-Castan, Agnès Resch-Genger, Ute Wegner, K. David Bailly, Sabine Usson, Yves Henry, Maxime Coll, Jean-Luc Le Guével, Xavier Yu, Zhixi Chovelon, Benoit Fertin, Arnold Josserand, Véronique |
| AuthorAffiliation | University of Grenoble Alpes, CNRS-UMR 5525 Biology of Cancer and Infection Laboratory Cancer Targets and Experimental Therapeutics, Institute for Advanced Biosciences (IAB) University Grenoble Alpes, INSERM, CEA Centre Hospitalier Universitaire (CHU) de Grenoble Alpes University of Grenoble Alpes (UGA)/ INSERM-U1209/CNRS-UMR 5309 Institut de Biologie et Pathologie TIMC-IMAG Laboratory |
| AuthorAffiliation_xml | – name: Cancer Targets and Experimental Therapeutics, Institute for Advanced Biosciences (IAB) – name: Centre Hospitalier Universitaire (CHU) de Grenoble Alpes – name: Biology of Cancer and Infection Laboratory – name: University Grenoble Alpes, INSERM, CEA – name: TIMC-IMAG Laboratory – name: Institut de Biologie et Pathologie – name: University of Grenoble Alpes (UGA)/ INSERM-U1209/CNRS-UMR 5309 – name: University of Grenoble Alpes, CNRS-UMR 5525 |
| Author_xml | – sequence: 1 givenname: Zhixi surname: Yu fullname: Yu, Zhixi organization: University of Grenoble Alpes (UGA)/ INSERM-U1209/CNRS-UMR 5309 – sequence: 2 givenname: Benjamin surname: Musnier fullname: Musnier, Benjamin organization: University of Grenoble Alpes (UGA)/ INSERM-U1209/CNRS-UMR 5309 – sequence: 3 givenname: K. David surname: Wegner fullname: Wegner, K. David – sequence: 4 givenname: Maxime surname: Henry fullname: Henry, Maxime organization: University of Grenoble Alpes (UGA)/ INSERM-U1209/CNRS-UMR 5309 – sequence: 5 givenname: Benoit surname: Chovelon fullname: Chovelon, Benoit organization: Centre Hospitalier Universitaire (CHU) de Grenoble Alpes – sequence: 6 givenname: Agnès surname: Desroches-Castan fullname: Desroches-Castan, Agnès organization: University Grenoble Alpes, INSERM, CEA – sequence: 7 givenname: Arnold surname: Fertin fullname: Fertin, Arnold organization: University of Grenoble Alpes, CNRS-UMR 5525 – sequence: 8 givenname: Ute orcidid: 0000-0002-0944-1115 surname: Resch-Genger fullname: Resch-Genger, Ute – sequence: 9 givenname: Sabine surname: Bailly fullname: Bailly, Sabine organization: University Grenoble Alpes, INSERM, CEA – sequence: 10 givenname: Jean-Luc orcidid: 0000-0002-2453-3552 surname: Coll fullname: Coll, Jean-Luc email: jean-luc.coll@univ-grenoble-alpes.fr organization: University of Grenoble Alpes (UGA)/ INSERM-U1209/CNRS-UMR 5309 – sequence: 11 givenname: Yves surname: Usson fullname: Usson, Yves organization: University of Grenoble Alpes, CNRS-UMR 5525 – sequence: 12 givenname: Véronique surname: Josserand fullname: Josserand, Véronique organization: University of Grenoble Alpes (UGA)/ INSERM-U1209/CNRS-UMR 5309 – sequence: 13 givenname: Xavier orcidid: 0000-0003-3634-7762 surname: Le Guével fullname: Le Guével, Xavier email: xavier.le-guevel@univ-grenoble-alpes.fr organization: University of Grenoble Alpes (UGA)/ INSERM-U1209/CNRS-UMR 5309 |
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| Cites_doi | 10.1038/s41551-016-0010 10.1021/acs.jpcc.7b09500 10.3390/cells8091079 10.1002/hep.30655 10.1002/anie.201609043 10.1038/nphoton.2014.166 10.1039/C9TB02767J 10.1073/pnas.1718917115 10.1021/acs.nanolett.7b03070 10.1182/blood-2012-12-472142 10.1039/C9NR04120F 10.1038/s41587-019-0262-4 10.1038/nnano.2017.170 10.1038/nm.2995 10.3389/fgene.2014.00456 10.1063/1.4977203 10.1364/JOSAA.3.000731 10.1007/BFb0056195 10.1039/C8NR05299A 10.1002/adma.201605497 10.1002/adma.201901015 10.1038/s41551-017-0056 |
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| Keywords | shortwave infrared fluorescence vascular disorder Monte Carlo restoration imaging processing bone morphogenetic protein 9 (Bmp9) gold nanoclusters |
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| Title | High-Resolution Shortwave Infrared Imaging of Vascular Disorders Using Gold Nanoclusters |
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