Photostable Small-Molecule NIR-II Fluorescent Scaffolds that Cross the Blood-Brain Barrier for Noninvasive Brain Imaging
The second near-infrared (NIR-II, 1000-1700 nm) fluorescent probes have significant advantages over visible or NIR-I (600-900 nm) imaging for both depth of penetration and level of resolution. Since the blood-brain barrier (BBB) prevents most molecules from entering the central nervous system, NIR-I...
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| Vydáno v: | Journal of the American Chemical Society Ročník 144; číslo 51; s. 23668 - 23676 |
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| Jazyk: | angličtina |
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Amer Chemical Soc
28.12.2022
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| ISSN: | 0002-7863, 1520-5126, 1520-5126 |
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| Abstract | The second near-infrared (NIR-II, 1000-1700 nm) fluorescent probes have significant advantages over visible or NIR-I (600-900 nm) imaging for both depth of penetration and level of resolution. Since the blood-brain barrier (BBB) prevents most molecules from entering the central nervous system, NIR-II dyes with large molecular frameworks have limited applications for brain imaging. In this work, we developed a series of boron difluoride (BF2) formazanate NIR-II dyes, which had tunable photophysical properties, ultrahigh photostability, excellent biological stability, and strong brightness. Modulation of the aniline moiety of BF2 formazanate dyes significantly enhances their abilities to cross the BBB for noninvasive brain imaging. Furthermore, the intact mouse brain imaging and dynamic dye diffusion across the BBB were monitored using these BF2 formazanate dyes in the NIR-II region. In murine glioblastoma models, these dyes can differentiate tumors from normal brain tissues. We anticipate that this new type of small molecule will find potential applications in creating probes and drugs relevant to theranostic for brain pathologies. |
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| AbstractList | The second near-infrared (NIR-II, 1000-1700 nm) fluorescent probes have significant advantages over visible or NIR-I (600-900 nm) imaging for both depth of penetration and level of resolution. Since the blood-brain barrier (BBB) prevents most molecules from entering the central nervous system, NIR-II dyes with large molecular frameworks have limited applications for brain imaging. In this work, we developed a series of boron difluoride (BF
) formazanate NIR-II dyes, which had tunable photophysical properties, ultrahigh photostability, excellent biological stability, and strong brightness. Modulation of the aniline moiety of BF
formazanate dyes significantly enhances their abilities to cross the BBB for noninvasive brain imaging. Furthermore, the intact mouse brain imaging and dynamic dye diffusion across the BBB were monitored using these BF
formazanate dyes in the NIR-II region. In murine glioblastoma models, these dyes can differentiate tumors from normal brain tissues. We anticipate that this new type of small molecule will find potential applications in creating probes and drugs relevant to theranostic for brain pathologies. The second near-infrared (NIR-II, 1000-1700 nm) fluorescent probes have significant advantages over visible or NIR-I (600-900 nm) imaging for both depth of penetration and level of resolution. Since the blood-brain barrier (BBB) prevents most molecules from entering the central nervous system, NIR-II dyes with large molecular frameworks have limited applications for brain imaging. In this work, we developed a series of boron difluoride (BF2) formazanate NIR-II dyes, which had tunable photophysical properties, ultrahigh photostability, excellent biological stability, and strong brightness. Modulation of the aniline moiety of BF2 formazanate dyes significantly enhances their abilities to cross the BBB for noninvasive brain imaging. Furthermore, the intact mouse brain imaging and dynamic dye diffusion across the BBB were monitored using these BF2 formazanate dyes in the NIR-II region. In murine glioblastoma models, these dyes can differentiate tumors from normal brain tissues. We anticipate that this new type of small molecule will find potential applications in creating probes and drugs relevant to theranostic for brain pathologies.The second near-infrared (NIR-II, 1000-1700 nm) fluorescent probes have significant advantages over visible or NIR-I (600-900 nm) imaging for both depth of penetration and level of resolution. Since the blood-brain barrier (BBB) prevents most molecules from entering the central nervous system, NIR-II dyes with large molecular frameworks have limited applications for brain imaging. In this work, we developed a series of boron difluoride (BF2) formazanate NIR-II dyes, which had tunable photophysical properties, ultrahigh photostability, excellent biological stability, and strong brightness. Modulation of the aniline moiety of BF2 formazanate dyes significantly enhances their abilities to cross the BBB for noninvasive brain imaging. Furthermore, the intact mouse brain imaging and dynamic dye diffusion across the BBB were monitored using these BF2 formazanate dyes in the NIR-II region. In murine glioblastoma models, these dyes can differentiate tumors from normal brain tissues. We anticipate that this new type of small molecule will find potential applications in creating probes and drugs relevant to theranostic for brain pathologies. The second near-infrared (NIR-II, 1000-1700 nm) fluorescent probes have significant advantages over visible or NIR-I (600-900 nm) imaging for both depth of penetration and level of resolution. Since the blood-brain barrier (BBB) prevents most molecules from entering the central nervous system, NIR-II dyes with large molecular frameworks have limited applications for brain imaging. In this work, we developed a series of boron difluoride (BF2) formazanate NIR-II dyes, which had tunable photophysical properties, ultrahigh photostability, excellent biological stability, and strong brightness. Modulation of the aniline moiety of BF2 formazanate dyes significantly enhances their abilities to cross the BBB for noninvasive brain imaging. Furthermore, the intact mouse brain imaging and dynamic dye diffusion across the BBB were monitored using these BF2 formazanate dyes in the NIR-II region. In murine glioblastoma models, these dyes can differentiate tumors from normal brain tissues. We anticipate that this new type of small molecule will find potential applications in creating probes and drugs relevant to theranostic for brain pathologies. |
| Author | Wu, William Xiao, Han Cheng, Zhen Wang, Shichao Shi, Hui Chen, Yuda Loredo, Axel Tian, Zeru Zhang, Xuanjun Bachilo, Sergei M. Weisman, R. Bruce Wang, Lushun |
| Author_xml | – sequence: 1 givenname: Shichao surname: Wang fullname: Wang, Shichao organization: Rice Univ, Dept Chem, Houston, TX 77005 USA – sequence: 2 givenname: Hui surname: Shi fullname: Shi, Hui organization: Chinese Acad Sci, Shanghai Inst Mat Med, Mol Imaging Ctr, State Key Lab Drug Res, Shanghai 201203, Peoples R China – sequence: 3 givenname: Lushun orcidid: 0000-0002-8373-2199 surname: Wang fullname: Wang, Lushun organization: Rice Univ, Dept Chem, Houston, TX 77005 USA – sequence: 4 givenname: Axel surname: Loredo fullname: Loredo, Axel organization: Rice Univ, Dept Chem, Houston, TX 77005 USA – sequence: 5 givenname: Sergei M. orcidid: 0000-0001-5236-1383 surname: Bachilo fullname: Bachilo, Sergei M. organization: Rice Univ, Dept Chem, Houston, TX 77005 USA – sequence: 6 givenname: William surname: Wu fullname: Wu, William organization: Rice Univ, Dept Chem, Houston, TX 77005 USA – sequence: 7 givenname: Zeru surname: Tian fullname: Tian, Zeru organization: Rice Univ, Dept Chem, Houston, TX 77005 USA – sequence: 8 givenname: Yuda orcidid: 0000-0002-5399-1720 surname: Chen fullname: Chen, Yuda organization: Rice Univ, Dept Chem, Houston, TX 77005 USA – sequence: 9 givenname: R. Bruce orcidid: 0000-0001-6452-1778 surname: Weisman fullname: Weisman, R. Bruce organization: Rice Univ, Dept Chem, Houston, TX 77005 USA – sequence: 10 givenname: Xuanjun orcidid: 0000-0001-6452-1778 surname: Zhang fullname: Zhang, Xuanjun organization: Univ Macau, Fac Hlth Sci, MOE Frontiers Sci Ctr Precis Oncol, Macau, Peoples R China – sequence: 11 givenname: Zhen orcidid: 0000-0001-8177-9463 surname: Cheng fullname: Cheng, Zhen email: zcheng@simm.ac.cn organization: Chinese Acad Sci, Shanghai Inst Mat Med, Mol Imaging Ctr, State Key Lab Drug Res, Shanghai 201203, Peoples R China – sequence: 12 givenname: Han orcidid: 0000-0002-4311-971X surname: Xiao fullname: Xiao, Han email: han.xiao@rice.edu organization: Rice Univ, Dept Chem, Houston, TX 77005 USA |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36511618$$D View this record in MEDLINE/PubMed |
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| SubjectTerms | Animals Blood-Brain Barrier Brain - diagnostic imaging Chemistry Chemistry, Multidisciplinary Fluorescent Dyes Mice Neoplasms Neuroimaging Optical Imaging - methods Physical Sciences Science & Technology |
| Title | Photostable Small-Molecule NIR-II Fluorescent Scaffolds that Cross the Blood-Brain Barrier for Noninvasive Brain Imaging |
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