Tracking Labile Copper Fluctuation In Vivo/Ex Vivo: Design and Application of a Ratiometric Near-Infrared Fluorophore Derived from 4‑Aminostyrene-Conjugated Boron Dipyrromethene

Specimen differences, tissue-dependent background fluorescence and scattering, and deviated specimen position and sensor concentration make optical imaging for labile copper fluctuation in animals questionable, and a signal comparison between specimens is infeasible. We proposed ratiometric optical...

Full description

Saved in:
Bibliographic Details
Published inInorganic chemistry Vol. 60; no. 24; pp. 18567 - 18574
Main Authors Xu, Hongxia, Yao, Shankun, Chen, Yuncong, Zhang, Changli, Zhang, Shuren, Yuan, Hao, Chen, Zhongyan, Bai, Yang, Yang, Tao, Guo, Zijian, He, Weijiang
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 20.12.2021
Subjects
Online AccessGet full text
ISSN0020-1669
1520-510X
1520-510X
DOI10.1021/acs.inorgchem.1c01779

Cover

Loading…
Abstract Specimen differences, tissue-dependent background fluorescence and scattering, and deviated specimen position and sensor concentration make optical imaging for labile copper fluctuation in animals questionable, and a signal comparison between specimens is infeasible. We proposed ratiometric optical imaging as an alternative to overcome these disadvantages, and a near-infrared (NIR) ratiometric sensor, BDPS1, was devised therefore by conjugating boron dipyrromethene (BODIPY) with 4-aminostyrene and modifying the 4-amino group as a Cu+ chelator. BDPS1 possessed an excitation ratiometric copper-sensing ability to show the ratio of NIR emission (710 nm) upon excitation at 600 nm to that at 660 nm, F ex600/F ex660, increasing from 2.8 to 10.7. This sensor displayed still the opposite copper response of its internal charge transfer (ICT; 670 nm) and local (581 nm) emission bands. Ratiometric imaging with this sensor disclosed a higher labile copper region near the nucleus apparatus, and HEK-293T cells were more sensitive to copper incubation than MCF-7 cells. Dual excitation ratiometric imaging with this sensor realized tracking of labile copper fluctuation in mice, and the whole-body imaging found that tail intravenous injection of CUTX-101, a therapeutical agent for Menkes disease, led to a distinct labile copper increase in the upper belly. The ex vivo imaging of the resected viscera of mice revealed that CUTX-101 injection enhanced the labile copper level in the liver, intestine, lung, and gall bladder in sequence, yet the kidney, heart, and spleen showed almost no response. This study indicated that modifying BODIPY as an extended ICT fluorophore, with its electron-donating group being derived as a metal chelator, is an effective design rationale of NIR ratiometric sensors for copper tracking in vivo/ex vivo.
AbstractList Specimen differences, tissue-dependent background fluorescence and scattering, and deviated specimen position and sensor concentration make optical imaging for labile copper fluctuation in animals questionable, and a signal comparison between specimens is infeasible. We proposed ratiometric optical imaging as an alternative to overcome these disadvantages, and a near-infrared (NIR) ratiometric sensor, BDPS1, was devised therefore by conjugating boron dipyrromethene (BODIPY) with 4-aminostyrene and modifying the 4-amino group as a Cu+ chelator. BDPS1 possessed an excitation ratiometric copper-sensing ability to show the ratio of NIR emission (710 nm) upon excitation at 600 nm to that at 660 nm, Fex600/Fex660, increasing from 2.8 to 10.7. This sensor displayed still the opposite copper response of its internal charge transfer (ICT; 670 nm) and local (581 nm) emission bands. Ratiometric imaging with this sensor disclosed a higher labile copper region near the nucleus apparatus, and HEK-293T cells were more sensitive to copper incubation than MCF-7 cells. Dual excitation ratiometric imaging with this sensor realized tracking of labile copper fluctuation in mice, and the whole-body imaging found that tail intravenous injection of CUTX-101, a therapeutical agent for Menkes disease, led to a distinct labile copper increase in the upper belly. The ex vivo imaging of the resected viscera of mice revealed that CUTX-101 injection enhanced the labile copper level in the liver, intestine, lung, and gall bladder in sequence, yet the kidney, heart, and spleen showed almost no response. This study indicated that modifying BODIPY as an extended ICT fluorophore, with its electron-donating group being derived as a metal chelator, is an effective design rationale of NIR ratiometric sensors for copper tracking in vivo/ex vivo.Specimen differences, tissue-dependent background fluorescence and scattering, and deviated specimen position and sensor concentration make optical imaging for labile copper fluctuation in animals questionable, and a signal comparison between specimens is infeasible. We proposed ratiometric optical imaging as an alternative to overcome these disadvantages, and a near-infrared (NIR) ratiometric sensor, BDPS1, was devised therefore by conjugating boron dipyrromethene (BODIPY) with 4-aminostyrene and modifying the 4-amino group as a Cu+ chelator. BDPS1 possessed an excitation ratiometric copper-sensing ability to show the ratio of NIR emission (710 nm) upon excitation at 600 nm to that at 660 nm, Fex600/Fex660, increasing from 2.8 to 10.7. This sensor displayed still the opposite copper response of its internal charge transfer (ICT; 670 nm) and local (581 nm) emission bands. Ratiometric imaging with this sensor disclosed a higher labile copper region near the nucleus apparatus, and HEK-293T cells were more sensitive to copper incubation than MCF-7 cells. Dual excitation ratiometric imaging with this sensor realized tracking of labile copper fluctuation in mice, and the whole-body imaging found that tail intravenous injection of CUTX-101, a therapeutical agent for Menkes disease, led to a distinct labile copper increase in the upper belly. The ex vivo imaging of the resected viscera of mice revealed that CUTX-101 injection enhanced the labile copper level in the liver, intestine, lung, and gall bladder in sequence, yet the kidney, heart, and spleen showed almost no response. This study indicated that modifying BODIPY as an extended ICT fluorophore, with its electron-donating group being derived as a metal chelator, is an effective design rationale of NIR ratiometric sensors for copper tracking in vivo/ex vivo.
Specimen differences, tissue-dependent background fluorescence and scattering, and deviated specimen position and sensor concentration make optical imaging for labile copper fluctuation in animals questionable, and a signal comparison between specimens is infeasible. We proposed ratiometric optical imaging as an alternative to overcome these disadvantages, and a near-infrared (NIR) ratiometric sensor, , was devised therefore by conjugating boron dipyrromethene (BODIPY) with 4-aminostyrene and modifying the 4-amino group as a Cu chelator. possessed an excitation ratiometric copper-sensing ability to show the ratio of NIR emission (710 nm) upon excitation at 600 nm to that at 660 nm, / , increasing from 2.8 to 10.7. This sensor displayed still the opposite copper response of its internal charge transfer (ICT; 670 nm) and local (581 nm) emission bands. Ratiometric imaging with this sensor disclosed a higher labile copper region near the nucleus apparatus, and HEK-293T cells were more sensitive to copper incubation than MCF-7 cells. Dual excitation ratiometric imaging with this sensor realized tracking of labile copper fluctuation in mice, and the whole-body imaging found that tail intravenous injection of CUTX-101, a therapeutical agent for Menkes disease, led to a distinct labile copper increase in the upper belly. The imaging of the resected viscera of mice revealed that CUTX-101 injection enhanced the labile copper level in the liver, intestine, lung, and gall bladder in sequence, yet the kidney, heart, and spleen showed almost no response. This study indicated that modifying BODIPY as an extended ICT fluorophore, with its electron-donating group being derived as a metal chelator, is an effective design rationale of NIR ratiometric sensors for copper tracking / .
Specimen differences, tissue-dependent background fluorescence and scattering, and deviated specimen position and sensor concentration make optical imaging for labile copper fluctuation in animals questionable, and a signal comparison between specimens is infeasible. We proposed ratiometric optical imaging as an alternative to overcome these disadvantages, and a near-infrared (NIR) ratiometric sensor, BDPS1, was devised therefore by conjugating boron dipyrromethene (BODIPY) with 4-aminostyrene and modifying the 4-amino group as a Cu+ chelator. BDPS1 possessed an excitation ratiometric copper-sensing ability to show the ratio of NIR emission (710 nm) upon excitation at 600 nm to that at 660 nm, F ex600/F ex660, increasing from 2.8 to 10.7. This sensor displayed still the opposite copper response of its internal charge transfer (ICT; 670 nm) and local (581 nm) emission bands. Ratiometric imaging with this sensor disclosed a higher labile copper region near the nucleus apparatus, and HEK-293T cells were more sensitive to copper incubation than MCF-7 cells. Dual excitation ratiometric imaging with this sensor realized tracking of labile copper fluctuation in mice, and the whole-body imaging found that tail intravenous injection of CUTX-101, a therapeutical agent for Menkes disease, led to a distinct labile copper increase in the upper belly. The ex vivo imaging of the resected viscera of mice revealed that CUTX-101 injection enhanced the labile copper level in the liver, intestine, lung, and gall bladder in sequence, yet the kidney, heart, and spleen showed almost no response. This study indicated that modifying BODIPY as an extended ICT fluorophore, with its electron-donating group being derived as a metal chelator, is an effective design rationale of NIR ratiometric sensors for copper tracking in vivo/ex vivo.
Author Chen, Yuncong
Zhang, Changli
Zhang, Shuren
Guo, Zijian
Yang, Tao
Yao, Shankun
Chen, Zhongyan
Yuan, Hao
Bai, Yang
He, Weijiang
Xu, Hongxia
AuthorAffiliation State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering
Chemistry and Biomedicine Innovation Center
School of Environmental Science
AuthorAffiliation_xml – name: Chemistry and Biomedicine Innovation Center
– name: State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering
– name: School of Environmental Science
Author_xml – sequence: 1
  givenname: Hongxia
  surname: Xu
  fullname: Xu, Hongxia
– sequence: 2
  givenname: Shankun
  surname: Yao
  fullname: Yao, Shankun
– sequence: 3
  givenname: Yuncong
  orcidid: 0000-0002-8406-4866
  surname: Chen
  fullname: Chen, Yuncong
  email: chenyc@nju.edu.cn
– sequence: 4
  givenname: Changli
  surname: Zhang
  fullname: Zhang, Changli
  organization: School of Environmental Science
– sequence: 5
  givenname: Shuren
  surname: Zhang
  fullname: Zhang, Shuren
– sequence: 6
  givenname: Hao
  surname: Yuan
  fullname: Yuan, Hao
– sequence: 7
  givenname: Zhongyan
  orcidid: 0000-0003-3446-0710
  surname: Chen
  fullname: Chen, Zhongyan
– sequence: 8
  givenname: Yang
  surname: Bai
  fullname: Bai, Yang
– sequence: 9
  givenname: Tao
  surname: Yang
  fullname: Yang, Tao
– sequence: 10
  givenname: Zijian
  orcidid: 0000-0003-4986-9308
  surname: Guo
  fullname: Guo, Zijian
  email: zguo@nju.edu.cn
– sequence: 11
  givenname: Weijiang
  orcidid: 0000-0002-3157-5769
  surname: He
  fullname: He, Weijiang
  email: heweij69@nju.edu.cn
BackLink https://www.ncbi.nlm.nih.gov/pubmed/34826221$$D View this record in MEDLINE/PubMed
BookMark eNqFkdFu0zAUhi00xLrBI4B8yU26Y8d1Ergq3QaVKpDQQNxFjuO0LomdHScTveMVeBbeiCfBXTsuuNmVj3z-77f8_2fkxHlnCHnJYMqAswulw9Q6j2u9Md2UaWBZVjwhEzbjkMwYfDshE4A4MymLU3IWwhYAilTIZ-Q0FTmXnLMJ-X2DSn-3bk1XqrKtoQvf9wbpdTvqYVSD9Y4uHf1q7_zF1Y_78w29NMGuHVWupvO-b60-6HxDFf28nzszoNX0o1GYLF2DCk29t_To-41HEx3Q3sW7Bn1HxZ-fv-Zd_EwYdmicSRbebce1GqLgXUQcvbT9DnFvu4n75-Rpo9pgXhzPc_Ll-upm8SFZfXq_XMxXiRIsGxIhDMCsFlLzOk8zyHLgaVUXWkIxK5pM1rmoa2ikbGTGBTe8SFMNvKogN5WQ6Tl5ffDt0d-OJgxlZ4M2bauc8WMouQQBMccsj9JXR-lYdaYue7Sdwl35EHQUvD0INPoQ0DSltsN9bAMq25YMyn2tZay1_Fdreaw10rP_6IcHHuPYgduvt35EF_N6hPkLxVTAHQ
CitedBy_id crossref_primary_10_1021_acs_accounts_2c00643
crossref_primary_10_1002_open_202300078
crossref_primary_10_1016_j_cbpa_2023_102321
crossref_primary_10_1021_acs_inorgchem_2c03349
crossref_primary_10_1016_j_ccr_2023_215130
crossref_primary_10_1021_acs_chemrev_3c00819
crossref_primary_10_1021_acs_inorgchem_3c04017
crossref_primary_10_1016_j_ccr_2022_214695
crossref_primary_10_1002_adma_202207546
crossref_primary_10_1021_acsnano_3c12716
crossref_primary_10_1515_ncrs_2024_0375
crossref_primary_10_1016_j_snb_2024_136982
crossref_primary_10_1021_jacsau_3c00062
Cites_doi 10.1016/0022-1902(78)80071-2
10.1021/ja100714p
10.1073/pnas.1904610116
10.1073/pnas.1613628113
10.1021/ja055064u
10.1021/acs.analchem.7b05297
10.1128/MCB.05722-11
10.1038/s41589-018-0062-z
10.1039/b901614g
10.1007/s41048-020-00118-7
10.1038/nchembio.2098
10.1038/nrneurol.2010.180
10.1039/C1CS15132K
10.1039/C6MT00083E
10.1016/0166-2236(88)90192-0
10.1021/jacs.9b09181
10.1073/pnas.1113729109
10.1007/s11426-018-9424-8
10.1073/pnas.1409796111
10.1002/1522-2675(20001108)83:11<2926::AID-HLCA2926>3.0.CO;2-6
10.1073/pnas.1900172116
10.1039/C9SC01153F
10.1074/jbc.M105361200
10.1093/ajcn/88.3.855S
10.1039/C7CC01430A
10.1039/D0SC03037F
10.1039/c2cs35363f
10.1016/j.dyepig.2016.03.017
10.1039/C3CC46262E
10.1016/S0021-9258(18)83589-X
10.1021/cr980446m
10.1039/b711118p
10.1016/j.ceb.2019.02.009
10.1007/s00418-013-1123-8
10.1073/pnas.0406547102
10.1523/JNEUROSCI.3699-04.2005
10.1021/ja907778b
10.1038/nature09018
10.1056/NEJMoa070613
10.1038/nchembio.1913
10.1073/pnas.1009932108
10.1002/1521-3773(20010119)40:2<385::AID-ANIE385>3.0.CO;2-F
10.1039/c3cc42069h
10.1016/j.cbpa.2010.01.003
10.1073/pnas.1111297109
10.1016/j.jphotochem.2006.03.015
10.1038/188150a0
ContentType Journal Article
Copyright 2021 American Chemical Society
Copyright_xml – notice: 2021 American Chemical Society
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1021/acs.inorgchem.1c01779
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
MEDLINE

Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1520-510X
EndPage 18574
ExternalDocumentID 34826221
10_1021_acs_inorgchem_1c01779
a423867509
Genre Journal Article
GroupedDBID -
02
4.4
53G
55A
5GY
5VS
7~N
85S
AABXI
ABFLS
ABFRP
ABMVS
ABPPZ
ABPTK
ABUCX
ACGFS
ACJ
ACNCT
ACS
AEESW
AENEX
AFEFF
AHGAQ
ALMA_UNASSIGNED_HOLDINGS
AQSVZ
BAANH
CS3
D0L
DU5
DZ
EBS
ED
F5P
GGK
GNL
IH2
IH9
IHE
JG
K2
LG6
ROL
RXW
TAE
TN5
TWZ
UI2
UKR
UPT
VF5
VG9
VQA
W1F
WH7
X
YZZ
---
-DZ
-~X
.K2
AAYXX
ABBLG
ABJNI
ABLBI
ABQRX
ADHLV
AGXLV
CITATION
CUPRZ
ED~
JG~
XSW
~02
CGR
CUY
CVF
ECM
EIF
NPM
YIN
7X8
ID FETCH-LOGICAL-a417t-44e005d46c2d837078023bd9c60959f76d84dd0f66f67242e2933c02bb08eb463
IEDL.DBID ACS
ISSN 0020-1669
1520-510X
IngestDate Fri Jul 11 06:05:45 EDT 2025
Wed Feb 19 02:09:16 EST 2025
Thu Apr 24 23:07:06 EDT 2025
Tue Jul 01 01:33:10 EDT 2025
Wed Dec 22 03:12:30 EST 2021
IsPeerReviewed true
IsScholarly true
Issue 24
Language English
License https://doi.org/10.15223/policy-029
https://doi.org/10.15223/policy-037
https://doi.org/10.15223/policy-045
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-a417t-44e005d46c2d837078023bd9c60959f76d84dd0f66f67242e2933c02bb08eb463
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0002-3157-5769
0000-0003-4986-9308
0000-0002-8406-4866
0000-0003-3446-0710
PMID 34826221
PQID 2604026278
PQPubID 23479
PageCount 8
ParticipantIDs proquest_miscellaneous_2604026278
pubmed_primary_34826221
crossref_citationtrail_10_1021_acs_inorgchem_1c01779
crossref_primary_10_1021_acs_inorgchem_1c01779
acs_journals_10_1021_acs_inorgchem_1c01779
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2021-12-20
PublicationDateYYYYMMDD 2021-12-20
PublicationDate_xml – month: 12
  year: 2021
  text: 2021-12-20
  day: 20
PublicationDecade 2020
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Inorganic chemistry
PublicationTitleAlternate Inorg. Chem
PublicationYear 2021
Publisher American Chemical Society
Publisher_xml – name: American Chemical Society
References ref9/cit9
ref45/cit45
ref6/cit6
ref36/cit36
ref3/cit3
ref27/cit27
ref18/cit18
ref11/cit11
ref25/cit25
ref16/cit16
ref29/cit29
ref32/cit32
ref23/cit23
ref39/cit39
ref14/cit14
ref8/cit8
ref5/cit5
ref31/cit31
ref2/cit2
ref43/cit43
ref34/cit34
ref37/cit37
ref28/cit28
ref40/cit40
ref20/cit20
ref17/cit17
ref10/cit10
ref26/cit26
ref35/cit35
ref19/cit19
ref21/cit21
ref12/cit12
ref15/cit15
ref42/cit42
ref46/cit46
ref41/cit41
ref22/cit22
ref13/cit13
ref33/cit33
ref4/cit4
ref30/cit30
ref47/cit47
ref1/cit1
ref24/cit24
ref38/cit38
ref44/cit44
ref7/cit7
References_xml – ident: ref11/cit11
  doi: 10.1016/0022-1902(78)80071-2
– ident: ref20/cit20
  doi: 10.1021/ja100714p
– ident: ref25/cit25
  doi: 10.1073/pnas.1904610116
– ident: ref36/cit36
  doi: 10.1073/pnas.1613628113
– ident: ref17/cit17
  doi: 10.1021/ja055064u
– ident: ref34/cit34
  doi: 10.1021/acs.analchem.7b05297
– ident: ref15/cit15
  doi: 10.1128/MCB.05722-11
– ident: ref14/cit14
  doi: 10.1038/s41589-018-0062-z
– ident: ref45/cit45
  doi: 10.1039/b901614g
– ident: ref19/cit19
  doi: 10.1007/s41048-020-00118-7
– ident: ref13/cit13
  doi: 10.1038/nchembio.2098
– ident: ref1/cit1
  doi: 10.1038/nrneurol.2010.180
– ident: ref39/cit39
  doi: 10.1039/C1CS15132K
– ident: ref24/cit24
  doi: 10.1039/C6MT00083E
– ident: ref29/cit29
  doi: 10.1016/0166-2236(88)90192-0
– ident: ref31/cit31
  doi: 10.1021/jacs.9b09181
– ident: ref35/cit35
  doi: 10.1073/pnas.1113729109
– ident: ref26/cit26
  doi: 10.1007/s11426-018-9424-8
– ident: ref10/cit10
  doi: 10.1073/pnas.1409796111
– ident: ref41/cit41
  doi: 10.1002/1522-2675(20001108)83:11<2926::AID-HLCA2926>3.0.CO;2-6
– ident: ref21/cit21
  doi: 10.1073/pnas.1900172116
– ident: ref30/cit30
  doi: 10.1039/C9SC01153F
– ident: ref46/cit46
  doi: 10.1074/jbc.M105361200
– ident: ref3/cit3
  doi: 10.1093/ajcn/88.3.855S
– ident: ref22/cit22
  doi: 10.1039/C7CC01430A
– ident: ref33/cit33
  doi: 10.1039/D0SC03037F
– ident: ref38/cit38
  doi: 10.1039/c2cs35363f
– ident: ref28/cit28
  doi: 10.1016/j.dyepig.2016.03.017
– ident: ref32/cit32
  doi: 10.1039/C3CC46262E
– ident: ref5/cit5
  doi: 10.1016/S0021-9258(18)83589-X
– ident: ref44/cit44
  doi: 10.1021/cr980446m
– ident: ref2/cit2
  doi: 10.1039/b711118p
– ident: ref27/cit27
  doi: 10.1016/j.ceb.2019.02.009
– ident: ref43/cit43
  doi: 10.1007/s00418-013-1123-8
– ident: ref16/cit16
  doi: 10.1073/pnas.0406547102
– ident: ref8/cit8
  doi: 10.1523/JNEUROSCI.3699-04.2005
– ident: ref18/cit18
  doi: 10.1021/ja907778b
– ident: ref6/cit6
  doi: 10.1038/nature09018
– ident: ref37/cit37
  doi: 10.1056/NEJMoa070613
– ident: ref7/cit7
  doi: 10.1038/nchembio.1913
– ident: ref9/cit9
  doi: 10.1073/pnas.1009932108
– ident: ref40/cit40
  doi: 10.1002/1521-3773(20010119)40:2<385::AID-ANIE385>3.0.CO;2-F
– ident: ref23/cit23
  doi: 10.1039/c3cc42069h
– ident: ref4/cit4
  doi: 10.1016/j.cbpa.2010.01.003
– ident: ref12/cit12
  doi: 10.1073/pnas.1111297109
– ident: ref42/cit42
  doi: 10.1016/j.jphotochem.2006.03.015
– ident: ref47/cit47
  doi: 10.1038/188150a0
SSID ssj0009346
Score 2.4475675
Snippet Specimen differences, tissue-dependent background fluorescence and scattering, and deviated specimen position and sensor concentration make optical imaging for...
SourceID proquest
pubmed
crossref
acs
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 18567
SubjectTerms Animals
Boron Compounds - chemistry
Copper - chemistry
Fluorescent Dyes - chemical synthesis
Fluorescent Dyes - chemistry
HEK293 Cells
Humans
Mice
Molecular Structure
Optical Imaging
Porphobilinogen - analogs & derivatives
Porphobilinogen - chemistry
Styrenes - chemistry
Title Tracking Labile Copper Fluctuation In Vivo/Ex Vivo: Design and Application of a Ratiometric Near-Infrared Fluorophore Derived from 4‑Aminostyrene-Conjugated Boron Dipyrromethene
URI http://dx.doi.org/10.1021/acs.inorgchem.1c01779
https://www.ncbi.nlm.nih.gov/pubmed/34826221
https://www.proquest.com/docview/2604026278
Volume 60
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3NbtQwELZKOcCl_NOlgIzECSm7a69jb7gtaVctggoBRb1F8Z8odJMo2SDoqa_QZ-GNeBJm8rMVQqvCKZElj-LMjGfsmfmGkOca6xnTaRiYVIlAqNQFWugw8Nx75rHBhcZ7yLeHcv9IvD4OjzfIaE0En7NRairwQWEEFrEYMgMipKJr5DqXoMjoC8UfLlF2J21lDp6JmJRRX7KzjgyaJFP9aZLW-JmNvZnfIu_6qp02zeTrsF7qoTn7G8TxX5dym2x1viedtcJyh2y47C65Efct3-6Rn2C5DN6d0zcIvOtonBeFK-n8tMY6E-QhPcjop5Nv-Wjve_N8SXebHBCaZpbOLqPhNPc0pe_xfYFNuww9BJ0KDjJfYso7kszLvPiclw4olLDnWoqlLlT8Or-YLeD7K7wfz1wQ59mXGi_7LH2FcAt096T4USLKAgI3uPvkaL73Md4Puq4OQSqYWgZCONB8K6ThFpF3FELQaRsZhL6LvJJ2Kqwdeym9VOBAOHBIJmbMtR5PnRZy8oBsZnnmtglVqYk040b7UAtmhDY-NMwZxOiT3tsBeQG_POm0skqagDtnCQ6u-JB0fBgQ0UtBYjp8dGzTcXrVtOFqWtEChFw14VkvYgmwF-MzaebyukrgaAmnecnVdEAetrK3IokYRJJz9uh_lrRDbnJMwWEcNsPHZHNZ1u4J-FBL_bTRm9-0XR3a
linkProvider American Chemical Society
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1Lj9MwELaW5bBceD_K00ickNKtXcdpuJXsVi10e4Bd2FsUv0Rh60RJi4ATf4Hfwj_ilzCTJq1AWq321MqSR3Zm7BnP4xtCXiisZ8wGYaCzSAQiymyghAoDx51jDhtcKPRDHs3k-ES8OQ1Pd4hsa2FgERVQquog_hZdgO3j2NzDKOxl0WUaJCmKr5CrYJBwlOxh8n4LtttfF-jg04hJGbeVO-eRQc2kq3810znmZq12RjfIx82C62yTL93VUnX1j_-wHC-_o5vkemOJ0uFadG6RHetvk72kbQB3h_wGPabRk06nCMNraZIXhS3p6GyFVSfIUTrx9MP8a75_-K3-fUUP6owQmnlDh9vYOM0dzeg7_L_AFl6azuCEBRPvSkyAR5J5mRef8tIChRJuYEOx8IWKPz9_DRew_gq95d4GSe4_r9D1Z-hrBF-gB_Pie4mYCwjjYO-Sk9HhcTIOmh4PQSZYtAyEsHAPGCE1N4jDEyEgnTKxRiC82EXSDIQxPSelkxGYExbMk77ucaV6A6uE7N8juz739gGhUaZjxbhWLlSCaaG0CzWzGhH7pHOmQ17CJ0-bM1qldfidsxQHN3xIGz50iGiFIdUNWjo27Ti7aFp3M61Yw4VcNOF5K2kpsBejNZm3-apK4aEJb3vJo0GH3F-L4IYkIhJJztnDy2zpGdkbHx9N0-lk9vYRucYxOYdxuCYfk91lubJPwLpaqqf1UfoLjokmOw
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1fb9MwELdgSLCX8X90_DMST0jpatdxGt5KumqFUSFgaBIPUfxP61idKGkQ8MRX4LPwjfgk3KVpJ5CmCZ4SOfLJju98Z9_d7wh5qjCfMRuEgc4iEYgos4ESKgwcd445LHCh8B7y9VTuH4qXR-FRG1WJuTAwiAooVY0TH6W6MK5FGGC72D7z8AXmM-8yDdwUxZfJFXTdIXcPk3dngLv9ZZIOHo-YlPEqe-c8MqiddPWndjrH5GxUz_g6-bgedBNx8qlbL1RXf_sLz_H_ZnWDbLUWKR0uWegmuWT9LXItWRWCu01-gj7TeKNODxCO19IkLwpb0vFpjdknuLJ04umH2ed8d-9L83xOR01kCM28ocMzHznNHc3oW3yfYykvTacgacHEuxID4ZFkXubFcV5aoFDCTmwoJsBQ8ev7j-Ecxl_hrbm3QZL7kxqvAA19gSAMdDQrvpaIvYBwDvYOORzvvU_2g7bWQ5AJFi0CISzsB0ZIzQ3i8UQITKdMrBEQL3aRNANhTM9J6WQEZoUFM6Wve1yp3sAqIft3yYbPvb1HaJTpWDGulQuVYFoo7ULNrEbkPumc6ZBn8MvTVlartHHDc5Zi43od0nYdOkSsGCLVLWo6Fu84vahbd92tWMKGXNThyYrbUlhe9Npk3uZ1lcKBE874kkeDDtlesuGaJCITSc7Zzr9M6TG5-mY0Tg8m01f3ySbHGB3GYbd8QDYWZW0fgpG1UI8aafoNxVoovg
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Tracking+Labile+Copper+Fluctuation+In+Vivo+%2F+Ex+Vivo+%3A+Design+and+Application+of+a+Ratiometric+Near-Infrared+Fluorophore+Derived+from+4-Aminostyrene-Conjugated+Boron+Dipyrromethene&rft.jtitle=Inorganic+chemistry&rft.au=Xu%2C+Hongxia&rft.au=Yao%2C+Shankun&rft.au=Chen%2C+Yuncong&rft.au=Zhang%2C+Changli&rft.date=2021-12-20&rft.eissn=1520-510X&rft.volume=60&rft.issue=24&rft.spage=18567&rft_id=info:doi/10.1021%2Facs.inorgchem.1c01779&rft_id=info%3Apmid%2F34826221&rft.externalDocID=34826221
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0020-1669&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0020-1669&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0020-1669&client=summon