Near-infrared fluorescent probes based on naphthyridine derivatives for mitochondrial nucleic acid imaging
Most current nucleic acid-responsive fluorescent probes are enhanced ones with short emission wavelengths. Therefore, the development of novel near-infrared, turn-on response nucleic acid fluorescent probes is of great significance. Herein, three cationic fluorescent dyes 1a-1c were synthesized by r...
Saved in:
Published in | Analyst (London) Vol. 15; no. 4; pp. 642 - 649 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
10.02.2025
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Most current nucleic acid-responsive fluorescent probes are enhanced ones with short emission wavelengths. Therefore, the development of novel near-infrared, turn-on response nucleic acid fluorescent probes is of great significance. Herein, three cationic fluorescent dyes
1a-1c
were synthesized by reacting naphthalidine salt with suitable aldehydes. These probes exhibited excellent photostability, maintaining over 95% of their absorption rate after 5 h of irradiation. Notably, probes
1a-1c
exhibited an OFF-ON fluorescence response to DNA and RNA. The maximum emission wavelength could reach the near-infrared region (661-762 nm), with large Stokes shifts (153-222 nm) upon binding to DNA/RNA. The fluorescence intensity was enhanced 143 fold and 127 fold for
1b
upon interaction with DNA and RNA, respectively. Co-staining and nucleic acid digestion assays showed that probes
1a-1c
could target the mitochondria of fixed cells with low cytotoxicity. These findings may be useful for the early screening of genetic mutations related to mitochondrial diseases.
Fluorescent probes based on naphthyridinium salt derivatives exhibit OFF-ON fluorescence response to DNA/RNA. |
---|---|
AbstractList | Most current nucleic acid-responsive fluorescent probes are enhanced ones with short emission wavelengths. Therefore, the development of novel near-infrared, turn-on response nucleic acid fluorescent probes is of great significance. Herein, three cationic fluorescent dyes 1a-1c were synthesized by reacting naphthalidine salt with suitable aldehydes. These probes exhibited excellent photostability, maintaining over 95% of their absorption rate after 5 h of irradiation. Notably, probes 1a-1c exhibited an OFF-ON fluorescence response to DNA and RNA. The maximum emission wavelength could reach the near-infrared region (661-762 nm), with large Stokes shifts (153-222 nm) upon binding to DNA/RNA. The fluorescence intensity was enhanced 143 fold and 127 fold for 1b upon interaction with DNA and RNA, respectively. Co-staining and nucleic acid digestion assays showed that probes 1a-1c could target the mitochondria of fixed cells with low cytotoxicity. These findings may be useful for the early screening of genetic mutations related to mitochondrial diseases. Most current nucleic acid-responsive fluorescent probes are enhanced ones with short emission wavelengths. Therefore, the development of novel near-infrared, turn-on response nucleic acid fluorescent probes is of great significance. Herein, three cationic fluorescent dyes 1a-1c were synthesized by reacting naphthalidine salt with suitable aldehydes. These probes exhibited excellent photostability, maintaining over 95% of their absorption rate after 5 h of irradiation. Notably, probes 1a-1c exhibited an OFF-ON fluorescence response to DNA and RNA. The maximum emission wavelength could reach the near-infrared region (661-762 nm), with large Stokes shifts (153-222 nm) upon binding to DNA/RNA. The fluorescence intensity was enhanced 143 fold and 127 fold for 1b upon interaction with DNA and RNA, respectively. Co-staining and nucleic acid digestion assays showed that probes 1a-1c could target the mitochondria of fixed cells with low cytotoxicity. These findings may be useful for the early screening of genetic mutations related to mitochondrial diseases.Most current nucleic acid-responsive fluorescent probes are enhanced ones with short emission wavelengths. Therefore, the development of novel near-infrared, turn-on response nucleic acid fluorescent probes is of great significance. Herein, three cationic fluorescent dyes 1a-1c were synthesized by reacting naphthalidine salt with suitable aldehydes. These probes exhibited excellent photostability, maintaining over 95% of their absorption rate after 5 h of irradiation. Notably, probes 1a-1c exhibited an OFF-ON fluorescence response to DNA and RNA. The maximum emission wavelength could reach the near-infrared region (661-762 nm), with large Stokes shifts (153-222 nm) upon binding to DNA/RNA. The fluorescence intensity was enhanced 143 fold and 127 fold for 1b upon interaction with DNA and RNA, respectively. Co-staining and nucleic acid digestion assays showed that probes 1a-1c could target the mitochondria of fixed cells with low cytotoxicity. These findings may be useful for the early screening of genetic mutations related to mitochondrial diseases. Most current nucleic acid-responsive fluorescent probes are enhanced ones with short emission wavelengths. Therefore, the development of novel near-infrared, turn-on response nucleic acid fluorescent probes is of great significance. Herein, three cationic fluorescent dyes 1a-1c were synthesized by reacting naphthalidine salt with suitable aldehydes. These probes exhibited excellent photostability, maintaining over 95% of their absorption rate after 5 h of irradiation. Notably, probes 1a-1c exhibited an OFF-ON fluorescence response to DNA and RNA. The maximum emission wavelength could reach the near-infrared region (661-762 nm), with large Stokes shifts (153-222 nm) upon binding to DNA/RNA. The fluorescence intensity was enhanced 143 fold and 127 fold for 1b upon interaction with DNA and RNA, respectively. Co-staining and nucleic acid digestion assays showed that probes 1a-1c could target the mitochondria of fixed cells with low cytotoxicity. These findings may be useful for the early screening of genetic mutations related to mitochondrial diseases. Fluorescent probes based on naphthyridinium salt derivatives exhibit OFF-ON fluorescence response to DNA/RNA. |
Author | Ni, Wen-Pei Ma, Huan Lin, Qi Sun, Ru Ge, Jian-Feng |
AuthorAffiliation | Chemical Engineering and Material Science Suzhou Institute of Biomedical Engineering and Technology College of Chemistry Jiangsu Key Laboratory of Medical Optics Soochow University Chinese Academy of Science |
AuthorAffiliation_xml | – name: Jiangsu Key Laboratory of Medical Optics – name: Soochow University – name: College of Chemistry – name: Chemical Engineering and Material Science – name: Suzhou Institute of Biomedical Engineering and Technology – name: Chinese Academy of Science |
Author_xml | – sequence: 1 givenname: Huan surname: Ma fullname: Ma, Huan – sequence: 2 givenname: Wen-Pei surname: Ni fullname: Ni, Wen-Pei – sequence: 3 givenname: Qi surname: Lin fullname: Lin, Qi – sequence: 4 givenname: Ru surname: Sun fullname: Sun, Ru – sequence: 5 givenname: Jian-Feng surname: Ge fullname: Ge, Jian-Feng |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39829413$$D View this record in MEDLINE/PubMed |
BookMark | eNpd0c1LHDEYBvAgiq62F-9KwEsRxuZzZnNcbauC6KU9D_l442aZTdZkRvC_b9r1AzyFl_wI75PnEO3GFAGhY0ouKOHquxM6EiokMTtoRnkrGinZfBfNCCG8Ya0UB-iwlFUdKZFkHx1wNWdKUD5Dq3vQuQnRZ53BYT9MKUOxEEe8yclAwUaXepEijnqzHJcvObgQATvI4VmP4bkSnzJehzHZZYouBz3gONkBgsXaBofDWj-G-PgF7Xk9FPj6eh6hP79-_r66ae4erm-vFneNZaodG6OpbaXStrWezDlliinQYJy1naSG8hrKAAgGhhEhHGOGeGcV7yh03nf8CH3bvlsDPE1Qxn4daqJh0BHSVHpOZSclaQmt9OwTXaUpx7pdVa1QrOsUq-r0VU1mDa7f5Joov_Rvv1jB-RbYnErJ4N8JJf2_ivofYnH_v6LLik-2OBf77j4q5H8BjweN7Q |
Cites_doi | 10.1021/acs.analchem.3c05629 10.1016/j.dyepig.2020.108222 10.1038/s42004-020-00362-5 10.1093/nar/gkv875 10.1039/D2OB01095J 10.1039/D2AN00547F 10.1039/C8QO00236C 10.3390/bios13070734 10.1021/ac101329h 10.1002/ijch.202400024 10.1016/j.dyepig.2016.11.041 10.1039/D2CC00668E 10.1002/anie.201007386 10.1002/cbdv.202101030 10.3389/fcell.2022.796066 10.1016/j.fitote.2021.104863 10.1002/anie.202320179 10.1002/chem.200902823 10.1016/j.saa.2019.117865 10.1016/j.jphotochem.2016.05.009 10.3389/fcell.2021.669379 10.1007/s10439-022-03051-7 10.1016/j.jphotochem.2022.114287 10.1021/acssensors.9b00464 10.1021/acs.chemrev.1c00241 10.1016/j.bmcl.2014.02.071 10.1016/j.jconrel.2020.03.011 10.1016/j.trac.2023.117272 10.1016/j.saa.2023.123216 |
ContentType | Journal Article |
Copyright | Copyright Royal Society of Chemistry 2025 |
Copyright_xml | – notice: Copyright Royal Society of Chemistry 2025 |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7SR 7U5 8BQ 8FD JG9 L7M 7X8 |
DOI | 10.1039/d4an01450b |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Engineered Materials Abstracts Solid State and Superconductivity Abstracts METADEX Technology Research Database Materials Research Database Advanced Technologies Database with Aerospace MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Materials Research Database Engineered Materials Abstracts Solid State and Superconductivity Abstracts Technology Research Database Advanced Technologies Database with Aerospace METADEX MEDLINE - Academic |
DatabaseTitleList | MEDLINE CrossRef MEDLINE - Academic Materials Research Database |
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 | 1364-5528 |
EndPage | 649 |
ExternalDocumentID | 39829413 10_1039_D4AN01450B d4an01450b |
Genre | Journal Article |
GroupedDBID | --- -~X .HR 0-7 0R~ 23M 4.4 5RE 705 70~ 7~J AAEMU AAIWI AAJAE AANOJ AAWGC AAXHV AAXPP ABASK ABDVN ABEMK ABJNI ABOCM ABPDG ABRYZ ABXOH ACGFS ACIWK ACLDK ADMRA ADSRN AEFDR AENEX AENGV AESAV AETIL AFLYV AFOGI AFRZK AFVBQ AGEGJ AGRSR AHGCF AKMSF ALMA_UNASSIGNED_HOLDINGS ANUXI APEMP ASKNT AUDPV AZFZN BLAPV BSQNT C6K COF CS3 EBS ECGLT EE0 EF- F5P GGIMP GNO HZ~ H~N IDZ J3I M4U N9A O9- P2P R56 R7B R7E RAOCF RCNCU RPMJG RRA RRC RSCEA SKM SKR SKZ SLC SLF TN5 UPT VH6 WH7 ~02 .GJ 0UZ 186 1TJ 2WC 3EH 3O- 53G 71~ AAMEH AAYXX ACHDF ACRPL ADNMO ADXHL AFFNX AGKEF AGQPQ AHGXI AIDUJ ALSGL ANBJS ANLMG AQHUZ ASPBG AVWKF BBWZM C1A CAG CITATION EEHRC EJD H13 IDY J3G J3H L-8 LPU MVM NDZJH RCLXC RIG RNS ROL RRXOS SC5 SLH XOL XXG ZCG ZKB ZXP CGR CUY CVF ECM EIF NPM 7SR 7U5 8BQ 8FD JG9 L7M 7X8 |
ID | FETCH-LOGICAL-c296t-ba1c659ac6cf08312929eaebdcc751b13003bee42eb2044d22b0fdc9371e7ff73 |
ISSN | 0003-2654 1364-5528 |
IngestDate | Fri Jul 11 15:54:40 EDT 2025 Mon Jun 30 12:44:16 EDT 2025 Mon Jul 21 05:33:52 EDT 2025 Tue Jul 01 01:57:23 EDT 2025 Tue May 27 12:02:03 EDT 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 4 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c296t-ba1c659ac6cf08312929eaebdcc751b13003bee42eb2044d22b0fdc9371e7ff73 |
Notes | https://doi.org/10.1039/d4an01450b Electronic supplementary information (ESI) available. See DOI ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0002-5660-2209 0000-0003-2479-7600 |
PMID | 39829413 |
PQID | 3164927792 |
PQPubID | 2047505 |
PageCount | 8 |
ParticipantIDs | proquest_journals_3164927792 pubmed_primary_39829413 rsc_primary_d4an01450b crossref_primary_10_1039_D4AN01450B proquest_miscellaneous_3157550601 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2025-02-10 |
PublicationDateYYYYMMDD | 2025-02-10 |
PublicationDate_xml | – month: 02 year: 2025 text: 2025-02-10 day: 10 |
PublicationDecade | 2020 |
PublicationPlace | England |
PublicationPlace_xml | – name: England – name: London |
PublicationTitle | Analyst (London) |
PublicationTitleAlternate | Analyst |
PublicationYear | 2025 |
Publisher | Royal Society of Chemistry |
Publisher_xml | – name: Royal Society of Chemistry |
References | Xu (D4AN01450B/cit28/1) 2021; 150 Xu (D4AN01450B/cit19/1) 2014; 24 Zhang (D4AN01450B/cit22/1) 2022; 147 Prunkl (D4AN01450B/cit12/1) 2010; 16 Filho (D4AN01450B/cit29/1) 2023; 435 Rong (D4AN01450B/cit9/1) 2021; 9 Peng (D4AN01450B/cit11/1) 2011; 50 Bosch (D4AN01450B/cit13/1) 2017; 138 Shi (D4AN01450B/cit3/1) 2024; 63 Luo (D4AN01450B/cit4/1) 2024; 64 Wang (D4AN01450B/cit21/1) 2023; 303 Chowdhury (D4AN01450B/cit10/1) 2022; 10 Bosch (D4AN01450B/cit15/1) 2018; 5 Narayanaswamy (D4AN01450B/cit25/1) 2015; 43 Mikhailov (D4AN01450B/cit7/1) 2024; 52 Sun (D4AN01450B/cit27/1) 2023; 167 Cao (D4AN01450B/cit18/1) 2019; 4 Li (D4AN01450B/cit23/1) 2022; 58 Domljanovic (D4AN01450B/cit2/1) 2020; 3 Wei (D4AN01450B/cit6/1) 2020; 229 You (D4AN01450B/cit16/1) 2020; 176 Li (D4AN01450B/cit1/1) 2021; 121 Zhang (D4AN01450B/cit8/1) 2020; 322 Wang (D4AN01450B/cit20/1) 2024; 96 Efimova (D4AN01450B/cit5/1) 2023; 13 Kang (D4AN01450B/cit24/1) 2022; 19 Rurack (D4AN01450B/cit17/1) 2011; 83 Peng (D4AN01450B/cit14/1) 2022; 20 Margar (D4AN01450B/cit26/1) 2016; 327 |
References_xml | – volume: 96 start-page: 9808 year: 2024 ident: D4AN01450B/cit20/1 publication-title: Anal. Chem. doi: 10.1021/acs.analchem.3c05629 – volume: 176 start-page: 108222 year: 2020 ident: D4AN01450B/cit16/1 publication-title: Dyes Pigm. doi: 10.1016/j.dyepig.2020.108222 – volume: 3 start-page: 111 year: 2020 ident: D4AN01450B/cit2/1 publication-title: Commun. Chem. doi: 10.1038/s42004-020-00362-5 – volume: 43 start-page: 8651 year: 2015 ident: D4AN01450B/cit25/1 publication-title: Nucleic Acids Res. doi: 10.1093/nar/gkv875 – volume: 20 start-page: 5558 year: 2022 ident: D4AN01450B/cit14/1 publication-title: Org. Biomol. Chem. doi: 10.1039/D2OB01095J – volume: 147 start-page: 2470 year: 2022 ident: D4AN01450B/cit22/1 publication-title: Analyst doi: 10.1039/D2AN00547F – volume: 5 start-page: 1916 year: 2018 ident: D4AN01450B/cit15/1 publication-title: Org. Chem. Front. doi: 10.1039/C8QO00236C – volume: 13 start-page: 734 year: 2023 ident: D4AN01450B/cit5/1 publication-title: Biosensors doi: 10.3390/bios13070734 – volume: 83 start-page: 1232 year: 2011 ident: D4AN01450B/cit17/1 publication-title: Anal. Chem. doi: 10.1021/ac101329h – volume: 64 start-page: e202400024 year: 2024 ident: D4AN01450B/cit4/1 publication-title: Isr. J. Chem. doi: 10.1002/ijch.202400024 – volume: 138 start-page: 135 year: 2017 ident: D4AN01450B/cit13/1 publication-title: Dyes Pigm. doi: 10.1016/j.dyepig.2016.11.041 – volume: 58 start-page: 4881 year: 2022 ident: D4AN01450B/cit23/1 publication-title: Chem. Commun. doi: 10.1039/D2CC00668E – volume: 50 start-page: 4180 year: 2011 ident: D4AN01450B/cit11/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201007386 – volume: 19 start-page: e202101030 year: 2022 ident: D4AN01450B/cit24/1 publication-title: Chem. Biodivers. doi: 10.1002/cbdv.202101030 – volume: 10 start-page: 796066 year: 2022 ident: D4AN01450B/cit10/1 publication-title: Front. Cell Dev. Biol. doi: 10.3389/fcell.2022.796066 – volume: 150 start-page: 104863 year: 2021 ident: D4AN01450B/cit28/1 publication-title: Fitoterapia doi: 10.1016/j.fitote.2021.104863 – volume: 63 start-page: 202320179 year: 2024 ident: D4AN01450B/cit3/1 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.202320179 – volume: 16 start-page: 3392 year: 2010 ident: D4AN01450B/cit12/1 publication-title: Chem. – Eur. J. doi: 10.1002/chem.200902823 – volume: 229 start-page: 117865 year: 2020 ident: D4AN01450B/cit6/1 publication-title: Spectrochim. Acta, Part A doi: 10.1016/j.saa.2019.117865 – volume: 327 start-page: 58 year: 2016 ident: D4AN01450B/cit26/1 publication-title: J. Photochem. Photobiol., A doi: 10.1016/j.jphotochem.2016.05.009 – volume: 9 start-page: 669379 year: 2021 ident: D4AN01450B/cit9/1 publication-title: Front. Cell Dev. Biol. doi: 10.3389/fcell.2021.669379 – volume: 52 start-page: 2627 year: 2024 ident: D4AN01450B/cit7/1 publication-title: Ann. Biomed. Eng. doi: 10.1007/s10439-022-03051-7 – volume: 435 start-page: 114287 year: 2023 ident: D4AN01450B/cit29/1 publication-title: J. Photochem. Photobiol., A doi: 10.1016/j.jphotochem.2022.114287 – volume: 4 start-page: 1409 year: 2019 ident: D4AN01450B/cit18/1 publication-title: ACS Sens. doi: 10.1021/acssensors.9b00464 – volume: 121 start-page: 10469 year: 2021 ident: D4AN01450B/cit1/1 publication-title: Chem. Rev. doi: 10.1021/acs.chemrev.1c00241 – volume: 24 start-page: 1654 year: 2014 ident: D4AN01450B/cit19/1 publication-title: Bioorg. Med. Chem. Lett. doi: 10.1016/j.bmcl.2014.02.071 – volume: 322 start-page: 157 year: 2020 ident: D4AN01450B/cit8/1 publication-title: J. Controlled Release doi: 10.1016/j.jconrel.2020.03.011 – volume: 167 start-page: 117272 year: 2023 ident: D4AN01450B/cit27/1 publication-title: TrAC, Trends Anal. Chem. doi: 10.1016/j.trac.2023.117272 – volume: 303 start-page: 123216 year: 2023 ident: D4AN01450B/cit21/1 publication-title: Spectrochim. Acta, Part A doi: 10.1016/j.saa.2023.123216 |
SSID | ssj0001050 |
Score | 2.4508064 |
Snippet | Most current nucleic acid-responsive fluorescent probes are enhanced ones with short emission wavelengths. Therefore, the development of novel near-infrared,... |
SourceID | proquest pubmed crossref rsc |
SourceType | Aggregation Database Index Database Publisher |
StartPage | 642 |
SubjectTerms | Acid digestion Aldehydes Deoxyribonucleic acid DNA DNA - chemistry DNA, Mitochondrial - analysis DNA, Mitochondrial - chemistry Emission Fluorescent dyes Fluorescent Dyes - chemical synthesis Fluorescent Dyes - chemistry Fluorescent Dyes - radiation effects Fluorescent Dyes - toxicity Fluorescent indicators HeLa Cells Humans Infrared imaging Mitochondria - metabolism Naphthyridines - chemical synthesis Naphthyridines - chemistry Naphthyridines - radiation effects Naphthyridines - toxicity Near infrared radiation Nucleic acids Optical Imaging - methods Ribonucleic acid RNA RNA - analysis RNA - chemistry RNA - metabolism Spectrometry, Fluorescence |
Title | Near-infrared fluorescent probes based on naphthyridine derivatives for mitochondrial nucleic acid imaging |
URI | https://www.ncbi.nlm.nih.gov/pubmed/39829413 https://www.proquest.com/docview/3164927792 https://www.proquest.com/docview/3157550601 |
Volume | 15 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lj9MwELage4AL4rUQWJAR3Kosqe04-FiWRQWxFYiu2FvlV0QR666yCQd-PWM7r2pBAi5RZbdp5PkyD3vmG4ReGJ0ZAK_feishQOEznorCqFTk1hglCFgZX5x8suSLU_b-LD8bak9CdUmtDvXP39aV_I9UYQzk6qtk_0Gy_U1hAD6DfOEKEobrX8l4CTBN4UZVyCIvvzfbKrIz-bQrZS-n3kYZfx7g5MVXEEm1Md6rNPBwPwLjd2BjmJ7Daw1q0JnQwsN5imNP46o3Zro5D22Mxj5s5DGpx81A-t2Ek-CLLpoBc8uQLvDFuvSj3fTpP5G54FM_8LmJewHNeBeChKruNh-106w0JTwSQh_aqEwpZ2met8XfnbbNR6hiI9XJI8tWa4V5JDK9ouAz6vlRDZPOn4dmajBjfXLhMHkd7RGIHsgE7c2PV-8-9CYanMqsa6XoH7rjraXi5fDrXU_lSvgBzkjVNYkJzsjqNrrVRhF4HiFxB12z7i66cdQ177uHvu1AA4-ggSM0cIAG3jq8Aw08ggYGaOAdaOAWGthDA7fQuI9O3x6vjhZp21Yj1UTwOlVypnkupOa69H3mCHjIVlpltC7ymfLnm1RZy4hVJGPMEKKy0mhPnGiLsizoPpq4rbMPES4NtSbPpZAsZ5aWKpOADQi5KZG2oDRBz7slXF9E9pR1yHqgYv2GzZdhoV8n6KBb3XX7dl2uKcTxAqQnSIKe9dOwiv5ASzq7bfx3INjwDJmzBD2IUun_hopXRICHlqB9EFM_PIj30Z8mHqObA8IP0KSuGvsEPM9aPW1x9AtfNoXU |
linkProvider | Royal Society of Chemistry |
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=Near-infrared+fluorescent+probes+based+on+naphthyridine+derivatives+for+mitochondrial+nucleic+acid+imaging&rft.jtitle=Analyst+%28London%29&rft.au=Ma%2C+Huan&rft.au=Ni%2C+Wen-Pei&rft.au=Lin%2C+Qi&rft.au=Sun%2C+Ru&rft.date=2025-02-10&rft.issn=0003-2654&rft.eissn=1364-5528&rft.volume=15&rft.issue=4&rft.spage=642&rft.epage=649&rft_id=info:doi/10.1039%2Fd4an01450b&rft.externalDocID=d4an01450b |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0003-2654&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0003-2654&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0003-2654&client=summon |