An activatable NIR turn-on fluorescent probe for copper (II) ion and live cell imaging.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
17 Aug 2024
Historique:
received: 10 06 2024
accepted: 12 08 2024
medline: 18 8 2024
pubmed: 18 8 2024
entrez: 17 8 2024
Statut: epublish

Résumé

Herein we have reported a fluorescent probe (MB-M) based on MB derivative for Cu

Identifiants

pubmed: 39154101
doi: 10.1038/s41598-024-70052-y
pii: 10.1038/s41598-024-70052-y
doi:

Substances chimiques

Copper 789U1901C5
Fluorescent Dyes 0
Ions 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

19068

Subventions

Organisme : King Saud University
ID : RSP2024R243
Organisme : King Saud University
ID : RSP2024R243
Organisme : King Saud University
ID : RSP2024R243
Organisme : King Saud University
ID : RSP2024R243
Organisme : King Saud University
ID : RSP2024R243
Organisme : King Saud University
ID : RSP2024R243
Organisme : King Saud University
ID : RSP2024R243
Organisme : King Saud University
ID : RSP2024R243
Organisme : King Saud University
ID : RSP2024R243
Organisme : King Saud University
ID : RSP2024R243
Organisme : King Saud University
ID : RSP2024R243

Informations de copyright

© 2024. The Author(s).

Références

Song, J., Liu, Y., Wang, C., Xu, B. & Zhao, L. A dipeptide-derived dansyl fluorescent probe for the detection of Cu
doi: 10.1007/s10895-023-03274-4
Du, B., Li, Q., Huang, K. & Liang, L. A quinoline-fluoran hybrid fluorescent probe for selectively and sensitively sensing copper ions and fluorescence imaging application. J. Mol. Struct. 1271, 134015 (2023).
doi: 10.1016/j.molstruc.2022.134015
Sun, Y.-X. et al. A turn-off fluorescent probe for the detection of copper (II) ion based on a salicylaldehyde derivatives Schiff-base. J. Mol. Struct. 1291, 136069 (2023).
doi: 10.1016/j.molstruc.2023.136069
Li, S. et al. A novel “on− off− on” fluorescent probe with high selectivity for continuous identification of Cu
doi: 10.1016/j.molstruc.2024.137899
Said, A. I., Georgiev, N. I. & Bojinov, V. B. Simple excited state intramolecular proton transfer (ESIPT) based probe for pH and selective detection of copper (II) ion in aqueous alkaline environment: Sensitivity, selectivity and logic behavior. J. Photochem. Photobiol. A 446, 115176 (2024).
doi: 10.1016/j.jphotochem.2023.115176
Wang, H. et al. Fluorescent detection of copper ions with acylhydrazine-based probes: Effects of substitute and its position. Dyes Pigm. 197, 109954 (2022).
doi: 10.1016/j.dyepig.2021.109954
Xiao, W. et al. Construction of a novel flavonol fluorescent probe for copper (II) ion detection and its application in actual samples. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 314, 124175 (2024).
doi: 10.1016/j.saa.2024.124175
Tsvetkov, P. et al. Copper induces cell death by targeting lipoylated TCA cycle proteins. Science 375, 1254–1261 (2022).
pubmed: 35298263 pmcid: 9273333 doi: 10.1126/science.abf0529
Ilakiyalakshmi, M. & Napoleon, A. A. Phenothiazine appended thiophene derivative: A trilateral approach to copper ion detection in living cells and aqueous samples. RSC Adv. 14, 8885–8895 (2024).
pubmed: 38500619 pmcid: 10945519 doi: 10.1039/D3RA07608C
Prajapati, M., Pandey, N., Kalla, S., Bandaru, S. & Sivaiah, A. Synthesis and characterization of a rhodamine derivative as a selective switch-on fluorescent sensor for Cu
doi: 10.1039/D3SD00291H
Wechakorn, K. et al. A highly sensitive and selective rhodamine-semicarbazide based fluorescent sensor for Cu
pubmed: 38091746 doi: 10.1016/j.talanta.2023.125530
Arumugaperumal, R. et al. Facile rhodamine-based colorimetric sensors for sequential detections of Cu (II) ions and pyrophosphate (P 2 O 7 4−) anions. RSC Adv. 6, 106631–106640 (2016).
doi: 10.1039/C6RA24472F
Gerdan, Z., Saylan, Y. & Denizli, A. Recent advances of optical sensors for copper ion detection. Micromachines 13, 1298 (2022).
pubmed: 36014218 pmcid: 9413819 doi: 10.3390/mi13081298
Shellaiah, M. et al. An AIE active anthracene-based Schiff base probe for “turn-on” detection of Cu
doi: 10.1016/j.molstruc.2023.137347
Vaneev, A. N., Timoshenko, R. V., Gorelkin, P. V., Klyachko, N. L. & Erofeev, A. S. Recent advances in nanopore technology for copper detection and their potential applications. Nanomaterials 13, 1573 (2023).
pubmed: 37177118 pmcid: 10181076 doi: 10.3390/nano13091573
Zhu, H. et al. Dual-mode optical chemodosimeter for detecting copper ions in the environment, food, and living organisms with smartphone. Chem. Eng. J. 471, 144442 (2023).
doi: 10.1016/j.cej.2023.144442
Deng, L., Xue, L., Gao, Y., Fu, S. & Wang, H. A coumarin based ratiometric fluorescent probe for the detection of Cu
doi: 10.1016/j.saa.2023.123479
Liu, L. et al. Theory and experiment: The synthesis and drug application of “ON-OFF-ON” fluorescent probes for copper and biothiols detection. J. Pharm. Biomed. Anal. 239, 115876 (2024).
pubmed: 38039872 doi: 10.1016/j.jpba.2023.115876
Wang, J. et al. A cyclodextrin-based turn-off fluorescent probe for naked-eye detection of copper ions in aqueous solution. Spectrochim. Acta Part A: Mol. Biomol. Spectrosc. 287, 122069 (2023).
doi: 10.1016/j.saa.2022.122069
Zhang, T., Chi, H., Guo, J., Lu, X. & Li, G. Construction of a Cu
doi: 10.1007/s10895-024-03610-2 pubmed: 39141276
Ahmed, N., Zareen, W., Zhang, D., Yang, X. & Ye, Y. Coumarin-based reversible fluorescent probe for selective detection of Cu
pubmed: 32683577 doi: 10.1007/s10895-020-02585-0
Ahmed, N., Zareen, W., Zhang, D., Yang, X. & Ye, Y. Irreversible coumarin based fluorescent probe for selective detection of Cu
doi: 10.1016/j.saa.2021.120313
Ding, P. et al. A highly selective and sensitive probe for Cu
pubmed: 25491377 doi: 10.1007/s10895-014-1480-2
Li, S. et al. Synthesis and properties of a novel FRET-based ratiometric fluorescent sensor for Cu 2+. J. Fluoresc. 26, 769–774 (2016).
pubmed: 26781110 doi: 10.1007/s10895-016-1768-5
Li, S. et al. A novel solvent-dependently bifunctional NIR absorptive and fluorescent ratiometric probe for detecting Fe
doi: 10.1016/j.snb.2015.10.086
Tang, J. et al. Highly sensitive and fast responsive ratiometric fluorescent probe for Cu
doi: 10.1016/j.snb.2016.05.144
Ahmed, N., Zareen, W., Yang, X., Shafiq, Z. & Ye, Y. Development in fluorescent OFF–ON probes based on Cu
Huang, X. et al. A methylene blue-based near-infrared fluorescent probe for rapid detection of hypochlorite in tap water and living cells. RSC Adv. 8, 14603–14608 (2018).
pubmed: 35540781 pmcid: 9079930 doi: 10.1039/C8RA01037D
Li, S. et al. Methylene blue-based near-infrared activatable probes for bioimaging. Dyes Pigm. 211, 111083 (2023).
doi: 10.1016/j.dyepig.2023.111083
Wei, H.-G., Liu, Y.-J. & Zhao, X.-D. Methylene blue-based 7-nitro-1, 2, 3-benzoxadiazole NIR fluorescent probe triggered by H2S. Bioorg. Med. Chem. Lett. 30, 127221 (2020).
pubmed: 32386977 doi: 10.1016/j.bmcl.2020.127221
Chang, I. J., Choi, M. G., Jeong, Y. A., Lee, S. H. & Chang, S.-K. Colorimetric determination of Cu
doi: 10.1016/j.tetlet.2016.12.066
Jiang, Q. et al. A nopinone based multi-functional probe for colorimetric detection of Cu
pubmed: 31793618 doi: 10.1039/c9pp00297a
Wang, Y. et al. A coumarin-containing Schiff base fluorescent probe with AIE effect for the copper (II) ion. RSC Adv. 10, 6109–6113 (2020).
pubmed: 35497414 pmcid: 9049598 doi: 10.1039/C9RA10632D
Zhu, D. et al. A novel ratiometric fluorescent probe for sensitive and selective detection of Cu2+ based on Boranil derivatives. Inorg. Chim. Acta 524, 120438 (2021).
doi: 10.1016/j.ica.2021.120438
Frisch, M. et al. Gaussian 09, revision B. 01, Gaussian Inc, Wallingford CT, 2209 Search PubMed;(b) NM O’Boyle AL Tenderholt and KM Langner. J. Comput. Chem. 29(2008), 839 (2009).
Sarikaya, E. K., Dereli, Ö. & Bahçeli, S. A comparative study of DFT/B3LYP/6–31G (d, p), RM062X/6–31G (d, p), B3LYP/6–311++ G (d, p) and HSEH1PBE/6–31G (d, p) methods applied to molecular geometry and electronic properties of Cs-C60Cl6 molecule. Adıyaman Univ. J. Sci. 11, 456–473 (2021).
Lu, T. & Chen, F. Multiwfn: A multifunctional wavefunction analyzer. J. Comput. Chem. 33, 580–592 (2012).
pubmed: 22162017 doi: 10.1002/jcc.22885
Humphrey, W., Dalke, A. & Schulten, K. VMD: Visual molecular dynamics. J. Mol. Graph. 14, 33–38 (1996).
pubmed: 8744570 doi: 10.1016/0263-7855(96)00018-5
Wick, C. R. & Clark, T. On bond-critical points in QTAIM and weak interactions. J. Mol. Model. 24, 1–9 (2018).
doi: 10.1007/s00894-018-3684-x
Alzahrani, A. Y. A. et al. Theoretical and experimental studies on mechanochromic triphenylamine based fluorescent “ON-OFF-ON” sensor for sequential detection of Fe3+ and deferasirox. Spectrochim. Acta Part A: Mol. Biomol. Spectrosc. 297, 122745 (2023).
doi: 10.1016/j.saa.2023.122745
Khaliq, F. et al. Surface functionalization of Si6Li6 cluster with superalkalis to achieve high nonlinear optical response: A DFT study. Colloids Surfaces A: Physicochem. Eng. Aspects 653, 129985 (2022).
doi: 10.1016/j.colsurfa.2022.129985
Bader, R., Nguyen-Dang, T. & Tal, Y. A topological theory of molecular structure. Rep. Progr. Phys. 44, 893 (1981).
doi: 10.1088/0034-4885/44/8/002
Basha, F., Khan, F. L. A., Muthu, S. & Raja, M. Computational evaluation on molecular structure (Monomer, Dimer), RDG, ELF, electronic (HOMO-LUMO, MEP) properties, and spectroscopic profiling of 8-Quinolinesulfonamide with molecular docking studies. Comput. Theor. Chem. 1198, 113169 (2021).
doi: 10.1016/j.comptc.2021.113169
Khan, S., Sajid, H., Ayub, K. & Mahmood, T. Adsorption behaviour of chronic blistering agents on graphdiyne; excellent correlation among SAPT, reduced density gradient (RDG) and QTAIM analyses. J. Mol. Liq. 316, 113860 (2020).
doi: 10.1016/j.molliq.2020.113860
Du, J., Sun, X. & Jiang, G. Exploring the interaction natures in plutonyl (VI) complexes with topological analyses of electron density. Int. J. Mol. Sci. 17, 414 (2016).
pubmed: 27077844 pmcid: 4848887 doi: 10.3390/ijms17040414
Ali, A. et al. Efficient synthesis SC-XRD, and theoretical studies of O-Benzenesulfonylated pyrimidines: Role of noncovalent interaction influence in their supramolecular network. ACS Omega 5(15115), 15128 (2020).
Gui, Y. et al. The sensing mechanism of N-doped SWCNTs toward SF6 decomposition products: A first-principle study. Appl. Surface Sci. 440, 846–852 (2018).
doi: 10.1016/j.apsusc.2018.01.247

Auteurs

Nadeem Ahmed (N)

College of Chemistry, Zhengzhou University, Zhengzhou, 450001, China.

Jianfei Liu (J)

College of Chemistry, Zhengzhou University, Zhengzhou, 450001, China.

Xiujuan Xu (X)

College of Chemistry, Zhengzhou University, Zhengzhou, 450001, China.

Ajaz Hussain (A)

Institute of Chemical Sciences, Bahauddin Zakariya University, Multan, 60800, Pakistan.

Aleena Mustafai (A)

Institute of Chemical Sciences, Bahauddin Zakariya University, Multan, 60800, Pakistan.

Muhammad Yar (M)

Department of Physiology and Biochemistry, Cholistan University of Veterinary and Anifmal Sciences, Bahawalpur, 63100, Pakistan.

Khurshid Ayub (K)

Department of Chemistry, COMSATS University, Abbottabad, 22060, Pakistan.

Asma A Alothman (AA)

Department of Chemistry, College of Science, King Saud University, 11451, Riyadh, Saudi Arabia.

Saikh Mohammad (S)

Department of Chemistry, College of Science, King Saud University, 11451, Riyadh, Saudi Arabia.

Yong Ye (Y)

College of Chemistry, Zhengzhou University, Zhengzhou, 450001, China. yeyong03@tsinghua.org.cn.

Zahid Shafiq (Z)

Institute of Chemical Sciences, Bahauddin Zakariya University, Multan, 60800, Pakistan. zahidshafiq@bzu.edu.pk.

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