TY - JOUR
T1 - Near-infrared pH responsive heptamethine cyanine platforms
T2 - Modulating the proton acceptor
AU - Kurutos, Atanas
AU - Shindo, Yutaka
AU - Hiruta, Yuki
AU - Oka, Kotaro
AU - Citterio, Daniel
N1 - Funding Information:
This study was supported by a Grant-in-Aid for the Japan Society for the Promotion of Science (JSPS) Postdoctoral Fellows (Grant No. 18F18767 ) to A.K. and D.C., Grant-in-Aid for Research Activity -Career Scientists (Grant No. 19K16339 ) to Y.H. from the Japan Society for the Promotion of Science (JSPS) , and AMED under Grant Number JP20lm0203012 to Y.H.
Funding Information:
This study was supported by a Grant-in-Aid for the Japan Society for the Promotion of Science (JSPS) Postdoctoral Fellows (Grant No. 18F18767) to A.K. and D.C. Grant-in-Aid for Research Activity-Career Scientists (Grant No. 19K16339) to Y.H. from the Japan Society for the Promotion of Science (JSPS), and AMED under Grant Number JP20lm0203012 to Y.H.
Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/10
Y1 - 2020/10
N2 - In this report, we wish to present the rational design, synthesis, and study of optical characteristics of near-infrared (NIR) molecular probes emitting over 800 nm. The title pH sensing platforms consist of a piperazine moiety serving as a hydronium ion receptor, coupled with a rigidified symmetric heptamethine backbone. The spectrally fine-tuned response of the fluorophores was studied in both organic solvents and aqueous buffer solutions, employing combined UV–Vis and steady state fluorimetric techniques. In parallel, computational approach and optical spectroscopy were employed aiming to ascribe the origin of spectral behavior of the amino-substituted heptamethines. Herein, we also investigated the halochromic effect of the differently substituted piperazines on the spectral properties of the NIR cyanine dyes. Under acidic conditions, the protonation of the piperazine moiety promoted a gradual bathochromic shift in the absorption spectra. The Δλ between the neutral and the protonated forms are indirectly related to the modifications applied to the proton acceptor. The calculated pKa values (5.13–7.06) were found to be dependent on the dye chemical structure. A good linear correlation was established between the pKa of the newly synthesized dyes and that of the reported piperazine moieties. This aspect allows the future expansion of the current facile strategy since sensing chromophores with predicted pH response could readily be designed based on pKa databases for substituted piperazine derivatives. A detailed literature study along with NMR and computational methods were found to be in agreement with our assumption, that both nitrogen atoms of the 1,4-disubstituted amine are involved in the sensing process. The covered pKa range allows us to recommend the title fluorophores as promising potential candidates for qualitative analysis of biological samples. A cytotoxicity study by the MTT assay showed that the NIR dyes are safe and applicable for bioanalytical purposes at dye concentrations up to 10 μM. Fluorescence imaging and cellular applications, including staining and visualization of HeLa cervical cancer cells was successfully demonstrated.
AB - In this report, we wish to present the rational design, synthesis, and study of optical characteristics of near-infrared (NIR) molecular probes emitting over 800 nm. The title pH sensing platforms consist of a piperazine moiety serving as a hydronium ion receptor, coupled with a rigidified symmetric heptamethine backbone. The spectrally fine-tuned response of the fluorophores was studied in both organic solvents and aqueous buffer solutions, employing combined UV–Vis and steady state fluorimetric techniques. In parallel, computational approach and optical spectroscopy were employed aiming to ascribe the origin of spectral behavior of the amino-substituted heptamethines. Herein, we also investigated the halochromic effect of the differently substituted piperazines on the spectral properties of the NIR cyanine dyes. Under acidic conditions, the protonation of the piperazine moiety promoted a gradual bathochromic shift in the absorption spectra. The Δλ between the neutral and the protonated forms are indirectly related to the modifications applied to the proton acceptor. The calculated pKa values (5.13–7.06) were found to be dependent on the dye chemical structure. A good linear correlation was established between the pKa of the newly synthesized dyes and that of the reported piperazine moieties. This aspect allows the future expansion of the current facile strategy since sensing chromophores with predicted pH response could readily be designed based on pKa databases for substituted piperazine derivatives. A detailed literature study along with NMR and computational methods were found to be in agreement with our assumption, that both nitrogen atoms of the 1,4-disubstituted amine are involved in the sensing process. The covered pKa range allows us to recommend the title fluorophores as promising potential candidates for qualitative analysis of biological samples. A cytotoxicity study by the MTT assay showed that the NIR dyes are safe and applicable for bioanalytical purposes at dye concentrations up to 10 μM. Fluorescence imaging and cellular applications, including staining and visualization of HeLa cervical cancer cells was successfully demonstrated.
KW - Cellular imaging
KW - Cyanine dyes
KW - Fluorescence microscopy
KW - NIR molecular Probes
KW - Optical properties
KW - pH response
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U2 - 10.1016/j.dyepig.2020.108611
DO - 10.1016/j.dyepig.2020.108611
M3 - Article
AN - SCOPUS:85086434994
SN - 0143-7208
VL - 181
JO - Dyes and Pigments
JF - Dyes and Pigments
M1 - 108611
ER -