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Communication

A Ratiometric Selective Fluorescent Probe Derived from Pyrene for Cu2+ Detection

1
School of Tropical Medicine, Hainan Medical University, Haikou 571199, China
2
Key Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou 571199, China
3
NHC Key Laboratory of Control of Tropical Diseases, School of Tropical Medicine, Hainan Medical University, Haikou 571199, China
4
School of Public Health and One Health, Hainan Medical University, Haikou 571101, China
5
School of Chemical Engineering and Environment, Weifang University of Science and Technology, Shouguang 262700, China
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Submission received: 3 May 2022 / Revised: 20 May 2022 / Accepted: 27 May 2022 / Published: 31 May 2022
(This article belongs to the Special Issue Fluorescent Sensors for Disease Diagnosis and Therapy)

Abstract

:
A novel ratiometric Cu2+-selective probe was rationally constructed based on pyrene derivative. Compared to other tested metal ions, the probe presented the selective recognition for Cu2+ which could be detected by a significant turn-on fluorescent response at 393 nm and 415 nm. Under the optimized conditions, a detection limit of 0.16 μM Cu2+ in aqueous media was found. Besides this, a 1:1 metal–ligand complex was confirmed by MS spectra and Job’s plot experiment, and the binding mode was also studied by 1H NMR experiment. Meanwhile, the fluorescence imaging in living cells was performed to detect Cu2+ with satisfactory results.

1. Introduction

Because of wide use of heavy metal ions, analysis and detection of them has been an important means of disease prevention and control in public health and environmental safety [1,2]. Cu2+, as an important heavy metal ion, is confirmed to be harmful to human health in that excessive concentration of Cu2+ is probably involved in the forming of reactive oxygen species to bring out neurodegenerative disorders, such as Wilson’s diseases [3]. To prevent Cu2+-related pollution and health problems, design of effective tools capable of detection of trace amounts of Cu2+ has inspired considerable interest. Due to these advantages, including rapid analysis, high sensitivity, real-time in situ monitoring, and high spatial resolution, fluorescence probe method is expected to be an ideal choice for sensing and bioimaging of analytes in a variety of samples [4,5,6]. To date, researchers have developed many Cu2+ fluorescent probes [7,8,9]. One of the most important approaches is that a specific group is grafted to a fluorophore by organic methods [10,11,12]. Zhao’s group developed a Cu2+ fluorescent probe by incorporating benzoyl hydrazone group as a receptor into the fluorophore hemicyanine, which could rapidly recognize Cu2+ and was also used for cell image [13]. Li et al. synthesized a Cu2+ fluorescent probe by combining a specific recognition unit phenol derivative with a cyanine dye [14]. However, because Cu2+ is a fluorescence quencher due to its paramagnetic through energy or electron transfer processes, these probes showed an “on-off” fluorescence response [15,16,17]. Based on sensitivity and selectivity considerations for practical applications, fluorescence quenching probes upon Cu2+ combination are not as popular as fluorescence enhancement probes under Cu2+ binding. In contrast, “turn-on” fluorescent probes by Cu2+-triggered have attracted special interest. A number of these fluorescent probes have been synthesized and characterized [18,19,20]. For example, You’s group reported a highly fluorescent probe derived from a quinoline moiety for Cu2+ in DMSO-Tris buffer and living cells [21]. In addition, some probes based on rhodamine derivatives could recognize Cu2+ with the aid of structural changes between spirolactam and ring-opened amide to gives rise to a stronger fluorescence emission and color change [22]. However, these limitations, including organic cosolvent dependence, poor photostability, poor cellular compatibility and pH dependence [23,24], to some extent, lowered the sensitivity and also restricted the practical applications because the recognition groups had drawbacks in selectivity and sensitivity. Therefore, development of highly selective and sensitive fluorescent probes for Cu2+ sensing with “off-on” response has been still of great challenge.
With this in mind, in this study, probe P was reasonably constructed by connecting an important fluorophore pyrene with 2-aminobenzhydrazide via –C=N– bond (Scheme 1). The responses of P toward Cu2+ were explored in detail by UV and fluorescence analysis. P was also demonstrated that it could react with Cu2+ and effectively turn on fluorescence in living cells. The design concept was explained as follows: (1) Pyrene was used as the fluorophore in view of its excellent photophysical properties and easy modification on the molecular structure [25,26]. In particular, its fine structures of excited state were the ideal signal units for construction of ratio-type fluorescent probes, which measure the ratio of fluorescence intensity at two different wavelengths as a signal parameter. This mode is not affected by the intensity of light source and instrument; (2) Acylhydrazone Schiff base was one of most selective π-conjugated reagents for Cu2+. In addition, this type of compound was characterized by ketone–enol tautomerism, and O atom of the carbonyl group (–C=O), N atom of the amino group (–NH2), and the imine group (–N=CH) could participate in coordination with Cu2+ and consequently produced stable coordination complexes according to HSAB principle [27]; (3) C=N isomerization and photoinduced electron-transfer (PET) phenomenon were introduced as common signaling mechanisms to play roles in photophysical processes upon binding of P with Cu2+, which was based on the following considerations. Firstly, the main advantage was that it was easy to prepare and design “off-on” probes based on the two mechanisms; furthermore, the affinity of the chelating group C=N for heavy metal ions was stronger than that for alkali metals and alkaline earth metals [28,29].

2. Materials and Methods

2.1. Materials and Instruments

All reagents used in our study were all analytically pure and used directly.
Fluorescence experiments were carried out by a Hitachi 4600 spectrofluometer (Japan). Absorption spectra were measured by a Hitachi U-2910 spectrophotometer (Japan). Confocal microscopy imaging was determined in an Olympus FluoView Fv3000 laser scanning microscope (Japan). Electrospray ionization (ESI) analyses were performed on a Thermo TSQ Quantum Mass Spectrometer (America), method parameters: Sheath Gas Flow Rate (arb): 30; Aux Gas Flow Rate (arb): 10; Capillary Temp. (°C): 275; Capillary Voltage (V): −45.00 (ES−)/10.00 (ES+); SpraVoltage (kV): 5.00. 1H NMR and 13C NMR spectra were performed by a Bruker AV 400 instrument with tetramethylsilane (TMS) as an internal standard and DMSO-d6 as a deuterium generation reagent (Switzerland).

2.2. Synthesis of P and P1

0.23 g (1 mmol) compound 1 and 0.158 g (1 mmol) compound 2 were stirred in ethanol (40 mL) and refluxed for 4 h, and then cooled slowly to 25 °C, followed by filtering precipitate so produced. The obtained yellow solid P was dried and used directly. Yields: 83.4%. MS (ESI+) m/z: 364.1 [M + H]+, 386.6 [M + Na]+. 1H NMR (δ ppm, d6-DMSO): 11.80 (s, 1H), 9.46 (s, 1H), 8.81 (d, 1H, J = 7.25), 8.58 (d, 1H, J = 7.72), 8.37 (d, 1H, J = 7.88), 8.27 (d, 1H, J = 8.88), 8.23 (d, 1H, J = 8.92), 8.13 (t, 1H, J = 7.62), 7.72 (d, 1H, J = 7.72), 7.28 (t, 1H, J = 7.60), 6.74 (d, 1H, J = 8.24), 6.67 (t, 1H, J = 7.42), 6.47 (b, 2H). 13C NMR (δ ppm, d6-DMSO): 151.11, 146.48, 133.27, 132.67, 131.78, 131.08, 129.57, 129.42, 129.19, 128.31, 128.12, 127.47, 126.94, 126.61, 126.13, 125.88, 125.09, 124.72, 123.41, 117.41, 115.59 (Figures S1–S3).
Compound P1 was synthesized similar to P. Yields: 87.2%. MS (ESI+) m/z: 349.3 [M + H]+, 371.2 [M + Na]+ (Figure S4).

2.3. Optical Experimental Method

Stock solutions of metal ions and compound P/P1 were prepared by dissolving appropriate amount in deionized water and DMSO, respectively. Slit widths of excitation and emission were 5 nm and 5 nm, respectively. Excitation wavelength was 350 nm.

2.4. Cell Culture

Hela cells were washed 3 times by PBS (phosphate-buffered saline), and incubated with 1 μM of Cu2+ (in PBS) for 30 min at 37 °C, followed by washing another 3 times with PBS. Then, 10 μM of probe P (in DMSO) was added. After treatment for 30 min in the same growth media, it was washed 3 times with PBS again.
Other cell culture experiments were completed according to this method mentioned above.
The cytotoxicity experiment of P in Hela cells was measured using MTT assay. Cells were seeded into 96-well cell culture plate at a rate of 4000/well in 5% CO2 at 37 °C for 24 h, followed by adding probe P (0, 0.1, 1, 10 µM), and then allowed to incubate for 24 h, respectively. Subsequently, each well was injected with 20 µL MTT (5 mg/mL) and cultured for another 4 h under the same conditions. After that, cells were lysed in the solution composed of 10% SDS, 0.012 M HCl, and 5% isopropanol. A570nm of each well was obtained on a microplate reader to calculate the amount of formazan.

3. Results

3.1. Effects of pH

Effect of pH was firstly investigated to evaluate the actual sensing for Cu2+. The results were displayed in Figure 1, when Cu2+ was not added to the P solution, the fluorescence intensity of P itself remained fairly static in the range of pH 4–10. However, after mixing P with Cu2+, the emission intensity gradually increased in the range of pH 4–7, which reached a maximum at pH 6.3. While pH > 7, the fluorescence intensity began to decrease, which tended to the formation of Cu(OH)2 precipitation. Thereby, the pH-control measurements revealed that P was stable in a wide range of pH, which also showed P had the best sensing response to Cu2+ at pH 6.3. All measurements were carried out in alcohol–aqueous media (v/v, 8:2, pH 6.3, 0.02 M HEPES).

3.2. UV-Vis Response of P

Absorption spectra of P to various common metal ions were illustrated in Figure 2. P exhibited three absorption bands with peaks at 400 nm, 380 nm and 280 nm, we attributed it to the electron transition of pyrene in the energy bond of π-π* and n-π*. Upon the addition of general metal ions (100 µM), such as K+, Na+, Ca2+, Mg2+, Zn2+, Pb2+, Cd2+, Cr3+, Co2+, Ni2+, Hg2+, Cu2+ and Ag+; only Cu2+ resulted in an appreciable spectral change with three new blue-shifted absorption peaks at 340 nm, 325 nm and 275 nm. In addition, absorbance enhancement at 275 nm was also obvious (Figure 2a). These results were enough to account for the binding between P and Cu2+.
The absorption titration experiment showed a significant decrease of absorbance at 400 nm, 380 nm, and an absorbance increase at 275 nm was observed simultaneously with three isosbestic points at 290 nm, 310 nm and 340 nm, which displayed an obvious ratiometric absorbance change (Figure 2b). These results indicated that P possessed the characteristic of recognizing Cu2+ by ratio absorption spectrum, and it also be concluded that Cu2+ binding with P blocked conjugation of the double bonds and resulted in the appearance of some shorter absorption wavelengths.

3.3. Characterization of Fluorescent Response of P

The selective properties of P for respective metal ions were further evaluated by fluorescence spectroscopy. P itself showed a very weak fluorescence response with the excitation wavelength 350 nm as seen in Figure 3a, the reason was explained by the transfer of the lone pair electrons from –C=N– group to benzoyl hydrazine unit. In addition, it was likely due to non-radiative decay of the C=N bond in excited state. When comparing Cu2+ with other examined metal ions, a remarkable “turn-on” fluorescence response generated at 393 nm and 415 nm by the addition of Cu2+, which was the typical monomer emission of pyrene. In this process, we surmised that the N and O atoms in Schiff base maybe participate in forming the complex P-Cu2+, and the isomerization of C=N bond and PET process were restricted, so the enhanced fluorescence intensity at 393 nm and 415 nm were induced significantly. These results suggested that P could act as an ideal fluorescent probe for Cu2+ over other metal ions. Competitive experiments were also employed to prove the practical application of P as a Cu2+-sensitive fluorescent probe. As shown in Figure S5, after Cu2+ was added to the mixture of P with different interfering substances, including Na+, K+, Mg2+, Ca2+, Pb2+, Zn2+, Cd2+, Co2+, Hg2+, Cr3+, Ag+ and Ni2+, an obvious enhancement of the fluorescence intensity ratio (I393nm/I415nm) was caused. These results displayed that the fluorescence signal of P toward Cu2+ was not susceptible remarkably to the coexistent metal ions, which further confirmed that P was a promising probe to sense Cu2+. Furthermore, to evaluate the role of amino group in P, the fluorescence signal of control compound P1 toward the above mentioned metal ions were also measured as seen in Figure 3b. No remarkable emission of P1 at 440 nm was observed, and an emission band at 393 nm and 415 nm was not shown upon addition of Cu2+ as found in P, which indicated the amino group played a crucial role in the formed chelating complex P-Cu2+.
The sensing ability of Cu2+ with P was also checked by the titration experiment with fluorescence spectroscopy. Along with the increasing concentration of Cu2+, the fluorescence intensity at 393 nm and 415 nm enhanced gradually (Figure 3c), which indicated a ratiometric fluorescence change. The linear fitting curve showed that a perfect linear relationship between the ratios of fluorescent emission intensity (I393nm/I415nm) and [Cu2+] within 0.5–8 μM, and LOD (a detection limit) of 0.16 μM was obtained, respectively. It exhibited that probe P could be used for qualitative and quantitative sensing of Cu2+, and the sensitivity reached 30 μM Cu2+ in drinking water in the standard of the WHO (World Health Organization) [30].

3.4. Reaction Mechanism Research

To explore the probable complexation between P and Cu2+, we conducted Job’s plot experiment as displayed in Figure 4 and Figure S6. A maximum emission intensity at 460 nm was found with the proportion of [P]/[Cu2+] of 0.5. As expected, a 1:1 stoichiometry for the complex p-Cu2+ was indicated. It was also proved using the Benesi–Hildebrand method [31], the association constant (Ka) was approximately equal to 6.5 × 105 M−1 from fluorescence titration experiments (Figure S7), compared with reported Cu2+-probe (2.18 × 104 M−1) [32], and it indicated that a stable complex was formed between P with Cu2+. Meanwhile, this 1:1 binding stoichiometric mode was also observed on MS spectra of P-Cu2+, a peak at m/z 425.06 (ESI+) belonged to ([P + Cu2+-H+]+) (Figure S8).
To explore the binding mode of complex P-Cu2+ and also to fully strengthen the sensing mechanism of P with Cu2+, 1H NMR experiment was carried out as shown in Scheme 2. Free P showed the NMR signal of Hb, Ha, Hc at 11.803, 9.485, 6.486 ppm. Upon the addition of 1.0 equiv Cu2+, the NMR signal of Hb (O=C–NH–) disappeared, while that of Ha (–CH=N), Hc (–NH2) downshifted to 9.639 and 7.912, respectively. Meanwhile, the addition of Cu2+ promoted the NMR peaks in the range of 6.5–9.0 ppm, which assigned to protons of pyrene and phenyl to widen and combine together. It suggested that the structure of P became more rigid after coordination with Cu2+.
Keeping these results in mind, a sensing mechanism for the complex P-Cu2+ was surmised as depicted as Scheme 2. According to the MS spectra of P-Cu2+ complex, 425.06 (ES+) belonged to [P + Cu2+-H+]+, which proved the result that the formation of –OH enhanced the coordination ability of O, and a stable five-membered ring formed in the P-Cu2+ complex. Thus, –C=O, –NH2 and –C=N groups participated in the coordination of P-Cu2+ complex. Moreover, the reaction of Cu2+ with P blocked the PET and C=N isomerization and greatly increased the emission intensity of pyrene moiety.

3.5. Cell Application

According to the excellent fluorescence properties of P, the application of P in living cells was explored. Firstly, cytotoxicity of P on Hela cells using a standard MTT assay was performed. As was shown in Figure S8, after the cells were incubated for 24 h with P concentrations within 0–10 μM, high celluar viability was still found to be about 95% (Figure S9), which demonstrated the low cytotoxicity and favorable biocompatibility of P to cultured Hela cells.
After that, the biological capability experiment of P to detect Cu2+ in Hela cells was conducted. When the Hela cells were supplemented with 10 μM of P at 37 °C for 30 min, a very faint fluorescence intensity was detected (Figure S5), suggesting that background signal in the cells was very feeble. In contrast, when cells treated with Cu2+ (1 µM) for 30 min, and then cultured upon addition of P (10 µM) for 30 min, a dramatic fluorescence change was triggered (Figure 5d), demonstrating that P had a good cell-membrane penetration, which also clearly displayed that the enhanced intracellular fluorescence change resulted from interaction of Cu2+ with P inside cells. We could deduce that P had low toxicity and good cytocompatibility in view of the morphology of cells. Hence, P may act as a prospective probe to image Cu2+ for bioanalysis.
In addition, fluorescence imaging of P (10 μM) with various [Cu2+] (0, 2, 4, 6, 8 μM) in Hela cells was measured. It could be seen that the fluorescence intensity was enhanced regularly with increasing concentration of Cu2+ as shown in Figure 6a–e, which also determined based on the average fluorescence intensity by confocal laser scanning microscopy as displayed in Figure 6f. These data also established that P could respond to intracellular Cu2+ level changes in living cells.
The subcellular localization of P in Hela cells was also conducted, Green 488 was selected as a nuclear dye. Afterwards, Hela cells were co-cultured with Cu2+ (10 μM), P (10 μM) and Green 488 in the growth medium as shown in Figure 5. The fluorescence imaging was recorded as represented in Figure 7, P (blue panel, Figure 7a) located in the periphery of Green 488 (green panel, Figure 7b); we concluded that P was mainly located in the cytoplasm of living cells as shown in Figure 7c.
Furthermore, the cytoplasm location of P in living Hela cells was also explored by conducting co-localization experiment (Figure 8). Mito Tracker Red and Green 488 were utilized as a mitochondria-specific dye and a nuclear-specific dye, respectively. The cell image of probe P (red panel, Figure 8a) and dye Mito Tracker Red (blue panel, Figure 8b) could not overlay completely in mitochondria (Figure 8d), so it could be concluded that probe P was not locate in mitochondria of Hela cells.

3.6. Method Performance Comparison

The photophysical properties of reported probes and our proposed P toward Cu2+ were summarized as displayed in Table 1. Probes derived from different fluorophores, including spiropyran, pyridine, naphthalene, rhodamine and pyrene, exhibited fluorescence enhancement or quench which possessed good selectivity and high sensitivity, low LOD [24,32,33,34,35], and meanwhile most Cu2+-probes can adopt dual signal changes towards Cu2+ except some probes [15,33,35,36]. Especially, some Cu2+ probes could display a ratiometric fluorescence change [32,35,37] as well as our proposed probe. Though the availability of fluorescence is increasing, there are still numerous challenges in developing new fluorescent probes for practical applications, such as unfavorable signal mode [15,34] rigorous testing media [15,36,37], no applicability [15,24,33,34,35,36,37] and narrow linear range [35]. Our newly designed pyrene-based probe possessed several advantages such as good selectivity and high sensitivity, a ratiometric dual fluorescence and wide linear range, encouraging applicability.

4. Conclusions

In summary, we took advantage of C=N isomerization and PET mechanism to design and synthesize facilely a newly pyrene-based probe for Cu2+. The formation of P-Cu2+ complex effectively led to the enhanced fluorescence response of pyrene moiety, which realized ratiometric detection of Cu2+. The probe exhibited an excellent feature of a dual-responsive colorimetric and fluorescent response to Cu2+, which showed a high selectivity for Cu2+ compared with other metal ions in alcohol–aqueous media (v/v, 8:2, pH 6.3, 0.02 M HEPES). The proposed probe can be applied to the quantification of Cu2+ with a linear range of 0.5–8 μM and the detection limit of 0.16 μM, and it was also applied for the imaging of Cu2+ in living cells, which showed P had low toxicity and good cytocompatibility. Further investigations on its applications in life science are still underway. We believe that the design concept should provide reference to develop new “off-on” probes for transition metal ions.

Supplementary Materials

The following supporting information can be downloaded at: https://0-www-mdpi-com.brum.beds.ac.uk/article/10.3390/chemosensors10060207/s1. Figure S1: MS spectra of P; Figure S2: 1H NMR spectrum of P; Figure S3: 13C NMR spectrum of P; Figure S4: MS spectra of P1; Figure S5: Fluorescence interfering experiment; Figure S6: Job’s plot for P and Cu2+; Figure S7: Benesi–Hildebrand plot between P and Cu2+. Figure S8: MS spectra of P-Cu2+; Figure S9: MTT experiment.

Author Contributions

Validation, data curation and writing—review and editing, C.Y.; Data curation, methodology and writing—original draft preparation, M.Y.; Validation, writing—original draft preparation and software, S.C.; Software, methodology and validation, Y.J.; Project management and funding acquisition, J.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financially supported by Hainan Province Science and Technology Special Fund (No. ZDYF2022SHFZ076) and the Natural Science Foundation of Hainan Province (No. 820RC626, No. 821RC559) and the National Natural Science Foundation of China (No. 81860381).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

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Scheme 1. Design and synthesis of compounds.
Scheme 1. Design and synthesis of compounds.
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Figure 1. pH-dependent fluorescence response of P (10 µM) and P (10 µM) toward Cu2+ (100 µM) under different HEPES buffers.
Figure 1. pH-dependent fluorescence response of P (10 µM) and P (10 µM) toward Cu2+ (100 µM) under different HEPES buffers.
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Figure 2. Absorption spectra. (a) absorption spectra of P (10 μM) toward metal ions (100 μM) in alcohol–aqueous media (v/v, 8:2, pH 6.3, 0.02 M HEPES); (b) absorption titration of P (10 μM) upon addition of increasing amounts of Cu2+ (0–10 μM) under the same conditions.
Figure 2. Absorption spectra. (a) absorption spectra of P (10 μM) toward metal ions (100 μM) in alcohol–aqueous media (v/v, 8:2, pH 6.3, 0.02 M HEPES); (b) absorption titration of P (10 μM) upon addition of increasing amounts of Cu2+ (0–10 μM) under the same conditions.
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Figure 3. Fluorescence spectra. (a) fluorescence response of P (10 μM) to different metal ions (100 μM) in alcohol–aqueous media (v/v, 8:2, pH 6.3, 0.02 M HEPES); (b) fluorescence emission of P1 (10 μM) for above-mentioned metal ions (100 μM) in alcohol–aqueous media (v/v, 8:2, pH 6.3, 0.02 M HEPES); (c) fluorescence titration of P (10 μM) with various [Cu2+], inset: the ratios of fluorescent emission intensity (I393nm/I415nm) of P (10 μM) as a function of [Cu2+] within 0.5–8 μM.
Figure 3. Fluorescence spectra. (a) fluorescence response of P (10 μM) to different metal ions (100 μM) in alcohol–aqueous media (v/v, 8:2, pH 6.3, 0.02 M HEPES); (b) fluorescence emission of P1 (10 μM) for above-mentioned metal ions (100 μM) in alcohol–aqueous media (v/v, 8:2, pH 6.3, 0.02 M HEPES); (c) fluorescence titration of P (10 μM) with various [Cu2+], inset: the ratios of fluorescent emission intensity (I393nm/I415nm) of P (10 μM) as a function of [Cu2+] within 0.5–8 μM.
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Figure 4. Stoichiometry for P and Cu2+ by Job’s plot in alcohol–aqueous media (v/v, 8:2, pH 6.3, 0.02 M HEPES). The total concentration of ([P] + [Cu2+]) was 10 μM.
Figure 4. Stoichiometry for P and Cu2+ by Job’s plot in alcohol–aqueous media (v/v, 8:2, pH 6.3, 0.02 M HEPES). The total concentration of ([P] + [Cu2+]) was 10 μM.
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Scheme 2. Recognization mode between P and Cu2+.
Scheme 2. Recognization mode between P and Cu2+.
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Figure 5. Hela cells fluorescence images. (a) cells cultured with 10 µM of P for 30 min in the growth medium; (b) image of bright field cells in panel (a); (c) images of overlay in panels (a,b); (d) after supplementing with 1 µM of Cu2+ for 30 min, Hl-7701 cells incubated with P (10 µM) for additional 30 min; (e) image of bright field cells in panel (d); (f) images of overlay in panels (d,e).
Figure 5. Hela cells fluorescence images. (a) cells cultured with 10 µM of P for 30 min in the growth medium; (b) image of bright field cells in panel (a); (c) images of overlay in panels (a,b); (d) after supplementing with 1 µM of Cu2+ for 30 min, Hl-7701 cells incubated with P (10 µM) for additional 30 min; (e) image of bright field cells in panel (d); (f) images of overlay in panels (d,e).
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Figure 6. Confocal fluorescence images of Hela cells. (ae): cells supplemented with 0, 2, 4, 6, 8 μM Cu2+ in the growth media for 30 min at 37 °C, and then incubated with 10 μM P for 30 min respectively; (f) fluorescence intensity of P with various [Cu2+] ((ae): 0, 2, 4, 6, 8 μM).
Figure 6. Confocal fluorescence images of Hela cells. (ae): cells supplemented with 0, 2, 4, 6, 8 μM Cu2+ in the growth media for 30 min at 37 °C, and then incubated with 10 μM P for 30 min respectively; (f) fluorescence intensity of P with various [Cu2+] ((ae): 0, 2, 4, 6, 8 μM).
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Figure 7. Subcellular localization of P in Hela cells. (a) cells supplemented with Cu2+ 10 μM) for 30 min, followed by the incubation with P 10 μM) for 30 min; (b) cells treated upon addition of Cu2+ (10 μM) for 30 min, P (10 μM) for another 30 min, and then cultured with Green 488 for 30 min; (c) images of overlay in panel (a,b).
Figure 7. Subcellular localization of P in Hela cells. (a) cells supplemented with Cu2+ 10 μM) for 30 min, followed by the incubation with P 10 μM) for 30 min; (b) cells treated upon addition of Cu2+ (10 μM) for 30 min, P (10 μM) for another 30 min, and then cultured with Green 488 for 30 min; (c) images of overlay in panel (a,b).
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Figure 8. Cell localization experiment. (a) Cells were incubated with P for 30 min, and then Cu2+ (10 μM) for 30 min; (b) cells were incubated with P for 30 min, Cu2+ (10 μM) for 30 min, and Mito Tracker Red for 20 min at 37 °C, subsequently; (c) cells were incubated with P for 30 min, Cu2+ (10 μM) for 30 min, and Mito Tracker Red for 20 min at 37 °C, Green-488 for 10 min at 37 °C subsequently; (d) overlay field image of cells in panels (ac).
Figure 8. Cell localization experiment. (a) Cells were incubated with P for 30 min, and then Cu2+ (10 μM) for 30 min; (b) cells were incubated with P for 30 min, Cu2+ (10 μM) for 30 min, and Mito Tracker Red for 20 min at 37 °C, subsequently; (c) cells were incubated with P for 30 min, Cu2+ (10 μM) for 30 min, and Mito Tracker Red for 20 min at 37 °C, Green-488 for 10 min at 37 °C subsequently; (d) overlay field image of cells in panels (ac).
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Table 1. Performances comparison of various fluorescent probes for Cu2+.
Table 1. Performances comparison of various fluorescent probes for Cu2+.
ModesReagentsSelectivityLinear Range (µM)LOD (µM)Testing MediaApplicationsRemarksRef.
Quenching
λex/em = 556/603 nm
Spiropyran derivativeGood0.75–3.60.15Ethanol or pH 6.98 (0.1 M Tris-HCl)NAFluorescence changes[15]
Enhancement
λex/em = 530/580 nm
Rhodaming
derivative
Good0.05–0.90.03Water/methanol (1:4, v/v, pH 6.0, 20 mM HEPES)NADual chromo- and fluorogenic changes[24]
Enhancement
λex/em = 342/375–460 nm
pyridine derivativeGood0.1–200.02Tris-HNO3 (9:1 v/v, pH 7.0)Water samples and living cellsDual chromo- and fluorogenic changes, ratiometric.[32]
Enhancement
λex/em = 370/410–415 nm
Pyrene derivativeGood0.1–1.90.000234Water/DMF solution (1:1, v/v)NAfluorogenic changes[33]
Quenching
λex/em = 355/565 nm
Coumarin derivativeGood0.5–4.50.0634HEPES aqueous buffer (pH 7.0)NADual chromo- and fluorogenic changes[34]
Enhancement
λex/em = 451/475–525 nm
Naphthalimide derivativeGood0–0.10.01Water-ethanol (6:4, v/v, pH 7.2, 50 mM HEPES)NAFluorescent change, ratiometric[35]
Enhancement
λex/em = 350/495 nm
Pyrene derivativeGoodNA0.15CH3CNNAfluorogenic changes[36]
Enhancement
λex/em = 360/430–489 nm
Naphthalimide
derivative
GoodNANACH3CNNADual chromo- and fluorogenic changes, ratiometric[37]
Enhancement
λex/em = 350/393–415 nm
Pyrene derivativeGood0.5–80.16Alcohol–water media (v/v, 8:2, pH 6.3, 20 mM HEPES)Cell imagingDual chromo-and fluorogenic changes, ratiometricThis work
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Yu, C.; Yang, M.; Cui, S.; Ji, Y.; Zhang, J. A Ratiometric Selective Fluorescent Probe Derived from Pyrene for Cu2+ Detection. Chemosensors 2022, 10, 207. https://0-doi-org.brum.beds.ac.uk/10.3390/chemosensors10060207

AMA Style

Yu C, Yang M, Cui S, Ji Y, Zhang J. A Ratiometric Selective Fluorescent Probe Derived from Pyrene for Cu2+ Detection. Chemosensors. 2022; 10(6):207. https://0-doi-org.brum.beds.ac.uk/10.3390/chemosensors10060207

Chicago/Turabian Style

Yu, Chunwei, Mei Yang, Shuhua Cui, Yuxiang Ji, and Jun Zhang. 2022. "A Ratiometric Selective Fluorescent Probe Derived from Pyrene for Cu2+ Detection" Chemosensors 10, no. 6: 207. https://0-doi-org.brum.beds.ac.uk/10.3390/chemosensors10060207

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