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Article

Visualization of Fluoride Ions In Vivo Using a Gadolinium(III)-Coumarin Complex-Based Fluorescence/MRI Dual-Modal Probe

by
Yue Wang
1,
Renfeng Song
2,
Huan Feng
1,
Ke Guo
2,
Qingtao Meng
1,*,
Haijun Chi
1,
Run Zhang
1,3,* and
Zhiqiang Zhang
1
1
School of Chemical Engineering, University of Science and Technology Liaoning, Anshan 114051, China
2
Ansteel Mining Engineering Corporation, Anshan 114002, China
3
Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane 4072, Australia
*
Authors to whom correspondence should be addressed.
Sensors 2016, 16(12), 2165; https://doi.org/10.3390/s16122165
Submission received: 17 November 2016 / Revised: 11 December 2016 / Accepted: 12 December 2016 / Published: 16 December 2016
(This article belongs to the Special Issue Colorimetric and Fluorescent Sensor)
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Abstract

:
A new Gadolinium(III)–coumarin complex, DO3A-Gd-CA, was designed and prepared as a dual-modal probe for simultaneous fluorescence and relaxivity responses to fluoride ions (F−) in aqueous media and mice. DO3A-Gd-CA was designed by using Gd(III) center as an MRI signal output unit and fluoride binding site, and the 4-(diethylamino)-coumarin-3-carboxylic acid (CA) as a fluorescence reporter. Upon the addition of fluoride ions to the solution of DO3A-Gd-CA, the liberation of the coordinated CA ligand led to a 5.7-fold fluorescence enhancement and a 75% increase in the longitudinal relaxivity (r1). The fluorescent detection limit for fluoride ions was determined to be 8 μM based on a 3σ/slope. The desirable features of the proposed DO3A-Gd-CA, such as high sensitivity and specificity, reliability at physiological pH and low cytotoxicity enable its application in visualization of fluoride ion in mice. The successful in vivo imaging indicates that DO3A-Gd-CA could be potentially used in biomedical diagnosis fields.

1. Introduction

Detection and diagnosis of diseases at early stage with a high level of accuracy is the key factor to be considered in biomedical and clinical researches on the treatment of diseases [1,2]. The disease biomarkers are often detected at all stages during diseases diagnostic and treatment, while such detection remains a challenge currently [3,4]. Molecular imaging enables visualization of disease biomarkers and their metabolisms in living systems in real time at various levels from molecules and single cells, to tissues, and organs, which allows detection and differential diagnosis of diseases [5,6]. Over the past decades, a variety of molecular imaging techniques, such as positron emission tomography (PET), X-ray computed tomography (CT), magnetic resonance imaging (MRI) and fluorescence imaging (FI), have been widely used in clinical diagnostics, biomedical research and molecular imaging fields [7,8,9,10]. Each method has its inherent advantages and considerations. For instance, a magnetic resonance imaging (MRI) technique is characterized by superb spatial resolution but low sensitivity and requires a high concentration of the contrast agent [11]. Fluorescence imaging, on the other hand, has much higher sensitivity and the potential for real-time imaging, but with limited penetration depth of optical photonics, which restricts their application in the detection of biomarkers in deep tissues [12].These limitations could be addressed by the dual-modal or multi-modal imaging techniques proposed recently [13,14,15]. A fluorescence/MRI dual-modal probe fabricated by integrating a fluorescent unit with a contrast agent could thus be used for imaging of biomarkers in vivo. With these dual-modal probes, detailed information on biomarkers in cells and organs within live bodies could be observed simultaneously employing fluorescence imaging and MRI techniques [16].Therefore, molecular probes, defined as a class of molecules that bind selectively to the analyte of interest with concomitant change in one or more properties of the system, such as fluorescence color [17,18,19], redox potential and magnetic resonance [20], plays fundamental roles in advanced imaging techniques [21]. In recent years, numerous efforts have been made for the development of molecular probes for the monitoring of biomarkers in biological systems [22]. Nevertheless, to the best of our knowledge, anions fluorescence/MRI dual-modal probes based on Gd(III) complex have been scarcely reported [23].
Due to the important roles of anions played in live organisms, environmental samples, and in the broad applications (e.g., catalysis, etc.), the development of molecular probes for the selective and sensitive sensing and quantification of anions of interest have attracted considerable interest [24]. Among various important anions in biological systems, fluoride ion, being the smallest and most electronegative anion, has particularly attracted attention due to its profound effects on human health. It is well known that intake of acute amount of fluoride ions is beneficial to the treatment of osteoporosis and dental health [25]. On the other hand, excessive intake of fluoride ions may induce various diseases, such as gastrointestinal dysfunction, dental fluorosis, bone fluorosis, and so on [26,27]. Accordingly, the development of molecule probes for the selective and sensitive detection of fluoride ion in biological systems is urgently needed.
In recent years, lanthanide (Ln) complexes have been reported to be an excellent candidate for the development of the responsive optical probes owing to their unique photophysical properties [28,29,30]. By virtue of the extremely high Ln–fluoride affinity, the coordinated molecules or fluorophores of Ln complexes can be displaced by fluoride ions. As the result of this interaction, the liberation of the coordinated ligands may lead to the changes in several observable signals, such as colour [31], fluorescence and MR [32,33]. Due to their high magnetic moment and symmetric electronic ground state, gadolinium(III) complexes have been frequently chosen as MRI contrast agents [34]. As a consequence of the fluoride ions-induced displacement, the relaxivity of Gd(III) complexes thus could be finely tuned by changing in q (number of coordinated water molecular) upon the addition of targeted fluoride ions in aqueous solution (Scheme 1) [35,36,37,38,39,40,41,42,43].

2. Materials and Methods

2.1. Materials and Instruments

4-Diethylaminosalicylaldehyde, diethylmalonate, piperidine and tetrabutylammonium salts of F−, Cl−, Br−, I−, HSO4−, NO3−, OH−, AcO−, PO43− and H2PO4− were purchased from Sinopharm Chemical Reagent Co., Ltd. (Shanghai, China). GdCl3, 1,4,7,10-Tetraazacyclododecane (Cyclen), tert-Butyl bromoacetate and trifluoroacetic acid were purchased from Alfa Aesar.
1H-NMR and 13C-NMR spectra were recorded with an AVANCE600MHZ spectrometer (BRUKER) with chemical shifts reported as ppm (in DMSO, TMS as internal standard). API-ES mass spectra were recorded on an Agilent 6530QTOF spectrometer. Fluorescence spectra were determined with LS 55 luminescence spectrometer (Perkin Elmer, Waltham, MA, USA). The absorption spectra were measured with a Lambda 900 UV/VIS/NIR spectrophotometer (Perkin Elmer, Waltham, MA, USA). Longitudinal relaxivity (r1) and MR imaging were performed on an MesoMR23-060H-I Analyst Analyzing & Imaging system (Shanghai Niumag Corp., Shanghai, China) using a 0.5 T magnet, point resolution = 256 × 128 mm, section thickness = 1 mm, TE = 18.2 ms, TR = 400 ms, and number of acquisitions = 4.

2.2. Synthesis and Characterization of 4-(Diethylamino)-coumarin-3-carboxylic acid (CA)

4-(diethylamino)-coumarin-3-carboxylic acid (CA) was synthesized according to the literature procedurein 78% yield [44]. 1H-NMR (DMSO-d, 600 MHz) δ (ppm): 12.52 (s, H), 8.59 (s, 1H), 7.64 (d, J = 12.0 Hz, 2H), 6.79 (d, J = 12.0 Hz, 2H), 6.57 (s, 1H), 3.49 (m, J = 9.0 Hz, 4H), 1.14 (t, J = 9.0 Hz, 6H). 13C-NMR (DMSO-d, 150 MHz) δ (ppm): 165.0, 160.0, 158.4, 153.4, 149.9, 132.3, 110.5, 107.8, 107.7, 96.4, 44.9, 12.8. ESI-HRMS (positive mode, m/z) Calcd for C14H15NO4: 261.1001 [CA − H]+; Found: 260.0995.

2.3. Synthesis and Characterization of DO3A-Gd

1,4,7-Tris(carboxymethyl)-1,4,7,10-tetraazacyclododecane (DO3A) and DO3A-Gd were synthesized according to the literature procedure [45,46]. ESI-HRMS (positive mode, m/z) of DO3A, Calcd for C14H27N4O6: 347.1931: [DO3A + H]+; Found: 347.1936; ESI-HRMS (positive mode, m/z) of DO3A-Gd, Calcd for C14H22GdN4O6: 500.0802 [DO3A-Gd]−; Found: 500.0781.

2.4. Synthesis and Characterization of DO3A-Gd-CA

DO3A-Gd-CA was prepared by addition of 1.0 equiv. of [DO3A-Gd]Na to CA (10 μM) solution in CH3CN-H2O (9:1, v/v, pH = 7.4). ESI-HRMS (positive mode, m/z) of [DO3A-Gd-CA]−, Calcd for C28H37GdN5O10: 761.1803, Found: 761.1778.

2.5. General Procedures of Spectroscopic Detection

Stock solutions of CA (1 mM) were prepared in CH3CN. Before spectroscopic measurements, the solution was freshly prepared by diluting the high concentration of stock solution to corresponding solution (10 μM, CH3CN:H2O = 9:1, pH = 7.4). DO3A-Gd-CA stock solution for anions sensing was prepared in situ by addition of 1.0 equiv. of [DO3A-Gd]Na to CA (10 μM) solution in CH3CN-H2O (9:1, v/v, pH = 7.4). Each time, a 3 mL solution of probe was filled in a quartz cell of 1 cm optical path length, and different stock solutions of cations were added into the quartz cell gradually by using a micro-syringe. Excitation wavelength for CA was 408 nm.

2.6. Association Constant Calculation

The Benesi-Hildebrand equation was used as shown below [47].
1 F 0 − F = 1 K a ( F 0 − F min ) [ DO 3 A -Gd ] + 1 F 0 − F min
where F and F0 represent the fluorescence emission at 460 nm of CA in the presence and absence of [DO3A-Gd]−, respectively, Fmin is the saturated fluorescence intensity.

2.7. MRI Experiment

Male 8-week-old mice were purchased from the Animal Experiment Center of Dalian Medical University. All live mice experiments were performed in compliance with the relevant laws and institutional guidelines.
All MR relaxivity measurements were performed on a MesoMR23-060H-I Analyzing & Imaging system (Shanghai Niumag Corp.). The specific relaxivity values of r1 were calculated through the curve fitting of 1/T1 (s−1) vs. the concentration of DO3A-Gd-CA (0.2 mM). T1-weighted MR images were acquired using a multi-slice gradient echo sequence.

3. Results

3.1. Synthesis and Photophysical Characterization of DO3A-Gd-CA in Solution

The formation of DO3A-Gd-CA was investigated by recording the changes in UV-Vis absorption and fluorescence spectra. As shown in Figure 1, consistent with the free coumarin derivative, CA displayed a major absorption maximum at 402 nm in aqueous medium (CH3CN:H2O = 9:1, pH = 7.4) [48]. In the presence of an increasing amount of [DO3A-Gd]− (0–15 µM), an obvious bathochromic-shift in the absorption band from 402 nm to 430 nm and an increase in the absorption at 430 nm were noted, which could be assigned to the complexation of CA with Gd(III) center.
The complexation of CA with [DO3A-Gd]− was further studied by the analysis of fluorescence titration. CA displayed strong fluorescence at 460 nm in CH3CN-H2O (9:1, v/v, pH = 7.4). As expected, the fluorescence intensity of CA decreased gradually with a 12 nm bathochromic-shift in the emission band in the presence of an incremental addition of [DO3A-Gd]−. The fluorescence intensity reached a constant value when 12 µM fluoride ion was added (Figure 2, insert). The decrease of fluorescence intensity (more than 81.5% fluorescence quenching) and bathochromic-shift of emission wavelength suggested the formation of the complex DO3A-Gd-CA [49,50]. Based on the 1:1 binding mode, the association constant (Ka) was evaluated to be 4.3 × 103 M−1 using the Benesi–Hildebrand method (Figure S6) [51]. Furthermore, no obvious changes of the fluorescent intensities within 13 h, indicating that DO3A-Gd-CA is reliable under the test condition (Figure S7). The proposed structure of DO3A-Gd-CA was further confirmed by ESI-HRMS. As shown in Figure S8, analysis of the solution of DO3A-Gd-CA revealed the presence of a peak assigned to [DO3A-Gd-CA]− at m/z = 761.1778, indicating the formation of the expected 1:1 stoichiometry complex between DO3A-Gd and CA.

3.2. Spectroscopic Studies of DO3A-Gd-CA towards Fluoride Ion in Aqueous Medium

By virtue of the high affinity of gadolinium(III) center and fluoride ions, fluoride is expected to replace the coordinated CA ligand [52], resulting the significant changes in UV-Vis and fluorescence spectra of CA, by which fluorescence detection of fluoride ion could be achieved. The stock solution of DO3A-Gd-CA for anion sensing was prepared in situ by the addition of 1.0 equiv. of [DO3A-Gd]− to CA solution (10 μM) in CH3CN-H2O (9:1, v/v, pH = 7.4). The displacement approach was firstly investigated by UV-Vis spectra titration analysis. The major absorption band of DO3A-Gd-CA (10 μM) at 430 nm decreased and the absorption peak assigned to free CA at 402 nm emerged by the addition of 0–200 μM tetrabutylammonium fluoride (n-Bu4NF) to the DO3A-Gd-CA solution (Figure 3). The final absorption spectrum was in agreement with the native CA in identical conditions (Figure S9a), which corroborated the results of the decomplexing of DO3A-Gd-CA in the presence of fluoride ion. The changes of absorption spectra ofDO3A-Gd-CA in the presence of other physiologically and environmentally important anions, such as Br−, I−, AcO−, HSO4−, NO3−, OH− and H2PO4− were then evaluated by UV-Vis analysis. As illustrated in Figure 4, obvious changes in UV-Vis spectra were obtained upon the addition of fluoride ions, instead of other anions even at high concentrations (concentration of Cl−, PO43− are 100 mM and 1 mM, respectively). This result indicates that DO3A-Gd-CA is specific toward fluoride ions over other competitive anions.
To evaluate the capability of DO3A-Gd-CA as the fluorescence probe for fluoride ions, emission spectra of DO3A-Gd-CA were then investigated. As shown in Figure 5, DO3A-Gd-CA presented a weak fluorescence emission. Upon the addition of fluoride ion, the maximum emission wavelength of DO3A-Gd-CA at 472 nm was gradually shifted to 460 nm, accompanied by an increase in fluorescence intensity. When 200 μM fluoride ion was added, the fluorescence intensity increased to a maximum value. The intensity and overall pattern of the emission spectrum closely match those of native CA state, indicating the liberation of coordinated CA ligand (Figure S9b). Job’s plots of the fluorescence emission variation at 460 nm against the mole fraction of fluoride ions clearly showed the inflection point at 0.67 (Figure S10), which supported that DO3A-Gd-CA binding fluoride ion with 1:2 binding stoichiometry. The fluoride-induced replacement process was further verified by HRMS. Upon the addition of fluoride ions into the aqueous solution of DO3A-Gd-CA, the peak of [DO3A-Gd-CA]− at m/z = 761.1778 disappeared, and a new peak at m/z = 260.0930 assigned to [CA–H+]− was emerged, indicating that the binding between fluoride ions with Gd(III) centers led to the release of CA (Figure S11). To evaluate the selectivity of DO3A-Gd-CA toward fluoride ion against other anions, the changes in fluorescence of DO3A-Gd-CA were examined in the presence of 0.2 mM various anions (Br−, I−, H2PO4−, HSO4−, AcO−, NO3−, OH−, AcO−) and 100 mM Cl−, 1 mM PO43−. The maximum emission of DO3A-Gd-CA significantly increased in the presence of fluoride ions exclusively, whereas other anions did not induce any detectable fluorescence enhancement (Figure 6). To further verify the excellent selectivity for fluoride ions, the competitive experiments were conducted by the addition of 0.2 mM fluoride ion to the mixture of DO3A-Gd-CA and diverse coexisting anions. As shown in Figure 6, negligible effects on the detection of fluoride ions were found in the presence of various completive anions, indicating DO3A-Gd-CA is a fluorescence probe specific for fluoride ion detection [53]. The excellent selectivity to fluoride ions is partly due to the highest affinity to gadolinium(III) center compared to other anionic analytes [54]. The relative fluorescence intensity of DO3A-Gd-CA is linearly proportional to fluoride ions concentration of 0–30 μM (Figure S12), and the detection limit was calculated to be 8 μM based on a 3σ/slope under experimental conditions, which is low enough for fluoride ion sensing in aqueous medium and biological systems [55].

3.3. MRI Responses of DO3A-Gd-CA towards Anions in Aqueous Medium and In Vivo

The longitudinal relaxivity (r1) of DO3A-Gd-CA towards fluoride ions was further investigated by a MesoMR23-060H-I Analyzing & Imaging system at 25 °C. As shown in Figure 7, DO3A-Gd-CA (0.2 mM) exhibited relatively low longitudinal relaxivity (r1 = 1.67 mM−1∙s−1), suggesting that no inner-sphere water molecule was bonded to Gd(III) ion arising from the complexation of EDTA-Gd with CA (q = 0) [56]. Upon the addition of fluoride ion into the aqueous solution containing EDTA-Gd-CA (0.2 mM), the relaxivity increased to 2.957 mM−1·s−1 (Figure 7), which closely matched the native EDTA-Gd state (Figure S13). The result demonstrated the replacement of coordination CA in the presence of fluoride ions. In addition, the corresponding T1-weighted images of DO3A-Gd-CA (0.2 mM) presented a continuous increase in spot brightness with increasing fluoride ion concentrations (Figure 7 insert). The increase in longitudinal relaxivity (r1) demonstrated the applicability of DO3A-Gd-CA as an efficient T1 MRI probe.
The changes in relaxivity of DO3A-Gd-CA were fluoride-specific over other physiologically important anions including Br−, I−, H2PO4−, HSO4−, AcO−, NO3−, OH−, AcO−, Cl− (100 mM) and PO43− (1 mM) (Figure 8). In addition, a distinctly increased imaging intensity in the presence of 0.5 mM fluoride ions was obtained, whereas no obvious differences were observed upon addition of other competitive anions (Figure 8, insert). In order to investigate the feasibility of DO3A-Gd-CA for the in vivo magnetic resonance imaging (MRI), the long-term cellular toxicity of DO3A-Gd-CA was evaluated by means of a MTT assay [57,58]. The MDA-MB-231 cell viabilities remained more than 80% at a high concentration of 200 µM even with an incubation time of 24 h, demonstrating the low cytotoxicity of DO3A-Gd-CA (Figure S14). In addition, the suitable pH range for DO3A-Gd-CA was evaluated to be 3.0–11.0, suggested that the probe is suitable for application under physiological conditions (Figure S15).
Then, in vivo MRI experiments were studied using a 0.5 T MRI instrument. As shown in Figure 9b, after the injection of DO3A-Gd-CA (0.2 mM), a 40.1% contrast enhancement at the site of injection was observed compared with the baseline of the pre-injection image (Figure 9a). Further injection of fluoride ions (0.2 mL, 0.5 mM) into the hind legs of the mice led to the significant contrast effect of T1-weighted MR images in the areas of interest (Figure 9c). To demonstrate the potential applications of DO3A-Gd-CA in biomedical diagnosis fields, the proposed probe was subcutaneously injected into one hind leg of mouse and then imaged at different time points, respectively. As shown in Figure S16, the successive bright MRI action of the DO3A-Gd-CA on mice model was achieved at four representative time points, even after 12 h, suggesting that the contrast agents could continuously improve contrast in tissues and have a relatively longer blood circulation time. The results of images demonstrated that DO3A-Gd-CA could serve as a MRI probe for imaging of fluoride ions in vivo.

4. Conclusions

In summary, we reported the design and synthesis of a novel mononuclear nine-coordinate complex, DO3A-Gd-CA as fluoride-specific fluorescence and MRI dual-modal probe. Upon the addition of fluoride ions to the aqueous solution of DO3A-Gd-CA, the replacement of the coordination aromatic carboxylic acid (CA) led an increase in longitudinal relaxivity (r1) and an enhancement in fluorescence intensity, realizing switch-on dual-modal responses towards fluoride ions in water medium. The desirable features of DO3A-Gd-CA, such as high sensitivity, suitability at physiological pH, favorable dynamical stability and low cytotoxicity encouraged us to further evaluate its potential biological applications. In vivo magnetic resonance imaging (MRI) in mice indicates that DO3A-Gd-CA can be potentially used as a powerful tool for the detection of fluoride ions in live systems. Given these promising results, we believe that DO3A-Gd-CA is valuable both in methodology and potential application, which provides a new flexible strategy for the rational design of bimodal or multimodal probes for anion sensing.

Supplementary Materials

The following are available online at https://www.mdpi.com/1424-8220/16/12/2165/s1, Figures S1 and S2: NMR of CA, Figure S3–S5, S8, S11: HR MS characterizations, Figure S6: Benesi-Hildebrand plot, Figure S7: Stability of DO3A-Gd-CA, Figure S9: UV-Vis and emission spectra of CA sequential upon addition of [DO3A-Gd]− and fluoride ion, Figure S10: Job’s plot, Figure S12: Linear relationship, Figure S13: Changes in the r1 of DO3A-Gd as a function of the CA concentration, Figure S14: Cell viabilities, Figure S15: Influence of pH on DO3A-Gd-CA, Figure S16: Resident time of DO3A-Gd-CA in mice.

Acknowledgments

This work is supported by the National Natural Science Foundation of China (No. 21301011, 21601076), the Key Laboratory Program of Educational Department of Liaoning Province (LZ2015047), Natural Science Foundation of Liaoning Province (No. 201602400).

Author Contributions

Qingtao Meng conceived and designed the experiments, wrote the paper; Yue Wang and Huan Feng performed the synthesis and test experiments; Run Zhang contributed the cytotoxicity measurement; Renfeng Song and Ke Guo were involved inanalyzing the data; Haijun Chi contributed to the high resolution MS spectra characterization; Zhiqiang Zhang contributed to manuscript revision.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Wang, H.; Wu, H.; Shen, H.; Geng, S.; Wang, B.; Wang, Y.; Ma, X.; Lid, G.; Tan, M. A bimodal MRI and NIR liposome nanoprobe for tumor targeted molecular imaging. J. Mater. Chem. B 2015, 3, 8832–8841. [Google Scholar] [CrossRef]
  2. Zheng, X.; Tang, H.; Xie, C.; Zhang, J.; Wu, W.; Jiang, X. Tracking cancer metastasis in vivo by using an iridium-based hypoxia-activated optical oxygen nanosensor. Angew. Chem. Int. Ed. 2015, 54, 8094–8099. [Google Scholar] [CrossRef] [PubMed]
  3. Zhou, Z.; Han, Z.; Lu, Z.-R. A targeted nanoglobular contrast agent from host-guest self-assembly for MR cancer molecular imaging. Biomaterials 2016, 85, 168–179. [Google Scholar] [CrossRef] [PubMed]
  4. Munge, B.S.; Coffey, A.L.; Doucette, J.M.; Somba, B.K.; Malhotra, R.; Patel, V.; Gutkind, J.S.; Rusling, J.F. Nanostructured immunosensor for attomolar detection of cancer biomarker interleukin-8 using massively labeled superparamagnetic particles. Angew. Chem. Int. Ed. 2011, 50, 7915–7918. [Google Scholar] [CrossRef] [PubMed]
  5. Pu, K.; Chattopadhyay, N.; Rao, J. Recent advances of semiconducting polymer nanoparticles in in vivo molecular imaging. J. Control. Release 2016, 240, 312–322. [Google Scholar] [CrossRef] [PubMed]
  6. Xie, Z.; Li, S.; Yang, K.; Xu, B.; Ren, Q. Evaluation of a wobbling method applied to correcting defective pixels of CZT detectors in SPECT imaging. Sensors 2016, 16, 772. [Google Scholar] [CrossRef] [PubMed]
  7. Lee, D.-E.; Koo, H.; Sun, I.-C.; Ryu, J.H.; Kim, K.; Kwon, I.C. Multifunctional nanoparticles for multimodal imaging and theragnosis. Chem. Soc. Rev. 2012, 41, 2656–2672. [Google Scholar] [CrossRef] [PubMed]
  8. Weissleder, R.; Pittet, M.J. Imaging in the era of molecular oncology. Nature 2008, 452, 580–589. [Google Scholar] [CrossRef] [PubMed]
  9. Pröhla, M.; Schuberta, U. S.; Weigand, W.; Gottschaldta, M. Metal complexes of curcumin and curcumin derivatives for molecular imaging and anticancer therapy. Coord. Chem. Rev. 2016, 307, 32–41. [Google Scholar] [CrossRef]
  10. Zhang, X.; Bi, A.; Gao, Q.; Zhang, S.; Huang, K.; Liu, Z.; Gao, T.; Zeng, W. Advances of molecular imaging for monitoring the anatomical and functional architecture of the olfactory system. ACS Chem. Neurosci. 2016, 7, 4–14. [Google Scholar] [CrossRef] [PubMed]
  11. Glunde, K.; Artemov, D.; Penet, M.-F.; Jacobs, M.A.; Bhujwalla, Z.M. Magnetic resonance spectroscopy in metabolic and molecular imaging and diagnosis of cancer. Chem. Rev. 2010, 110, 3043–3059. [Google Scholar] [CrossRef] [PubMed]
  12. Yang, T.; Liu, Q.; Pu, S.; Dong, Z.; Huang, C.; Li, F. Fluorophore-photochrome co-embedded polymer nanoparticles for photoswitchable fluorescence bioimaging. Nano Res. 2012, 5, 494–503. [Google Scholar] [CrossRef]
  13. Jennings, L.E.; Long, N.J. ‘Two is better than one’—Probes for dual-modality molecular imaging. Chem. Commun. 2009, 3511–3524. [Google Scholar] [CrossRef] [PubMed]
  14. Guo, K.; Berezin, M.Y.; Zheng, J.; Akers, W.; Lin, F.; Teng, B.; Vasalatiy, O.; Gandjbakhche, A.; Griffiths, G.L.; Achilefu, S. Near infrared-fluorescent and magnetic resonance imaging molecular probe with high T1 relaxivity for in vivo multimodal imaging. Chem. Commun. 2010, 46, 3705–3707. [Google Scholar] [CrossRef] [PubMed]
  15. Quea, E.L.; Chang, C.J. Responsive magnetic resonance imaging contrast agents as chemical sensors for metals in biology and medicine. Chem. Soc. Rev. 2010, 39, 51–60. [Google Scholar] [CrossRef] [PubMed]
  16. Berdichevski, A.; Yameen, H.S.; Dafni, H.; Neeman, M.; Seliktar, D. Precise and in situ genetic humanization of 6 Mb of mouse immunoglobulin genes. Proc. Natl. Acad. Sci. USA 2015, 112, 5147–5152. [Google Scholar] [CrossRef] [PubMed]
  17. Meng, Q.T.; Jia, H.M.; Succar, P.; Zhao, L.; Zhang, R.; Duan, C.Y.; Zhang, Z.Q. A highly selective and sensitive ON–OFF–ON fluorescen cechemosensor for cysteine detection in endoplasmic reticulum. Biosens. Bioelectron. 2015, 74, 461–468. [Google Scholar] [CrossRef] [PubMed]
  18. Lei, Z.; Yang, Y. A concise colorimetric and fluorimetric probe for sarin related threats designed via the “Covalent-Assembly” approach. J. Am. Chem. Soc. 2014, 136, 6594–6597. [Google Scholar] [CrossRef] [PubMed]
  19. Lee, K.; Dzubeck, V.; Latshaw, L.; Schneider, J.P. De novo designed peptidic redox potential probe: Linking sensitized emission to disulfide bond formation. J. Am. Chem. Soc. 2004, 126, 13616–13617. [Google Scholar] [CrossRef] [PubMed]
  20. Babailov, S.P. Thulium diketonate as NMR paramagnetic probe for moderately fast molecular dynamics and supersensitive reagent for in situ control of temperature. Sens. Actuators B 2016, 233, 476–478. [Google Scholar] [CrossRef]
  21. Louie, A. Multimodality Imaging Probes: Design and Challenges. Chem. Rev. 2010, 110, 3146–3195. [Google Scholar] [CrossRef] [PubMed]
  22. Kobayashi, H.; Longmire, M.R.; Ogawa, M.; Choyke, P.L. Rational chemical design of the next generation of molecular imaging probes based on physics and biology: Mixing modalities, colors and signals. Chem. Soc. Rev. 2011, 40, 4626–4648. [Google Scholar] [CrossRef] [PubMed]
  23. Wang, Y.; Song, R.F.; Guo, K.; Meng, Q.T.; Zhang, R.; Kong, X.; Zhang, Z.Q. A gadolinium(III) complex based dual-modal probefor MRI and fluorescence sensing of fluoride ions in aqueous medium and in vivo. Dalton Trans. 2016, 45, 17616–17623. [Google Scholar] [CrossRef] [PubMed]
  24. Ngo, H.T.; Liu, X.; Jolliffe, K.A. Anion recognition and sensing with Zn(II)–dipicolylamine complexes. Chem. Soc. Rev. 2012, 41, 4928–4965. [Google Scholar] [CrossRef] [PubMed]
  25. Gupta, A.S.; Paul, K.; Luxami, V. Ratiometric fluorescent chemosensor for fluoride ion based on inhibition of excited state intramolecular proton transfer. Spectrochim. Aata A 2015, 138, 67–72. [Google Scholar] [CrossRef] [PubMed]
  26. Pillai, A.B.; Varghese, B.; Madhusoodanan, K.N. Design and Development of Novel Sensors for the Determination of Fluoride in Water. Environ. Sci. Technol. 2012, 46, 404–409. [Google Scholar] [CrossRef] [PubMed]
  27. Ren, X.X.; Wang, Y.; Meng, Q.T.; Jia, H.M.; Wang, Y.F.; Kong, X.F.; Duan, C.Y.; Zhang, Z.Q. A Coumarin–based Colorimetric and Fluorescent Chemosensor for the “Naked–eye” Detection of Fluoride ion in 100% Natural Water Medium Using Coated Chromatography Plates. ChemistrySelect 2016, 1, 4397–4402. [Google Scholar] [CrossRef]
  28. Liu, X.; Xu, J.; Lv, Y.; Wu, W.; Liu, W.; Tang, Y. An ATP-selective, lanthanide complex luminescent probe. Dalton Trans. 2013, 42, 9840–9846. [Google Scholar] [CrossRef] [PubMed]
  29. Mizukami, S.; Tonai, K.; Kaneko, M.; Kikuchi, K. Lanthanide-Based Protease Activity Sensors for Time-Resolved Fluorescence Measurements. J. Am. Chem. Soc. 2008, 130, 14376–14377. [Google Scholar] [CrossRef] [PubMed]
  30. Efimov, N.N.; Koroteev, P.S.; Gavrikov, A.V.; Ilyukhin, A.B.; Dobrokhotova, Z.V.; Novotortsev, V.M. Magnetic Behavior of Carboxylate and β-Diketonate Lanthanide Complexes Containing Stable Organometallic Moieties in the Core-Forming Ligand. Magnetochemistry 2016, 2, 38. [Google Scholar] [CrossRef]
  31. Vaněk, J.; Lubal, P.; Ševčíková, R.; Polášek, M.; Hermann, P. Mono(pyridine-N-oxide) analog of DOTA as a suitable organic reagent for a sensitive and selective fluorimetric determination of Ln(III) ions. J. Lumin. 2012, 132, 2030–2035. [Google Scholar] [CrossRef]
  32. Tripier, R.; Platas-Iglesias, C.; Boos, A.; Morfin, J.-F.; Charbonnière, L. Towards Fluoride Sensing with Positively Charged Lanthanide Complexes. Eur. J. Inorg. Chem. 2010, 2735–2745. [Google Scholar] [CrossRef]
  33. Li, W.; Fraser, E.; Meade, T.J. A Calcium-Sensitive Magnetic Resonance Imaging Contrast Agent. J. Am. Chem. Soc. 1999, 121, 1413–1414. [Google Scholar] [CrossRef]
  34. Major, J.L.; Boiteau, R.M.; Meade, T.J. Mechanisms of ZnII-Activated Magnetic Resonance Imaging Agents. Inorg. Chem. 2008, 47, 10788–10795. [Google Scholar] [CrossRef] [PubMed]
  35. Louie, Y.; Huber, M.M.; Ahrens, E.T.; Rothbacher, U.; Moats, R.; Jacobs, R.E.; Fraser, S.E.; Meade, T.J. In vivo visualization of gene expression using magnetic resonance imaging. Nat. Biotechnol. 2000, 18, 321–325. [Google Scholar] [PubMed]
  36. Gunnlaugsson, T.; Harte, A.J.; Leonard, J.P.; Nieuwenhuyzen, M. Delayed lanthanide luminescence sensing of aromatic carboxylates using heptadentate triamide Tb(III) cyclen complexes: The recognition of salicylic acid in water. Chem. Commun. 2002, 18, 2134–2135. [Google Scholar] [CrossRef]
  37. Wang, Y.; Jin, C.-W.; He, S.-M.; Ren, N.; Zhang, J.-J. Five novel lanthanide complexes with 2-chloroquinoline-4-carboxylic acid and 1,10-phenanthroline: Crystal structures, molecular spectra, thermal properties. J. Mol. Struct. 2016, 1125, 383–390. [Google Scholar] [CrossRef]
  38. Girginova, P.I.; Pereira, L.C.J.; Coutinho, J.T.; Santos, I.C.; Almeida, M. Slow magnetic relaxation in lanthanide ladder type coordination polymers. Dalton Trans. 2014, 43, 1897–1903. [Google Scholar] [CrossRef] [PubMed]
  39. Wang, Q.; Fan, Y.; Song, T.; Xu, J.; Wang, J.; Chai, J.; Liu, Y.; Wang, L.; Zhang, L. In situ synthesis of a series of lanthanide coordination polymers based on N-heterocyclic carboxylate ligands: Crystal structure and luminescence. Inorg. Chim. Acta 2015, 438, 128–134. [Google Scholar] [CrossRef]
  40. Gai, Y.-L.; Xiong, K.-C.; Chen, L.; Bu, Y.; Li, X.-J.; Jiang, F.-L.; Hong, M.-C. Visible and NIR Photoluminescence Properties of a Series of Novel Lanthanide–Organic Coordination Polymers Based on Hydroxyquinoline–Carboxylate Ligands. Inorg. Chem. 2012, 51, 13128–13137. [Google Scholar] [CrossRef] [PubMed]
  41. Choi, C.-L.; Yen, Y.-F.; Sung, H.H.-Y.; Siu, A.W.-H.; Jayarathne, S.T.; Wong, K.S.; Williams, I.D. Quantifying enhanced photoluminescence in mixed-lanthanide carboxylate polymers: Sensitizationversusreduction of self-quenching. J. Mater. Chem. 2011, 21, 8547–8549. [Google Scholar] [CrossRef]
  42. Plush, S.E.; Gunnlaugsson, T. Luminescent Sensing of Dicarboxylates in Water by a Bismacrocyclic Dinuclear Eu(III) Conjugate. Org. Lett. 2007, 9, 1919–1922. [Google Scholar] [CrossRef] [PubMed]
  43. Lo, L.-C.; Liao, Y.-C.; Kuo, C.-H.; Chen, C.-T. A Novel Coumarin-Type Derivatizing Reagent of Alcohols: Application in the CD Exciton Chirality Method for Microscale Structural Determination. Org. Lett. 2000, 2, 683–685. [Google Scholar] [CrossRef] [PubMed]
  44. Nithyakumar, A.; Alexander, V. Synthesis, relaxivity, and in vitro fluorescence imaging studies of a novel d–f heterometallic trinuclear complex as a potential bimodal imaging probe for MRI and optical imaging. Dalton Trans. 2015, 44, 17800–17809. [Google Scholar] [CrossRef] [PubMed]
  45. Faulkner, S.; Carrié, M.-C.; Pope, S.J.A.; Squire, J.; Beeby, A.; Sammes, P.G. Pyrene-sensitised near-IR luminescence from ytterbium and neodymium complexes. Dalton Trans. 2004, 15, 1405–1409. [Google Scholar] [CrossRef] [PubMed]
  46. Meng, Q.T.; Shi, Y.; Wang, C.P.; Jia, H.M.; Gao, X.; Zhang, R.; Wang, Y.F.; Zhang, Z.Q. NBD-based fluorescent chemosensor for theselective quantification of copper and sulfide inan aqueous solution and living cells. Org. Biomol. Chem. 2015, 13, 2918–2926. [Google Scholar] [CrossRef] [PubMed]
  47. Ishikawa, N.; Sugita, M.; Wernsdorfer, W. Quantum Tunneling of Magnetization in Lanthanide Single-Molecule Magnets: Bis(phthalocyaninato)terbium and Bis(phthalocyaninato)dysprosium Anions. Angew. Chem. Int. Ed. 2005, 44, 2931–2935. [Google Scholar] [CrossRef] [PubMed]
  48. Wei, C.; Wang, R.; Wei, L.; Cheng, L.; Li, Z.; Xi, Z.; Yi, L. o-Fluorination of Aromatic Azides Yields Improved Azido-Based Fluorescent Probes for Hydrogen Sulfide: Synthesis, Spectra, and Bioimaging. Chem. Asian J. 2014, 9, 3586–3592. [Google Scholar] [CrossRef] [PubMed]
  49. Choi, M.G.; Cha, S.; Lee, H.; Jeon, H.L.; Chang, S.-K. Sulfide-selective chemosignaling by a Cu2+ complex of dipicolylamine appended fluorescein. Chem. Comm. 2009, 47, 7390–7392. [Google Scholar] [CrossRef] [PubMed]
  50. Peng, B.; Chen, W.; Liu, C.; Rosser, E.W.; Pacheco, A.; Zhao, Y.; Aguilar, H.C.; Xian, M. Fluorescent Probes Based on Nucleophilic Substitution-Cyclization for Hydrogen Sulfide Detection and Bioimaging. Chem. Eur. J. 2014, 20, 1010–1016. [Google Scholar] [CrossRef] [PubMed]
  51. Meng, Q.T.; Jia, H.M.; Gao, X.; Wang, Y.; Zhang, R.; Wang, R.J.; Zhang, Z.Q. Reversible and Selective Fluorescence Detection of HistidineUsing a Naphthalimide-Based Chemosensing Ensemble. Chem. Asian J. 2015, 10, 2411–2418. [Google Scholar] [CrossRef] [PubMed]
  52. Blackburn, O.A.; Routledge, J.D.; Jennings, L.B.; Rees, N.H.; Kenwright, A.M.; Beer, P.D.; Faulkner, S. Substituent effects on fluoride binding by lanthanide complexes of DOTA-tetraamides. Dalton Trans. 2016, 45, 3070–3077. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Wang, F.; Wu, J.; Zhuang, X.; Zhang, W.; Liu, W.; Wang, P.; Wu, S. A highly selective fluorescent sensor for fluoride in aqueous solution based on the inhibition of excited-state intramolecular proton transfer. Sens. Actuators B 2010, 146, 260–265. [Google Scholar] [CrossRef]
  54. Mizukami, S.; Nagano, T.; Urano, Y.; Odani, A.; Kikuchi, K. A fluorescent anion sensor that works in neutral aqueous solution for bioanalytical application. J. Am. Chem. Soc. 2002, 124, 3920–3925. [Google Scholar] [CrossRef] [PubMed]
  55. Koteeswari, R.; Ashokkumar, P.; Malar, E.J.P.; Ramakrishnan, V.T.; Ramamurthy, P. Highly selective, sensitive and quantitative detection of Hg2+ in aqueous medium under broad pH range. Chem. Commun. 2011, 47, 7695–7697. [Google Scholar] [CrossRef] [PubMed]
  56. Shen, C.; New, E.J. Promising strategies for Gd-based responsive magnetic resonance imaging contrast agents. Curr. Opin. Chem. Biol. 2013, 17, 158–166. [Google Scholar] [CrossRef] [PubMed]
  57. Xie, N.; Feng, K.; Chen, B.; Zhao, M.; Peng, S.; Zhang, L.-P.; Tung, C.-H.; Wu, L.-Z. Water-soluble copolymeric materials: Switchable NIR two-photon fluorescence imaging agents for living cancer cells. J. Mater. Chem. B 2014, 2, 502–510. [Google Scholar] [CrossRef]
  58. Shibu, E.S.; Sugino, S.; Ono, K.; Saito, H.; Nishioka, A.; Yamamura, S.; Sawada, M.; Nosaka, Y.; Biju, V. Singlet-oxygen-sensitizing near-infrared-fluorescent multimodal nanoparticles. Angew. Chem. Int. Ed. 2013, 52, 10559–10563. [Google Scholar] [CrossRef] [PubMed]
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Scheme 1. Proposed dual-modal responses mechanism of DO3A-Gd-CA towards fluoride ion.
Scheme 1. Proposed dual-modal responses mechanism of DO3A-Gd-CA towards fluoride ion.
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Figure 1. UV-Vis absorption spectra of CA (10 μM) in the presence of increasing amount of DO3A-Gd (0–15.0 μM) in CH3CN-H2O (9:1, v/v, pH = 7.4). Insert: The maximum absorbance band of CA at 430 nm against the concentrations of DO3A-Gd.
Figure 1. UV-Vis absorption spectra of CA (10 μM) in the presence of increasing amount of DO3A-Gd (0–15.0 μM) in CH3CN-H2O (9:1, v/v, pH = 7.4). Insert: The maximum absorbance band of CA at 430 nm against the concentrations of DO3A-Gd.
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Figure 2. Fluorescence spectra of CA (10 μM) in CH3CN-H2O (9:1, v/v, pH = 7.4) in the presence of different amounts of DO3A-Gd (0–15.0 μM). Insert: Fluorescence intensities of CA at 460 nm as a function of the concentration of DO3A-Gd. Excitation was performed at 408 nm.
Figure 2. Fluorescence spectra of CA (10 μM) in CH3CN-H2O (9:1, v/v, pH = 7.4) in the presence of different amounts of DO3A-Gd (0–15.0 μM). Insert: Fluorescence intensities of CA at 460 nm as a function of the concentration of DO3A-Gd. Excitation was performed at 408 nm.
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Figure 3. UV-Vis absorption spectra of DO3A-Gd-CA (10 μM) in the presence of increasing concentrations of fluoride ions (0–200 μM) in CH3CN-H2O (9:1, v/v, pH = 7.4). Insert: Ratiometric changes of absorbance band of CA (A430/A402) as a function of fluoride ions concentrations.
Figure 3. UV-Vis absorption spectra of DO3A-Gd-CA (10 μM) in the presence of increasing concentrations of fluoride ions (0–200 μM) in CH3CN-H2O (9:1, v/v, pH = 7.4). Insert: Ratiometric changes of absorbance band of CA (A430/A402) as a function of fluoride ions concentrations.
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Figure 4. UV-Vis absorption spectra of DO3A-Gd-CA (10 μM) in the presence of various anions (200 μM) in CH3CN-H2O (9:1, v/v, pH = 7.4): H2PO4− (0.2 mM), PO43− (1 mM), HSO4− (0.2 mM), Br−(0.2 mM), I− (0.2 mM), NO3− (0.2 mM), OH− (0.2 mM), AcO− (0.2 mM), Cl− (100 mM), F− (0.2 mM).
Figure 4. UV-Vis absorption spectra of DO3A-Gd-CA (10 μM) in the presence of various anions (200 μM) in CH3CN-H2O (9:1, v/v, pH = 7.4): H2PO4− (0.2 mM), PO43− (1 mM), HSO4− (0.2 mM), Br−(0.2 mM), I− (0.2 mM), NO3− (0.2 mM), OH− (0.2 mM), AcO− (0.2 mM), Cl− (100 mM), F− (0.2 mM).
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Figure 5. Fluorescence spectra of DO3A-Gd-CA (10 μM) in the presence of different concentrations of fluoride ion (0–200 μM). Insert: Fluorescence intensities of DO3A-Gd-CA (10 μM) at 460 nm as a function of fluoride ions concentration (0–200 μM). Excitation was performed at 408 nm.
Figure 5. Fluorescence spectra of DO3A-Gd-CA (10 μM) in the presence of different concentrations of fluoride ion (0–200 μM). Insert: Fluorescence intensities of DO3A-Gd-CA (10 μM) at 460 nm as a function of fluoride ions concentration (0–200 μM). Excitation was performed at 408 nm.
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Figure 6. Changes in fluorescence intensity of DO3A-Gd-CA (10 μM) toward fluoride ion in the presence of various competing anions in CH3CN-H2O (9:1, v/v, pH = 7.4): 1. H2PO4− (0.2 mM), 2. PO43− (1 mM), 3. HSO4− (0.2 mM), 4. Br− (0.2 mM), 5. I− (0.2 mM), 6. NO3− (0.2 mM), 7. OH− (0.2 mM), 8. AcO− (0.2 mM), 9. Cl− (100 mM), 10. F− (0.2 mM), and 11. All anions mixed. The intensities were recorded at 460 nm, excitation at 408 nm.
Figure 6. Changes in fluorescence intensity of DO3A-Gd-CA (10 μM) toward fluoride ion in the presence of various competing anions in CH3CN-H2O (9:1, v/v, pH = 7.4): 1. H2PO4− (0.2 mM), 2. PO43− (1 mM), 3. HSO4− (0.2 mM), 4. Br− (0.2 mM), 5. I− (0.2 mM), 6. NO3− (0.2 mM), 7. OH− (0.2 mM), 8. AcO− (0.2 mM), 9. Cl− (100 mM), 10. F− (0.2 mM), and 11. All anions mixed. The intensities were recorded at 460 nm, excitation at 408 nm.
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Figure 7. Changes in the longitudinal relaxivity (r1) of DO3A-Gd-CA (0.2 mM) as a function of the fluoride ion concentration (0–0.5 mM) in CH3CN-H2O (9:1, v/v, pH = 7.4). Insert: T1-weighted MR images of DO3A-Gd-CA recorded versus different concentrations of fluoride ion: (a) 0 mM; (b) 0.1 mM; (c) 0.3 mM; (d) 0.5 mM.
Figure 7. Changes in the longitudinal relaxivity (r1) of DO3A-Gd-CA (0.2 mM) as a function of the fluoride ion concentration (0–0.5 mM) in CH3CN-H2O (9:1, v/v, pH = 7.4). Insert: T1-weighted MR images of DO3A-Gd-CA recorded versus different concentrations of fluoride ion: (a) 0 mM; (b) 0.1 mM; (c) 0.3 mM; (d) 0.5 mM.
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Figure 8. Longitudinal relaxivity (r1) responses of DO3A-Gd-CA (0.2 mM) to various anions of interest (0.5 mM) in CH3CN-H2O (9:1, v/v, pH = 7.4). Insert: T1-weighted MR images (T1 measurements at a proton frequency of 20 MHz) of DO3A-Gd-CA (0.2 mM ) in the presence of (1) Br− (0.5 mM); (2) I− (0.5 mM); (3) Cl− (100 mM); (4) PO43− (1.0 mM); (5) H2PO4− (0.5 mM); (6) HSO4− (0.5 mM); (7) NO3− (0.5 mM); (8) OH− (0.5 mM); (9) AcO− (0.5 mM); (10) F− (0.5 mM); and (11) All anions mixture.
Figure 8. Longitudinal relaxivity (r1) responses of DO3A-Gd-CA (0.2 mM) to various anions of interest (0.5 mM) in CH3CN-H2O (9:1, v/v, pH = 7.4). Insert: T1-weighted MR images (T1 measurements at a proton frequency of 20 MHz) of DO3A-Gd-CA (0.2 mM ) in the presence of (1) Br− (0.5 mM); (2) I− (0.5 mM); (3) Cl− (100 mM); (4) PO43− (1.0 mM); (5) H2PO4− (0.5 mM); (6) HSO4− (0.5 mM); (7) NO3− (0.5 mM); (8) OH− (0.5 mM); (9) AcO− (0.5 mM); (10) F− (0.5 mM); and (11) All anions mixture.
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Figure 9. T1-weighted MR pseudocolor images of living white mice injection of: (a) Control group; (b) DO3A-Gd-CA (0.2 mL, 0.2 mM) only; (c) DO3A-Gd-CA (0.2 mL, 0.2 mM) + 0.5 mM fluoride ions.
Figure 9. T1-weighted MR pseudocolor images of living white mice injection of: (a) Control group; (b) DO3A-Gd-CA (0.2 mL, 0.2 mM) only; (c) DO3A-Gd-CA (0.2 mL, 0.2 mM) + 0.5 mM fluoride ions.
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MDPI and ACS Style

Wang, Y.; Song, R.; Feng, H.; Guo, K.; Meng, Q.; Chi, H.; Zhang, R.; Zhang, Z. Visualization of Fluoride Ions In Vivo Using a Gadolinium(III)-Coumarin Complex-Based Fluorescence/MRI Dual-Modal Probe. Sensors 2016, 16, 2165. https://doi.org/10.3390/s16122165

AMA Style

Wang Y, Song R, Feng H, Guo K, Meng Q, Chi H, Zhang R, Zhang Z. Visualization of Fluoride Ions In Vivo Using a Gadolinium(III)-Coumarin Complex-Based Fluorescence/MRI Dual-Modal Probe. Sensors. 2016; 16(12):2165. https://doi.org/10.3390/s16122165

Chicago/Turabian Style

Wang, Yue, Renfeng Song, Huan Feng, Ke Guo, Qingtao Meng, Haijun Chi, Run Zhang, and Zhiqiang Zhang. 2016. "Visualization of Fluoride Ions In Vivo Using a Gadolinium(III)-Coumarin Complex-Based Fluorescence/MRI Dual-Modal Probe" Sensors 16, no. 12: 2165. https://doi.org/10.3390/s16122165

APA Style

Wang, Y., Song, R., Feng, H., Guo, K., Meng, Q., Chi, H., Zhang, R., & Zhang, Z. (2016). Visualization of Fluoride Ions In Vivo Using a Gadolinium(III)-Coumarin Complex-Based Fluorescence/MRI Dual-Modal Probe. Sensors, 16(12), 2165. https://doi.org/10.3390/s16122165

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