英语专业论文翻译

A smart copper(II)-responsive binucleargadolinium(III) complex-based magnetic resonanceimaging contrast agent†

Yan-meng Xiao,ab Gui-yan Zhao,ab Xin-xiu Fang,ab Yong-xia Zhao,ab Guan-hua Wang,c Wei Yang*a and Jing-wei Xu*a A novel Gd-DO3A-type bismacrocyclic complex, [Gd2(DO3A)2BMPNA], with a Cu2+-selective binding unitwas synthesized as a potential “smart” copper(II)-responsive magnetic resonance imaging (MRI) contrast agent.The relaxivity of the complex was modulated by the presence or absence of Cu2+; in the absence of Cu2+, the complex exhibited a relatively low relaxivity value (6.40 mM1 s1), while the addition of Cu2+ triggered an approximately 76% enhancement in relaxivity (11.28 mM1 s1).Moreover, this Cu2+- responsive contrast agent was highly selective in its response to Cu2+ over other biologically-relevant metal ions.The influence of some common biological anions on the Cu2+-responsive contrast agent and the luminescence lifetime of the complex were also studied.The results of the luminescence lifetime measurements indicated that the enhancement in relaxivity was mainly ascribed to the increased number of inner-sphere water molecules binding to the paramagnetic Gd3+ core upon the addition of Cu2+.In addition, the visual change aociated with the significantly enhanced relaxivity due to the addition of Cu2+ was observed from T1-weighted phantom images.Introduction Copper(II) ion is a vital metal nutrient for the metabolism of life and plays a critical role in various biological procees.1,2 Its homeostasis is critical for the metabolism and development of living organisms.3,4 On the other hand, the disruption of its homeostasis may lead to a variety of physical diseases and neurological problems such as Alzheimer\'s disease,5 Menkes and Wilson\'s disease,6 amyotrophic lateral sclerosis,7,8 and prion disease.9,10 Therefore, the aement and understanding of the distribution of biological copper in living systems by noninvasive imaging is crucial to provide more insight into copper homeostasis and better understand the relationship between copper regulation and its physiological function.A wide variety of organic uorescent dyes have been exploited for the optical detection of ions in the last few decades.11–13However, optical imaging using organic uorescent dyes haeveral limitations such as photobleaching, light scattering,limited penetration, low spatial resolution and the disturbance of auto uorescence.14 By comparison, magnetic resonance imaging (MRI) is an increasingly acceible technique used as a noninvasive clinical diagnostic modality for medical diagnosis and biomedical research.15 It can provide high spatial resolution three-dimensional anatomical images with information about physiological signals and biochemical events.16 As a powerful diagnostic imaging tool in medicine, MRI can distinguish normal tiue from diseased tiue and lesions in a noninvasive manner,17–19 which avoids diagnostic thoracotomy or laparotomy surgery for medical diagnoses and greatly improves the diagnostic efficiency.Multiple MRI imaging parameters can provide a wealth of diagnostic information.In addition, the desired cro-section for acquiring multi-angle and multi-planar images of various parts of the entire body can be freely chosen by adjusting the MRI magnetic eld; this ability makes medical diagnostics and studies of the body\'s metabolism and function more and more effective and convenient.

Contrast agents are often used in MRI examinations to improve the resolution and sensitivity; the image quality can be signicantly improved by applying contrast agents which enhance the MRI signal intensity by increasing the relaxation rates of the surrounding water protons.20 Due to the high magnetic moment (seven unpaired electrons) and slow electronic relaxation of the

paramagnetic gadolinium(III) ion, gadolinium(III)-based MRI contrast agents are commonly employed to increase the relaxation rate of the surrounding water protons.16,21 However, most of these contrast agents are nonspecific and provide only anatomical information.On the basis of Solomon–Bloembergen–Morgan theory,22–24 several parameters can be manipulated to alter the relaxivity of gadolinium(III)-based MRI contrast agents.These parameters include the number of coordinated water molecules (q), the rotational correlation time (sR) and the residence lifetime of coordinated water molecules bound to the paramagnetic Gd3+ center (sM).Adjusting any of these three factors provides the opportunity to design “smart” MRI contrast agents for specific biochemical events.25–27 In recent years, there have been many studies on the development of responsive gadolinium(III)-based MRI contrast agents; most of them have focused on the development of targeted, high relaxivity and bioactivated contrast agents.These responsive gadolinium(III)-based MRI contrast agents can be modulated by particular in vivo stimuli including pH,28–35 metal ion concentration36–43 and enzyme activity.44–50 Notably, a number of copper-responsive MRI contrast agents have been reported to detect uctuations of copper ions in vivo.51–58 These activated contrast agents exploit the modulation of the number of coordinated water molecules to generate distinct enhancements in longitudinal relaxivity in response to copper ions (Cu+ or Cu2+).In this study, we designed and synthesized a binuclear gadolinium-based MRI contrast agent, [Gd2(DO3A)2BMPNA], that is specically responsive to Cu2+ over other biologicallyrelevant metal ions.The new copper-responsive MRI contrast agent comprises two Gd-DO3A cores connected by a 2,6-bis(3- methyl-1H-pyrazol-1-yl)isonicotinic acid scaffold59,60 (BMPNA), which functions as a receptor for copper-induced relaxivity switching.The synthetic strategy for [Gd2(DO3A)2BMPNA] is depicted in Scheme 1.Subsequently, the T1 relaxivity of [Gd2(DO3A)2BMPNA] was studied at 25 C and 60 MHz in the absence or presence of Cu2+.Experiments to determine the selectivity of [Gd2(DO3A)2BMPNA] towards Cu2+ over other biologically-relevant ions were carried out as well.Luminescence lifetime was measured to determine the number of coordinated water molecules (q) of [Gd2(DO3A)2BMPNA] in the absence or presence of Cu2+.In addition, T1-weighted phantom images were collected to visualize the relaxivity enhancement caused by Cu2+, suggesting potential in vivo applications.Experimental section

Materials and instruments

All materials for synthesis were purchased from commercial suppliers and used without further purication.1H and 13C NMR spectra were taken on an AMX600 Bruker FT-NMR spectrometer with tetramethylsilane (TMS) as an internal standard.Luminescence measurements were performed on a Hitachi Fluorescence spectrophotometer-F-4600.The time-resolved luminescence emiion spectra were recorded on a Perkin- Elmer LS-55 uorimeter with the following conditions: excitation wavelength, 295 nm; emiion wavelength, 545 nm; dela time, 0.02 ms; gate time, 2.00 ms; cycle time, 20 ms; excitation slit, 5 nm; emiion slit, 10 nm.The luminescence lifetime was measured on a Lecroy Wave Runner 6100 Digital Oscilloscope (1 GHz) using a tunable laser (pulse width ¼ 4 ns, gate ¼ 50 ns) as the excitation (Continuum Sunlite OPO).Ma spectra (MS) were obtained on an auto ex III TOF/TOF MALDI-MS and anIonSpec ESI-FTICR ma spectrometer.Elemental analyses were performed on a Vario EL Element Analyzer. Synthesis Synthesis of compound 3.Methyl 2,6-bis(3-(bromomethyl)-1H-pyrazol-1-yl) isonicotinate (Compound1)59,60 and 4,7,10- tris(2-(tert-butoxy)-2-oxoethyl)-4,7,10-triaza-azoniacyclododecan-1-ium bromide (Compound 2)61 were prepared following thereported methods.Compound 2 (0.25 g, 0.296 mmol) was suspended in 2 ml anhydrous acetonitrile with 6 equivalents of NaHCO3 (0.1492 g) and the mixture was stirred at room temperature for 0.5 h.Compound 1 (0.0675 g, 0.148 mmol) was added, and the mixture was slowly heated to reflux (80 C) and stirred overnight.After the reaction was terminated, the mixture was cooled to room temperature, and the solution was ltered.The precipitate was washed several times with anhydrous acetonitrile, and the collected ltrate solution was evaporated under reduced preure.The residue was puried using silicagel column chromatography eluted with CH2Cl2–n-hexane–CH3OH (10 : 3 : 1, v/v/v) to afford Compound 3 (0.1038 g, 53%) as a pale yellow solid.1H NMR (600 MHz, DMSO): 8.22 (s, 2H), 8.15 (s, 2H), 6.62 (s, 2H), 4.53 (s, 4H), 3.82 (s, 3H), 3.42 (m, 4H), 2.98 (m, 8H), 2.85 (s, 8H), 2.71 (m, 24H), 1.33 (s, 54H) (Fig.S1†).13C NMR (151 MHz, CDCl3): d 173.21, 172.44, 163.99, 152.38, 150.11, 143.13, 128.07, 109.83, 108.36, 82.59, 57.84, 56.52, 56.06, 55.56, 52.98, 50.55, 48.91, 47.30, 27.96 (Fig.S2†).HRMS (ESI): m/z calc.for C67H111N13O14 [M + 2H]2+ 661.92650, [M + H + Na]2+ 672.91747, [M + 2Na]2+ 683.90844, found [M + 2H]2+ 661.92584, [M+ H + Na]2+ 672.91690, [M + 2Na]2+ 683.90682 (Fig.S3†).

Synthesis of compound 4.Compound 3 (0.1 g, 0.0756 mmol) was stirred with triuoroacetic acid in methylene chloride solution (2 ml) at room temperature for 24 h.The solvent was then evaporated under reduced preure, and the residue was washed three times in CH3OH and CH2Cl2 to eliminate exce acid.The obtained residue was diolved with a minimum volume of CH3OH and precipitated with cold Et2O.The precipitate was ltered to afford a brown yellow solid (0.1022 g).1H NMR (600 MHz, DMSO): 9.06 (s, 2H), 8.17 (s, 2H), 6.84 (s, 2H), 4.33 (s, 4H), 3.98 (s, 3H), 3.56 (b, 20H), 3.09 (m, 24H) (Fig.S4†).13C NMR (151 MHz, D2O): d 174.11, 169.13, 164.64, 150.75, 148.85, 142.10, 129.88, 109.75, 107.99, 55.69, 54.01, 53.10, 52.43, 51.15, 49.59, 48.22, 47.69 (Fig.S5†).MALDI-TOFMS spectrum (CH3OH): m/z calc.for C43H63N13O14 [M H] 984.46, found 984.7 (Fig.S6†).Anal calc.for C43H63N13O14- $3CF3COOH$2H2O: C, 43.14; H, 5.17; N, 13.35; found C, 42.34; H, 4.999; N, 13.29%.Preparation of [Gd2(DO3A)2BMPNA] and [Tb2(DO3A)2- BMPNA].Compound 4 (0.05 mmol) was diolved in 2 ml of highly-puried water.GdCl3 or TbCl3 (0.1 mmol) was added dropwise.The pH was maintained at 6.5–7.0 with NaOH during the whole proce.The solution was then stirred at 75 C for 24 h.MALDI-MS (H2O): m/z calc.for C42H55N13O14Gd2 [M + H]+ 1281.46, found 1281.4 (Fig.S7†).MALDI-MS (H2O): m/z calc.for C42H55N13O14Tb2 [M + H]+ 1284.3, found 1284.4 (Fig.S8†).

T1 measurements.The longitudinal relaxation times (T1) of aqueous solutions of [Gd2(DO3A)2BMPNA] were measured on an HT-MRSI60-25 spectrometer (Shanghai Shinning Globe Science and Education Equipment Co., Ltd) at 1.5 T.All of the tested samples were prepared in HEPES-buffered aqueous solutions at pH 7.4.All of the metal ions (Na+, K+, Ca2+, Mg2+, Cu2+, Zn2+, Fe3+, Fe2+) were used as chloride salts.Concentrations of Gd3+ were determined by ICP-OES.Relaxivities were determined from the slope of the plot of 1/T1 vs.[Gd].The data were tted to the following eqn (1),20

(1/T1)obs ¼ (1/T1)d + r1[M] (1)

where (1/T1)obs and (1/T1)d are the observed values in the presence and absence of the paramagnetic species, respectively, and [M] is the concentration of paramagnetic [Gd].

Luminescence measurements.Luminescence emiion spectra were collected on a Hitachi uorescence spectrophotometer-F-4600.The luminescence lifetime was measured on a Lecroy Wave Runner 6100 Digital Oscilloscope (1 GHz) using a tunable laser (pulse width ¼ 4 ns, gate ¼ 50 ns) as the excitation (Continuum Sunlite OPO).Samples were excited at 290 nm, and the emiion maximum (545 nm) was used to determine luminescence lifetimes.The Tb(III)-based emiion spectra were measured using 0.1 mM solutions of Tb complex analog in 100 mM HEPES buffer at pH 7.4 in H2O and D2O in the absence and presence of Cu2+.The number of coordinated water molecules (q) was calculated according to eqn (2):62,63 q= ¼ 5(sH2O1 sD2O1 0.06) (2) T1-weighted MRI phantom images.Phantom images were collected on a 1.5 T HT-MRSI60-25 spectrometer (Shanghai Shinning Globe Science and Education Equipment Co., Ltd).Instrument parameter settings were as follows: 1.5 T magnet; matrix =256 256; slice thickne =1 mm; TE= 13 ms; TR= 100 ms; and number of acquisitions =1.Results and discuion Longitudinal relaxivity of [Gd2(DO3A)2BMPNA] in response to copper(II) ion To investigate the inuence of Cu2+ on the relaxivity of [Gd2(DO3A)2BMPNA], the longitudinal relaxivity r1 for the [Gd2(DO3A)2BMPNA] contrast agent was determined using T1 measurements in the absence or presence of Cu2+ at 60 MHz and 25 C using a 0.2mMGd3+ solution of [Gd2(DO3A)2BMPNA] in 100 mM HEPES buffer (pH 7.4) under simulated physiological conditions.The concentrations of Gd3+ were determined by ICP-OES.The relaxivity r1 was calculated from eqn (1).In the absence of Cu2+, the relaxivity of [Gd2(DO3A)2BMPNA] was 6.40 mM1 s1, which was higher than that of [Gd(DOTA)(H2O)] (4.2 mM1 s1, 20 MHz, 25 C) and Gd(DO3A)(H2O)2 (4.8 mM1 s1, 20 MHz, 40 C).64 Upon addition of up to 1 equiv.of Cu2+, the relaxivity of [Gd2(DO3A)2BMPNA] increased to 11.28 mM1 s1 (76% relaxivity enhancement).As shown in Fig.1, the relaxivity gradually increased with the copper ion concentration, reaching a maximum value of approximately 1.2 equivalents of Cu2+.Due to the use of triuoroacetic acid in the synthesis of Compound 4, triuoroacetic acid residues produced CF3COO in the [Gd2(DO3A)2BMPNA] solution, allowing CF3COO to partially coordinate with Cu2+ to form “Chinese lantern” type structure complexes.65 When the amount of added copper ions was further increased to above 1.2 equiv., the relaxivity was maintained at the same level.The observed difference in Cu2+-triggered relaxivity enhancement demonstrated the ability of this contrast agent to sense Cu2+ in vivo by means of MRI.Our designed contrast agent not only exhibited a higher relaxivity, but also displayed a Cu2+-responsive relaxivity enhancement.

Selectivity studies The relaxivity response of [Gd2(DO3A)2BMPNA] exhibited excellent selectivity for Cu2+ over a variety of other competing, biologically-relevant metal ions at physiological levels.As depicted in Fig.2 (white bars), the addition of alkali metal cations (10 mM Na+, 2 mM K+) and alkaline earth metal cations (2 mM Mg2+, 2 mM Ca2+) did not generate an increase in relaxivity compared to the copper ion turn-on response; even the introduction of d-block metal cations (0.2 mM Fe2+, 0.2 mM Fe3+, 0.2 mM or 2 mM Zn2+) did not trigger relaxivity enhancements.We noted that Zn2+ is also known to replace Gd3+ in transmetalation experiments; however, studies with analogous Gd3+-DO3A complexes demonstrated that this ligand is more kinetically inert to metal-ion exchange.66 To ensure the kinetic stability of the complex, we used MS to monitor [Gd2(DO3A)2BMPNA] in the presence of 1 equiv.of Zn2+.No metal-ion exchange was observed at room temperature after 7 days (Fig.S13†).Relaxivity interference experiments for [Gd2(DO3A)2BMPNA] in the presence of both Cu2+ (0.2 mM) and other biologically-relevant metal ions were also conducted; the results are shown as black bars in Fig.2, indicating that these biologically-relevant metal ions (Na+, K+, Mg2+, Ca2+, Fe2+, Fe3+, Zn2+) had no interference on the Cu2+-triggered relaxivity enhancement.

In addition, we also tested the Cu2+ response for [Gd2(DO3A)2BMPNA] in the presence of physiologically-relevant concentrations of common biological anions to determine whether the Cu2+-triggered relaxivity enhancement was affected by biological anions at physiological levels.As previously mentioned, Cu2+ binding induced an enhancement in relaxivity from 6.40 mM1 s1 to 11.28 mM1 s1 (a 76% increase).As shown in Fig.3, in the presence of citrate (0.13 mM), lactate (0.9 mM), H2PO4 (0.9 mM), or HCO3 (10 mM), the Cu2+-triggered relaxivity enhancement was approximately 61% (from 6.01 mM1 s1 to 9.66mM1 s1), 66% (from 6.13mM1 s1 to 10.16 mM1 s1), 20% (from 5.88 mM1 s1 to 7.02 mM1 s1), or 55% (from 6.15 mM1 s1 to 9.55 mM1 s1), respectively.Additionally, 100 mM NaCl had almost no effect (an approximately 75% increase), and a simulated extracellular anion solution (EAS, contain 30 mM NaHCO3, 100 mM NaCl, 0.9 mM KH2PO4, 2.3 mM sodium lactate, and 0.13 mM sodium citrate, pH =7),67 resulted in a Cu2+-triggered relaxivity enhancement of approximately 26% (from 6.02 mM1 s1 to 7.56 mM1 s1).Generally, the results revealed that lactate, citrate, and HCO3 had slight impacts on the Cu2+-triggered relaxivity enhancement, while H2PO4 and EAS influenced the enhancement to a greater degree.As shown in Scheme 2, [Gd2(DO3A)2BMPNA] poeed two water molecules after the addition of 1 equiv.Of Cu2+.According to the work of Dickins and coworkers, in lanthanide complexes with two water molecules, the waters can be partially displaced by phosphate, carbonate, acetate, carboxylate, lactate and citrate at different levels.68–70 The influence of these anions on the Cu2+-triggered relaxivity enhancement may be attributed to the partial replacement of coordinated water molecules by these anions.The relatively high concentration of phosphate could likely replace coordinated water molecules to reduce the increased number of water molecules surrounding the paramagnetic Gd3+ centre induced by Cu2+.As shown in Table 1, we measured the number of water molecules in the rst coordination sphere of Tb3+ in the presence of phosphate; the number of coordinated water molecules (q) decreased from 1.5 to 0.8.

Coordination features Luminescence lifetime experiments were performed to explore the mechanism of the Cu2+-triggered relaxivity enhancement.Luminescence lifetime measurements of lanthanide complexes have been widely used to quantify the number of inner-sphere water molecules.71 In particular, Tb3+ and Eu3+ have commonly been applied for lifetime measurements because their emiion spectra are in the visible region when their 4f electrons are relaxed from higher energy levels to the lowest energy multiplets.72,73 Therefore, the Tb3+ analogue of [Gd2(DO3A)2BMPNA], [Tb2(DO3A)2BMPNA], was prepared according to a similar method, and the luminescence lifetimes of the Tb3+ analogue in HEPES-buffered H2O and D2O in the absence and presence of Cu2+ were measured.As shown in Fig.S9,† the luminescence decay curve of [Tb2(DO3A)2BMPNA] was tted to obtain the luminescence lifetimes74 (Table 1), and the number of coordinated water molecules (q) was calculated by eqn (2).The analysis results (Table 1) for [Tb2(DO3A)2BMPNA] in HEPES-bufferedH2OandD2O in the absence and presence of Cu2+ indicated that q increased from 0.6 to 1.5 upon the addition of 1 equiv.of Cu2+; this result indicated that the Cu2+-triggered relaxivity enhancement for [Gd2(DO3A)2BMPNA] was most likely due to the increased number of coordinated water molecules around the Gd3+ ion upon Cu2+ binding to the pyrazole centre (Scheme 2).Aer the addition of Cu2+, Cu2+ removed the pyrazole centre N atom from the paramagnetic Gd3+ ion to generate an open coordination site available for a water molecule.Luminescence emiion titrations of [Tb2(DO3A)2BMPNA] towards Cu2+ were also performed to investigate the binding properties of the contrast agent towards Cu2+.Upon addition of 1 equiv.Cu2+, the luminescence of [Tb2(DO3A)2BMPNA] at 545 nm decreased gradually and reached a minimum due to the quenching nature of the paramagnetic Cu2+ (Fig.S10†).The titration data indicated a 1 : 1 binding stoichiometry (Scheme 2) Copper-responsive T1-weighted phantom MRI in vitro To demonstrate the potential feasibility of this Cu2+-responsive [Gd2(DO3A)2BMPNA] for copper-imaging applications, T1- weighted phantom images of [Gd2(DO3A)2BMPNA] were acquired in the absence and presence of copper ions.The phantom images depicted in Fig.4 displayed distinct increases in image intensity in the presence of 1 equiv.Cu2+ compared with those without Cu2+ (Fig.4D).Moreover, some of the other competing metal ions were also tested to further verify the selectivity of [Gd2(DO3A)2BMPNA] towards Cu2+.Discernible differences were not observed upon the addition of Mg2+ (Fig.4C), Zn2+ (Fig.4E), or Ca2+ (Fig.4F).In addition, we also tested the clinical contrast agent Magnevist (Fig.4G); the image intensity was a bit darker than that of our contrast agent.Conclusions

In conclusion, we designed and synthesized a novel bismacrocyclic DO3A-type Cu2+-responsive MRI contrast agent, [Gd2(DO3A)2BMPNA].The new Cu2+-responsive MRI contrast agent comprised two Gd-DO3A cores connected by a 2,6-bis(3-methyl-1H-pyrazol-1-yl)isonicotinic acid scaffold (BMPNA) that functioned as a Cu2+ receptor switch to induce a distinct relaxivity enhancement in response to Cu2+; the relaxivity was increased up to 76%.Importantly, the complex exhibited high selectivity for Cu2+ over a range of other biologically-relevant metal ions at physiological levels.Luminescence lifetime experiment results showed that the number of inner-sphere water molecules (q) increased from 0.6 to 1.5 upon the addition of 1 equiv.Cu2+.When Cu2+ was coordinated in the central part of the complex, the donor N atom of the pyrazole centre was removed from the paramagnetic Gd3+ ion and replaced by a water molecule (Scheme 2).Consequently, the Cu2+-triggered relaxivity enhancement could be ascribed to the increase in the number of inner-sphere water molecules.The designed contrast agent had a longitudinal relaxivity of 6.40 mM1 s1, which was higher than that of [Gd(DOTA)(H2O)] (4.2 mM1 s1, 20 MHz, 25 C) and Gd(DO3A)(H2O)2 (4.8 mM1 s1, 20 MHz, 40 C).In addition, the visual change aociated with the signicantly enhanced relaxivity from the addition of Cu2+ was observed in T1-weighted phantom images.Acknowledgements We are grateful to the State Key Laboratory of Electroanalytical Chemistry for nancial support.Notes and references 1 S.Puig and D.J.Thiele, Curr.Opin.Chem.Biol., 2002, 6, 171.2 S.C.Leary, D.R.Winge and P.A.Cobine, Biochim.Biophys.Acta, Gen.Subj., 2009, 146, 1793.3 D.D.Agranoff and S.Krishna, Mol.Microbiol., 1998, 28, 403.4 H.Kozlowski, A.Janicka-Klos, J.Brasun, E.Gaggelli, D.Valensin and G.Valensin, Coord.Chem.Rev., 2009, 253, 2665.5 K.J.Barnham, C.L.Masters and A.I.Bush, Nat.Rev.Drug Discovery, 2004, 3, 205.6 D.J.Waggoner, T.B.Bartnikas and J.D.Gitlin, Neurobiol.Dis., 1999, 6, 221.7 J.S.Valentine and P.J.Hart, Proc.Natl.Acad.Sci.U.S.A., 2003, 100, 3617.8 L.I.Bruijn, T.M.Miller and D.W.Cleveland, Annu.Rev.Neurosci., 2004, 27, 723.9 G.L.Millhauser, Acc.Chem.Res., 2004, 37, 79.10 D.R.Brown and H.Kozlowski, Dalton Trans., 2004, 1907.11 A.W.Czarnik, Acc.Chem.Res., 1994, 27, 302.12 L.Prodi, F.Bolletta, M.Montalti and N.Zaccheroni, Coord.Chem.Rev., 2000, 205, 59.13 H.N.Kim, M.H.Lee, H.J.Kim, J.S.Kim and J.Yoon, Chem.Soc.Rev., 2008, 37, 1465.14 M.Mahmoudi, V.Serpooshan and S.Laurent, Nanoscale, 2011, 3, 3007.15 P.A.Rinck, Magnetic Resonance Imaging, Blackwell Science, Berlin, 4th edn, 2001, p.149.16 A.E.Merbach and ´E.T´oth, The Chemistry of Contrast Agents in Medical Magnetic Resonance Imaging, John Wiley & Sons, Ltd., New York, 2001.17 S.Aime, E.Terreno, D.D.Castelli and A.Viale, Chem.Rev., 2010, 110, 3019.18 S.Aime, M.Fasano and E.Terreno, Chem.Soc.Rev., 1998, 27, 19.19 M.Woods, D.E.Woener and A.D.Sherry, Chem.Soc.Rev., 2006, 35, 500.20 R.B.Lauffer, Chem.Rev., 1987, 87, 901.21 J.Kowalewski, D.Kruk and J.Parigi, Adv.Inorg.Chem., 2005, 57, 42.22 I.Solomon, Phys.Rev., 1955, 99, 559.23 N.Bloembergen, J.Chem.Phys., 1957, 27, 572.24 N.Bloembergen and L.O.Morgan, J.Chem.Phys., 1961, 34, 842.25 E.L.Que and C.J.Chang, Chem.Soc.Rev., 2010, 39, 51.26 C.S.Bonnet and ´E.T´oth, Future Med.Chem., 2010, 2, 367.27 L.Prodi, F.Bolletta, M.Montalti and N.Zaccheroni, Coord.Chem.Rev., 2000, 205, 59.28 S.Aime, S.G.Crich, M.Botta, G.Giovenzana, G.Palmisano and M.Sisti, Chem.Commun., 1999, 1577.29 J.Hall, R.Haner, S.Aime, M.Botta, S.Faulkner, D.Parker and A.S.de Sousa, New J.Chem., 1998, 22, 627.30 M.P.Lowe and D.Parker, Chem.Commun., 2000, 707.31 S.Aime, A.Barge, M.Botta, D.Parker and A.S.De Sousa, J.Am.Chem.Soc., 1997, 119, 4767.32 S.Aime, F.Fedeli, A.Sanino and E.Terreno, J.Am.Chem.Soc., 2006, 128, 11326.33 M.P.Lowe, D.Parker, O.Reany, S.Aime, M.Botta, G.Castellano, E.Gianolio and R.Pagliarin, J.Am.Chem.Soc., 2001, 123, 7601.34 R.Hovland, C.Glogard, A.J.Aasen and J.Klavene, J.Chem.Soc., Perkin Trans.2, 2001, 929.35 ´E.T´oth, R.D.Bolskar, A.Borel, G.Gonz´alez, L.Helm, A.E.Merbach, B.Sitharaman and L.J.Wilson, J.Am.Chem.Soc., 2004, 127, 799.36 W.H.Li, S.E.Fraser and T.J.Meade, J.Am.Chem.Soc., 1999, 121, 1413.37 K.Dhingra, M.E.Maier, M.Beyerlein, G.Angelovski and N.K.Logothetis, Chem.Commun., 2008, 3444.38 H.Hifumi, A.Tanimoto, D.Citterio, H.Komatsu and K.Suzuki, Analyst, 2007, 132, 1153.39 L.M.De Le´on-Rodr´ıguez, A.J.M.Lubag, J.A.L´opez, G.Andreu-de-Riquer, J.C.Alvarado-Monz´on and A.D.Sherry, MedChemComm, 2012, 3, 480.40 R.Trokowski, J.Ren, F.K.Kalman and A.D.Sherry, Angew.Chem., Int.Ed., 2005, 44, 6920.41 W.S.Li, J.Luo, F.Jiang and Z.N.Chen, Dalton Trans., 2012, 41, 9405.42 K.Hanaoka, K.Kikuchi, Y.Urano and T.Nagano, J.Chem.Soc., Perkin Trans.2, 2001, 1840.43 R.Ruloff, G.v.Koten and A.E.Merbach, Chem.Commun., 2004, 842.44 M.Giardiello, M.P.Lowe and M.Botta, Chem.Commun., 2007, 4044.45 M.Andrews, A.J.Amoroso, L.P.Harding and S.J.A.Pope, Dalton Trans., 2010, 3407.46 W.Xu and Y.Lu, Chem.Commun., 2011, 47, 4998.47 R.A.Moats, S.E.Fraser and T.J.Meade, Angew.Chem., Int.Ed., 1997, 36, 726.48 A.Y.Louie, M.M.Huber, E.T.Ahrens, U.Rothbacher, R.Moats, R.E.Jacobs, S.E.Fraser and T.J.Meade, Nat.Biotechnol., 2000, 18, 321.49 B.Yoo and M.D.Pagel, J.Am.Chem.Soc., 2006, 128, 14032.50 Q.Wei, G.K.Seward, P.A.Hill, B.Patton, I.E.Dimitrov, N.N.Kuzma and I.J.Dmochowski, J.Am.Chem.Soc., 2006, 128, 13274.51 E.L.Que and C.J.Chang, J.Am.Chem.Soc., 2006, 128, 15942.52 E.L.Que, E.Gianolio, S.L.Baker, A.P.Wong, S.Aime and C.J.Chang, J.Am.Chem.Soc., 2009, 131, 8527.53 E.L.Que, E.Gianolio, S.L.Baker, S.Aime and C.J.Chang, Dalton Trans., 2010, 39, 469.54 W.S.Li, J.Luo and Z.N.Chen, Dalton Trans., 2011, 484.55 E.L.Que, E.J.New and C.J.Chang, Chem.Sci., 2012, 3, 1829.56 M.Andrews, A.J.Amoroso, L.P.Harding and S.J.A.Pope, Dalton Trans., 2010, 3407.57 D.Kasala, T.S.Lin, C.Y.Chen, G.C.Liu, C.L.Kao, T.L.Cheng and Y.M.Wang, Dalton Trans., 2011, 5018.58 D.Patel, A.Kell, B.Simard, B.Xiang, H.Y.Lin and G.Tian, Biomaterials, 2011, 32, 1167.59 E.Brunet, O.Juanes, R.Sedano and J.C.Rodr´ıguez-Ubis, Photochem.Photobiol.Sci., 2002, 1, 613.60 Z.Q.Ye, G.L.Wang, J.X.Chen, X.Y.Fu, W.Z.Zhang and J.L.Yuan, Biosens.Bioelectron., 2010, 26, 1043.61 S.Mizukami, K.Tonai, M.Kaneko and K.Kikuchi, J.Am.Chem.Soc., 2008, 130, 14376.62 W.D.Horrocks and D.R.Sudnick, Acc.Chem.Res., 1981, 14, 384.63 S.Quici, M.Cavazzini, G.Marzanni, G.Accorsi, N.Armaroli, B.Vcntura and F.Barigelletti, Inorg.Chem., 2005, 44, 529.64 P.Caravan, J.J.Ellison, T.J.McMurry and R.B.Laufer, Chem.Rev., 1999, 99, 2293.65 O.G.Polyakov, B.G.Nolan, B.P.Fauber, S.M.Miller, O.P.Anderson and S.H.Strau, Inorg.Chem., 2000, 39, 1735.66 M.F.Tweedle, J.J.Hagan, K.Kumar, S.Mantha and C.A.Chang, Magn.Reson.Imaging, 1991, 9, 409.67 D.Parker, Coord.Chem.Rev., 2000, 205, 109.68 R.S.Dickins, T.Gunnlaugon, D.Parker and R.D.Peacock, Chem.Commun., 1998, 1643.69 J.I.Bruce, R.S.Dickins, L.J.Govenlock, T.Gunnlaugon, S.Lopinski, M.P.Lowe, D.Parker, R.D.Peacock, J.J.B.Perry, S.Aime and M.Botta, J.Am.Chem.Soc., 2000, 122, 9674.70 R.S.Dickins, S.Aime, A.S.Batsanov, A.Beeby, M.Botta, J.I.Bruce, J.A.K.Howard, C.S.Love, D.Parker, R.D.Peacock and H.Puschmann, J.Am.Chem.Soc., 2002, 124, 12697–12705.71 W.D.Horrocks and D.R.Sudnick, Acc.Chem.Res., 1981, 14, 384.72 C.C.Bryden and C.N.Reilley, Anal.Chem., 1982, 54, 610.73 K.Binnemans, Chem.Rev., 2009, 109, 4283.74 S.Quici, M.Cavazzini, G.Marzanni, G.Accorsi, N.Armaroli, B.Vcntura and F.Barigelletti, Inorg.Chem., 2005, 44, 529.This journal is © The Royal Society of Chemistry 2014 RSC Adv., 2014, 4, 34421–34427 | 34427

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