Water soluble, cyclometalated Pt( II )–Ln( III ) conjugates towards novel bimodal imaging agents †

Facile conjugation of a luminescent cyclometalated Pt II complex with a DO3A-derived Gd III moiety yields a hybrid species with visible luminescence and enhanced relaxivity.

A number of imaging techniques (MRI, CT, ultrasound, PET, SPECT, optical) are available at a biomedical level with various pros and cons for each regarding image resolution, depth of tissue penetration, acquisition time, and sensitivity.Therefore combining two or more imaging modalities into a single molecule agent can circumvent many limitations associated with a particular technique, whilst simplifying aspects of the agent administration and biodistribution characteristics (pharmacodynamics). 1 It is very well known that trivalent lanthanide ions (Ln III ) offer remarkable opportunities in the design of biological imaging agents. 2 With dual applications in optical (luminescence) 3 and magnetic resonance imaging (MRI), 4 Ln III complexes have been extensively studied and a range of ligand systems investigated.Therefore Ln III moieties are particularly useful as a component of a bi-or multimodal single molecule imaging agent. 5In this context, systems based on Gd III have attracted most attention, with covalent coupling of organic fluorophores (MR/optical), 6 labelling with 18 F (MR/PET) 7 and 99m Tc chelation (MR/SPECT) 8 providing prospective agents.
We are particularly interested in the use of phosphorescent metal-based luminophores 9 as components of dual MR/optical imaging agents.Such species offer distinct photophysical advantages (tunable emission wavelengths, large Stokes' shifts, long emission lifetimes) over fluorescent variants and can be very effective in cellular imaging studies using confocal fluorescence microscopy. 10Cyclometalated Pt II complexes can possess many of these beneficial luminescent properties and have been successfully applied to biological imaging. 11In tandem with such physical attributes, interest in the use of Pt II complexes with therapeutic benefits also continues. 12Indeed one of the challenges of probing the (non)-specific biological action of Pt II therapeutics often lies in the difficulty of directly imaging the biological action.In this context, Pt II complexes can be tagged with fluorophores, such as anthraquinone, providing a means for identifying the intracellular fate of such compounds and understanding the role of targeting vectors. 13Recent studies into Pt II complexes of 2-phenylpyridine (ppy), have also explored binding with amyloid b peptide. 14The influences of the Pt complexes on protein aggregation, via the inhibition of Cu and Zn peptide complex formation, have been suggested as an approach to the study of Alzheimer's disease.
In this work, we describe the development of water soluble Pt II -Ln III hybrid systems wherein the cyclometalated Pt II moiety is luminescent.Previous work has described the synthesis of mixed Pt II /Ln III species and their photophysical properties, where the Pt II chelate acts as an antenna for sensitised Ln III emission within donor (Pt)-acceptor (Ln) assemblies. 15However, such systems are often not water soluble or water stable, and thus, to the best of our knowledge, there are no reports on the water relaxometric properties of Pt II -Gd III heterometallic species.A number of other water stable d-f hybrids employing Ru II , Re I and Os II as MLCT-based sensitisers have also been reported, 16 with Re I /Ru II -Gd III hybrids demonstrating the physical properties for potential in dual MR/optical imaging. 17The aim of this work was to synthesise a water-soluble Pt II -Ln III complex with favourable luminescence and relaxivity properties.
Two new ligands were required for the assembly of the Pt II -Ln III targets.Firstly, for the macrocyclic complex (Ln-py), a route was utilised 18 to give the ethylamine amide derivative (P1, ESI †), which subsequently reacted with 4-pyridinecarboxaldehyde using a reductive amination procedure (P2, ESI †); was not amenable to this synthetic pathway, giving a poor yield of the desired Pt II complex.However, the methoxy analogue [PtCl(pq-2)(DMSO)], which would be expected to be slightly less hydrophilic than pq-1, was successfully isolated as an orange solid suggesting that the terminal hydroxyl group of pq-1 may interfere with the coordination chemistry of Pt II .[PtCl(pq-2)(DMSO)] was characterised via a range of techniques including 195 Pt{ 1 H} NMR which revealed a resonance at À3665 ppm.An X-ray crystal structure (Fig. 1) of [PtCl(pq-2)(DMSO)] was also obtained (crystal structure data and refinement parameters are contained in the ESI †) and revealed the anticipated coordination environment for Pt II , with typical Pt-L bond lengths and angles for the coordinated atoms (ESI, † Table S1) and a distortion of ca.71 in the phenylquinoline unit.The packing structure also revealed a head-to-toe arrangement, with some p-stacking between the phenylquinoline moieties; there are no intermolecular Pt-Pt interactions.
Finally, the two complexes Ln-py and [PtCl(pq-2)(DMSO)] were dissolved in a minimum volume of acetone and reacted at 40 1C for 48 h.The resultant Pt-Ln dimetallic complexes were obtained as extremely hygroscopic orange powders and the formation confirmed using HRMS (ESI, † Fig. S2), which revealed the distinct and appropriate isotopic distribution corresponding to the loss of the chloride ligand to give the cationic dimer as [M À Cl] + .
The electronic properties of [PtCl(pq-2)(DMSO)] show that the complex absorbs in the UV region, with 1 p-p* transitions associated with the phenylquinoline unit, and in the visible region with l max at 424 nm, which probably corresponds to a 1 MLCT type transition.Supporting theoretical (TD-DFT) calculations on the model complexes [PtCl(epqc)(DMSO)] (where epqc = 4-ethyl-2-phenylquinoline carboxylate) and [PtCl(epqc)(py)] (where py = pyridine) show that the majority of the electron density in the HOMO lies across both the phenyl moiety of the cyclometalated ligand and the 5d-orbitals of the platinum.The orbital representations of the calculated lowest energy HOMO-LUMO transitions are shown in the ESI, † (Fig. S3).The percentage contribution to the energy levels for the Pt II 5d-orbitals (ESI, † Table S2) were calculated from the theoretical data showing that for both model complexes the HOMO comprises ca.25% 5d-orbital character and is consistent, therefore, with a MLCT contribution.
The UV-vis spectra (Fig. 2) of the Pt-Ln hybrids are closely comparable to [PtCl(pq-2)(DMSO)], with the visible MLCT absorption characteristics retained for both Pt-Gd and Pt-Yb.The luminescence properties of [PtCl(pq-2)(DMSO)] revealed a broad, featureless emission band at 625 nm (l ex = 425 nm) with a corresponding lifetime of 116 ns, which are attributed to an excited state of triplet character which is likely to encompass a strong 3

MLCT component. The properties of the corresponding
Scheme 1 Route to the heterometallic targets.Pt-Gd adduct were obtained in aqueous solution: the UV-vis spectrum shares all of the same features as [PtCl(pq-2)(DMSO)] with 1 MLCT absorption retained ca.425 nm and visible luminescence observed at 617 nm (Table 1).
In comparison, the steady state luminescence spectrum (l ex = 425 nm) of Pt-Yb displayed dual emission comprised of 3 MLCT character at ca. 620 nm and Yb III centred emission (inset, Fig. 2) in the near-IR region around 980 nm (corresponding to 2 F 5/2 -2 F 7/2 ).Since absorption at 425 nm is dominated by the Pt II chromophore this observation suggests that the Yb III emission must be sensitised and therefore confirms the formation of the heterometallic dimer.For completeness, lifetime measurements on the donor component of the two Pt-Ln complexes were recorded in water to estimate the through-space Pt -Yb energy transfer rate, k ET , (using k ET = (t q ) À1 À (t ref ) À1 where t q is the 3 MLCT lifetime in the presence of Yb III and t ref is the lifetime in the presence of Gd III ).The value for k ET was calculated to be ca.3 Â 10 6 s À1 , which is similar to the rate of 2 Â 10 6 s À1 for a previously reported Pt II -Yb III complex. 19he lifetimes of the Yb III emission were also obtained in H 2 O (0.90 ms) and D 2 O (5.46 ms) to give an approximate inner sphere hydration (q = k H 2 O À k D 2 O À 0.1) 20 of 0.8, which is consistent with an octadentate Yb III complex, implying that the amide carbonyl participates in the coordination sphere of Yb III , as observed in related lanthanide complexes of mono-amide DO3A derivatives. 21he relaxivity properties of the Gd III containing species were determined using field-cycling relaxometry. 1 H NMRD plots (ESI, † Fig. S4) were obtained for Gd-py and Pt-Gd (at field strengths between 1 Â 10 À2 À 30 MHz) to give bulk relaxivities, r 1 , in water per mM of complex per second.The relaxivity of Gd-py was obtained as 3.8 mM À1 s À1 (30 MHz, 37 1C, pH 6.5), which is in accordance with the literature values for [Gd(DOTA)(H 2 O)] À , where r 1 was recorded as 3.8 mM À1 s À1 (20 MHz, 37 1C) and consistent with a q = 1 species. 22Interestingly, the r 1 value for Pt-Gd was 7.1 mM À1 s À1 (30 MHz, 37 1C, pH 6.7), which shows that, upon formation of the dimetallic species, r 1 increases by 86%.This is most likely due to the increase in the molecular weight of the dimer resulting in a longer rotational correlation time, t R .The plots also demonstrate the temperature dependence of r 1 with relaxivities at 25 1C approximately 10-25% higher than at 37 1C (1 Â 10 À2 to 30 MHz).
Preliminary optical imaging studies were attempted with Pt-Gd using both MCF7 cells and Schizosaccharomyces pombe (fission yeast).Confocal fluorescence microscopy revealed that MCF7 cells poorly took up the complex with little evidence for internalisation.However, with S. pombe the images (ESI, † Fig. S5 and S6) clearly showed characteristic red emission from the cells, particularly those that were dividing, consistent with the Pt II -based chromophore, showing that these species are compatible with confocal fluorescence microscopy.
Our studies have shown how a luminescent, amphiphilic cyclometalated Pt(II) chelate can be coupled with a macrocyclic hydrophilic Ln(III) species to give a water soluble dimetallic construct.Such an approach has allowed the study of heterometallic Pt-Yb and Pt-Gd species: sensitised Yb III emission of the former corroborates the integrity of the dimer, while the latter reveals a bimetallic complex with visible luminescence properties and enhanced water relaxivity.Preliminary studies reveal that these complexes can be applied to the confocal fluorescence microscopy of cells, but that a careful balance of charge and amphiphilicity, and an understanding of cytotoxicity, will be required for future studies with different cell lines.
The EPSRC UK National Mass Spectrometry Facility (NMSF) at Swansea University, and the EPSRC UK National Crystallographic Service at the University of Southampton 23 are gratefully acknowledged.

Notes and references
deprotection of the tert-butyl esters with trifluoroacetic acid and complexation with either Gd(OTf) 3 or Yb(OTf) 3 gave the monometallic Ln III complexes, Ln-py (Scheme 1) possessing a pendant pyridine donor.Formation of the lanthanide complexes was confirmed by HRMS with additional 1 H NMR data for Yb-py (ESI, † Fig. S1) showing the pronounced chemical shifts of the azamacrocycle and arm protons between +135 and À80 ppm.For the hydrophilic Pt II component, two 2-phenylquinoline derivatives incorporating a PEG-like functionality were synthesised, yielding both amide (pq-1, ESI †) and ester linked (pq-2, ESI †) derivatives from either 2-(2-aminoethoxy)ethanol or 2-(2-methoxyethoxy)ethanol, respectively.The attempted synthesis of the Pt II complexes was undertaken via the splitting of dimeric [(L)Pt(m-Cl 2 )Pt(L)] with DMSO to form the monometallic species [PtCl(pq)(DMSO)].In our hands, the use of the hydroxyl terminated PEG derivative (pq-1)

Fig. 2
Fig. 2 Main: UV-vis absorption spectra of the complexes.Inset: Near-IR emission spectrum of Pt-Yb recorded in D 2 O (l ex = 425 nm).