Anticancer Potential of Diruthenium Complexes with Bridging Hydrocarbyl Ligands from Bioactive Alkynols

Diruthenacyclopentenone complexes of the general composition [Ru2Cp2(CO)2{μ–η1:η3-CH=C(C(OH)(R))C(=O)}] (2a–c; Cp = η5-C5H5) were synthesized in 94–96% yields from the reactions of [Ru2Cp2(CO)2{μ–η1:η3-C(Ph)=C(Ph)C(=O)}] (1) with 1-ethynylcyclopentanol, 17α-ethynylestradiol, and 17-ethynyltestosterone, respectively, in toluene at reflux. Protonation of 2a–c by HBF4 afforded the corresponding allenyl derivatives [Ru2Cp2(CO)3{μ–η1:η2-CH=C=R}]BF4 (3a–c) in 85–93% yields. All products were thoroughly characterized by elemental analysis, mass spectrometry, and IR, UV–vis, and nuclear magnetic resonance spectroscopy. Additionally, 2a and 3a were investigated by cyclic voltammetry, and the single-crystal diffraction method was employed to establish the X-ray structures of 2b and 3a. The cytotoxicity in vitro of 2b and 3a–c was evaluated against nine human cancer cell lines (A2780, A2780R, MCF-7, HOS, A549, PANC-1, Caco-2, PC-3, and HeLa), while the selectivity was assessed on normal human lung fibroblast (MRC-5). Overall, complexes exert stronger cytotoxicity than cisplatin, and 3b (comprising 17α-estradiol derived ligand) emerged as the best-performing complex. Inductively coupled plasma mass spectrometry cellular uptake studies in A2780 cells revealed a higher level of internalization for 3b and 3c compared to 2b, 3a, and the reference compound RAPTA-C. Experiments conducted on A2780 cells demonstrated a noteworthy impact of 3a and 3b on the cell cycle, leading to the majority of the cells being arrested in the G0/G1 phase. Moreover, 3a moderately induced apoptosis and oxidative stress, while 3b triggered autophagy and mitochondrial membrane potential depletion.


INTRODUCTION
−19 Since the Cp ligand is formally anionic, the bond with the ruthenium is strengthened by an electrostatic contribution, supplying robustness to the overall structure.In the pursuit of novel and potent metallodrugs, dinuclear metal complexes could offer significant advantages compared to their corresponding monometallic counterparts. 20,21In this regard, several complexes containing two ruthenium(II) arene fragments connected by variable linkers 22−28 and a diversity of other diruthenium species 29−32 have been evaluated, showing an interesting activity in several cases.We note that the "diruthenium approach" is not always favorable; for instance, the assembly of two {RuCp(CO) 2 } units with diamine linkers resulted in the absence of cytotoxicity on human cancer cell lines. 33,34o the best of our knowledge, diorganoruthenium compounds bearing a direct metal−metal bond have been almost unexplored for their anticancer potential; the commercial [Ru 2 Cp 2 (CO) 4 ] serves as a convenient initial compound for synthesizing a wide range of [RuRu] organometallics, 35−38 for which biological investigations are almost absent in the literature.There are some substantial reasons for encouraging the advance of this piece of chemistry.−41 This synthetic strategy offers advantageous opportunities in view of a drug design, such as the facile incorporation within the dimetallic framework of organic fragments playing a specific biological role, and the introduction of a net positive charge enhancing the water solubility of the complex. 35−44 In this work, we present the synthesis, characterization, and evaluation of the anticancer potential of a novel series of diruthenium complexes derived from [Ru 2 Cp 2 (CO) 4 ] via the incorporation of alkynes, including two estradiol-containing alkynes.−49 This field of research has included the conjugation of metal structures with, inter alia, steroid hormone derivatives, and related examples have appeared in the literature concerning platinum(II), 50,51 ferrocene, 52 and ruthenium arene complexes. 53Steroidal units may enhance the antiproliferative activity especially against hormone-dependent cancer cells (e.g., breast cancer cells), by facilitating the intracellular drug uptake through steroid receptor systems. 54

Synthesis and Characterization of Complexes.
We synthesized the diruthenacyclopentenone complex 1 using a recently published procedure, starting from commercial [Ru 2 Cp 2 (CO) 4 ]. 55It has been established that the {PhCCPh} fragment within 1 is susceptible to thermal exchange with a variety of alkynes. 38,55,56−60 Then, addition of a strong protonating agent leads to cationic

Inorganic Chemistry
7][58][59]61 We exploited this strategy to conjugate 17αethynylestradiol and 17-ethynyltestosterone with the {Ru 2 Cp 2 (CO) 3 } scaffold (Scheme 1). Thu, the reactions of 1 with an excess of such two alkynes and 1-ethynylcyclopentanol, which was used as a nonbioactive analog, were carried out in toluene solution under reflux conditions.These reactions resulted in the formation of unprecedented diruthenacyclopentenone species 2a−c in almost quantitative yields.Following this, 2a−c was subjected to reactions with tetrafluoroboric acid in dichloromethane, leading to the corresponding allenyl derivatives 3a−c in high yields.
The IR spectra of 2a−c (dissolved in CH 2 Cl 2 ) exhibit a consistent pattern comprising three distinct absorptions, associated with the terminal and bridging carbonyl ligands, as well as the acyl moiety (e.g., for 2b, at 1976, 1803, and 1751 cm −1 , respectively).The NMR spectra of 2a−c (in acetone-d 6 , Figures S1 and S6) reveal singular sets of resonances.In the 1 H NMR spectra, the Cp ligands resonate at ca. 5.5 and 5.2 ppm; these values indicate a cis configuration with respect to the Ru 2 -μ-CO plane, as previously observed for analogous complexes. 37,59The hydroxyl group adjacent to the dimetallacycle manifests itself with a broad 1 H signal around 3.5 ppm.The alkenyl CH moiety is observed at characteristic low chemical shift values [δ( 1 H) = 10.70−10.87ppm, δ( 13 C) = 151.9−156.0−66 In the 13 C NMR spectrum of 2b, the CO units have been detected at 237.1 (bridging CO), 219.6 (acyl), and 201.5 ppm (terminal CO), in agreement with literature data on similar complexes. 37,59,67he molecular structure of 2b was determined through Xray diffraction analysis (Figure 2, Table 1).Coherently with the NMR data, the structure consists of a cis-Ru 2 Cp 2 (CO)(μ-CO) core bonded to μ−η 1 :η 3 -CH = C(R)C(�O) with R being an estradiol fragment.The presence of the bulky steroid moiety does not significantly affect the geometry of the dimetallacyclopentenone core compared to analogous bimetallic complexes containing less hindered substituents. 37,58,60,68,69he C(3) carbon is positioned almost equidistantly between the two ruthenium atoms [Ru(1)−C(3) 2.054 (14) and Ru(2)−C(3) 2.137(14) Å), reflecting its bridging alkylidene nature, in agreement with NMR spectroscopy.
The IR spectra of 3a−c (dissolved in CH 2 Cl 2 ) display three bands corresponding to two terminal and one bridging CO ligands (e.g., for 3a, at 2039, 2018, and 1871 cm −1 ).On the other hand, the NMR spectra of 3a−c (recorded in acetoned 6 ) at room temperature exhibit broad signals that could not be assigned, implying the occurrence of a fluxional process.There is large evidence in the literature that analogous diiron and diruthenium complexes containing a bridging η 1 :η 2 -allenyl ligand experience rapid oscillation of the allenyl moiety between the two metal atoms (σ−π fluxionality, Scheme 2). 57,58,60The same process is common to diiron and diruthenium μ−η 1 :η 2 -alkenyl compounds. 70,71esolved 1 H NMR spectra for 3a−c (Figures S7−S9) were recorded at −20 °C, and they unveiled the existence of two distinct resonance sets.The two resonance sets were assigned to cis and trans isomers in 3a [δ = 6.12, and 5.98 ppm (cis); δ = 5.95 and 5.80 ppm (trans), with the former largely prevailing.Note that analogous μ-allenyl complexes usually display cis configuration of the Cp rings. 57,59,72Besides, in diruthenium μ−η 1 :η 2 -alkenyl species, it is common to observe one Cp 1 H NMR resonance at a higher chemical shift in the trans isomer compared to the cis isomer. 58,73According to low-temperature 1 H NMR data, it can be inferred that 3b and 3c exist in solution as a combination of two isomers, both featuring cis geometry of the Cp ligands [e.g., for 3b: δ = 6.19, 5.99 ppm and 6.18, 6.01 ppm for the two isomers, respectively].It is presumable that this isomerism arises from the two possible orientations adopted by the cyclic substituent on the allenyl.Consistently, two isomers were previously reported for [Ru 2 (CO) 2 (μ-CO){μ−η 1 :η 2 -CH�C�C(Me)-(Ph)}(Cp) 2 ] + , varying in the orientations of the Me and Ph groups (Scheme 3). 59n the 1 H spectra, the ruthenium-bound CH undergoes a minor shift ongoing from 2a−c to 3a−c (e.g., from 10.87 ppm in 2a to 10.80 ppm in the cis isomer of 3a), thus indicating that the bridging alkylidene character of such CH carbon is maintained upon dimetallacyclopentenone to allenyl conversion.
The structure of 3a was elucidated by single-crystal X-ray diffraction studies (Figure 3, Table 2).It may be described as a diruthenium complex consisting of a cis-Ru 2 Cp 2 (CO) 2 (μ-CO) core linked to a μ−η 1 :η 2 -CH�C�C(C 5 H 9 ) allenyl.The overall structure and bonding values closely resemble those observed in similar diiron and diruthenium allenyl complexes. 57,58,72 3).As a starting point, octanol/water partition coefficients (Log P ow ) were determined using a UV−vis method.In general, the cationic allenyl complexes 3a−c display a balanced hydrophilic/ hydrophobic character, which is a favorable prerequisite for biological applications, with 3a being more hydrophilic compared to the estradiol-containing analogue 3b and the testosterone-derivative 3c.On the other hand, the neutral compounds 2a−c possess a marked lipophilicity (Log P ow > 1.5).Because of their limited solubility in water, the stability of the complexes was gauged in a methanol/water mixture (ca.1:5 v/v) through UV−vis spectroscopy at various time intervals (Figures S10−S19).In general, cationic complexes 3a−c were substantially more stable than the neutral ones 2a− c.On account of the Log P ow and stability data, we decided to focus the biological studies on the allenyl complexes 3a−c, with 2b selected as a representative species of the series 2a−c.The stability assessment was replicated in the presence of a cell culture medium (DMEM), revealing a gradual degradation of the complexes over an 18 h period, with 3c emerging as the most robust species (67% residual complex after 18 h).It is presumable that the modification of diruthenium complexes in aqueous solution is facilitated by the displacement of the C� C moiety coordinated to ruthenium by the solvent, in line with previous findings concerning diiron μ-allenyl complexes. 74In any case, the released organic species are expected to differ significantly from the alkynol reactants, which reasonably form an irreversible C−C bond in 2a−c and further undergo the loss of the hydroxyl moiety to give 3a−c (Scheme 1).
The ESI-MS spectra of complexes 3a−c, in methanol/water mixture after 24 h, confirmed their substantial stability, each spectrum showing the peak of the cation as the main species (Figures S20−S22).Next, the representative compounds 3a and 3b were incubated in methanol/water solutions in the presence of selected biomolecules, i.e., reduced glutathione (GSH) and L-cysteine, respectively.The resulting ESI-MS spectra did not evidence the formation of any product ascribable to the interaction with 10 mM GSH (Figures S23−S24).Note that the selected GSH concentration is expected to mimic the intracellular level in cancer cells. 75,76On the other hand, a mixture of nonidentified diruthenium species was produced from the reaction of 3a with L-cysteine (120 μM 77 ), after 24 h incubation (Figure S25).We expanded this study to assess the potential interaction of 3a−b with bovine serum albumin (BSA) as a representative protein model (48 h incubation at 37 °C), using the MALDI-TOF MS technique (Figure S26).Complex 3a showed a notable affinity toward BSA, and an adduct was detected apparently comprising more than six 3a cations (resulting in a mass variation of 3434 Da Table 1.Selected Bond Lengths (Å) and Angles (°) for 2b with respect to BSA).On the other hand, the interaction of 3b with BSA involves the binding of a unit likely originating from the cleavage of the diruthenium structure (leading to a mass variation of 483 Da compared to BSA).Taking into account the uncertainty of the measurement, this unit might correspond to a mononuclear ruthenium complex with the allenylsteroidal moiety coordinated to the {RuCp(CO) 2 } scaffold.
2.3.Electrochemistry.The electrochemical behavior of neutral complex 2a and cationic 3a was comparatively studied in CH 2 Cl 2 /[N n Bu 4 ]PF 6 solution, where both complexes are sufficiently soluble.The voltammetric profiles of the compounds (Figure S27) show two irreversible processes, namely, one reduction and one oxidation.According to the nature of the complexes, these processes are shifted toward more cathodic (for the neutral 2a) or anodic (for the cationic 3a) potentials (Table 4).While both reduction and oxidation do not seem viable in a biological environment in the case of 3a, in principle, the oxidation of 2a could be accessible.In fact, the biologically relevant range of potentials spans from −0.4 to +0.8 V vs SHE. 78,79Nevertheless, the low stability of 2a in aqueous solutions (see above) suggests that its electrochemistry cannot play a significant role.

Biological Studies.
To the best of our knowledge, biological studies on dimetallacyclopentenone compounds have been limited to iron−platinum complexes, investigated for their interactions with cancer-relevant proteins. 80We conducted an in vitro cytotoxicity screening of selected complexes on a panel of nine human cancer cell lines, while the selectivity was evaluated on the normal cell line MRC-5.Cisplatin and RAPTA-C 13 were employed as standards for comparative purposes.The obtained IC 50 values are compiled in Table 5, highlighting the promising antiproliferative potential of diruthenium complexes with IC 50 values generally lower than those measured for cisplatin.Overall, complex 3b demonstrated the best performance, excelling in terms of both antiproliferative efficacy and selectivity; specifically, the IC 50 value on the healthy MRC-5 cell line is approximately 2-fold compared to the average IC 50 values referred to the cancer cell lines.The comparable antiproliferative activity exhibited by 3a−c on the cell lines expressing the estrogen receptors (dominantly A2780, cisplatin-resistant A2780R and MCF-7) 81 suggests that the presence of the bioactive fragment in 3b and 3c does not provide a substantial effect.Nevertheless, it is possible that the estrogen-ligand, which is expected to be gradually released from 3b−c in a physiological solution (see stability studies), may partially contribute to the overall mechanism of antiproliferative effect by exerting its intrinsic biological activity. 82Despite the superior lipophilicity, complex 2b is inactive toward A549, PANC-1, and Caco-2 cells and less cytotoxic than 3a−c against HOS and PC-3 cell lines.The lower performance of 2b might be associated with its relatively fast degradation (Table 3).The cytotoxicity was then determined on the A2780 cell line at different incubation times (Table 6), pointing out that the activity of diruthenium

Inorganic Chemistry
compounds takes place primarily within the initial 24 h.In fact, the IC 50 values did not significantly decrease after additional 24 and 48 h.Conversely, a progressive decrease in IC 50 over 72 h was detected on cisplatin under identical conditions.2.4.1.Cellular Uptake.The uptake in A2780 cells was determined for complexes 2b, 3a, 3b, and 3c at the respective IC 50 concentrations at different times by ICP-MS measurement of the intracellular ruthenium level (Figure 4).RAPTA-C, for which a negligible in vitro internalization in cancer cells is documented, 11,83 was employed as a reference.
In general, the internalization of ruthenium species in the cancer cells increases during the initial 12 h and then remains approximately unchanged, presumably due to the occurrence of disassembly of the organometallic scaffold as suggested by the stability studies.The further increase of cellular uptake observed for 3c after 12 h may be ascribable to the formation of ruthenium-containing fragmentation products with a specific ability to cross the cell membrane.The degree of internalization in the first 12 h follows the order: RAPTA-C < 2b < 3a < 3c < 3b.Concerning allenyl complexes 3a−c, this order is in alignment with the Log P ow values and the cytotoxicity data.Conversely, the reduced intracellular accumulation of lipophilic compound 2b reflects its minor antiproliferative efficacy.

Cell Cycle Analysis.
The performant cationic complexes 3a and 3b underwent a targeted study to assess their influence on the cell cycle of A2780 cells.Both compounds showed a profound effect (Figure 5), characterized by strong depression of the cell number in the synthetic (S) phase and second gap and mitotic phases (G2/M) of the cycle, thereby increasing the population of nondividing cells (in the G0/G1 phase).Cisplatin was analyzed as a reference drug, known for its primary mechanism of action involving the covalent alteration of DNA, 84 thereby halting cell progression in the synthetic phase of the cell cycle. 85On the other hand, the studied diruthenium complexes probably act at different sites and through different modes of action, possibly associated with the lowering of the metabolic activity and consequently the dividing capacity of the target cells.Numerous previous studies (for more details, see e.g., Zaki et al. 86 ) pointed out the  The values are presented as the mean ± standard deviation (SD).capability of organo-ruthenium complexes to affect the metabolic activity of cancer cells through the interference with several metabolic pathways, such as iron and ATP metabolism, 87 calcium metabolism in mitochondria 88,89 and various enzymatic routes.

Induction of Apoptosis and Autophagy.
The proapoptotic effects of 3a−b and cisplatin were assessed on A2780 cells through flow cytometry using Annexin V/ propidium iodide (PI) staining (Figure 6).The findings indicate a relatively low effect on the raising of the cell count during the initial phases of apoptosis (Annexin positive/PI negative) and an even lower effect in the advanced stages of apoptosis (Annexin positive/PI positive).Although the effect provided by 3a is quantitatively stronger than that of 3b, overall the proapoptotic activities of 3a and 3b are much less effective than that of cisplatin, which elicited apoptotic changes in ca.40% of the cells.
The results of Annexin V/PI staining were confirmed by the selective flow cytometric identification of the cells with active executioner caspase 3/7, which are activated at the late stages of apoptosis and induce the degradation of intracellular matrix and cytoskeleton and DNA fragmentation (Figure 7).As a matter of fact, 3a−b negligibly increased the cell population with the activated caspase 3/7, unlike cisplatin for which apoptosis induction represents a major mode of action. 84utophagy represents another type of cell death, usually associated with the physiological response of the cells to uncontrollable cellular stress and, often, with cancer tissue survival.The autophagy level (Figure 8) was significantly enhanced in cisplatin-treated cells, but only moderately in the    cells treated with 3b, whereas the effect of 3a was not appreciable.Nevertheless, the induction of autophagy by 3b may be triggered by the release of the bioactive loading and could considerably contribute to the antiproliferative effect of this complex.A similar behavior was previously reported for an estradiol-platinum(II) complex. 90.4.4.Intracellular Oxidative Stress and Mitochondrial Membrane Damage.Due to the availability of adjacent, relatively stable oxidation states, associated with a versatile redox chemistry, transition metal complexes may be prone to induce intracellular oxidative stress. 91This may occur via direct production of an excess of reactive oxygen species (ROS) or by depleting the capacity of natural intracellular defenses against oxidative stress (e.g., by direct inhibition of antioxidant enzymes or inhibition of small antioxidant molecules such as GSH).Thus, incubation of A2780 cells with representative complex 3a resulted in a noteworthy elevation of intracellular ROS levels (Figure 9); interestingly, no appreciable effect was detected for 3b under the same experimental conditions.
One of the consequences of localized intracellular overproduction of ROS is the damaging of cell membrane structures. 92Concerning mitochondrial membranes, this phenomenon depletes oxidative metabolism and cellular respiration.An additional plausible consequence of mitochondrial membrane damage is the liberation of cytochrome c from the inner mitochondrial membrane, leading to an intrinsic pathway of apoptosis by apoptosome sequestration and subsequent activation of executioner caspases.Both cisplatin and the diruthenium complexes 3a and 3b led to a notable augmentation in the cell count with damaged mitochondrial membranes (Figure 10).Consequently, this biological process could potentially contribute to the mechanism of action of diruthenium complexes.According to literature findings, 93 also the elimination of carbon monoxide from the complexes, as indirectly outlined by the stability studies (see above), may contribute to intracellular metabolic stress, although additional targeted investigations are needed to confirm this hypothesis.
2.4.5.Concluding Remarks.Ruthenium complexes are pivotal in the quest for novel and efficacious anticancer metallodrugs, with the aim of surpassing the constraints of currently used platinum drugs in chemotherapy.So far, research efforts have been primarily focused on mononuclear complexes based on the ruthenium-arene framework.Meanwhile, diruthenium complexes, despite their potential benefits stemming from metal−metal cooperative phenomena, have received less attention.In this work, we present the synthesis and evaluation of the anticancer capabilities of novel diruthenium complexes featuring diverse bridging hydrocarbyl ligands.These complexes represent rare derivatives of the commercial [Ru 2 Cp 2 (CO) 4 ] evaluated in the biological field.We provide evidence that a simple synthetic protocol enables the incorporation of various substituents on the bridging ligand, including steroidal fragments, thus modulating the physicochemical characteristics and cytotoxicity of the complexes.Cationic diruthenium μ-allenyl complexes were revealed to be promising, in that they display a strong antiproliferative potency against a spectrum of cancer cell lines (typically exhibiting IC 50 values lower than those associated with cisplatin).This potency is accompanied by a propensity for selectivity.Targeted experiments suggest a multimodal mechanism of action, which seems sensitive to local structural variations.We recognized, for the most active compounds, a significant influence on the cell cycle and the interference with the cellular metabolism at different levels, resulting in the enhancement of ROS production, the depletion of mitochondrial membrane potential, and the induction of autophagy.It is likely that the activity is ascribable, at least in part, to the modification of the complexes in the biological environment, including the gradual release of ligands (estradiol-molecules and CO).It is also conceivable that protein binding plays some role, as suggested by ESI-MS interaction studies with a model protein.Nevertheless, an accelerated decomposition, as evidenced for neutral diruthenacyclopentenone complexes, is  detrimental to the activity.Since the here proposed synthetic strategy possesses a general character, a broad scope is offered for the future development of diruthenium allenyl complexes with optimized properties and activities.

Synthesis and Structural
Characterization of Diruthenium Complexes.3.1.1.General Details.Reagents and solvents were obtained from different sources (Merck, Alfa Aesar, TCI Chemicals or Strem) and were of the utmost purity commercially attainable.Complex 1 was synthesized using the literature procedure. 55The reactions were performed within a N 2 atmosphere by employing conventional Schlenk techniques.After isolation, the products were stored in ambient air conditions.Dichloromethane and tetrahydrofuran were dried using the solvent purification system mBraun MB SPS5, whereas acetonitrile was distilled over calcium hydride.Infrared spectra of solutions were acquired by using a CaF 2 liquid transmission cell (2300−1500 cm −1 ) through a PerkinElmer Spectrum 100 FT-IR spectrometer.Spectragryph software was used for processing the infrared spectra. 94NMR spectra were recorded on a Jeol JNM-ECZ500R instrument equipped with a Royal HFX Broadband probe (at a temperature of 298 K, unless otherwise specified).Chemical shifts are expressed in parts per million and referenced to the residual solvent peaks. 95NMR spectra were assigned with the assistance of 1 H− 13 C (gs-HSQC and gs-HMBC) correlation experiments. 96NMR signals related to secondary isomeric forms (where detectable) are denoted in italics.Elemental analyses were conducted by using a Vario MICRO cube instrument (Elementar).ESI-MS analyses were performed with the Bruker amaZon SL ion-trap mass spectrometer using the ESI ion source in positive ionization mode, except for experiments with GSH which were performed on a Shimadzu Liquid Chromatograph Mass Spectrometer LCMS-8050 using the ESI-8050 ionization unit in positive ionization mode.MALDI-TOF MS analyses were performed using a Microflex LRF20 (Bruker Daltonik, Germany) mass spectrometer.ICP-MS analyses were performed on an Agilent 7700× mass spectrometer with the external calibration, using the Merck Transition metal mix 3 for ICP standard solution.

Synthesis and Characterization of Diruthenacyclopentenone Complexes (2a−c). 3.1.3. General Procedure.
A solution of (ca.0.15 mmol) in toluene (30 mL) was treated with an excess (ca. 5 equiv) of the selected propargyl alcohol.The resultant mixture was stirred at reflux temperature for a duration of 1 h.The resulting solution was then permitted to cool to room temperature and the solvent was subsequently evaporated under reduced pressure at 50 °C.The residue was subjected to washing with pentane (3 × 20 mL) and then dried under vacuum.(15 mL) was treated with HBF 4 •Et 2 O (1 equiv) which was added dropwise at room temperature; stirring was maintained for 15 min.Subsequently, H 2 O (ca. 5 mL) was added, and the resultant mixture was vigorously agitated.The organic phase was isolated and desiccated under a reduced pressure.The resulting solid residue was dissolved in CH 2 Cl 2 (4 mL), and precipitation occurred upon the addition of diethyl ether (60 mL).The resultant solid was subjected to washing with diethyl ether (3 × 15 mL) and then dried under vacuum.
3  7. Experimental data were collected on a Bruker APEX II diffractometer equipped with a PHOTON2 detector, utilizing Mo−Kα radiation.The structures were initially resolved through direct methods and subsequently refined by full-matrix leastsquares involving all the collected data using F 2 . 97Hydrogen atoms were positioned at computed coordinates and subjected to refinement using a riding model except for those connected to the H 2 O molecule of 2b•H 2 O.The latter was identified in the Fourier Difference Map and then refined isotropically using the 1.5-fold U iso parameter of the parent O atom.

Behavior in Aqueous Media. 3.2.1. Determination of Partition Coefficients (Log P ow ).
Partition coefficients (P ow ), defined by the formula P ow = c org /c aq , wherein c org and c aq denote the molar concentrations of the specific compound in octanol and aqueous phases, respectively, were obtained using the shake-flask method with UV−vis measurements, following a previously described procedure (Table 3). 98All the operations were carried out at 21 ± 1 °C.The wavelength corresponding to the maximum absorption of each compound within the range 350−430 nm was employed for quantifying using UV−vis techniques.

Stability in Aqueous Solutions (UV−Vis).
Solutions with an approximate concentration of 10 −5 M diruthenium complexes, formulated in a mixture of MeOH and H 2 O (about 1:5 v/v), underwent UV−vis spectroscopic analysis immediately after sample preparation (t 0 ) and after storage for 4 h at room temperature.The percentage of remaining complex in the solution was calculated by considering the change in absorbance at the characteristic wavelength.The identical procedure was employed to evaluate stability in MeOH and DMEM (about 1:5 v/v) solutions.DMEM stands for the cell culture medium (containing 1000 mg/L glucose and L-glutamine, excluding sodium bicarbonate and phenol red; reference D2902-Merck).
3  Inorganic Chemistry complexes (3a or 3b, 10 μM) were mixed with an equal volume of an aqueous solution of either L-cysteine (to produce the final concentration of 120 μM) or GSH (to produce the final concentration of 10 mM).The resulting solutions were maintained in the dark.Afterward, aliquots of the final solutions were injected, using the autosampler of the LC−MS system with bypassed separation column, into the stream of 1:1 v/v methanol/water at 0.2 mL/min flow rate and immediately analyzed by ESI-MS in a positive ionization mode (mass range 100−1500 m/z).Samples from L-cysteine were analyzed on a Bruker amaZon SL mass spectrometer, while samples from GSH were analyzed on a Shimadzu LC−MS 8050 Liquid Chromatograph Mass Spectrometer.The obtained data were processed using the dedicated software provided by each respective manufacturer (Bruker, Data Analysis 4.4; Shimadzu, LabSolutions Connect software).

Interaction with BSA (MALDI-TOF MS).
Bovine serum albumin (BSA, 30 μM in 50 mM NH 4 HCO 3 ) was incubated with the selected complexes (3a or 3b, 1 mM) at 37 °C for 48 h.Each complex was preliminarily dissolved in 50 μL of methanol.Following the incubation, an aliquot of the protein was adsorbed by repeated aspiration and release (20 times, 10-μL volume) into a ZipTip-C4 pipet tip (Merck, Darmstadt, Germany) that had been preequilibrated in 0.1% trifluoroacetic acid (TFA), washed by the equilibrating solution, and eluted into 10 μL of 70% acetonitrile containing 0.1% TFA.The eluate was subsequently subjected to evaporation using a vacuum centrifuge, and the residue was dissolved in 3 μL of 0.1% TFA.A 1 μL aliquot of this solution was deposited on an MSP Big Anchor 96 target plate (Bruker Daltonik, Bremen, Germany), onto which 1 μL of the matrix solution (sinapinic acid, 12 mg/mL in 0.1% TFA and 50% acetonitrile) was immediately superimposed.The sample was then allowed to dry.Mass spectra were acquired using a Microflex LRF20 MALDI-TOF mass spectrometer operated in a linear positive ion mode and controlled using flexControl 3.4 software from Bruker Daltonik).Protein Standard II, from Bruker Daltonik, was used for external calibration.All spectra were subjected to processing by using flexAnalysis 3.4 software from Bruker Daltonik.
3.3.Electrochemistry.Cyclic voltammetry measurements were conducted by using a PalmSens4 instrument connected to a computer operating with the PSTrace5 electrochemical software.Prior to use, anhydrous CH 2 Cl 2 (Merck) was stored under argon over 3 Å molecular sieves.Both [N n Bu 4 ]PF 6 (electrochemical grade) and FeCp 2 , obtained from Fluka, were utilized without requiring additional purification.Cyclic voltammetries were carried out under argon by utilizing a 0.2 M solution of [N n Bu 4 ]PF 6 in CH 2 Cl 2 as the supporting electrolyte.The working electrode and the counter electrode were comprised of a platinum disk and a platinum gauze, respectively, both enclosed within a glass tube.A leakage-free miniature electrode of Ag/AgCl/KCl (from eDAQ) was employed as a reference.The three-electrode designed cell was subjected to predrying via vacuum heating and then filled with argon gas.The Schlenk-type design of the cell was effective in upholding both anhydrous and anaerobic conditions.Subsequently, a solution of supporting electrolyte, prepared under argon, was introduced into the cell, and the CV of the solvent was acquired.Afterward, the analyte was introduced, and voltammograms were recorded.Under the selected experimental conditions, the one-electron oxidation of ferrocene occurred at a standard potential of E°= +0.45 V relative to Ag/AgCl/KCl.
3.4.Biological Studies.3.4.1.In Vitro Cytotoxicity.The in vitro cytotoxicity of complexes (2b, 3a, 3b, 3c, RAPTA-C, and cisplatin) was evaluated using the MTT assay with different incubation times.The cytotoxicity assessment was conducted on various human cancer cell lines, including A2780 ovarian carcinoma, A2780R cisplatinresistant ovarian carcinoma, MCF-7 breast, HOS osteosarcoma, A549 epithelial lung, PANC-1 pancreatic, Caco-2 colorectal, PC-3 prostate adenocarcinoma, and HeLa cervical cell lines.Additionally, the assessment extended to a normal human fetal fibroblast cell line (MRC-5).Cells were obtained from ATCC collection and cultivated according to the producer's instructions.Stock solutions of the compounds were prepared in DMF immediately before application, and diluted with H 2 O to achieve the final concentration of 0.1% v/v DMF. 99The culture media were enriched with 10% fetal calf serum.Subsequently, the cells were exposed to the tested compounds, vehicle (0.1% v/v DMF) and Triton X-100 (1% v/v), during incubation.The conventional MTT assay was carried out following different incubation periods (Tables 5-6).The absorbance was measured at 570 nm by using a spectrophotometer (Infinite M200, Schoeller Instruments, Prague, Czech Republic).The obtained data are presented as the percentage of cell viability with 100% representing negative control treatment (0.1% v/v DMF) and 0% representing the positive control (Triton X-100).The half-maximal inhibitory concentrations (IC 50 ) were determined from dose−response curves using GraphPad Prism 6 software (GraphPad Software, San Diego, USA).
3.4.2.Mechanism Studies.3.4.2.1.Cell Culture.The A2780 ovarian carcinoma cell line was received from Merck (reference 93112519−1VL) and cultured at 37 °C in an environment with 5% CO 2 .The cultivation was carried out in complete cell culture medium (RPMI-1640 medium, Merck), which was supplemented with 10% fetal bovine serum (FBS, Merck), 1% L-glutamine (Merck) and 1% penicillin−streptomycin−neomycin (PSN, Merck).For the flow cytometry experiments, three independent duplicates were analyzed using a BD FACSVerse flow cytometer (Becton Dickinson, USA).At least 5 × 10 3 events were recorded for each sample.The same procedure was replicated for the experiments described below.Solutions of the complexes were formulated using the stock solutions (Section 5.1).The reference sample for the drug was a solution of cisplatin at a concentration of 15 μM, whereas the negative control sample consisted of the vehicle alone (0.1% DMF).These studies were conducted on A2780 cells using the BD Cycletest Plus DNA kit (from Becton Dickinson, USA).Thus, cells were seeded in 96-well plates (10 4 cells/ well) and treated with 4 μM complexes 3a and 3b for 24 h.Following the incubation period, cells underwent a series of procedural steps.Initially, they were rinsed using PBS (0.1 M, pH 7.4).Subsequently, Solution A (comprising trypsin within a detergent buffer containing spermine tetrahydrochloride), Solution B (containing trypsin inhibitor and ribonuclease A within a citrate-stabilizing buffer with spermine tetrahydrochloride) and Solution C (comprising propidium iodide, PI, along with spermine tetrahydrochloride within a citrate stabilizing buffer) were sequentially introduced in accordance with the manufacturer's instructions.A sample of cisplatin was employed as a positive control.
3.4.2.3.Apoptosis and Caspase 3/7 Activation Analysis.Apoptosis assay was performed using an Annexin V-FITC/PI commercial kit (V13242, Thermo Fisher Scientific, USA), while caspase 3/7 activation assay was performed with a CellEvent Caspase-3/7 Green Flow Cytometry Assay Kit (C10427, Thermo Fisher Scientific, USA).A2780 cells were seeded in 24-well plates at a density of 5 × 10 4 cells per well; after 24 h, the cells were exposed to 4 μM solution of the selected complex for 24 h.The drug-reference sample consisted of 15 μM solution of cisplatin, while vehicle (0.1% DMF) was employed as a negative control.The supernatant was collected, cells were washed with PBS (0.1 M, pH 7.4), and trypsin was added (0.25% trypsin-EDTA, GibcoTM).Finally, complete cell culture medium was added to stop the trypsinization, and a final volume of 500 μL was divided into two 250 μL aliquots, following the protocol provided by the manufacturer.Samples were centrifuged, treated with the respective buffers, and then incubated in the dark at room temperature for 10 min (Annexin V-FITC/PI) or at 37 °C for 30 min (CellEventTM Caspase-3/7 Green Detection Reagent).Heatdamaged cells (10 min, 60 °C) were used as a positive control for caspase 3/7 activation, while cisplatin was used as a positive control in the apoptosis assay.
3.4.2.4.Autophagy Analysis.The potential induction of autophagy by 3a and 3b in A2780 cells was studied with the kit CYTO-ID Autophagy Detection 2.0 (from Enzo Life Sciences, USA), following the protocol provided by the manufacturer.Hence, a total of 5 × 10 4 A2780 cells per well were seeded into a 24-well plate and after 24 h incubated with 4 μM solutions of the complexes, for 24 h.A 15 μM solution of cisplatin and vehicle (0.1% DMF) were employed as the positive and the negative control, respectively.The supernatant was collected, cells were washed with warm PBS, detached using 0.25% trypsin-EDTA (Gibco) and resuspended in a cell culture medium.Diluted CYTO-ID Green stain solution (according to the protocol) was used to stain the samples.Following incubation for 30 min in a light-protected environment, the samples were washed with PBS (phosphate-buffered saline).Subsequently, a flow cytometry experiment was conducted.A mixture of chloroquine (10 μM) and rapamycin (0.5 μM) was used as positive control.
3.4.2.5.Mitochondrial Membrane Potential (MMP) Analysis.To investigate the effects on mitochondrial membrane potential of A2780 cells, an MITO-ID Membrane potential detection kit (Enzo Life Sciences, USA) was used.Cells were seeded in a 24-well (5 × 10 4 cells/well), and then incubated with 4 μM solution of complexes for 24 h.The supernatant was collected, cells were washed with warm PBS, detached using 0.25% trypsin-EDTA (Gibco) and resuspended in a cell culture medium.Then, samples were stained with diluted MITO-ID MP Detection Reagent (according to the protocol) at RT for 15 min, prior to flow cytometry analysis.A positive control was established by treating the samples with 2 μM carbonyl cyanide 3chlorophenylhydrazone.
3.4.2.6.ROS production Assessment.ROS-ID Total ROS/ Superoxide detection kit (from Enzo Life Sciences, US) was employed to quantify ROS and superoxide generation in A2780 cells following the treatment with the tested compounds.Thus, cells were seeded in a 96-well plate (10 4 cells/well) and incubated with 4 μM solution of complexes for 24 h.A 100 μM solution of pyocyanin, which is a known oxidative-stress inducer, was used as a positive control.Following the treatment, the supernatant was aspirated, and the cells were subsequently rinsed with buffer (1X).The next step involved staining with the ROS/Superoxide Detection Solution, containing Oxidative Stress Detection Reagent (Green) and Superoxide Detection Reagent (Orange), both at 1:2500 dilution in wash buffer, at 37 °C in the dark for 60 min.Finally, a microplate reader Infinite M200Pro (Tecan, Switzerland) was used to measure sample fluorescence (green: Ex. 488 nm/Em.520 nm, and red: Ex. 550 nm/ Em. 610 nm) and three independent experiments were done in triplicates.
3.4.2.7.Statistical Analysis.Three separate experiments were conducted, and the mean values along with the standard deviation (SD) were computed.Subsequently, statistical analysis was carried out using Statistica software 100 involving One-way ANOVA followed by Dunnet post hoc test.Significant differences in comparison to the untreated control were denoted with asterisks (*p < 0.05, **p < 0.01, ***p < 0.001).

Figure 2 .
Figure 2. View of the molecular structure of 2b.Displacement ellipsoids are presented at the 50% probability level.Hydrogen atoms have been excluded for the sake of clarity, with the exception of those attached to oxygen atoms and C(3).

Figure 4 .
Figure 4. Ruthenium cellular uptake in A2780 cells after different times of incubation at different IC 50 concentrations.

Figure 5 .
Figure 5.Effect of cationic diruthenium complexes 3a and 3b and cisplatin on the cell cycle in A2780 cells.The results labeled with *** denote a statistically significant distinction between the designated cell population and the control group at the significance level of p < 0.001.

Figure 6 .
Figure 6.Effect of diruthenium complexes 3a and 3b and cisplatin on apoptosis in A2780 cells.The results marked with an asterisk represent a statistically significant difference between the specific population of cells and the control group at *p < 0.05, **p < 0.01, and ***p < 0.001 levels.

Figure 7 .
Figure 7. Stimulation of caspases 3/7 in A2780 cells induced by 3a and 3b and cisplatin.The results marked with an asterisk represent a statistically significant difference between the specific population of cells and the control group at ***p < 0.001 level.

Figure 8 .
Figure 8. Activation of Autophagy in A2780 cells induced by 3a and 3b and cisplatin.The results marked with an asterisk represent a statistically significant difference between the specific population of cells and the control group at *p < 0.05 and ***p < 0.001 levels.

Figure 9 .
Figure 9. Induction of oxidative stress in A2780 cells by treatment with 3a and 3b and the drug cisplatin.As a positive control, the wellknown ROS inducer pyocyanin was used in 100 μM concentration.The results marked with an asterisk represent a statistically significant difference between the specific population of cells and the control group at *p < 0.05 and ***p < 0.001 levels.

Figure 10 .
Figure 10.Effect of 3a and 3b and cisplatin on the mitochondrial membrane integrity in A2780 cells.The results marked with an asterisk represent a statistically significant difference between the specific population of cells and the control group at: *p < 0.05, **p < 0.01, and ***p < 0.001 levels.

Chart 4 .
Structure of the Cation of 3a Chart 5. Structure of the Cation of 3b Chart 6. Structure of the cation of 3c

Table 3 .
Behavior of Diruthenium Complexes in Aqueous Media: Octanol/Water Partition Coefficients (Log P ow , based on UV−Vis Spectroscopy) at 21 °C and Stability in H 2 O/CH 3 OH and DMEM/CH 3 OH Solutions at Different Times (ca. 5:1 v/v, UV−Vis Analyses)

Table 4 .
Formal Electrode Potentials (V, Referenced to Ag/ AgCl/KCl and, in Parentheses, to FeCp 2 ) for the Redox Transformations Displayed by 2a and 3a When Dissolved in CH 2 Cl 2 /[N n Bu 4 ]PF 6 0.2 M a Peak potential value for irreversible processes.

Table 7 .
Crystal Data and Measurement Details for 2b•H 2 O and 3a a Goodness on fit on