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Referencias:

• Miller, M.R., Megson, I.L., Recent developments in nitric oxide donor drugs (2007) Br J Pharmacol, 151 (3), pp. 305-321. , PID: 17401442
• Bonavida, B., (2010) Nitric oxide (NO) and cancer: prognosis, prevention, and therapy, , (ed), Springer Science and Business Media, New York
• Serafim, R.A., Primi, M.C., Trossini, G.H., Ferreira, E.I., Nitric oxide: state of the art in drug design (2012) Curr Med Chem, 19 (3), pp. 386-405. , PID: 22335514
• Tfouni, E., Truzzi, D.R., Tavares, A., Gomes, A.J., Figueiredo, L.E., Franco, D.W., Biological activity of ruthenium nitrosyl complexes (2012) Nitric Oxide, 26 (1), pp. 38-53. , PID: 22178685
• de Lima, R.G., Silva, B.R., da Silva, R.S., Bendhack, L.M., Ruthenium complexes as NO donors for vascular relaxation induction (2014) Molecules, 19 (7), pp. 9628-9654. , PID: 25004072
• Szabo, C., Gasotransmitters in cancer: from pathophysiology to experimental therapy (2016) Nat Rev Drug Discovery, 15, pp. 185-203. , PID: 26678620
• Lundberg, J.O., Gladwin, M.T., Weitzberg, E., Strategies to increase nitric oxide signalling in cardiovascular disease (2015) Nat Rev Drug Discov, 14 (9), pp. 623-641. , PID: 26265312
• Paulo, M., Banin, T.M., de Andrade, F.A., Bendhack, L.M., Enhancing vascular relaxing effects of nitric oxide-donor ruthenium complexes (2014) Future Med Chem, 6 (7), pp. 825-838. , PID: 24941875
• Liu, J., Duan, Q., Wang, J., Song, Z., Qiao, X., Wang, H., Photocontrolled nitric oxide release from two nitrosylruthenium isomer complexes and their potential biomedical applications (2015) J Biomed Opt, 20 (1), p. 015004. , PID: 25621873
• Carneiro, Z.A., Biazzotto, J.C., Alexiou, A.D., Nikolaou, S., Nitric oxide photorelease from a trinuclear ruthenium nitrosyl complex and its in vitro cytotoxicity against melanoma cells (2014) J Inorg Biochem, 134, pp. 36-38. , PID: 24522147
• Castro, P.F.D.S., Andrade, D.L., Reis, C.D.F., Costa, S.H.N., Batista, A.C., Silva, R.S., Rocha, M.L., Relaxing effect of a new ruthenium complex nitric oxide donor on airway smooth muscle of an experimental model of asthma in rats (2016) Clin Exp Pharmacol Physiol, 43 (2), pp. 221-229. , PID: 26662887
• Rodrigues, F.P., Carneiro, Z.A., Mascharak, P., Curti, C., da Silva, R.S., Incorporation of a ruthenium nitrosyl complex into liposomes, the nitric oxide released from these liposomes and HepG2 cell death mechanism (2016) Coord Chem Rev, 306, pp. 701-707
• Ramos, L.C.B., Marchesi, M.S.P., Callejon, D., Baruffi, M.D., Lunardi, C.N., Slep, L.D., Bendhack, L.M., da Silva, R.S., Enhanced antitumor activity against melanoma cancer cells by nitric oxide release and photosensitized generation of singlet oxygen from ruthenium complexes (2016) Eur J Inorg Chem, 22, pp. 3592-3597
• Negri, L.B., Martins, T.J., Ramos, L.C.B., da Silva, R.S., Nitric oxide derivative ruthenium compounds as NO-based chemotherapeutic and phototherapeutic agents (2017) Nitric oxide donors: novel biomedical applications and perspectives, pp. 1-24. , Sebara AB, (ed), 1, Elsevier, New York
• Toledo, J.C., de França Lopes, L.G., Alves, A.A., da Silva, L.P., Franco, D.W., Release of NO by a nitrosyl complex upon activation by the mitochondrial reducing power (2002) J Inorg Biochem, 89 (3), pp. 267-271. , PID: 12062131
• Rodrigues, F.P., Pestana, C.R., Polizello, A.C., Pardo-Andreu, G.L., Uyemura, S.A., Santos, A.C., Alberici, L.C., Curti, C., Release of NO from a nitrosyl ruthenium complex through oxidation of mitochondrial NADH and effects on mitochondria (2012) Nitric Oxide, 26 (3), pp. 174-181. , PID: 22349020
• Pereira, A.D.C., Ford, P.C., da Silva, R.S., Bendhack, L.M., Ruthenium-nitrite complex as pro-drug releases NO in a tissue and enzyme-dependent way (2011) Nitric Oxide, 24 (4), pp. 192-198
• Fry, N.L., Mascharak, P.K., Photoactive ruthenium nitrosyls as NO donors: how to sensitize them toward visible light (2011) Acc Chem Res, 44 (4), pp. 289-298. , PID: 21361269
• Smith, N.A., Sadler, P.J., Photoactivatable metal complexes: from theory to applications in biotechnology and medicine (2013) Philos Trans R Soc A, 371, p. 20120519
• da Silva, R.S., Marchesi, M.S., Khin, C., Lunardi, C.N., Bendhack, L.M., Ford, P.C., Photoinduced electron transfer between the cationic complexes [Ru(NH3)5pz]2+ and trans-[RuCl([15]aneN4)NO]+ mediated by phosphate ion: visible light generation of nitric oxide for biological targets (2007) J Phys Chem B, 111 (24), pp. 6962-6968. , PID: 17439277
• Cicillini, S.A., Prazias, A.C.L., Tedesco, A.C., Serra, O.A., da Silva, R.S., Nitric oxide and singlet oxygen photo-generation by light irradiation in the phototherapeutic window of a nitrosyl ruthenium conjugated with a phthalocyanine rare earth complex (2009) Polyhedron, 28 (13), pp. 2766-2770
• Da Rocha, Z.N., Marchesi, M.S.P., Molin, J.C., Lunardi, C.N., Miranda, K.M., Bendhack, L.M., Ford, P.C., da Silva, R.S., The inducing NO-vasodilation by chemical reduction of coordinated nitrite ion in cis-[Ru(NO2)L(bpy)2]+ complex (2008) Dalton Trans, 32, pp. 4282-4287
• Sarniguet, C., Toloza, J., Cipriani, M., Lapier, M., Vieites, M., Toledano-Magaña, Y., García-Ramos, J.C., Otero, L., Water-soluble ruthenium complexes bearing activity against protozoan parasites (2014) Biol Trace Elem Res, 159 (1-3), pp. 379-392. , PID: 24740394
• Sesti-Costa, R., Carneiro, Z.A., Silva, M.C., Santos, M., Silva, G.K., Milanezi, C., da Silva, R.S., Silva, J.S., Ruthenium complex with benznidazole and nitric oxide as a new candidate for the treatment of chagas disease (2014) PLoS Negl Trop Dis, 8 (10), p. 3207
• Iniguez, E., Sánchez, A., Vasquez, M.A., Martínez, A., Olivas, J., Sattler, A., Sánchez-Delgado, R.A., Maldonado, R.A., Metal–drug synergy: new ruthenium (II) complexes of ketoconazole are highly active against Leishmania major and Trypanosoma cruzi and nontoxic to human or murine normal cells (2013) J Biol Inorg Chem, 18 (7), pp. 779-790. , PID: 23881220
• Ridnour, L.A., Thomas, D.D., Switzer, C., Flores-Santana, W., Isenberg, J.S., Ambs, S., Roberts, D.D., Wink, D.A., Molecular mechanisms for discrete nitric oxide levels in cancer (2008) Nitric Oxide, 19 (2), pp. 73-76. , PID: 18472020
• Thomas, D.D., Ridnour, L.A., Isenberg, J.S., Flores-Santana, W., Switzer, C.H., Donzelli, S., Colton, C., Wink, D.A., The chemical biology of nitric oxide: implications in cellular signaling (2008) Free Radic Biol Med, 45 (1), pp. 18-31. , PID: 18439435
• Stevens, E.V., Wells, A., Shin, J.H., Liu, J., Der, C.J., Schoenfisch, M.H., Nitric oxide-releasing silica nanoparticle inhibition of ovarian cancer cell growth (2010) Mol Pharm, 7 (3), pp. 775-785. , PID: 20205473
• Hirst, D., Robson, T., Targeting nitric oxide for cancer therapy (2007) J Pharm Pharmacol, 59 (1), pp. 3-13. , PID: 17227615
• Xiang, H.J., Deng, Q., An, L., Guo, M., Yang, S.P., Liu, J.G., Tumor cell specific and lysosome-targeted delivery of nitric oxide for enhanced photodynamic therapy triggered by 808 nm near-infrared light (2016) Chem Commun, 52 (1), pp. 148-151
• Park, J., Pramanick, S., Kim, J., Leeab, J., Kim, W.J., Nitric oxide-activatable gold nanoparticles for specific targeting and photo-thermal ablation of macrophages (2017) Chem Commun, 53 (81), pp. 11229-11232
• Safdar, S., Payne, C.A., Tu, N.H., Taite, L.J., Targeted nitric oxide delivery preferentially induces glioma cell chemosensitivity via altered p53 and O6-methylguanine-DNA methyltransferase activity (2013) Biotechnol Bioeng, 110 (4), pp. 1211-1220. , PID: 23125026
• Li, Y.H., Guo, M., Shi, S.W., Zhang, Q.L., Yang, S.P., Liu, J.G., A ruthenium-nitrosyl-functionalized nanoplatform for the targeting of liver cancer cells and NIR-light-controlled delivery of nitric oxide combined with photothermal therapy (2017) J Mater Chem B, 5 (38), pp. 7831-7838
• Deng, Q., Xiang, H.J., Tang, W.W., An, L., Yang, S.P., Zhang, Q.L., Liu, J.G., Ruthenium nitrosyl grafted carbon dots as a fluorescence-trackable nanoplatform for visible light-controlled nitric oxide release and targeted intracellular delivery (2016) J Inorg Biochem, 165, pp. 152-158. , PID: 27324826
• Wyland, K.R., Hoffman, E.E., Jain, A., DNA interaction studies and photoinduced ligand exchange kinetics of a sterically strained Ruthenium(II) complex (2017) Inorg Chim Acta, 454, pp. 62-66
• Campagna, S., Puntoriero, F., Nastasi, F., Bergamini, G., Balzani, V., Photochemistry and photophysics of coordination compounds: ruthenium (2007) Photochemistry and photophysics of coordination compounds I, pp. 117-214. , Balzani V, Campagna S, (eds), Springer, Berlin
• Sauaia, M.G., de Lima, R.G., Tedesco, A.C., da Silva, R.S., Nitric oxide production by visible light irradiation of aqueous solution of nitrosyl ruthenium complexes (2005) Inorg Chem, 44 (26), pp. 9946-9951. , PID: 16363866
• Meyer, T.J., Godwin, J.B., Preparation of ruthenium nitrosyl complexes containing 2, 2′-bipyridine and 1, 10-phenanthroline (1971) Inorg Chem, 10 (3), pp. 471-474
• Sauaia, M.G., Oliveira, F.S., Tedesco, A.C., da Silva, R.S., Control of NO release by light irradiation from nitrosyl-ruthenium complexes containing polypyridyl ligands (2003) Inorg Chim Acta, 355, pp. 191-196
• Ghosh, K., Kumar, S., Kumar, R., Synthesis and characterization of a novel ruthenium nitrosyl complex and studies on photolability of coordinated NO (2011) Inorg Chem Commun, 14 (1), p. 146
• Elmore, S., Apoptosis: a review of programmed cell death (2007) Toxicol Pathol, 35 (4), pp. 495-516. , PID: 17562483
• Grau-Campistany, A., Massaguer, A., Carrion-Salip, D., Barragán, F., Artigas, G., López-Senín, P., Moreno, V., Marchán, V., Conjugation of a Ru(II) arene complex to neomycin or to guanidinoneomycin leads to compounds with differential cytotoxicities and accumulation between cancer and normal cells (2013) Mol Pharm, 10 (5), pp. 1964-1976. , PID: 23510087
• Wang, T., Zabarska, N., Wu, Y., Lamla, M., Fischer, S., Monczak, K., Ng, D.Y.W., Weil, T., Receptor selective ruthenium-somatostatin photosensitizer for cancer targeted photodynamic applications (2015) Chem Commun, 51, pp. 12552-12555
• Becke, A.D.J., Density functional calculations of molecular bond energies (1988) J Chem Phys, 84, pp. 4524-4529
• Becke, A.D.J., Density-functional thermochemistry. III. The role of exact exchange (1993) J Chem Phys, 98, pp. 5648-5652
• Lee, C., Yang, W., Parr, R.G., Development of the Colle–Salvetti correlation-energy formula into a functional of the electron density (1988) Phys Rev B, 37 (2), pp. 785-789
• Perdew, J.P., Density-functional approximation for the correlation energy of the inhomogeneous electron gas (1986) Phys Rev B, 33, pp. 8822-8824
• Dunning, T.H., Jr., Hay, P.J., Modern theoretical chemistry (1976) Modern theoretical chemistry, pp. 1-28. , Schaefer HF, (ed), Plenum, New York
• Hay, P.J., Wadt, W.R.J., Ab initio effective core potentials for molecular calculations. Potentials for the transition metal atoms Sc to Hg (1985) J Chem Phys, 82, pp. 270-283
• Hay, P.J., Wadt, W.R.J., Ab initio effective core potentials for molecular calculations. Potentials for K to Au including the outermost core orbitals (1985) J Chem Phys, 82, pp. 299-310
• Wadt, W.R., Hay, P.J.J., Ab initio effective core potentials for molecular calculations. Potentials for main group elements Na to Bi (1985) J Chem Phys, 82, pp. 284-298
• Pedersen, P.L., Greenawalt, J.W., Reynafarje, B., Hullihen, J., Decker, G.L., Soper, J.W., Bustamente, E., Preparation and characterization of mitochondria and submitochondrial particles of rat liver and liver-derived tissues (1978) Methods Cell Biol, 20, pp. 411-481. , PID: 151184
• Åkerman, K.E., Wikström, M.K., Safranine as a probe of the mitochondrial membrane potential (1976) FEBS Lett, 68 (2), pp. 191-197. , PID: 976474
• Wrona, M., Patel, K., Wardman, P., Reactivity of 2′, 7′-dichlorodihydrofluorescein and dihydrorhodamine 123 and their oxidized forms toward carbonate, nitrogen dioxide, and hydroxyl radicals (2005) Free Radic Biol Med, 38 (2), pp. 262-270. , PID: 15607909
• Blondin, G.A., Green, D.E., The mechanism of mitochondrial swelling (1967) Proc Natl Acad Sci USA, 58 (2), pp. 612-619. , PID: 5233462
• Terpetschnig, E., Szmacinski, H., Malak, H., Lakowicz, J.R., Metal–ligand complexes as a new class of long-lived fluorophores for protein hydrodynamics (1995) Biophys J, 68 (1), pp. 342-350. , PID: 7711260
• Mosmann, T., Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays (1983) J Immunol Methods, 65, pp. 55-63. , PID: 6606682
• Tfouni, E., Krieger, M., McGarvey, B.R., Franco, D.W., Structure, chemical and photochemical reactivity and biological activity of some ruthenium amine nitrosyl complexes (2003) Coord Chem Rev, 236 (1-2), pp. 57-69
• Caramori, G.F., Frenking, G., The nature of the Ru–NO bond in ruthenium tetraammine nitrosyl complexes (2007) Organometallics, 26 (24), pp. 5815-5825
• Videla, M., Jacinto, J.S., Baggio, R., Garland, M.T., Singh, P., Kaim, W., Slep, L.D., Olabe, J.A., Structure, spectroscopy, and electrophilic and nucleophilic reactivities of bound nitrosyl (2006) Inorg Chem, 45, pp. 8608-8617. , PID: 17029371
• Cohen, A.J., Mori-Sánchez, P., Yang, W., Insights into current limitations of density functional theory (2008) Science, 321 (5890), pp. 792-794. , PID: 18687952
• Coropceanu, V., Malagoli, M., André, J.M., Brédas, J.L., Charge-transfer transitions in triarylamine mixed-valence systems: a joint density functional theory and vibronic coupling study (2002) J Am Chem Soc, 124 (35), pp. 10519-10530. , PID: 12197754
• Renz, M., Kaupp, M., Predicting the localized/delocalized character of mixed-valence diquinone radical anions. Toward the right answer for the right reason (2012) J Phys Chem A, 116 (43), pp. 10629-10637. , PID: 23025699
• Shimidzu, T., Iyoda, T., Izaki, K., Photoelectrochemical properties of bis (2,2′-bipyridine)(4,4′-dicarboxy-2,2′-bipyridine) ruthenium(II) chloride (1985) J Phys Chem, 89 (4), pp. 642-645
• Borges, S.D.S., Davanzo, C.U., Castellano, E.E., Zukerman-Schpector, J., Silva, S.C., Franco, D.W., Ruthenium nitrosyl complexes with N-heterocyclic ligands (1998) Inorg Chem, 37 (11), pp. 2670-2677. , PID: 11670402
• Calandreli, I., Oliveira, F.D., Liang, G.G., da Rocha, Z.N., Tfouni, E., Synthesis and characterization of trans-[Ru(NO)Cl(L)4](PF6)2(L = isonicotinamide; 4-acetylpyridine) and related species (2009) Inorg Chem Commun, 12 (7), pp. 591-595
• Sauaia, M.G., da Silva, R.S., The reactivity of nitrosyl ruthenium complexes containing polypyridyl ligands (2003) Transit Met Chem, 28 (3), pp. 254-259
• Zoratti, M., Szabò, I., The mitochondrial permeability transition (1995) Biochim Biophys Acta, 1241 (2), pp. 139-176. , PID: 7640294
• Halestrap, A.P., What is the mitochondrial permeability transition pore (2009) J Mol Cell Cardiol, 46 (6), pp. 821-831. , PID: 19265700
• Petronilli, V., Cola, C., Massari, S., Colonna, R., Bernardi, P., Physiological effectors modify voltage sensing by the cyclosporin A-sensitive permeability transition pore of mitochondria (1993) J Biol Chem, 268 (29), pp. 21939-21945. , PID: 8408050
• Petronilli, V., Costantini, P., Scorrano, L., Colonna, R., Passamonti, S., Bernardi, P., The voltage sensor of the mitochondrial permeability transition pore is tuned by the oxidation-reduction state of vicinal thiols. Increase of the gating potential by oxidants and its reversal by reducing agents (1994) J Biol Chem, 269 (24), pp. 16638-16642. , PID: 7515881
• Brown, G.C., Nitric oxide and mitochondria (2007) Front Biosci, 12 (6), pp. 1024-1033. , PID: 17127357
• Brown, G.C., Borutaite, V., Nitric oxide, mitochondria, and cell death (2001) IUBMB Life, 52 (3-5), pp. 189-195. , PID: 11798032
• Kroemer, G., Galluzzi, L., Brenner, C., Mitochondrial membrane permeabilization in cell death (2007) Physiol Rev, 87 (1), pp. 99-163. , PID: 17237344
• Gogvadze, V., Orrenius, S., Zhivotovsky, B., Mitochondria as targets for chemotherapy (2009) Apoptosis, 14 (4), pp. 624-640. , PID: 19205885

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