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Trichomonacidal Activity of 3,3′-Diindolylmethane (DIM) Is Additive to Metronidazole (MTZ) In Vitro, Supporting Future Oral/Topical Use Ibáñez Escribano, Alexandra Lau, Leyre Pernaute Nogal Ruiz, Juan José Gómez Barrio, Alicia Escario García-Trevijano, José Antonio Zeligs, Michael A. New, safe, well tolerated, and versatile anti-trichomonal agents for oral and topical use are needed to combat spreading resistance of Trichomonas vaginalis to metronidazole (MTZ). Diindolylmethane (DIM) is a non-toxic, cruciferous indole under pharmaceutical development for treatment of cervical and prostatic pre-cancers. Present work reports anti-trichomonal activity of DIM with IC50 hundreds of times below the DIM concentration provided in a clinic-ready, sustainedrelease, vaginal-topical formulation (BR-DIM-VC™ 2%) which has passed vaginal tolerance testing in rabbits. Present in vitro findings against T. vaginalis exhibit additive effects of DIM with MTZ, significantly reducing the IC50 for MTZ (p < 0.05). Combinatorial activity with MTZ was demonstrated using DIM dissolved in DMSO and in a novel self-emulsifying lipid-based formulation, BR-9001, showing a statistically significant enhanced effect of BR-9001 over DIM (DMSO) (p < 0.05). Improved bio-delivery of DIM from BR-9001 confirmed DIM’s concentration-dependent trichomonacidal activity. Performed in triplicate, the anti-parasitic results are: IC50 DIM-DMSO = 91.8 μM, IC50 BR-9001 = 30.65 μM *, IC50 MTZ = 2.34 μM, IC50 MTZ(0.75uM)+DIM(37.5uM) = 1.6 μM * and IC50 MTZ(0.75uM)+BR9-001(37.5uM) = 0.8 μM *, * =p < 0.05. Considering the nonexistent therapeutic alternatives for trichomonosis treatment in patients with hypersensitivity to 5-nitroimidazoles or against resistant cases, the combined use of DIM + MTZ for oral and topical administration provides a promising new therapeutic opportunity. 2023-06-18T00:06:47Z 2023-06-18T00:06:47Z 2017-10-19 journal article Ibáñez Escribano, A., Lau, L. P., Nogal Ruiz, J. J. et al. «Trichomonacidal Activity of 3,3′-Diindolylmethane (DIM) Is Additive to Metronidazole (MTZ) In Vitro, Supporting Future Oral/Topical Use». Proceedings of the 1st Molecules Medicinal Chemistry Symposium, Barcelona, Spain, MDPI, 2017, p. 645. DOI.org (Crossref), https://doi.org/10.3390/proceedings1060645. 2504-3900 10.3390/proceedings1060645 https://hdl.handle.net/20.500.14352/19270 https://doi.org/10.3390/proceedings1060645 eng SAF2015-66690-R UCM (911120) https://creativecommons.org/licenses/by/3.0/es/ open access Atribución 3.0 España MDPI