Evaluación de la actividad de nanoencapsulados de Anfotericina B en aislamientos ambientales de Mucorales con impacto clínico
ilustraciones, diagramas, fotografías
- Autores:
-
Gutiérrez Pardo, Yinneth Marcela
- Tipo de recurso:
- Fecha de publicación:
- 2023
- Institución:
- Universidad Nacional de Colombia
- Repositorio:
- Universidad Nacional de Colombia
- Idioma:
- spa
- OAI Identifier:
- oai:repositorio.unal.edu.co:unal/85611
- Palabra clave:
- Infecciones Fúngicas Invasoras
Antifúngicos
Anticuerpos Antifúngicos
Invasive Fungal Infections
Antifungal Agents
Antibodies, Fungal
Mucorales
Anfotericina B
Nanoencapsulación
Susceptibilidad antifúngica
Galleria mellonella
- Rights
- openAccess
- License
- Atribución-NoComercial-CompartirIgual 4.0 Internacional
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oai:repositorio.unal.edu.co:unal/85611 |
network_acronym_str |
UNACIONAL2 |
network_name_str |
Universidad Nacional de Colombia |
repository_id_str |
|
dc.title.spa.fl_str_mv |
Evaluación de la actividad de nanoencapsulados de Anfotericina B en aislamientos ambientales de Mucorales con impacto clínico |
dc.title.translated.eng.fl_str_mv |
Evaluation of the activity of amphotericin B nanoencapsulated on environmental isolates of Mucorales with clinical impact |
title |
Evaluación de la actividad de nanoencapsulados de Anfotericina B en aislamientos ambientales de Mucorales con impacto clínico |
spellingShingle |
Evaluación de la actividad de nanoencapsulados de Anfotericina B en aislamientos ambientales de Mucorales con impacto clínico Infecciones Fúngicas Invasoras Antifúngicos Anticuerpos Antifúngicos Invasive Fungal Infections Antifungal Agents Antibodies, Fungal Mucorales Anfotericina B Nanoencapsulación Susceptibilidad antifúngica Galleria mellonella |
title_short |
Evaluación de la actividad de nanoencapsulados de Anfotericina B en aislamientos ambientales de Mucorales con impacto clínico |
title_full |
Evaluación de la actividad de nanoencapsulados de Anfotericina B en aislamientos ambientales de Mucorales con impacto clínico |
title_fullStr |
Evaluación de la actividad de nanoencapsulados de Anfotericina B en aislamientos ambientales de Mucorales con impacto clínico |
title_full_unstemmed |
Evaluación de la actividad de nanoencapsulados de Anfotericina B en aislamientos ambientales de Mucorales con impacto clínico |
title_sort |
Evaluación de la actividad de nanoencapsulados de Anfotericina B en aislamientos ambientales de Mucorales con impacto clínico |
dc.creator.fl_str_mv |
Gutiérrez Pardo, Yinneth Marcela |
dc.contributor.advisor.none.fl_str_mv |
Ceballos Garzón, Ándres |
dc.contributor.author.none.fl_str_mv |
Gutiérrez Pardo, Yinneth Marcela |
dc.contributor.researchgroup.spa.fl_str_mv |
Enfermedades Infecciosas: Unidad de Investigación en Proteómica y Micosis Humana Pontificia Universidad Javeriana PUJ Macromoléculas, Departamento de Quìmica |
dc.subject.decs.spa.fl_str_mv |
Infecciones Fúngicas Invasoras Antifúngicos Anticuerpos Antifúngicos |
topic |
Infecciones Fúngicas Invasoras Antifúngicos Anticuerpos Antifúngicos Invasive Fungal Infections Antifungal Agents Antibodies, Fungal Mucorales Anfotericina B Nanoencapsulación Susceptibilidad antifúngica Galleria mellonella |
dc.subject.decs.eng.fl_str_mv |
Invasive Fungal Infections Antifungal Agents Antibodies, Fungal |
dc.subject.proposal.spa.fl_str_mv |
Mucorales Anfotericina B Nanoencapsulación Susceptibilidad antifúngica Galleria mellonella |
description |
ilustraciones, diagramas, fotografías |
publishDate |
2023 |
dc.date.issued.none.fl_str_mv |
2023-07-26 |
dc.date.accessioned.none.fl_str_mv |
2024-02-05T16:59:28Z |
dc.date.available.none.fl_str_mv |
2024-02-05T16:59:28Z |
dc.type.spa.fl_str_mv |
Trabajo de grado - Maestría |
dc.type.driver.spa.fl_str_mv |
info:eu-repo/semantics/masterThesis |
dc.type.version.spa.fl_str_mv |
info:eu-repo/semantics/acceptedVersion |
dc.type.content.spa.fl_str_mv |
Other |
dc.type.redcol.spa.fl_str_mv |
http://purl.org/redcol/resource_type/TM |
status_str |
acceptedVersion |
dc.identifier.uri.none.fl_str_mv |
https://repositorio.unal.edu.co/handle/unal/85611 |
dc.identifier.instname.spa.fl_str_mv |
Universidad Nacional de Colombia |
dc.identifier.reponame.spa.fl_str_mv |
Repositorio Institucional Universidad Nacional de Colombia |
dc.identifier.repourl.spa.fl_str_mv |
https://repositorio.unal.edu.co/ |
url |
https://repositorio.unal.edu.co/handle/unal/85611 https://repositorio.unal.edu.co/ |
identifier_str_mv |
Universidad Nacional de Colombia Repositorio Institucional Universidad Nacional de Colombia |
dc.language.iso.spa.fl_str_mv |
spa |
language |
spa |
dc.relation.references.spa.fl_str_mv |
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Retrieved from http://dx.doi.org/10.3390/jof5010026 Skiada, A., Pavleas, I., & Drogari-Apiranthitou, M. (2020). Epidemiology and Diagnosis of Mucormycosis: An Update. Journal of Fungi, 6(4), 265. MDPI AG. Retrieved from http://dx.doi.org/10.3390/jof6040265 Garg, D., Muthu, V., Sehgal, I. S., Ramachandran, R., Kaur, H., Bhalla, A., Puri, G. D., Chakrabarti, A., & Agarwal, R. (2021). Coronavirus Disease (Covid-19) Associated Mucormycosis (CAM): Case Report and Systematic Review of Literature. Mycopathologia, 186(2), 289–298. https://doi.org/10.1007/s11046-021-00528-2 Macedo, D., Leonardelli, F., Dudiuk, C., Vitale, R. G., Del Valle, E., Giusiano, G., Gamarra, S., et al. (2019). In Vitro and In Vivo Evaluation of Voriconazole-Containing Antifungal Combinations against Mucorales Using a Galleria mellonella Model of Mucormycosis. Journal of Fungi, 5(1), 5. MDPI AG. Retrieved from http://dx.doi.org/10.3390/jof5010005 Sipsas, N. V., Gamaletsou, M. N., Anastasopoulou, A., & Kontoyiannis, D. P. (2018). Therapy of Mucormycosis. Journal of fungi (Basel, Switzerland), 4(3), 90. https://doi.org/10.3390/jof4030090 Cavassin, F.B., Baú-Carneiro, J.L., Vilas-Boas, R.R. Queiroz-Telles, F . (2021). Sixty years of Amphotericin B: An Overview of the Main Antifungal Agent Used to Treat Invasive Fungal Infections. Infect Dis Ther 10, 115–147 https://doi.org/10.1007/s40121-020-00382-7 Palmis, B., Alanio, A., Lortholary, O., & Lanternier, F. (2018). Recent advances in the understanding and management of mucormycosis. F1000Research, 7, F1000 Faculty Rev-1429. https://doi.org/10.12688/f1000research.15081.1 Villamil-Poveda, J.C. (2019). Evaluación de la eficacia de formulaciones de Anfotericina B encapsulada en micelas poliméricas como opción terapéutica en un modelo de Candidiasis en larvas de Galleria mellonella. Tesis de Maestría, Universidad Nacional de Colombia. https://repositorio.unal.edu.co/bitstream/handle/unal/75903/1019014737.2019.pdf?sequence=1&isAllowed=y Richardson, M.D.; Rautemaa-Richardson, R. (2020). Biotic Environments Supporting the Persistence of Clinically Relevant Mucormycetes. J. Fungi, 6 (1), 4. https://doi.org/10.3390/jof6010004 Walther, Wagner, & Kurzai. (2019). Updates on the Taxonomy of Mucorales with an Emphasis on Clinically Important Taxa. Journal of Fungi, 5(4), 106. MDPI AG. Retrieved from http://dx.doi.org/10.3390/jof5040106 Borman, A. M., Fraser, M., Patterson, Z., Palmer, M. D., & Johnson, E. M. (2021). In Vitro Antifungal Drug Resistance Profiles of Clinically Relevant Members of the Mucorales (Mucoromycota) Especially with the Newer Triazoles. Journal of fungi (Basel, Switzerland), 7(4), 271. https://doi.org/10.3390/jof7040271 Garre,V. (2022). Recent Advances and Future Directions in the Understanding of Mucormycosis. Frontiers in Cellular and Infection Microbiology vo.12 10.3389/fcimb.2022.850581, 2235-2988 Castrejón-Pérez, A. D., Welsh, E. C., Miranda, I., Ocampo-Candiani, J., & Welsh, O. (2017). Cutaneous mucormycosis. Anais brasileiros de dermatologia, 92(3), 304–311. https://doi.org/10.1590/abd1806-4841.20176614 CDC (2020). Mucormycosis Statistics. Centers for Disease Control and Prevention. https://www.cdc.gov/fungal/diseases/mucormycosis/statistics.html Serris, A., Danion, F., & Lanternier, F. (2019). Disease Entities in Mucormycosis. Journal of Fungi, 5(1), 23. MDPI AG. Retrieved from http://dx.doi.org/10.3390/jof5010023 Morales-López, S., Ceballos-Garzón, A. & Parra-Giraldo, C.M. Zygomycete Fungi Infection in Colombia: Literature Review. Curr Fungal Infect Rep 12, 149–154 (2018). https://doi.org/10.1007/s12281-018-0326-9 Spatafora, J. W., Chang, Y., Benny, G. L., Lazarus, K., Smith, M. E., Berbee, M. L., Bonito, G., Corradi, N., Grigoriev, I., Gryganskyi, A., James, T. Y., O'Donnell, K., Roberson, R. W., Taylor, T. N., Uehling, J., Vilgalys, R., White, M. M., & Stajich, J. E. (2016). A phylum-level phylogenetic classification of zygomycete fungi based on genome-scale data. Mycologia, 108(5), 1028–1046. https://doi.org/10.3852/16-042 Badali, H. Cañete-Gibas, C. McCarthy, D. Patterson, H, Sanders, C. David, M. Mele, J. Fan, H. Wiederhold, N. (2021). Epidemiology and Antifungal Susceptibilities of Mucoralean Fungi in Clinical Samples from the United States. Journal of clinical Microbiology . Vol 59 (9). https://doi.org/10.1128/JCM.01230-21 Nucci,M. Engelhardt, M. Hamed, K.(2019). Mucormycosis in South America: A review of 143 reported cases. Mycoses vol. 62(9) . https://doi.org/10.1111/myc.12958 García-Carnero, L. C., & Mora-Montes, H. M. (2022). Mucormycosis and COVID-19-Associated Mucormycosis: Insights of a Deadly but Neglected Mycosis. Journal of fungi (Basel, Switzerland), 8(5), 445. https://doi.org/10.3390/jof8050445 Brinder, U. Maurer, E. Lass-Flor. C. (2014). Mucormycosis–from the pathogens to the disease. Clin Microbiol Infect; 20(6): 60–66. https://doi.org/10.1111/1469-0691.12566 Katragkou,A. Walsh, J. Roilides, E. (2014). Why is mucormycosis more difficult to cure than more common mycoses?. European Society of Clinical Infectious Diseases. https://doi.org/10.1111/1469-0691.12466 Petrikkos, G. Tsioutis, C.(2018). Recent Advances in the Pathogenesis of Mucormycosis. Clinical Therapeutics. https://doi.org/10.1016/j.clinthera.2018.03.009. Ibrahim,A.S. Spellberg, B. Walsh,T. Kontoyiannis, D. (2012). Pathogenesis of Mucormycosis, Clinical Infectious Diseases, Volume 54, Issue suppl_1, Pages S16–S22, https://doi.org/10.1093/cid/cir865 García-Vidal, C. Salavert, M. (2014). Inmunopatología de las micosis invasivas por hongos filamentosos.Revista Iberoamericana de Micología. Vol. 31. Núm. 4. páginas 219-228 10.1016/j.riam.2014.09.001 Álvarez,F. Fernández-Ruiz, M. Aguado, J. M. ( 2013). Hierro e infección fúngica invasiva. Revista Iberoamericana de Microbiología. 30 (4): 217-225. DOI: 10.1016/j.riam.2013.04.002 Tahiri, G., Lax, C., Cánovas-Márquez, J. T., Carrillo-Marín, P., Sanchis, M., Navarro, E., Garre, V., et al. (2023). Mucorales and Mucormycosis: Recent Insights and Future Prospects. Journal of Fungi, 9(3), 335. MDPI AG. Retrieved from http://dx.doi.org/10.3390/jof9030335 Lugito, N. P. H., & Cucunawangsih, C. (2021). How Does Mucorales Benefit from the Dysregulated Iron Homeostasis During SARS-CoV-2 Infection?. Mycopathologia, 186(6), 877–882. https://doi.org/10.1007/s11046-021-00594-6 Singh, A. Ahmad, N. Varadarajan, Naval Vikram,A. Singh, T.P. Sharma, S. Sharma, P. (2021). Lactoferrin, a potential iron-chelator as an adjunct treatment for mucormycosis – A comprehensive review. International Journal of Biological Macromolecules. Volume 187,Pages 988-998, https://doi.org/10.1016/j.ijbiomac.2021.07.156. Challa, S. (2019). Mucormycosis: Pathogenesis and Pathology. Curr Fungal Infect Rep 13, 11–20. https://doi.org/10.1007/s12281-019-0337-1 Lui, M. Spellberg, B. Phan, Q. Fu,Y. Fu,Y. Lee, A.S. Edwards Jr, J.E. Filler,S.G. Ibrahim, A.S. (2010). The endothelial cell receptor GRP78 is required for mucormycosis pathogenesis in diabetic mice. Clin Invest. 2010;120(6):1914–1924. https://doi.org/10.1172/JCI42164. Abdelwahab, M.I, Voigt,K. (2019). Pathogenicity patterns of mucormycosis: epidemiology, interaction with immune cells and virulence factors, Medical Mycology, Volume 57, Issue Supplement_2, Pages S245–S256, https://doi.org/10.1093/mmy/myz011 Lax, C., Pérez-Arques, C., Navarro-Mendoza, M., Cánovas-Márquez, J., Tahiri, G., Pérez-Ruiz, J., Osorio-Concepción, M., et al. (2020). Genes, Pathways, and Mechanisms Involved in the Virulence of Mucorales. Genes, 11(3), 317. MDPI AG. Retrieved from http://dx.doi.org/10.3390/genes11030317 Biswas, D., Kotwal, A., Kakati, B., & Ahmad, S. (2015). 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The family structure of the Mucorales: a synoptic revision based on comprehensive multigene-genealogies. Persoonia, 30, 57–76. https://doi.org/10.3767/003158513X666259) Cruz-Lachica, I. Marquez, I. García-Estrada, R.S. Carrillo-Fasio,J.A. León-Félix, J. Allende-Molar, R. (2017). Identificación de hongos mucorales causantes de la pudrición blanda en frutos de papaya (Carica papaya L.) en México. Rev. mex. fitopatol vol.35 no.3 Texcoco sep. https://doi.org/10.18781/r.mex.fit.1611-3 Mendoza L, Vilela R, Voelz K, Ibrahim AS, Voigt K, Lee SC. Human Fungal Pathogens of Mucorales and Entomophthorales. Cold Spring Harb Perspect Med. 2014 Nov 6;5(4):a019562. doi: 10.1101/cshperspect.a019562. PMID: 25377138; PMCID: PMC4382724. Lackner, N., Posch, W., & Lass-Flörl, C. (2021). Microbiological and Molecular Diagnosis of Mucormycosis: From Old to New. Microorganisms, 9(7), 1518. MDPI AG. Retrieved from http://dx.doi.org/10.3390/microorganisms9071518 Dadwal, S. Kontoyiannis, D. (2018). 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A Revised Species Concept for Opportunistic Mucor Species Reveals Species-Specific Antifungal Susceptibility Profiles. Danion, F., Coste, A., Le Hyaric, C., Melenotte, C., Lamoth, F., Calandra, T., Garcia-Hermoso, D., et al. (2023). What Is New in Pulmonary Mucormycosis? Journal of Fungi, 9(3), 307. MDPI AG. Retrieved from http://dx.doi.org/10.3390/jof9030307 Muthu, V., Rudramurthy, S.M., Chakrabarti, A. Agarwal, R. (2021). Epidemiology and Pathophysiology of COVID-19-Associated Mucormycosis: India Versus the Rest of the World. Mycopathologia 186, 739–754. https://doi.org/10.1007/s11046-021-00584-8 Mahalaxmi,I. Jayaramayya, K. Venkatesan, D. Subramaniam, M.D. Renu, K. Vijayakumar, P. Narayanasamy,A. Gopalakrishnan, A. Kumar, N. Sivaprakash, P. Sambasiva Rao, K. Vellingiri, B. (2021). Mucormycosis: An opportunistic pathogen during COVID-19. Environmental Research, Volume 201, 111643, ,https://doi.org/10.1016/j.envres.2021.111643. Chandley, P., Subba, P., & Rohatgi, S. (2022). 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It only takes one to do many jobs: Amphotericin B as antifungal and immunomodulatory drug. Frontiers in microbiology, 3, 286. https://doi.org/10.3389/fmicb.2012.00286 Sangalli-Leite, F. Scorzoni,L. Mesa-Arango, A.C. Casas,C. Herrero,E. Soares Mendes Gianinni,M.J. Rodríguez-Tudela,J. Cuenca-Estrella,M. Zaragoza,O. (2011). Amphotericin B mediates killing in Cryptococcus neoformans through the induction of a strong oxidative burst, Microbes and Infection, Volume 13, Issue 5,Pages 457-467,https://doi.org/10.1016/j.micinf.2011.01.015. Hamill, R.J. Amphotericin B Formulations: A Comparative Review of Efficacy and Toxicity. Drugs 73, 919–934 (2013). https://doi.org/10.1007/s40265-013-0069-4 Noor A, Preuss CV. (2023). Amphotericin B. In: Stat Pearls [Internet]. Treasure Island (FL): Obtenido de: https://www.ncbi.nlm.nih.gov/books/NBK482327/ Tonin, F. Steimbach,L. Borba,H. Sanches, A. Wiens,A. Pontarolo, R. Fernandez-Llimos, F. (2017). 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Modeling and interactions of Aspergillus fumigatus lanosterol 14-α demethylase `A' with azole antifungals, Bioorganic & Medicinal Chemistry, Volume 12, Issue 11, Pages 2937-2950, https://doi.org/10.1016/j.bmc.2004.03.034. Ganesan, P., Ganapathy, D., Sekaran, S., Murthykumar, K., Sundramoorthy, A. K., Pitchiah, S., & Shanmugam, R. (2022). Molecular Mechanisms of Antifungal Resistance in Mucormycosis. BioMed research international, 2022, 6722245. https://doi.org/10.1155/2022/6722245 Chang Z, Billmyre RB, Lee SC, Heitman J (2019) Broad antifungal resistance mediated by RNAi-dependent epimutation in the basal human fungal pathogen Mucor circinelloides. PLoS Genet 15(2): e1007957. https://doi.org/10.1371/journal.pgen.1007957 Begines, B., Ortiz, T., Pérez-Aranda, M., Martínez, G., Merinero, M., Argüelles-Arias, F., & Alcudia, A. (2020). Polymeric Nanoparticles for Drug Delivery: Recent Developments and Future Prospects. Nanomaterials, 10(7), 1403. MDPI AG. 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Correlation between hemolytic activity, cytotoxicity and systemic in vivo toxicity of synthetic antimicrobial peptides. Sci Rep 10, 13206 https://doi.org/10.1038/s41598-020-69995-9 Brunet, K., Diop, C. A. B., Chauzy, A., Prébonnaud, N., Marchand, S., Rammaert, B., & Tewes, F. (2022). Improved In Vitro Anti-Mucorales Activity and Cytotoxicity of Amphotericin B with a Pegylated Surfactant. Journal of Fungi, 8(2), 121. MDPI AG. Retrieved from http://dx.doi.org/10.3390/jof8020121 Vandermeulen,G., Rouxhet,L.,Arien,A., Brewster,M.E., Préat,V. (2006). Encapsulation of amphotericin B in poly(ethylene glycol) -block-poly (ɛ-caprolactone-co-trimethylenecarbonate) polymeric micelles. Volume 309, Pages 234-240, https://doi.org/10.1016/j.ijpharm.2005.11.031. Klepser,M. (2011): The value of amphotericin B in the treatment of invasive fungal infections, Journal of Critical Care, Volume 26, Issue 2,Pages 225.e1-225.e10, https://doi.org/10.1016/j.jcrc.2010.08.005.) Abu Ammar, A., Nasereddin, A., Ereqat, S. Dan-Goor, M. Jaffe, C. Zussman, E. Abdeen, Z. (2019). Amphotericin B-loaded nanoparticles for local treatment of cutaneous leishmaniasis. Drug Deliv. and Transl. Res. 9, 76–84. https://doi.org/10.1007/s13346-018-00603-0 Haley, R. M., Zuckerman, S. T., Gormley, C. A., Korley, J. N., & von Recum, H. A. (2019). Local delivery polymer provides sustained antifungal activity of amphotericin B with reduced cytotoxicity. Experimental biology and medicine (Maywood, N.J.), 244(6), 526–533. https://doi.org/10.1177/1535370219837905 Ménard, G., Rouillon, A., Cattoir, V., & Donnio, P. Y. (2021). Galleria mellonella as a Suitable Model of Bacterial Infection: Past, Present and Future. Frontiers in cellular and infection microbiology, 11, 782733. https://doi.org/10.3389/fcimb.2021.782733 Bastidas, R. Shertz, C. Chan Lee, S. Heitman, J. Cardenas, M. (2012).Rapamycin Exerts Antifungal Activity In Vitro and In Vivo against Mucor circinelloides via FKBP12-Dependent Inhibition of Tor. ASM Journals Eukaryotic Cell. Vol. 11, No. 3. doi: https://doi.org/10.1128/ec.05284-11 |
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Universidad Nacional de Colombia |
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Bogotá - Ciencias - Maestría en Ciencias - Microbiología |
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Facultad de Ciencias |
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Universidad Nacional de Colombia - Sede Bogotá |
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Atribución-NoComercial-CompartirIgual 4.0 Internacionalhttp://creativecommons.org/licenses/by-nc-sa/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Ceballos Garzón, Ándres9681a65a70cf8c2e757b3704a46d5399Gutiérrez Pardo, Yinneth Marcelaf1ecf8227103ace3b7dc741e1a9da0fdEnfermedades Infecciosas: Unidad de Investigación en Proteómica y Micosis Humana Pontificia Universidad Javeriana PUJ Macromoléculas, Departamento de Quìmica2024-02-05T16:59:28Z2024-02-05T16:59:28Z2023-07-26https://repositorio.unal.edu.co/handle/unal/85611Universidad Nacional de ColombiaRepositorio Institucional Universidad Nacional de Colombiahttps://repositorio.unal.edu.co/ilustraciones, diagramas, fotografíasLa mucormicosis es una infección fúngica causada por hongos del orden Mucorales, estos hongos se caracterizan por ser ubicuos. Sin embargo, algunas especies tienen factores de virulencia que les han permitido colonizar hospederos humanos, en su mayoría con un sistema inmune debilitado. Las tasas de mortalidad asociadas pueden alcanzar hasta el 90% en los casos de infección diseminada. Estas elevadas tasas de mortalidad se deben en gran medida a la resistencia innata a los fármacos antifúngicos, la dificultad para identificar el agente causal de esta micosis y la toxicidad que genera la anfotericina B (AMB), el cual es el antifúngico de mayor eficiencia contra estos hongos. Entre las nuevas estrategias terapéuticas, las nanopartículas parecen ser prometedoras, debido a que estas permiten aumentar el tiempo de vida media de los fármacos y mejoran la liberación de estos disminuyendo así la toxicidad. Este estudio tuvo como objetivo evaluar nanoencapsulados de AMB contra especies de Mucorales ambientales que tienen impacto clínico, con el fin de establecer su efectividad In vitro e In vivo. Para ello se utilizó la metodología de microdilución en caldo siguiendo los lineamientos del European Committee on Antimicrobial Susceptibility Testing (EUCAST), lo cual permitió obtener y comparar las concentraciones mínimas inhibitorias (CMIs) entre la formulación tradicional vs los encapsulados de AMB (Pol I, Pol II, Pol III, Pol IV y Pol V). Se evidencio que el nanoencapsulado AMB Pol III permitió reducir los valores de CMI en comparación con la AMB convencional para los aislamientos de Mucor circinelloides aquí evaluados. Además, en el modelo In vivo (Galleria mellonella), se observó una reducción en la mortalidad de las larvas infectadas con Mucor circinelloides en comparación con las larvas que no recibieron tratamiento y que fueron tratadas con AMB convencional. (Texto tomado de la fuente)Mucormycosis is a fungal infection caused by fungi of the order Mucorales, these fungi are characterized by being ubiquitous. However, some species have virulence factors that have allowed them to colonize human hosts, mostly with a weakened immune system. Associated mortality rates can reach up to 90% in cases of disseminated infection. These high mortality rates are largely due to the innate resistance to antifungal drugs, the difficulty in identifying the causal agent of this mycosis and the toxicity generated by amphotericin B (AMB), which is the most efficient antifungal drug against these fungi. Among the new therapeutic strategies, nanoparticles seem to be promising, since they increase the half-life of drugs and improve drug release, thus reducing toxicity. The objective of this study was to evaluate nanoencapsulated AMB against environmental Mucorales species with clinical impact, in order to establish their effectiveness In vitro and In vivo. For this purpose, the broth microdilution methodology was used following the guidelines of the European Committee on Antimicrobial Susceptibility Testing (EUCAST), which allowed obtaining and comparing the minimum inhibitory concentrations (MICs) between the traditional formulation vs. the AMB encapsulates (Pol I, Pol II, Pol III, Pol IV and Pol V). It was evidenced that the AMB Pol III nanoencapsulated allowed to reduce MIC values compared to conventional AMB for the Mucor circinelloides isolates evaluated here. 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Mediterranean journal of hematology and infectious diseases, 3(1), e2011001. https://doi.org/10.4084/MJHID.2011.001Hoenigl, M., Seidel, D., Sprute, R., Cunha, C., Oliverio, M., Goldman, G., Ibrahim, A., Carvalho, A. (2022) . COVID-19-associated fungal infections. Nat Microbiol 7, 1127–1140. https://doi.org/10.1038/s41564-022-01172-2Martin Gomez, M.T., Salavert Lletib, M. (2021). Mucormycosis: Current and future management perspective. Revista Iberoamericana de Micología, 38 (2), 91-100. https://doi.org/10.1016/j.riam.2021.04.003Zamudio, A; Vargas, MC; Camacho, F. (2021). Cutaneous Mucormycosis, life–threatening unsuspected mycosis, case report and review. Rev Asoc Colomb Dermatol. Vol 29(4):282-294Prakash, H., & Chakrabarti, A. (2019). Global Epidemiology of Mucormycosis. Journal of Fungi, 5(1), 26. MDPI AG. Retrieved from http://dx.doi.org/10.3390/jof5010026Skiada, A., Pavleas, I., & Drogari-Apiranthitou, M. (2020). Epidemiology and Diagnosis of Mucormycosis: An Update. Journal of Fungi, 6(4), 265. MDPI AG. Retrieved from http://dx.doi.org/10.3390/jof6040265Garg, D., Muthu, V., Sehgal, I. S., Ramachandran, R., Kaur, H., Bhalla, A., Puri, G. D., Chakrabarti, A., & Agarwal, R. (2021). Coronavirus Disease (Covid-19) Associated Mucormycosis (CAM): Case Report and Systematic Review of Literature. Mycopathologia, 186(2), 289–298. https://doi.org/10.1007/s11046-021-00528-2Macedo, D., Leonardelli, F., Dudiuk, C., Vitale, R. G., Del Valle, E., Giusiano, G., Gamarra, S., et al. (2019). In Vitro and In Vivo Evaluation of Voriconazole-Containing Antifungal Combinations against Mucorales Using a Galleria mellonella Model of Mucormycosis. Journal of Fungi, 5(1), 5. MDPI AG. Retrieved from http://dx.doi.org/10.3390/jof5010005Sipsas, N. V., Gamaletsou, M. N., Anastasopoulou, A., & Kontoyiannis, D. P. (2018). Therapy of Mucormycosis. Journal of fungi (Basel, Switzerland), 4(3), 90. https://doi.org/10.3390/jof4030090Cavassin, F.B., Baú-Carneiro, J.L., Vilas-Boas, R.R. Queiroz-Telles, F . (2021). Sixty years of Amphotericin B: An Overview of the Main Antifungal Agent Used to Treat Invasive Fungal Infections. Infect Dis Ther 10, 115–147 https://doi.org/10.1007/s40121-020-00382-7Palmis, B., Alanio, A., Lortholary, O., & Lanternier, F. (2018). Recent advances in the understanding and management of mucormycosis. F1000Research, 7, F1000 Faculty Rev-1429. https://doi.org/10.12688/f1000research.15081.1Villamil-Poveda, J.C. (2019). Evaluación de la eficacia de formulaciones de Anfotericina B encapsulada en micelas poliméricas como opción terapéutica en un modelo de Candidiasis en larvas de Galleria mellonella. Tesis de Maestría, Universidad Nacional de Colombia. https://repositorio.unal.edu.co/bitstream/handle/unal/75903/1019014737.2019.pdf?sequence=1&isAllowed=yRichardson, M.D.; Rautemaa-Richardson, R. (2020). Biotic Environments Supporting the Persistence of Clinically Relevant Mucormycetes. J. 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(2011): The value of amphotericin B in the treatment of invasive fungal infections, Journal of Critical Care, Volume 26, Issue 2,Pages 225.e1-225.e10, https://doi.org/10.1016/j.jcrc.2010.08.005.)Abu Ammar, A., Nasereddin, A., Ereqat, S. Dan-Goor, M. Jaffe, C. Zussman, E. Abdeen, Z. (2019). Amphotericin B-loaded nanoparticles for local treatment of cutaneous leishmaniasis. Drug Deliv. and Transl. Res. 9, 76–84. https://doi.org/10.1007/s13346-018-00603-0Haley, R. M., Zuckerman, S. T., Gormley, C. A., Korley, J. N., & von Recum, H. A. (2019). Local delivery polymer provides sustained antifungal activity of amphotericin B with reduced cytotoxicity. Experimental biology and medicine (Maywood, N.J.), 244(6), 526–533. https://doi.org/10.1177/1535370219837905Ménard, G., Rouillon, A., Cattoir, V., & Donnio, P. Y. (2021). Galleria mellonella as a Suitable Model of Bacterial Infection: Past, Present and Future. Frontiers in cellular and infection microbiology, 11, 782733. https://doi.org/10.3389/fcimb.2021.782733Bastidas, R. Shertz, C. Chan Lee, S. Heitman, J. Cardenas, M. (2012).Rapamycin Exerts Antifungal Activity In Vitro and In Vivo against Mucor circinelloides via FKBP12-Dependent Inhibition of Tor. ASM Journals Eukaryotic Cell. 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