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dc.contributor.advisorDe la Cruz Flores, Mario Javier
dc.contributor.advisorGarcía de Sotero, Dora Enith
dc.contributor.authorAlva Ochavano, Magaly Eusebia
dc.contributor.authorGolac Linares, Gessica Jhoana
dc.date.accessioned2022-09-26T18:01:28Z
dc.date.available2022-09-26T18:01:28Z
dc.date.issued2022
dc.identifier.urihttps://hdl.handle.net/20.500.12737/8372
dc.description.abstractAntioxidants have the ability to protect biological systems against reactions that can produce potentially harmful effects, such as reactive oxygen species (EROS or ROS). The objective was to determine secondary metabolites by spectrophotometric methods and in vitro antioxidant activity of the bark of Cecropia strigosa Trécul and Matisia cordata Bonpl by the DPPH method. The samples were conditioned, dried in a dehumidifier at 40°C for seven days, sprayed. In phenolic compounds, C. strigosa Trécul presented 14940.562 mg/100g in total phenols; flavonoids 21,027 mg/100g; anthocyanins 13.073 mg/100g and catechins 0.002 mg/100g; M. cordata Bonpl 19842.523 mg/100g in total phenols; flavonoids 31,842mg/100g; anthocyanins 13.880 mg/100g and catechins 0.004 mg/100g. For Alkaloids, C. strigosa Trécul presented 23.14 mg/100g; while M. cordata Bonpl 37.42 mg/100g. For Saponins, C. strigosa Trécul 178.620 mg/100g and M. cordata Bonpl 442.110 mg/100g. The antioxidant activity of C. strigosa Trécul showed inhibition percentages of 19.65%, 33.71%, 39.54%, 42.16%, 45.72%, 94.29%; while M. cordata Bonpl showed 32.97%, 61.54%, 83.53%, 89.49%, 98.14% and 98.57% at concentrations of 1, 2, 4, 8, 16 and 25 mg/mL respectively. M. cordata Bonpl, compared to C. strigosa Trécul, showed a better result in IC50, because it obtained the lowest value (1.46 mg/mL) compared to the IC50=16.79mg/mL of C. strigosa Trecul; being identified, as well as the one with the best antioxidant activity in vitro.en_US
dc.description.abstractLos antioxidantes tienen la capacidad de proteger los sistemas biológicos contra reacciones que pueden producir efectos potencialmente dañinos, como las especies reactivas del oxígeno (EROS o ROS). El objetivo fue determinar metabolitos secundarios por métodos espectrofotométricos y actividad antioxidante in vitro de corteza de Cecropia strigosa Trécul y Matisia cordata Bonpl por el método DPPH. Las muestras fueron acondicionadas, secadas en deshumecedor a 40°C por siete días, pulverizadas. La especie C. strigosa Trécul presentó 14940,562 mg/100g de fenoles totales; flavonoides 21,027 mg/100g; antocianinas 13,073 mg/100g y catequinas 0,002 mg/100g; M. cordata Bonpl 19842,523 mg/100g en fenoles totales; flavonoides 31,842 mg/100g; antocianinas 13,880 mg/100g y catequinas 0,004 mg/100g. Para Alcaloides, C. strigosa Trécul presentó 23,14 mg/100g y M. cordata Bonpl 37,42 mg/100g, Para Saponinas, C. strigosa Trécul 178,620 mg/100g y M. cordata Bonpl 442,110 mg/100g. La actividad antioxidante de C. strigosa Trécul mostró porcentajes de inhibición de 19,65%, 33,71%, 39,54%, 42,16%, 45,72%, 94,29%; mientras que M. cordata Bonpl mostró 32,97%, 61,54%, 83,53%, 89,49%, 98,14% y 98,57% a concentraciones de 1, 2, 4, 8, 16 y 25 mg/mL respectivamente. M. cordata Bonpl, en comparación con C. strigosa Trécul, mostró una mejor actividad antioxidante in vitro con un menor valor de IC50 de 1,46 mg/mL; en comparación con la IC50=16,79mg/mL de C. strigosa Trécul.es_PE
dc.formatapplication/pdfes_PE
dc.language.isospaes_PE
dc.publisherUniversidad Nacional de la Amazonía Peruanaes_PE
dc.rightsinfo:eu-repo/semantics/openAccess*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subjectAntioxidantees_PE
dc.subjectCortezaes_PE
dc.subjectCecropia strigosaes_PE
dc.subjectMatisia cordataes_PE
dc.subjectIn vitroes_PE
dc.subjectEquipo de laboratorioes_PE
dc.titleMetabolitos secundarios y actividad antioxidante in vitro de corteza de Cecropia strigosa Trécul y Matisia cordata Bonpl por el método 1,1-difenil-2-picril-hidrazilo-DPPHes_PE
dc.typeinfo:eu-repo/semantics/bachelorThesises_PE
thesis.degree.disciplineFarmacia y Bioquímicaes_PE
thesis.degree.grantorUniversidad Nacional de la Amazonía Peruana. Facultad de Farmacia y Bioquímicaes_PE
thesis.degree.nameQuímico(a) Farmacéutico(a)es_PE
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.01.05es_PE
renati.author.dni71928688
renati.author.dni70600483
renati.advisor.orcidhttps://orcid.org/0000-0003-2212-3936
renati.advisor.orcidhttps://orcid.org/0000-0002-9501-1372
renati.advisor.dni40553043
renati.advisor.dni05236520
renati.typehttps://purl.org/pe-repo/renati/type#tesises_PE
renati.discipline917046es_PE
renati.levelhttps://purl.org/pe-repo/renati/level#bachilleres_PE
renati.jurorRuiz Vásquez, Liliana
renati.jurorJara Herrera, Cleto
renati.jurorAlvarez Marreros, Roy Alexander
dc.publisher.countryPEes_PE


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