Synthesis and characterization of type B gelatin and silica nanoparticles with a novel rational designed translocating and antifungal peptide

Gelatin and silica nanoparticles have been developed as nanocarriers of drug delivery systems because of their high biocompatibility. This study aims to synthesize type B gelatin (GNPs) and silica nanoparticles (SNPs) with a novel rational designed peptide to be use as translocating and antifungal a...

Full description

Autores:
Sánchez Betancourt, Melisa
Segura Rodríguez, Daniel Mateo
Tipo de recurso:
Trabajo de grado de pregrado
Fecha de publicación:
2022
Institución:
Universidad de los Andes
Repositorio:
Séneca: repositorio Uniandes
Idioma:
eng
OAI Identifier:
oai:repositorio.uniandes.edu.co:1992/63985
Acceso en línea:
http://hdl.handle.net/1992/63985
Palabra clave:
Gelatin
Silica
Nanoparticle
Hemolysis
Antifungal Activity
Nanobioconjugate
Ingeniería
Rights
openAccess
License
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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oai_identifier_str oai:repositorio.uniandes.edu.co:1992/63985
network_acronym_str UNIANDES2
network_name_str Séneca: repositorio Uniandes
repository_id_str
dc.title.none.fl_str_mv Synthesis and characterization of type B gelatin and silica nanoparticles with a novel rational designed translocating and antifungal peptide
title Synthesis and characterization of type B gelatin and silica nanoparticles with a novel rational designed translocating and antifungal peptide
spellingShingle Synthesis and characterization of type B gelatin and silica nanoparticles with a novel rational designed translocating and antifungal peptide
Gelatin
Silica
Nanoparticle
Hemolysis
Antifungal Activity
Nanobioconjugate
Ingeniería
title_short Synthesis and characterization of type B gelatin and silica nanoparticles with a novel rational designed translocating and antifungal peptide
title_full Synthesis and characterization of type B gelatin and silica nanoparticles with a novel rational designed translocating and antifungal peptide
title_fullStr Synthesis and characterization of type B gelatin and silica nanoparticles with a novel rational designed translocating and antifungal peptide
title_full_unstemmed Synthesis and characterization of type B gelatin and silica nanoparticles with a novel rational designed translocating and antifungal peptide
title_sort Synthesis and characterization of type B gelatin and silica nanoparticles with a novel rational designed translocating and antifungal peptide
dc.creator.fl_str_mv Sánchez Betancourt, Melisa
Segura Rodríguez, Daniel Mateo
dc.contributor.advisor.none.fl_str_mv Reyes Barrios, Luis Humberto
dc.contributor.author.none.fl_str_mv Sánchez Betancourt, Melisa
Segura Rodríguez, Daniel Mateo
dc.subject.keyword.none.fl_str_mv Gelatin
Silica
Nanoparticle
Hemolysis
Antifungal Activity
Nanobioconjugate
topic Gelatin
Silica
Nanoparticle
Hemolysis
Antifungal Activity
Nanobioconjugate
Ingeniería
dc.subject.themes.es_CO.fl_str_mv Ingeniería
description Gelatin and silica nanoparticles have been developed as nanocarriers of drug delivery systems because of their high biocompatibility. This study aims to synthesize type B gelatin (GNPs) and silica nanoparticles (SNPs) with a novel rational designed peptide to be use as translocating and antifungal agent. Also, the physical, chemical and biocompatibility properties of the obtained nanoparticles were compared. Gelatin nanoparticles were synthesized by the double desolvation method and the silica nanoparticles by the hydrolysis and polycondensation of TEOS in a mixture of ammonia, alcohol, and water. The obtained nanobioconjugates were characterized by thermogravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FTIR). FTIR results show that the peptide was immobilized correctly in both nanoparticles. Furthermore, the NPs were tested for their ability to induce hemolysis and platelet aggregation. The obtained NPs with the KS-peptide show a low hemolytic percentage (less than 5%) and a lower tendency to induce platelet aggregation. Finally, they were tested upon an antifungal assay with C. tropicalis, C. krusei, C. albicans and Cryptococcus neoformans; the NPs show a tendency to not inhibit the growth of fungi.
publishDate 2022
dc.date.issued.none.fl_str_mv 2022-06
dc.date.accessioned.none.fl_str_mv 2023-01-19T12:47:10Z
dc.date.available.none.fl_str_mv 2023-01-19T12:47:10Z
dc.type.es_CO.fl_str_mv Trabajo de grado - Pregrado
dc.type.driver.none.fl_str_mv info:eu-repo/semantics/bachelorThesis
dc.type.version.none.fl_str_mv info:eu-repo/semantics/acceptedVersion
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dc.language.iso.es_CO.fl_str_mv eng
language eng
dc.rights.license.spa.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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dc.format.extent.es_CO.fl_str_mv 16 páginas
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dc.publisher.es_CO.fl_str_mv Universidad de los Andes
dc.publisher.program.es_CO.fl_str_mv Ingeniería Química
dc.publisher.faculty.es_CO.fl_str_mv Facultad de Ingeniería
dc.publisher.department.es_CO.fl_str_mv Departamento de Ingeniería Química y de Alimentos
institution Universidad de los Andes
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Also, the physical, chemical and biocompatibility properties of the obtained nanoparticles were compared. Gelatin nanoparticles were synthesized by the double desolvation method and the silica nanoparticles by the hydrolysis and polycondensation of TEOS in a mixture of ammonia, alcohol, and water. The obtained nanobioconjugates were characterized by thermogravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FTIR). FTIR results show that the peptide was immobilized correctly in both nanoparticles. Furthermore, the NPs were tested for their ability to induce hemolysis and platelet aggregation. The obtained NPs with the KS-peptide show a low hemolytic percentage (less than 5%) and a lower tendency to induce platelet aggregation. 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