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...
- 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:repositorio.uniandes.edu.co:1992/63985 |
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Séneca: repositorio Uniandes |
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|
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 |
dc.type.coar.none.fl_str_mv |
http://purl.org/coar/resource_type/c_7a1f |
dc.type.content.es_CO.fl_str_mv |
Text |
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http://purl.org/redcol/resource_type/TP |
format |
http://purl.org/coar/resource_type/c_7a1f |
status_str |
acceptedVersion |
dc.identifier.uri.none.fl_str_mv |
http://hdl.handle.net/1992/63985 |
dc.identifier.instname.es_CO.fl_str_mv |
instname:Universidad de los Andes |
dc.identifier.reponame.es_CO.fl_str_mv |
reponame:Repositorio Institucional Séneca |
dc.identifier.repourl.es_CO.fl_str_mv |
repourl:https://repositorio.uniandes.edu.co/ |
url |
http://hdl.handle.net/1992/63985 |
identifier_str_mv |
instname:Universidad de los Andes reponame:Repositorio Institucional Séneca repourl:https://repositorio.uniandes.edu.co/ |
dc.language.iso.es_CO.fl_str_mv |
eng |
language |
eng |
dc.rights.license.spa.fl_str_mv |
Attribution-NonCommercial-NoDerivatives 4.0 Internacional |
dc.rights.uri.*.fl_str_mv |
https://repositorio.uniandes.edu.co/static/pdf/aceptacion_uso_es.pdf |
dc.rights.accessrights.spa.fl_str_mv |
info:eu-repo/semantics/openAccess |
dc.rights.coar.spa.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
rights_invalid_str_mv |
Attribution-NonCommercial-NoDerivatives 4.0 Internacional https://repositorio.uniandes.edu.co/static/pdf/aceptacion_uso_es.pdf http://purl.org/coar/access_right/c_abf2 |
eu_rights_str_mv |
openAccess |
dc.format.extent.es_CO.fl_str_mv |
16 páginas |
dc.format.mimetype.es_CO.fl_str_mv |
application/pdf |
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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Attribution-NonCommercial-NoDerivatives 4.0 Internacionalhttps://repositorio.uniandes.edu.co/static/pdf/aceptacion_uso_es.pdfinfo:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Reyes Barrios, Luis Humberto62fecea0-8853-433b-97b3-fef038cdd5c2600Sánchez Betancourt, Melisa1035ce99-56ce-46d4-8e01-fbdd0681ac52600Segura Rodríguez, Daniel Mateo23b1d64a-cadf-4f28-b7cf-95fc193be09a6002023-01-19T12:47:10Z2023-01-19T12:47:10Z2022-06http://hdl.handle.net/1992/63985instname:Universidad de los Andesreponame:Repositorio Institucional Sénecarepourl:https://repositorio.uniandes.edu.co/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. 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