Cargando…
Release profile and stability evaluation of optimized chitosan/alginate nanoparticles as EGFR antisense vector
Chitosan/alginate nanoparticles which had been optimized in our previous study using two different N/P ratios were chosen and their ability to release epidermal growth factor receptor (EGFR) antisense was investigated. In addition, the stability of these nanoparticles in aqueous medium and after fre...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2950403/ https://www.ncbi.nlm.nih.gov/pubmed/20957167 |
_version_ | 1782187652869521408 |
---|---|
author | Azizi, Ebrahim Namazi, Alireza Haririan, Ismaeil Fouladdel, Shamileh Khoshayand, Mohammad R Shotorbani, Parisa Y Nomani, Alireza Gazori, Taraneh |
author_facet | Azizi, Ebrahim Namazi, Alireza Haririan, Ismaeil Fouladdel, Shamileh Khoshayand, Mohammad R Shotorbani, Parisa Y Nomani, Alireza Gazori, Taraneh |
author_sort | Azizi, Ebrahim |
collection | PubMed |
description | Chitosan/alginate nanoparticles which had been optimized in our previous study using two different N/P ratios were chosen and their ability to release epidermal growth factor receptor (EGFR) antisense was investigated. In addition, the stability of these nanoparticles in aqueous medium and after freeze-drying was investigated. In the case of both N/P ratios (5, 25), nanoparticles started releasing EGFR antisense as soon as they were exposed to the medium and the release lasted for approximately 50 hours. Nanoparticle size, shape, zeta potential, and release profile did not show any significant change after the freeze-drying process (followed by reswelling). The nanoparticles were reswellable again after freeze-drying in phosphate buffer with a pH of 7.4 over a period of six hours. Agarose gel electrophoresis of the nanoparticles with the two different N/P ratios showed that these nanoparticles could protect EGFR antisense molecules for six hours. |
format | Text |
id | pubmed-2950403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-29504032010-10-18 Release profile and stability evaluation of optimized chitosan/alginate nanoparticles as EGFR antisense vector Azizi, Ebrahim Namazi, Alireza Haririan, Ismaeil Fouladdel, Shamileh Khoshayand, Mohammad R Shotorbani, Parisa Y Nomani, Alireza Gazori, Taraneh Int J Nanomedicine Original Research Chitosan/alginate nanoparticles which had been optimized in our previous study using two different N/P ratios were chosen and their ability to release epidermal growth factor receptor (EGFR) antisense was investigated. In addition, the stability of these nanoparticles in aqueous medium and after freeze-drying was investigated. In the case of both N/P ratios (5, 25), nanoparticles started releasing EGFR antisense as soon as they were exposed to the medium and the release lasted for approximately 50 hours. Nanoparticle size, shape, zeta potential, and release profile did not show any significant change after the freeze-drying process (followed by reswelling). The nanoparticles were reswellable again after freeze-drying in phosphate buffer with a pH of 7.4 over a period of six hours. Agarose gel electrophoresis of the nanoparticles with the two different N/P ratios showed that these nanoparticles could protect EGFR antisense molecules for six hours. Dove Medical Press 2010 2010-08-09 /pmc/articles/PMC2950403/ /pubmed/20957167 Text en © 2010 Azizi et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Azizi, Ebrahim Namazi, Alireza Haririan, Ismaeil Fouladdel, Shamileh Khoshayand, Mohammad R Shotorbani, Parisa Y Nomani, Alireza Gazori, Taraneh Release profile and stability evaluation of optimized chitosan/alginate nanoparticles as EGFR antisense vector |
title | Release profile and stability evaluation of optimized chitosan/alginate nanoparticles as EGFR antisense vector |
title_full | Release profile and stability evaluation of optimized chitosan/alginate nanoparticles as EGFR antisense vector |
title_fullStr | Release profile and stability evaluation of optimized chitosan/alginate nanoparticles as EGFR antisense vector |
title_full_unstemmed | Release profile and stability evaluation of optimized chitosan/alginate nanoparticles as EGFR antisense vector |
title_short | Release profile and stability evaluation of optimized chitosan/alginate nanoparticles as EGFR antisense vector |
title_sort | release profile and stability evaluation of optimized chitosan/alginate nanoparticles as egfr antisense vector |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2950403/ https://www.ncbi.nlm.nih.gov/pubmed/20957167 |
work_keys_str_mv | AT aziziebrahim releaseprofileandstabilityevaluationofoptimizedchitosanalginatenanoparticlesasegfrantisensevector AT namazialireza releaseprofileandstabilityevaluationofoptimizedchitosanalginatenanoparticlesasegfrantisensevector AT haririanismaeil releaseprofileandstabilityevaluationofoptimizedchitosanalginatenanoparticlesasegfrantisensevector AT fouladdelshamileh releaseprofileandstabilityevaluationofoptimizedchitosanalginatenanoparticlesasegfrantisensevector AT khoshayandmohammadr releaseprofileandstabilityevaluationofoptimizedchitosanalginatenanoparticlesasegfrantisensevector AT shotorbaniparisay releaseprofileandstabilityevaluationofoptimizedchitosanalginatenanoparticlesasegfrantisensevector AT nomanialireza releaseprofileandstabilityevaluationofoptimizedchitosanalginatenanoparticlesasegfrantisensevector AT gazoritaraneh releaseprofileandstabilityevaluationofoptimizedchitosanalginatenanoparticlesasegfrantisensevector |