Cargando…
Nanoparticle-Mediated Angiotensin-(1-9) Drug Delivery for the Treatment of Cardiac Hypertrophy
Ang-(1-9) peptide is a bioactive vasodilator peptide that prevents cardiomyocyte hypertrophy in vitro and in vivo as well as lowers blood pressure and pathological cardiovascular remodeling; however, it has a reduced half-life in circulation, requiring a suitable carrier for its delivery. In this wo...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8228229/ https://www.ncbi.nlm.nih.gov/pubmed/34206106 http://dx.doi.org/10.3390/pharmaceutics13060822 |
_version_ | 1783712694274097152 |
---|---|
author | Sepúlveda-Rivas, Sabrina Leal, Matías S. Pedrozo, Zully Kogan, Marcelo J. Ocaranza, María Paz Morales, Javier O. |
author_facet | Sepúlveda-Rivas, Sabrina Leal, Matías S. Pedrozo, Zully Kogan, Marcelo J. Ocaranza, María Paz Morales, Javier O. |
author_sort | Sepúlveda-Rivas, Sabrina |
collection | PubMed |
description | Ang-(1-9) peptide is a bioactive vasodilator peptide that prevents cardiomyocyte hypertrophy in vitro and in vivo as well as lowers blood pressure and pathological cardiovascular remodeling; however, it has a reduced half-life in circulation, requiring a suitable carrier for its delivery. In this work, hybrid nanoparticles composed of polymeric nanoparticles (pNPs) based on Eudragit(®) E/Alginate (EE/Alg), and gold nanospheres (AuNS), were developed to evaluate their encapsulation capacity and release of Ang-(1-9) under different experimental conditions. Hybrid pNPs were characterized by dynamic light scattering, zeta potential, transmission and scanning electron microscopy, size distribution, and concentration by nanoparticle tracking analysis. Nanometric pNPs, with good polydispersity index and colloidally stable, produced high association efficiency of Ang-(1-9) and controlled release. Finally, the treatment of neonatal cardiomyocytes in culture with EE/Alg/AuNS 2% + Ang-(1-9) 20% pNPs decreased the area and perimeter, demonstrating efficacy in preventing norepinephrine-induced cardiomyocyte hypertrophy. On the other hand, the incorporation of AuNS did not cause negative effects either on the cytotoxicity or on the association capacity of Ang-(1-9), suggesting that the hybrid carrier EE/Alg/AuNS pNPs could be used for the delivery of Ang-(1-9) in the treatment of cardiovascular hypertrophy. |
format | Online Article Text |
id | pubmed-8228229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82282292021-06-26 Nanoparticle-Mediated Angiotensin-(1-9) Drug Delivery for the Treatment of Cardiac Hypertrophy Sepúlveda-Rivas, Sabrina Leal, Matías S. Pedrozo, Zully Kogan, Marcelo J. Ocaranza, María Paz Morales, Javier O. Pharmaceutics Article Ang-(1-9) peptide is a bioactive vasodilator peptide that prevents cardiomyocyte hypertrophy in vitro and in vivo as well as lowers blood pressure and pathological cardiovascular remodeling; however, it has a reduced half-life in circulation, requiring a suitable carrier for its delivery. In this work, hybrid nanoparticles composed of polymeric nanoparticles (pNPs) based on Eudragit(®) E/Alginate (EE/Alg), and gold nanospheres (AuNS), were developed to evaluate their encapsulation capacity and release of Ang-(1-9) under different experimental conditions. Hybrid pNPs were characterized by dynamic light scattering, zeta potential, transmission and scanning electron microscopy, size distribution, and concentration by nanoparticle tracking analysis. Nanometric pNPs, with good polydispersity index and colloidally stable, produced high association efficiency of Ang-(1-9) and controlled release. Finally, the treatment of neonatal cardiomyocytes in culture with EE/Alg/AuNS 2% + Ang-(1-9) 20% pNPs decreased the area and perimeter, demonstrating efficacy in preventing norepinephrine-induced cardiomyocyte hypertrophy. On the other hand, the incorporation of AuNS did not cause negative effects either on the cytotoxicity or on the association capacity of Ang-(1-9), suggesting that the hybrid carrier EE/Alg/AuNS pNPs could be used for the delivery of Ang-(1-9) in the treatment of cardiovascular hypertrophy. MDPI 2021-06-01 /pmc/articles/PMC8228229/ /pubmed/34206106 http://dx.doi.org/10.3390/pharmaceutics13060822 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sepúlveda-Rivas, Sabrina Leal, Matías S. Pedrozo, Zully Kogan, Marcelo J. Ocaranza, María Paz Morales, Javier O. Nanoparticle-Mediated Angiotensin-(1-9) Drug Delivery for the Treatment of Cardiac Hypertrophy |
title | Nanoparticle-Mediated Angiotensin-(1-9) Drug Delivery for the Treatment of Cardiac Hypertrophy |
title_full | Nanoparticle-Mediated Angiotensin-(1-9) Drug Delivery for the Treatment of Cardiac Hypertrophy |
title_fullStr | Nanoparticle-Mediated Angiotensin-(1-9) Drug Delivery for the Treatment of Cardiac Hypertrophy |
title_full_unstemmed | Nanoparticle-Mediated Angiotensin-(1-9) Drug Delivery for the Treatment of Cardiac Hypertrophy |
title_short | Nanoparticle-Mediated Angiotensin-(1-9) Drug Delivery for the Treatment of Cardiac Hypertrophy |
title_sort | nanoparticle-mediated angiotensin-(1-9) drug delivery for the treatment of cardiac hypertrophy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8228229/ https://www.ncbi.nlm.nih.gov/pubmed/34206106 http://dx.doi.org/10.3390/pharmaceutics13060822 |
work_keys_str_mv | AT sepulvedarivassabrina nanoparticlemediatedangiotensin19drugdeliveryforthetreatmentofcardiachypertrophy AT lealmatiass nanoparticlemediatedangiotensin19drugdeliveryforthetreatmentofcardiachypertrophy AT pedrozozully nanoparticlemediatedangiotensin19drugdeliveryforthetreatmentofcardiachypertrophy AT koganmarceloj nanoparticlemediatedangiotensin19drugdeliveryforthetreatmentofcardiachypertrophy AT ocaranzamariapaz nanoparticlemediatedangiotensin19drugdeliveryforthetreatmentofcardiachypertrophy AT moralesjaviero nanoparticlemediatedangiotensin19drugdeliveryforthetreatmentofcardiachypertrophy |