Cargando…

Preparation, Optimization and Activity Evaluation of PLGA/Streptokinase Nanoparticles Using Electrospray

Purpose: PLGA nanoparticles (NPs) have been extensively investigated as carriers of different drug molecules to enhance their therapeutic effects or preserve them from the aqueous environment. Streptokinase (SK) is an important medicine for thrombotic diseases. Methods: In this study, we used electr...

Descripción completa

Detalles Bibliográficos
Autores principales: Yaghoobi, Nasrin, Faridi Majidi, Reza, Faramarzi, Mohammad ali, Baharifar, Hadi, Amani, Amir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5426726/
https://www.ncbi.nlm.nih.gov/pubmed/28507947
http://dx.doi.org/10.15171/apb.2017.017
_version_ 1783235538516443136
author Yaghoobi, Nasrin
Faridi Majidi, Reza
Faramarzi, Mohammad ali
Baharifar, Hadi
Amani, Amir
author_facet Yaghoobi, Nasrin
Faridi Majidi, Reza
Faramarzi, Mohammad ali
Baharifar, Hadi
Amani, Amir
author_sort Yaghoobi, Nasrin
collection PubMed
description Purpose: PLGA nanoparticles (NPs) have been extensively investigated as carriers of different drug molecules to enhance their therapeutic effects or preserve them from the aqueous environment. Streptokinase (SK) is an important medicine for thrombotic diseases. Methods: In this study, we used electrospray to encapsulate SK in PLGA NPs and evaluate its activity. This is the first paper which investigates activity of an electrosprayed enzyme. Effect of three input parameters, namely, voltage, internal diameter of needle (nozzle) and concentration ratio of polymer to protein on size and size distribution (SD) of NPs was evaluated using artificial neural networks (ANNs). Optimizing the SD has been rarely reported so far in electrospray. Results: From the results, to obtain lowest size of nanoparticles, ratio of polymer/enzyme and needle internal diameter (ID) should be low. Also, minimum SD was obtainable at high values of voltage. The optimum preparation had mean (SD) size, encapsulation efficiency and loading capacity of 37 (12) nm, 90% and 8.2%, respectively. Nearly, 20% of SK was released in the first 30 minutes, followed by cumulative release of 41% during 72 h. Activity of the enzyme was also checked 30 min after preparation and 19.2% activity was shown. Conclusion: Our study showed that electrospraying could be an interesting approach to encapsulate proteins/enzymes in polymeric nanoparticles. However, further works are required to assure maintaining the activity of the enzyme/protein after electrospray.
format Online
Article
Text
id pubmed-5426726
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Tabriz University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-54267262017-05-15 Preparation, Optimization and Activity Evaluation of PLGA/Streptokinase Nanoparticles Using Electrospray Yaghoobi, Nasrin Faridi Majidi, Reza Faramarzi, Mohammad ali Baharifar, Hadi Amani, Amir Adv Pharm Bull Research Article Purpose: PLGA nanoparticles (NPs) have been extensively investigated as carriers of different drug molecules to enhance their therapeutic effects or preserve them from the aqueous environment. Streptokinase (SK) is an important medicine for thrombotic diseases. Methods: In this study, we used electrospray to encapsulate SK in PLGA NPs and evaluate its activity. This is the first paper which investigates activity of an electrosprayed enzyme. Effect of three input parameters, namely, voltage, internal diameter of needle (nozzle) and concentration ratio of polymer to protein on size and size distribution (SD) of NPs was evaluated using artificial neural networks (ANNs). Optimizing the SD has been rarely reported so far in electrospray. Results: From the results, to obtain lowest size of nanoparticles, ratio of polymer/enzyme and needle internal diameter (ID) should be low. Also, minimum SD was obtainable at high values of voltage. The optimum preparation had mean (SD) size, encapsulation efficiency and loading capacity of 37 (12) nm, 90% and 8.2%, respectively. Nearly, 20% of SK was released in the first 30 minutes, followed by cumulative release of 41% during 72 h. Activity of the enzyme was also checked 30 min after preparation and 19.2% activity was shown. Conclusion: Our study showed that electrospraying could be an interesting approach to encapsulate proteins/enzymes in polymeric nanoparticles. However, further works are required to assure maintaining the activity of the enzyme/protein after electrospray. Tabriz University of Medical Sciences 2017-04 2017-04-13 /pmc/articles/PMC5426726/ /pubmed/28507947 http://dx.doi.org/10.15171/apb.2017.017 Text en ©2017 The Authors. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, as long as the original authors and source are cited. No permission is required from the authors or the publishers.
spellingShingle Research Article
Yaghoobi, Nasrin
Faridi Majidi, Reza
Faramarzi, Mohammad ali
Baharifar, Hadi
Amani, Amir
Preparation, Optimization and Activity Evaluation of PLGA/Streptokinase Nanoparticles Using Electrospray
title Preparation, Optimization and Activity Evaluation of PLGA/Streptokinase Nanoparticles Using Electrospray
title_full Preparation, Optimization and Activity Evaluation of PLGA/Streptokinase Nanoparticles Using Electrospray
title_fullStr Preparation, Optimization and Activity Evaluation of PLGA/Streptokinase Nanoparticles Using Electrospray
title_full_unstemmed Preparation, Optimization and Activity Evaluation of PLGA/Streptokinase Nanoparticles Using Electrospray
title_short Preparation, Optimization and Activity Evaluation of PLGA/Streptokinase Nanoparticles Using Electrospray
title_sort preparation, optimization and activity evaluation of plga/streptokinase nanoparticles using electrospray
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5426726/
https://www.ncbi.nlm.nih.gov/pubmed/28507947
http://dx.doi.org/10.15171/apb.2017.017
work_keys_str_mv AT yaghoobinasrin preparationoptimizationandactivityevaluationofplgastreptokinasenanoparticlesusingelectrospray
AT faridimajidireza preparationoptimizationandactivityevaluationofplgastreptokinasenanoparticlesusingelectrospray
AT faramarzimohammadali preparationoptimizationandactivityevaluationofplgastreptokinasenanoparticlesusingelectrospray
AT baharifarhadi preparationoptimizationandactivityevaluationofplgastreptokinasenanoparticlesusingelectrospray
AT amaniamir preparationoptimizationandactivityevaluationofplgastreptokinasenanoparticlesusingelectrospray