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Development of a Parenteral Formulation of NTS-Polyplex Nanoparticles for Clinical Purpose

Neurotensin (NTS)-polyplex is a nanoparticle system for targeted gene delivery that holds great promise for treatment of Parkinson’s disease and various types of cancer. However, the high instability in aqueous suspension of NTS-polyplex nanoparticles is a major limitation for their widespread clini...

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Autores principales: Aranda-Barradas, María E., Márquez, Maripaz, Quintanar, Liliana, Santoyo-Salazar, Jaime, Espadas-Álvarez, Armando J., Martínez-Fong, Daniel, García-García, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5874818/
https://www.ncbi.nlm.nih.gov/pubmed/29301386
http://dx.doi.org/10.3390/pharmaceutics10010005
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author Aranda-Barradas, María E.
Márquez, Maripaz
Quintanar, Liliana
Santoyo-Salazar, Jaime
Espadas-Álvarez, Armando J.
Martínez-Fong, Daniel
García-García, Elizabeth
author_facet Aranda-Barradas, María E.
Márquez, Maripaz
Quintanar, Liliana
Santoyo-Salazar, Jaime
Espadas-Álvarez, Armando J.
Martínez-Fong, Daniel
García-García, Elizabeth
author_sort Aranda-Barradas, María E.
collection PubMed
description Neurotensin (NTS)-polyplex is a nanoparticle system for targeted gene delivery that holds great promise for treatment of Parkinson’s disease and various types of cancer. However, the high instability in aqueous suspension of NTS-polyplex nanoparticles is a major limitation for their widespread clinical use. To overcome this obstacle, we developed a clinical formulation and a lyophilization process for NTS-polyplex nanoparticles. The reconstituted samples were compared with fresh preparations by using transmission electron microscopy, dynamic light scattering, electrophoretic mobility, circular dichroism and transfection assays in vitro and in vivo. Our formulation was able to confer lyoprotection and stability to these nanoparticles. In addition, transmission electron microscopy (TEM) and size exclusion-high performance liquid chromatography (SEC-HPLC) using a radioactive tag revealed that the interaction of reconstituted nanoparticles with fetal bovine or human serum did not alter their biophysical features. Furthermore, the formulation and the lyophilization procedure guaranteed functional NTS-polyplex nanoparticles for at least six months of storage at 25 °C and 60% relative humidity. Our results offer a pharmaceutical guide for formulation and long-term storage of NTS-polyplex nanoparticles that could be applied to other polyplexes.
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spelling pubmed-58748182018-04-02 Development of a Parenteral Formulation of NTS-Polyplex Nanoparticles for Clinical Purpose Aranda-Barradas, María E. Márquez, Maripaz Quintanar, Liliana Santoyo-Salazar, Jaime Espadas-Álvarez, Armando J. Martínez-Fong, Daniel García-García, Elizabeth Pharmaceutics Article Neurotensin (NTS)-polyplex is a nanoparticle system for targeted gene delivery that holds great promise for treatment of Parkinson’s disease and various types of cancer. However, the high instability in aqueous suspension of NTS-polyplex nanoparticles is a major limitation for their widespread clinical use. To overcome this obstacle, we developed a clinical formulation and a lyophilization process for NTS-polyplex nanoparticles. The reconstituted samples were compared with fresh preparations by using transmission electron microscopy, dynamic light scattering, electrophoretic mobility, circular dichroism and transfection assays in vitro and in vivo. Our formulation was able to confer lyoprotection and stability to these nanoparticles. In addition, transmission electron microscopy (TEM) and size exclusion-high performance liquid chromatography (SEC-HPLC) using a radioactive tag revealed that the interaction of reconstituted nanoparticles with fetal bovine or human serum did not alter their biophysical features. Furthermore, the formulation and the lyophilization procedure guaranteed functional NTS-polyplex nanoparticles for at least six months of storage at 25 °C and 60% relative humidity. Our results offer a pharmaceutical guide for formulation and long-term storage of NTS-polyplex nanoparticles that could be applied to other polyplexes. MDPI 2018-01-03 /pmc/articles/PMC5874818/ /pubmed/29301386 http://dx.doi.org/10.3390/pharmaceutics10010005 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Aranda-Barradas, María E.
Márquez, Maripaz
Quintanar, Liliana
Santoyo-Salazar, Jaime
Espadas-Álvarez, Armando J.
Martínez-Fong, Daniel
García-García, Elizabeth
Development of a Parenteral Formulation of NTS-Polyplex Nanoparticles for Clinical Purpose
title Development of a Parenteral Formulation of NTS-Polyplex Nanoparticles for Clinical Purpose
title_full Development of a Parenteral Formulation of NTS-Polyplex Nanoparticles for Clinical Purpose
title_fullStr Development of a Parenteral Formulation of NTS-Polyplex Nanoparticles for Clinical Purpose
title_full_unstemmed Development of a Parenteral Formulation of NTS-Polyplex Nanoparticles for Clinical Purpose
title_short Development of a Parenteral Formulation of NTS-Polyplex Nanoparticles for Clinical Purpose
title_sort development of a parenteral formulation of nts-polyplex nanoparticles for clinical purpose
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5874818/
https://www.ncbi.nlm.nih.gov/pubmed/29301386
http://dx.doi.org/10.3390/pharmaceutics10010005
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