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A Quality by Design Approach in Pharmaceutical Development of Non-Viral Vectors with a Focus on miRNA
Cancer is the leading cause of death worldwide. Tumors consist of heterogeneous cell populations that have different biological properties. While conventional cancer therapy such as chemotherapy, radiotherapy, and surgery does not target cancer cells specifically, gene therapy is attracting increasi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322860/ https://www.ncbi.nlm.nih.gov/pubmed/35890377 http://dx.doi.org/10.3390/pharmaceutics14071482 |
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author | Toma, Ioana Porfire, Alina Silvia Tefas, Lucia Ruxandra Berindan-Neagoe, Ioana Tomuță, Ioan |
author_facet | Toma, Ioana Porfire, Alina Silvia Tefas, Lucia Ruxandra Berindan-Neagoe, Ioana Tomuță, Ioan |
author_sort | Toma, Ioana |
collection | PubMed |
description | Cancer is the leading cause of death worldwide. Tumors consist of heterogeneous cell populations that have different biological properties. While conventional cancer therapy such as chemotherapy, radiotherapy, and surgery does not target cancer cells specifically, gene therapy is attracting increasing attention as an alternative capable of overcoming these limitations. With the advent of gene therapy, there is increasing interest in developing non-viral vectors for genetic material delivery in cancer therapy. Nanosystems, both organic and inorganic, are the most common non-viral vectors used in gene therapy. The most used organic vectors are polymeric and lipid-based delivery systems. These nanostructures are designed to bind and protect the genetic material, leading to high efficiency, prolonged gene expression, and low toxicity. Quality by Design (QbD) is a step-by-step approach that investigates all the factors that may affect the quality of the final product, leading to efficient pharmaceutical development. This paper aims to provide a new perspective regarding the use of the QbD approach for improving the quality of non-viral vectors for genetic material delivery and their application in cancer therapy. |
format | Online Article Text |
id | pubmed-9322860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93228602022-07-27 A Quality by Design Approach in Pharmaceutical Development of Non-Viral Vectors with a Focus on miRNA Toma, Ioana Porfire, Alina Silvia Tefas, Lucia Ruxandra Berindan-Neagoe, Ioana Tomuță, Ioan Pharmaceutics Review Cancer is the leading cause of death worldwide. Tumors consist of heterogeneous cell populations that have different biological properties. While conventional cancer therapy such as chemotherapy, radiotherapy, and surgery does not target cancer cells specifically, gene therapy is attracting increasing attention as an alternative capable of overcoming these limitations. With the advent of gene therapy, there is increasing interest in developing non-viral vectors for genetic material delivery in cancer therapy. Nanosystems, both organic and inorganic, are the most common non-viral vectors used in gene therapy. The most used organic vectors are polymeric and lipid-based delivery systems. These nanostructures are designed to bind and protect the genetic material, leading to high efficiency, prolonged gene expression, and low toxicity. Quality by Design (QbD) is a step-by-step approach that investigates all the factors that may affect the quality of the final product, leading to efficient pharmaceutical development. This paper aims to provide a new perspective regarding the use of the QbD approach for improving the quality of non-viral vectors for genetic material delivery and their application in cancer therapy. MDPI 2022-07-16 /pmc/articles/PMC9322860/ /pubmed/35890377 http://dx.doi.org/10.3390/pharmaceutics14071482 Text en © 2022 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 | Review Toma, Ioana Porfire, Alina Silvia Tefas, Lucia Ruxandra Berindan-Neagoe, Ioana Tomuță, Ioan A Quality by Design Approach in Pharmaceutical Development of Non-Viral Vectors with a Focus on miRNA |
title | A Quality by Design Approach in Pharmaceutical Development of Non-Viral Vectors with a Focus on miRNA |
title_full | A Quality by Design Approach in Pharmaceutical Development of Non-Viral Vectors with a Focus on miRNA |
title_fullStr | A Quality by Design Approach in Pharmaceutical Development of Non-Viral Vectors with a Focus on miRNA |
title_full_unstemmed | A Quality by Design Approach in Pharmaceutical Development of Non-Viral Vectors with a Focus on miRNA |
title_short | A Quality by Design Approach in Pharmaceutical Development of Non-Viral Vectors with a Focus on miRNA |
title_sort | quality by design approach in pharmaceutical development of non-viral vectors with a focus on mirna |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322860/ https://www.ncbi.nlm.nih.gov/pubmed/35890377 http://dx.doi.org/10.3390/pharmaceutics14071482 |
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