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Pilot Production of Mesenchymal Stem/Stromal Freeze-Dried Secretome for Cell-Free Regenerative Nanomedicine: A Validated GMP-Compliant Process
In this paper, a pilot production process for mesenchymal stem/stromal freeze-dried secretome was performed in a validated good manufacturing practice (GMP)-compliant cell factory. Secretome was purified from culture supernatants by ultrafiltration, added to cryoprotectant, lyophilized and character...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262564/ https://www.ncbi.nlm.nih.gov/pubmed/30380806 http://dx.doi.org/10.3390/cells7110190 |
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author | Bari, Elia Perteghella, Sara Di Silvestre, Dario Sorlini, Marzio Catenacci, Laura Sorrenti, Milena Marrubini, Giorgio Rossi, Rossana Tripodo, Giuseppe Mauri, Pierluigi Marazzi, Mario Torre, Maria Luisa |
author_facet | Bari, Elia Perteghella, Sara Di Silvestre, Dario Sorlini, Marzio Catenacci, Laura Sorrenti, Milena Marrubini, Giorgio Rossi, Rossana Tripodo, Giuseppe Mauri, Pierluigi Marazzi, Mario Torre, Maria Luisa |
author_sort | Bari, Elia |
collection | PubMed |
description | In this paper, a pilot production process for mesenchymal stem/stromal freeze-dried secretome was performed in a validated good manufacturing practice (GMP)-compliant cell factory. Secretome was purified from culture supernatants by ultrafiltration, added to cryoprotectant, lyophilized and characterized. We obtained a freeze-dried, “ready-off-the-shelf” and free soluble powder containing extracellular vesicles and proteins. In the freeze-dried product, a not-aggregated population of extracellular vesicles was detected by nanoparticle tracking analysis; Fourier transform infrared spectra showed the simultaneous presence of protein and lipids, while differential scanning calorimetry demonstrated that lyophilization process successfully occurred. A proteomic characterization allowed the identification of proteins involved in immune response, response to stress, cytoskeleton and metabolism. Moreover, the product was not cytotoxic up to concentrations of 25 mg/mL (on human fibroblasts, chondrocytes and nucleus pulposus cells by MTT assay) and was blood compatible up to 150 mg/mL. Finally, at concentrations between 5 and 50 mg/mL, freeze-dried secretome showed to in vitro counteract the oxidative stress damage induced by H(2)O(2) on nucleus pulposus cells by MTT assay. |
format | Online Article Text |
id | pubmed-6262564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62625642018-12-03 Pilot Production of Mesenchymal Stem/Stromal Freeze-Dried Secretome for Cell-Free Regenerative Nanomedicine: A Validated GMP-Compliant Process Bari, Elia Perteghella, Sara Di Silvestre, Dario Sorlini, Marzio Catenacci, Laura Sorrenti, Milena Marrubini, Giorgio Rossi, Rossana Tripodo, Giuseppe Mauri, Pierluigi Marazzi, Mario Torre, Maria Luisa Cells Article In this paper, a pilot production process for mesenchymal stem/stromal freeze-dried secretome was performed in a validated good manufacturing practice (GMP)-compliant cell factory. Secretome was purified from culture supernatants by ultrafiltration, added to cryoprotectant, lyophilized and characterized. We obtained a freeze-dried, “ready-off-the-shelf” and free soluble powder containing extracellular vesicles and proteins. In the freeze-dried product, a not-aggregated population of extracellular vesicles was detected by nanoparticle tracking analysis; Fourier transform infrared spectra showed the simultaneous presence of protein and lipids, while differential scanning calorimetry demonstrated that lyophilization process successfully occurred. A proteomic characterization allowed the identification of proteins involved in immune response, response to stress, cytoskeleton and metabolism. Moreover, the product was not cytotoxic up to concentrations of 25 mg/mL (on human fibroblasts, chondrocytes and nucleus pulposus cells by MTT assay) and was blood compatible up to 150 mg/mL. Finally, at concentrations between 5 and 50 mg/mL, freeze-dried secretome showed to in vitro counteract the oxidative stress damage induced by H(2)O(2) on nucleus pulposus cells by MTT assay. MDPI 2018-10-30 /pmc/articles/PMC6262564/ /pubmed/30380806 http://dx.doi.org/10.3390/cells7110190 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 Bari, Elia Perteghella, Sara Di Silvestre, Dario Sorlini, Marzio Catenacci, Laura Sorrenti, Milena Marrubini, Giorgio Rossi, Rossana Tripodo, Giuseppe Mauri, Pierluigi Marazzi, Mario Torre, Maria Luisa Pilot Production of Mesenchymal Stem/Stromal Freeze-Dried Secretome for Cell-Free Regenerative Nanomedicine: A Validated GMP-Compliant Process |
title | Pilot Production of Mesenchymal Stem/Stromal Freeze-Dried Secretome for Cell-Free Regenerative Nanomedicine: A Validated GMP-Compliant Process |
title_full | Pilot Production of Mesenchymal Stem/Stromal Freeze-Dried Secretome for Cell-Free Regenerative Nanomedicine: A Validated GMP-Compliant Process |
title_fullStr | Pilot Production of Mesenchymal Stem/Stromal Freeze-Dried Secretome for Cell-Free Regenerative Nanomedicine: A Validated GMP-Compliant Process |
title_full_unstemmed | Pilot Production of Mesenchymal Stem/Stromal Freeze-Dried Secretome for Cell-Free Regenerative Nanomedicine: A Validated GMP-Compliant Process |
title_short | Pilot Production of Mesenchymal Stem/Stromal Freeze-Dried Secretome for Cell-Free Regenerative Nanomedicine: A Validated GMP-Compliant Process |
title_sort | pilot production of mesenchymal stem/stromal freeze-dried secretome for cell-free regenerative nanomedicine: a validated gmp-compliant process |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262564/ https://www.ncbi.nlm.nih.gov/pubmed/30380806 http://dx.doi.org/10.3390/cells7110190 |
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