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Exosome-Coated tPA/Catalase Nanoformulation for Thrombolytic Therapy

Current tissue plasminogen-based therapeutic strategies for stroke suffer from systemic side effects and poor efficacy. Hence, novel drug delivery methods are needed to overcome these shortcomings. Exosome-based drug formulations have been shown to have superior therapeutic outcomes compared to conv...

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Detalles Bibliográficos
Autores principales: Khalil, Sara, Kanapathipillai, Mathumai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9952084/
https://www.ncbi.nlm.nih.gov/pubmed/36829671
http://dx.doi.org/10.3390/bioengineering10020177
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author Khalil, Sara
Kanapathipillai, Mathumai
author_facet Khalil, Sara
Kanapathipillai, Mathumai
author_sort Khalil, Sara
collection PubMed
description Current tissue plasminogen-based therapeutic strategies for stroke suffer from systemic side effects and poor efficacy. Hence, novel drug delivery methods are needed to overcome these shortcomings. Exosome-based drug formulations have been shown to have superior therapeutic outcomes compared to conventional systemic drug delivery approaches. In this paper, we report exosome surface-coated tissue plasminogen activator (tPA)/catalase nanoformulations with improved thrombolytic efficacy compared to free tPA, which also reduce side effects. The results showed that the tPA exosome formulations retained tPA activity, improved tPA stability, exhibited significant fibrinolysis, and showed no significant toxicity effects. Further, when combined with antioxidant enzyme catalase, the formulation was able to inhibit hydrogen peroxide-mediated oxidative stress and toxicity. Hence, exosome-based tPA/catalase nanoformulations could have the potential to offer a safer and effective thrombolytic therapy.
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spelling pubmed-99520842023-02-25 Exosome-Coated tPA/Catalase Nanoformulation for Thrombolytic Therapy Khalil, Sara Kanapathipillai, Mathumai Bioengineering (Basel) Article Current tissue plasminogen-based therapeutic strategies for stroke suffer from systemic side effects and poor efficacy. Hence, novel drug delivery methods are needed to overcome these shortcomings. Exosome-based drug formulations have been shown to have superior therapeutic outcomes compared to conventional systemic drug delivery approaches. In this paper, we report exosome surface-coated tissue plasminogen activator (tPA)/catalase nanoformulations with improved thrombolytic efficacy compared to free tPA, which also reduce side effects. The results showed that the tPA exosome formulations retained tPA activity, improved tPA stability, exhibited significant fibrinolysis, and showed no significant toxicity effects. Further, when combined with antioxidant enzyme catalase, the formulation was able to inhibit hydrogen peroxide-mediated oxidative stress and toxicity. Hence, exosome-based tPA/catalase nanoformulations could have the potential to offer a safer and effective thrombolytic therapy. MDPI 2023-01-31 /pmc/articles/PMC9952084/ /pubmed/36829671 http://dx.doi.org/10.3390/bioengineering10020177 Text en © 2023 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
Khalil, Sara
Kanapathipillai, Mathumai
Exosome-Coated tPA/Catalase Nanoformulation for Thrombolytic Therapy
title Exosome-Coated tPA/Catalase Nanoformulation for Thrombolytic Therapy
title_full Exosome-Coated tPA/Catalase Nanoformulation for Thrombolytic Therapy
title_fullStr Exosome-Coated tPA/Catalase Nanoformulation for Thrombolytic Therapy
title_full_unstemmed Exosome-Coated tPA/Catalase Nanoformulation for Thrombolytic Therapy
title_short Exosome-Coated tPA/Catalase Nanoformulation for Thrombolytic Therapy
title_sort exosome-coated tpa/catalase nanoformulation for thrombolytic therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9952084/
https://www.ncbi.nlm.nih.gov/pubmed/36829671
http://dx.doi.org/10.3390/bioengineering10020177
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