Investigating the Potential of Extracellular Vesicles as Delivery Systems for Chemotherapeutics

Background/Objectives: Standard chemotherapy is generally considered the best approach to treat many solid cancers, even accounting for severe side effects. Therefore, the development of a drug delivery system for chemotherapeutic administration could significantly improve standard chemotherapy by m...

ver descrição completa

Detalhes bibliográficos
Main Authors: Alessia Brancolini, Riccardo Vago
Formato: Artigo
Idioma:English
Publicado em: MDPI AG 2024-12-01
Colecção:Biomedicines
Assuntos:
Acesso em linha:https://www.mdpi.com/2227-9059/12/12/2863
_version_ 1826918006394978304
author Alessia Brancolini
Riccardo Vago
author_facet Alessia Brancolini
Riccardo Vago
author_sort Alessia Brancolini
collection DOAJ
description Background/Objectives: Standard chemotherapy is generally considered the best approach to treat many solid cancers, even accounting for severe side effects. Therefore, the development of a drug delivery system for chemotherapeutic administration could significantly improve standard chemotherapy by maintaining the cytotoxic effects of the drugs while decreasing the inherent side effects of the treatment. The aim of our study is the optimization of a loading strategy that conjugates the use of extracellular vesicles (EVs) as drug delivery carriers, by preserving their integrity, with the loading efficiency and activity maintenance of chemotherapeutics. Methods: We compared the EV loading of the chemotherapeutics epirubicin, mitomycin, methotrexate and mitoxantrone by co-incubation. Once loaded, the activity of drug-carrying EVs was tested on cancer cells and compared to that of free chemotherapeutics. Results: We defined a linear correlation between chemotherapeutics’ concentration and their absorbance at the drug-specific wavelength, which allowed the definition of a highly sensitive absorbance-based spectrophotometric quantification system, enabling the assessment of drug loading efficiency. Co-incubation of EVs and chemotherapeutics was sufficient to obtain quantifiable drug loading, and the efficacy of EV loading was drug-dependent. Epirubicin-loaded vesicles showed increased toxicity to bladder cancer cells with respect to the free chemotherapeutic. The cytotoxicity was maintained even upon 6-month storage at −80 °C of loaded EVs. Conclusion: We established an absorbance-based spectrophotometric quantification system that enables a straightforward measure of drug loading efficiency into EVs, and we demonstrated that chemotherapeutic-carrying EVs can be obtained by co-incubation, preserving and increasing drug cytotoxicity.
first_indexed 2025-02-17T12:42:02Z
format Article
id doaj.art-e7d3d7e1001643c6943b7cdd3dc6f8f6
institution Directory Open Access Journal
issn 2227-9059
language English
last_indexed 2025-02-17T12:42:02Z
publishDate 2024-12-01
publisher MDPI AG
record_format Article
series Biomedicines
spelling doaj.art-e7d3d7e1001643c6943b7cdd3dc6f8f62024-12-27T14:13:05ZengMDPI AGBiomedicines2227-90592024-12-011212286310.3390/biomedicines12122863Investigating the Potential of Extracellular Vesicles as Delivery Systems for ChemotherapeuticsAlessia Brancolini0Riccardo Vago1Faculty of Medicine and Surgery, Università Vita-Salute San Raffaele, 20132 Milano, ItalyFaculty of Medicine and Surgery, Università Vita-Salute San Raffaele, 20132 Milano, ItalyBackground/Objectives: Standard chemotherapy is generally considered the best approach to treat many solid cancers, even accounting for severe side effects. Therefore, the development of a drug delivery system for chemotherapeutic administration could significantly improve standard chemotherapy by maintaining the cytotoxic effects of the drugs while decreasing the inherent side effects of the treatment. The aim of our study is the optimization of a loading strategy that conjugates the use of extracellular vesicles (EVs) as drug delivery carriers, by preserving their integrity, with the loading efficiency and activity maintenance of chemotherapeutics. Methods: We compared the EV loading of the chemotherapeutics epirubicin, mitomycin, methotrexate and mitoxantrone by co-incubation. Once loaded, the activity of drug-carrying EVs was tested on cancer cells and compared to that of free chemotherapeutics. Results: We defined a linear correlation between chemotherapeutics’ concentration and their absorbance at the drug-specific wavelength, which allowed the definition of a highly sensitive absorbance-based spectrophotometric quantification system, enabling the assessment of drug loading efficiency. Co-incubation of EVs and chemotherapeutics was sufficient to obtain quantifiable drug loading, and the efficacy of EV loading was drug-dependent. Epirubicin-loaded vesicles showed increased toxicity to bladder cancer cells with respect to the free chemotherapeutic. The cytotoxicity was maintained even upon 6-month storage at −80 °C of loaded EVs. Conclusion: We established an absorbance-based spectrophotometric quantification system that enables a straightforward measure of drug loading efficiency into EVs, and we demonstrated that chemotherapeutic-carrying EVs can be obtained by co-incubation, preserving and increasing drug cytotoxicity.https://www.mdpi.com/2227-9059/12/12/2863extracellular vesicledrug deliveryepirubicinbladder cancerchemotherapeutic agents
spellingShingle Alessia Brancolini
Riccardo Vago
Investigating the Potential of Extracellular Vesicles as Delivery Systems for Chemotherapeutics
Biomedicines
extracellular vesicle
drug delivery
epirubicin
bladder cancer
chemotherapeutic agents
title Investigating the Potential of Extracellular Vesicles as Delivery Systems for Chemotherapeutics
title_full Investigating the Potential of Extracellular Vesicles as Delivery Systems for Chemotherapeutics
title_fullStr Investigating the Potential of Extracellular Vesicles as Delivery Systems for Chemotherapeutics
title_full_unstemmed Investigating the Potential of Extracellular Vesicles as Delivery Systems for Chemotherapeutics
title_short Investigating the Potential of Extracellular Vesicles as Delivery Systems for Chemotherapeutics
title_sort investigating the potential of extracellular vesicles as delivery systems for chemotherapeutics
topic extracellular vesicle
drug delivery
epirubicin
bladder cancer
chemotherapeutic agents
url https://www.mdpi.com/2227-9059/12/12/2863
work_keys_str_mv AT alessiabrancolini investigatingthepotentialofextracellularvesiclesasdeliverysystemsforchemotherapeutics
AT riccardovago investigatingthepotentialofextracellularvesiclesasdeliverysystemsforchemotherapeutics