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Dual-functionalized nanoliposomes achieve a synergistic chemo-phototherapeutic effect

Author
Lázaro Carrillo, Anauntranslated; Rodríguez-Amigo, Beatriz; Mora, Margarita; Sagristá, Maria Lluïsa; Cañete Gugel, Magdalenauntranslated; Nonell, Santi; Villanueva Oroquieta, Ángelesuntranslated
Entity
UAM. Departamento de Biología
Publisher
MDPI
Date
2022-11-01
Citation
10.3390/ijms232112817
International Journal of Molecular Sciences 23.21 (2022): 12817
 
 
 
ISSN
1661-6596 (print); 1422-0067 (online)
DOI
10.3390/ijms232112817
Project
Gobierno de España. CTQ2016-78454-C2-1-R; Gobierno de España. CTQ2016-78454-C2-2-R; Gobierno de España. PID2020-115801RB-C22; Gobierno de España. SEV-2016-0686
Editor's Version
https://doi.org/10.3390/ijms232112817
Subjects
Cancer; Photoacoustics; Theranostic Nanomedicine; Biología y Biomedicina / Biología
URI
http://hdl.handle.net/10486/706577
Rights
: © 2022 by the authors

Licencia Creative Commons
Esta obra está bajo una Licencia Creative Commons Atribución 4.0 Internacional.

Abstract

The enhancement of photodynamic therapy (PDT) effectiveness by combining it with other treatment modalities and improved drug delivery has become an interesting field in cancer research. We have prepared and characterized nanoliposomes containing the chemotherapeutic drug irinotecan (CPT11lip), the photodynamic agent protoporphyrin IX (PpIXlip), or their combination (CPT11-PpIXlip). The effects of individual and bimodal (chemo-phototherapeutic) treatments on HeLa cells have been studied by a combination of biological and photophysical studies. Bimodal treatments show synergistic cytotoxic effects on HeLa cells at relatively low doses of PpIX/PDT and CPT11. Mechanistic cell inactivation studies revealed mitotic catastrophe, apoptosis, and senescence contributions. The enhanced anticancer activity is due to a sustained generation of reactive oxygen species, which increases the number of double-strand DNA breaks. Bimodal chemo-phototherapeutic liposomes may have a very promising future in oncological therapy, potentially allowing a reduction in the CPT11 concentration required to achieve a therapeutic effect and overcoming resistance to individual cancer treatments
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Google™ Scholar:Lázaro Carrillo, Ana - Rodríguez-Amigo, Beatriz - Mora, Margarita - Sagristá, Maria Lluïsa - Cañete Gugel, Magdalena - Nonell, Santi - Villanueva Oroquieta, Ángeles

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  • Producción científica en acceso abierto de la UAM [16828]

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