Photosensitive EGFR-Targeted Nanocarriers for Combined Photodynamic and Local Chemotherapy

The major limitation of any cancer therapy lies in the difficulty of precisely controlling the localization of the drug in the tumor cells. To improve this drawback, our study explores the use of actively-targeted chemo-photo-nanocarriers that recognize and bind to epidermal growth factor receptor-o...

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Main Authors: Elena de las Heras (Author), M. Lluïsa Sagristá (Author), Montserrat Agut (Author), Santi Nonell (Author)
Format: Book
Published: MDPI AG, 2022-02-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Elena de las Heras  |e author 
700 1 0 |a M. Lluïsa Sagristá  |e author 
700 1 0 |a Montserrat Agut  |e author 
700 1 0 |a Santi Nonell  |e author 
245 0 0 |a Photosensitive EGFR-Targeted Nanocarriers for Combined Photodynamic and Local Chemotherapy 
260 |b MDPI AG,   |c 2022-02-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics14020405 
500 |a 1999-4923 
520 |a The major limitation of any cancer therapy lies in the difficulty of precisely controlling the localization of the drug in the tumor cells. To improve this drawback, our study explores the use of actively-targeted chemo-photo-nanocarriers that recognize and bind to epidermal growth factor receptor-overexpressing cells and promote the local on-demand release of the chemotherapeutic agent doxorubicin triggered by light. Our results show that the attachment of high concentrations of doxorubicin to cetuximab-IRDye700DX-mesoporous silica nanoparticles yields efficient and selective photokilling of EGFR-expressing cells mainly through singlet oxygen-induced release of the doxorubicin from the nanocarrier and without any dark toxicity. Therefore, this novel triply functionalized nanosystem is an effective and safe nanodevice for light-triggered on-demand doxorubicin release. 
546 |a EN 
690 |a mesoporous silica nanoparticles 
690 |a photodynamic therapy 
690 |a chemotherapy 
690 |a cetuximab 
690 |a EGFR 
690 |a singlet oxygen 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 14, Iss 2, p 405 (2022) 
787 0 |n https://www.mdpi.com/1999-4923/14/2/405 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/dcad8b14c32e4caeac133ea6aafe20c6  |z Connect to this object online.