Marcelo, GA.; Montpeyó, D.; Galhano, J.; Martínez-Máñez, R.; Capelo-Martínez, JL.; Lorenzo, J.; Lodeiro, C.... (2023). Development of New Targeted Nanotherapy Combined with Magneto-Fluorescent Nanoparticles against Colorectal Cancer. International Journal of Molecular Sciences. 24(7). https://doi.org/10.3390/ijms24076612
Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/204091
Título:
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Development of New Targeted Nanotherapy Combined with Magneto-Fluorescent Nanoparticles against Colorectal Cancer
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Autor:
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Marcelo, Goncalo A.
Montpeyó, David
Galhano, Joana
Martínez-Máñez, Ramón
Capelo-Martínez, José Luis
Lorenzo, Julia
Lodeiro, Carlos
Oliveira, Elisabete
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Entidad UPV:
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Universitat Politècnica de València. Escuela Técnica Superior de Ingenieros Industriales - Escola Tècnica Superior d'Enginyers Industrials
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Fecha difusión:
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Resumen:
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[EN] The need for non-invasive therapies capable of conserving drug efficiency and stability while having specific targetability against colorectal cancer (CRC), has made nanoparticles preferable vehicles and principal ...[+]
[EN] The need for non-invasive therapies capable of conserving drug efficiency and stability while having specific targetability against colorectal cancer (CRC), has made nanoparticles preferable vehicles and principal building blocks for the development of complex and multi-action anti-tumoral approaches. For that purpose, we herein report the production of a combinatory anti-tumoral nanotherapy using the production of a new targeting towards CRC lines. To do so, Magneto-fluorescent NANO3 nanoparticles were used as nanocarriers for a combination of the drugs doxorubicin (DOX) and ofloxacin (OFLO). NANO3 nanoparticles' surface was modified with two different targeting agents, a newly synthesized (anti-CA IX acetazolamide derivative (AZM-SH)) and a commercially available (anti-epidermal growth factor receptor (EGFR), Cetuximab). The cytotoxicity revealed that only DOX-containing nanosystems showed significant and even competitive cytotoxicity when compared to that of free DOX. Interestingly, surface modification with AZM-SH promoted an increased cellular uptake in the HCT116 cell line, surpassing even those functionalized with Cetuximab. The results show that the new target has high potential to be used as a nanotherapy agent for CRC cells, surpassing commercial targets. As a proof-of-concept, an oral administration form of NANO3 systems was successfully combined with Eudragit (R) enteric coating and studied under extreme conditions.
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Palabras clave:
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Target nanocarriers
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Oral formulations
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Colorectal cancer
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Target drug delivery
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Targeted
anticancer therapy
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Derechos de uso:
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Reconocimiento (by)
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Fuente:
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International Journal of Molecular Sciences. (eissn:
1422-0067
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DOI:
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10.3390/ijms24076612
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Editorial:
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MDPI AG
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Versión del editor:
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https://doi.org/10.3390/ijms24076612
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Código del Proyecto:
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info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-126304OB-C41/ES/NUEVOS MATERIALES Y SONDAS PARA EL RECONOCIMIENTO, LIBERACION DE FARMACOS, NANOMOTORES Y COMUNICACION/
...[+]
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-126304OB-C41/ES/NUEVOS MATERIALES Y SONDAS PARA EL RECONOCIMIENTO, LIBERACION DE FARMACOS, NANOMOTORES Y COMUNICACION/
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-127983OB-C22/ES/EVALUACION IN VITRO E IN VIVO DE NUEVOS NANOPORTADORES PARA ADMINISTRACION INTRANASAL EN EL TRATAMIENTO Y DIAGNOSTICO DE ENFERMEDADES CEREBRALES./
info:eu-repo/grantAgreement/FCT//PD%2FBD%2F142865%2F2018/PT/Biodegradable Magneto-Luminescent Mesopourous Nanoparticles as new Nano BioMedical tools in Cancer Treatment/
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID%2FQUI%2F50006%2F2013/PT/Clean Technologies and Processes/
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50006%2F2020/PT/Clean Technologies and Processes/
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50006%2F2020/PT/Clean Technologies and Processes/
info:eu-repo/grantAgreement/FCT/CEEC IND 2017/CEECIND%2F00648%2F2017%2FCP1462%2FCT0014/PT
info:eu-repo/grantAgreement/FCT/OE/2022.09495.BD/PT/NEWPATH: New Advances on Synergistic Antibacterial Coatings Against Pathogenic Bacteria./
info:eu-repo/grantAgreement/FEDER//POCI-01-0145-FEDER-007265/
info:eu-repo/grantAgreement/GVA//CIPROM%2F2021%2F007/
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Agradecimientos:
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This work received financial support from PT national funds (FCT/MCTES, Fundacao para a Ciencia e Tecnologia and Ministerio da Ciencia, Tecnologia e Ensino Superior) through the projects UIDB/50006/2020 and UIDP/50006/2020. ...[+]
This work received financial support from PT national funds (FCT/MCTES, Fundacao para a Ciencia e Tecnologia and Ministerio da Ciencia, Tecnologia e Ensino Superior) through the projects UIDB/50006/2020 and UIDP/50006/2020. G.M. acknowledges the financial support by the Associate Laboratory Research Unit for Green Chemistry-Clean Processes and Technologies-LAQV, which is financed by national funds from FCT/MEC (UID/QUI/50006/2013) and co-financed by the ERDF under the PT2020 Partnership Agreement (POCI-01-0145-FEDER-007265), as well as the Scientific Society PROTEOMASS (Portugal) for funding support (General Funding Grant). G.M. and J.G. thank FCT/MEC (Portugal) for their doctoral grant PD/BD/142865/2018 and 2022.09495.BD, respectively. E.O. thanks FCT (Fundacao para a Ciencia e Tecnologia) for funding through the Scientific Employment Stimulus-Individual Call (Ref. CEECIND/00648/2017). J.L. acknowledges the funding received from the Ministerio de Ciencia, Innovacion y Universidades, Spain, grant PID2021-127983OB-C22 funded by MCIN/AEI/10.13039/501100011033. RMM acknowledges the funding received from project PID2021-126304OB-C41 funded by MCIN/AEI /10.13039/501100011033/ and by European Regional Development Fund-A way of doing Europe and Generalitat Valenciana (CIPROM/2021/007).
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Tipo:
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Artículo
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