2 research outputs found

    Luminescent silicon-based nanocarrier for drug delivery in colorectal cancer cells

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    Nanocarriers sensitive to exogenous or endogenous stimuli emerged as an attractive alternative to target drug delivery, with inorganic silica mesoporous nanoparticles (MNs) playing a core role in the development of a new generation of non-toxic and tuneable nanocarriers. A sensitive nanovector (NANO1) comprising luminescent silicon quantum dots (SiQDs) and functionalized with MNs was synthesised and loaded with doxorubicin (DOX). NANO1 nanoparticles have a size of 74 ± 10 nm and DOX loading percentages of ca. 43%. As a control sample, a similar nanocarrier (NANO2), without SiQDs, was also synthesised and loaded with DOX. Release profile studies, in PBS, revealed the strong NANO1@DOX pH-dependant behaviour, with a pH 5.0 favouring the release of DOX to percentages of ca. 70%. Cytotoxicity assessments of both free and DOX-loaded nanocarriers were evaluated in human cell lines of colon, revealing both free drug and drug-loaded nanoparticles to be concentration-dependent.This work was supported 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); by the Scientific Society PROTEOMASS (Portugal) (General Funding Grant) and by the Spanish Ministry of Science, Innovation and Universities project RTI2018-098027-B-C22. This work was also supported by grant RTI2018-098027-B-C21 and RTI2018-088027-B-C22 from the Spanish Government funds and by the European Regional Development Fund (ERDF). The ICN2 is funded by the CERCA programme/Generalitat de Catalunya. The ICN2 is supported by the Severo Ochoa Centres of Excellence programme, funded by the Spanish Research Agency (AEI, grant no. SEV-2017-0706). F. N thanks to COST Action CA17121. F. N and J. L thanks to COST Action CA15138. G.M thanks to FCT/MEC (Portugal) for his doctoral grant PD/BD/142865/2018. E. O thanks FCT/MEC (Portugal) for the individual contract, CEECIND/00648/2017.Peer reviewe
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