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Τύπος: Άρθρο σε επιστημονικό περιοδικό
Τίτλος: Rational design of aqueous conjugated polymer nanoparticles as potential theranostic agents of breast cancer
Συγγραφέας: [EL] Κοράλλη, Παναγιώτα[EN] Koralli, Panagiotasemantics logo
[EL] Τσικαλάκης, Σπυρίδων[EN] Tsikalakis, Spyridonsemantics logo
[EL] Γουλιελμάκη, Μαρία[EN] Goulielmaki, Mariasemantics logo
[EL] Αρελάκη, Στέλλα[EN] Arelaki, Stellasemantics logo
[DE] Müller, Janinasemantics logo
[EL] Νέγκα, Αλκμήνη[EN] Negka, Alkminisemantics logo
[DE] Herbst, Friederikesemantics logo
[EN] Ball, Claudiasemantics logo
[EL] Γρηγορίου, Βασίλειος[EN] Gregoriou, Vasilissemantics logo
[EL] Δημητρακοπούλου, Αντωνία[DE] Dimitrakopoulou - Strauss, Antoniasemantics logo
[DE] Wiemann, Stefansemantics logo
[EL] Χώχος, Χρήστος[EN] Chochos, Christossemantics logo
Ημερομηνία: 07/05/2021
Περίληψη: Conjugated polymer nanoparticles (CPNs) have emerged as a new promising class of cancer theranostic agents due to their desirable optical features, such as high absorption coefficient and photoluminescence quantum yields, spanning from the ultraviolet to the near infrared, along with their photothermal and photodynamic properties. However, limited studies have been demonstrated up to now on the rational design of CPNs for specific biological purposes. In particular, it is not well understood how exactly the chemical structure of the conjugated polymer and the nanoparticle formulation approach (encapsulation versus nanoprecipitation) associates with the cytotoxicity, the intracellular uptake in vitro and the therapeutic behavior. For this reason, nanoprecipitated and encapsulated aqueous CPNs were formulated consisting of thiophene–quinoxaline type conjugated polymers varying as regards the number of the fluorine atoms (three versus four) on the repeat unit. The obtained CPNs were systematically examined in terms of cytotoxicity and intracellular uptake in vitro in three epithelial breast cell lines represented by one normal cell line, and two breast cancer cell lines composed of one luminal and one triple negative line. From the obtained results, it is presented that only the nanoprecipitated CPNs with the three fluorine atoms exhibited efficient intracellular uptake to all the epithelial cell lines tested, in addition to the visible fluorescence on the triple negative breast cancer cells. Moreover, evaluation of the comparison of the effect of the CPNs on cell proliferation and apoptosis of all cell lines with the corresponding antibiotic staurosporine was performed, indicating a putative therapeutic potential of nanoparticles under study
Γλώσσα: Αγγλικά
Σελίδες: 13
DOI: 10.1039/D1QM00479D
EISSN: 2052-1537
Θεματική κατηγορία: [EL] Νανοεπιστήμη και Νανοτεχνολογία[EN] Nanoscience and Nanotechnologysemantics logo
[EL] Νανοϋλικά[EN] Nano-materialssemantics logo
Κάτοχος πνευματικών δικαιωμάτων: © The Author(s) 2021
Όροι και προϋποθέσεις δικαιωμάτων: This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.
Ηλεκτρονική διεύθυνση του τεκμηρίου στον εκδότη: https://pubs.rsc.org/en/content/articlelanding/2021/qm/d1qm00479d
Ηλεκτρονική διεύθυνση περιοδικού: https://pubs.rsc.org/en/journals/journalissues/qm#!recentarticles&adv
Τίτλος πηγής δημοσίευσης: Materials Chemistry Frontiers
Τεύχος: 13
Τόμος: 5
Σελίδες τεκμηρίου (στην πηγή): 4950-4962
Σημειώσεις: This research has received funding by the Helmholtz European partnering program for the cooperation between German Cancer Research Center (DKFZ) and National Hellenic Research Foundation (NHRF) to build the Athens Comprehensive Cancer Center (ACCC). P. K. acknowledges the Operational Programme ‘‘Human Resources Development, Education and Lifelong Learning’’ in the context of the project ‘‘Reinforcement of Postdoctoral Researchers – 2nd Cycle’’ (MIS-5033021), implemented by the State Scholarships Foundation (IKY) cofinanced by Greece and the European Union (European Social Fund-ESF).
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