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Název: | Smart co-delivery of miR-34a and cytotoxic peptides (LTX-315 and melittin) by chitosan based polyelectrolyte nanocarriers for specific cancer cell death induction | ||||||||||
Autor: | Motiei, Marjan; Aboutalebi, Fatemeh; Forouzanfar, Mahboobeh; Dormiani, Kianoush; Nasr-Esfahani, Mohammad Hossein; Mirahmadi-Zare, Seyede Zohreh | ||||||||||
Typ dokumentu: | Recenzovaný odborný článek (English) | ||||||||||
Zdrojový dok.: | Materials Science & Engineering C-Materials For Biological Applications. 2021, vol. 128 | ||||||||||
ISSN: | 0928-4931 (Sherpa/RoMEO, JCR) | ||||||||||
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DOI: | https://doi.org/10.1016/j.msec.2021.112258 | ||||||||||
Abstrakt: | A novel polyelectrolyte nanocarrier was synthesized via layer-by-layer self-assembly of polycationic and polyanionic chains. The nanocarrier is composed of polyglutamate grafted chitosan core, dextran sulfate as a complexing agent, and polyethyleneimine shell decorated with folic acid. This polyelectrolyte complex has unique physicochemical properties so that the core is considered as an efficient carrier for LTX-315 and melittin peptides, and the shell is suitable for delivery of miR-34a. The spherical nanocarriers with an average size of 123 ± 5 nm and a zeta potential of −36 ± 1 mV demonstrated controlled-release of gene and peptides ensured a synergistic effect in establishing multiple cell death pathways on chemoresistance human breast adenocarcinoma cell line, MDA-MB-231. In vitro cell viability assays also revealed no cytotoxicity for the nanocarriers, and an IC50 of 15 μg/mL and 150 μg/mL for melittin and LTX-315, respectively, after 48 h, whereas co-delivery of melittin with miR-34a increased smart death induction by 54%. © 2021 Elsevier B.V. | ||||||||||
Plný text: | https://www.sciencedirect.com/science/article/pii/S0928493121003970 | ||||||||||
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