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Smart co-delivery of miR-34a and cytotoxic peptides (LTX-315 and melittin) by chitosan based polyelectrolyte nanocarriers for specific cancer cell death induction

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dc.title Smart co-delivery of miR-34a and cytotoxic peptides (LTX-315 and melittin) by chitosan based polyelectrolyte nanocarriers for specific cancer cell death induction en
dc.contributor.author Motiei, Marjan
dc.contributor.author Aboutalebi, Fatemeh
dc.contributor.author Forouzanfar, Mahboobeh
dc.contributor.author Dormiani, Kianoush
dc.contributor.author Nasr-Esfahani, Mohammad Hossein
dc.contributor.author Mirahmadi-Zare, Seyede Zohreh
dc.relation.ispartof Materials Science & Engineering C-Materials For Biological Applications
dc.identifier.issn 0928-4931 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2021
utb.relation.volume 128
dc.type article
dc.language.iso en
dc.publisher Elsevier Ltd
dc.identifier.doi 10.1016/j.msec.2021.112258
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0928493121003970
dc.subject polyelectrolyte nanocarrier en
dc.subject polyglutamate grafted chitosan en
dc.subject gene-peptide co-delivery en
dc.subject miR-34a en
dc.subject LTX-315 en
dc.subject melittin en
dc.subject active targeting en
dc.description.abstract 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. en
utb.faculty University Institute
dc.identifier.uri http://hdl.handle.net/10563/1010385
utb.identifier.obdid 43883278
utb.identifier.scopus 2-s2.0-85108444179
utb.identifier.wok 000691786400003
utb.source j-scopus
dc.date.accessioned 2021-07-01T21:14:23Z
dc.date.available 2021-07-01T21:14:23Z
dc.description.sponsorship Iran's National Elites Foundation (INEF)
utb.ou Centre of Polymer Systems
utb.contributor.internalauthor Motiei, Marjan
utb.fulltext.sponsorship The authors would like to thank Iran's National Elites Foundation (INEF) for financial support. We are also grateful to Professor Iraj Mohammadpoor-Baltork for the gift of fluorophore phenylxanthene dye.
utb.wos.affiliation [Motiei, Marjan; Aboutalebi, Fatemeh; Forouzanfar, Mahboobeh; Dormiani, Kianoush; Nasr-Esfahani, Mohammad Hossein; Mirahmadi-Zare, Seyede Zohreh] ACECR, Royan Inst Biotechnol, Cell Sci Res Ctr, Dept Anim Biotechnol, Esfahan 8159358686, Iran; [Motiei, Marjan] Tomas Bata Univ Zlin, Ctr Polymer Syst, Trida Tomase Bati 5678, Zlin 76001, Czech Republic
utb.scopus.affiliation Department of Animal Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, 8159358686, Iran; Centre of Polymer Systems, Tomas Bata University in Zlín, Třída Tomáše Bati 5678, Zlín, 76001, Czech Republic
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