Development of chitosan-pullulan composite nanoparticles for nasal delivery of vaccines: Optimisation and cellular studies
dc.contributor.author | Cevher, Erdal | |
dc.contributor.author | Salomon, Stefan K. | |
dc.contributor.author | Makrakis, Apostolos | |
dc.contributor.author | Li, Xiong Wei | |
dc.contributor.author | Brocchini, Steve | |
dc.contributor.author | Alpar, H. Oya | |
dc.date.accessioned | 2021-05-15T12:40:39Z | |
dc.date.available | 2021-05-15T12:40:39Z | |
dc.date.issued | 2015 | |
dc.department | Eczacılık Fakültesi | en_US |
dc.description | Cevher, Erdal/0000-0002-0486-2252; | |
dc.description.abstract | Nasal immunisation with nanoparticles has already shown promising results. In this study, nanoparticle composites carrying BSA for nasal vaccination prepared using electrostatic interaction process between polycation N-trimethyl chitosan chloride (TMC), chitosan glutamate (CG), chitosan chloride (CCl) and polyanion carboxymethyl pullulan (CMP). A mass ratio of 2:1 for TMC-CMP combination produced stable nanocarriers. For CCl-CMP and CG-CMP formulations needed a mass ratio of 3:1. Loading efficiency was >90% for all formulations. Nanoparticles' size ranged from 207 to 603 nm. The surface charge of the complexes varied between +14 and +33 mV. SDS-PAGE integrity of the model antigen was also demonstrated. MTT studies showed that nanoparticle composites were less toxic to Calu-3 cells than the particles of cationic polymers alone. FITC-BSA loaded nanoparticles efficiently taken up by J774A.1 macrophages as confirmed by confocal microscopy highlighting the potential of these novel nanoparticulate carriers' use for nasal vaccination. | en_US |
dc.identifier.doi | 10.3109/02652048.2015.1073392 | |
dc.identifier.endpage | 768 | en_US |
dc.identifier.issn | 0265-2048 | |
dc.identifier.issn | 1464-5246 | |
dc.identifier.issue | 8 | en_US |
dc.identifier.pmid | 26480961 | |
dc.identifier.scopus | 2-s2.0-84945471005 | |
dc.identifier.scopusquality | Q2 | |
dc.identifier.startpage | 755 | en_US |
dc.identifier.uri | https://doi.org/10.3109/02652048.2015.1073392 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12939/645 | |
dc.identifier.volume | 32 | en_US |
dc.identifier.wos | WOS:000369970100004 | |
dc.identifier.wosquality | Q2 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.institutionauthor | Alpar, H. Oya | |
dc.language.iso | en | |
dc.publisher | Taylor & Francis Ltd | en_US |
dc.relation.ispartof | Journal of Microencapsulation | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Carboxymethyl Pullulan | en_US |
dc.subject | Cellular Uptake | en_US |
dc.subject | Chitosan Derivatives | en_US |
dc.subject | Nanoparticles | en_US |
dc.subject | Nasal Vaccination | en_US |
dc.subject | N-Trimethyl Chitosan Chloride | en_US |
dc.subject | Polyion Complexation | en_US |
dc.title | Development of chitosan-pullulan composite nanoparticles for nasal delivery of vaccines: Optimisation and cellular studies | |
dc.type | Article |