Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.
Introduction: The researches have shown that the potential of virus antigen encapsulation in Chitosan Nanoparticles is higher
and more efficient than the whole virus. Hence in this study, the effect of Ether treatment of A/H9N2 sub type of Influenza
virus on Efficiency of Chitosan nanoparticles encapsulation was investigated.
Methods: A/H9N2 Virus was purified from allantoic fluid by Sucrose gradient (20-60%). Then, the part of purified virus was
mixed by Tween- 80- 10% for 5 min. This mixture was combined with equal volume of ether and incubated in 4Ă?ÂșC. After
15 min, the upper layer that contain ether and virus envelops were eliminate and the virus capsid and spikes were collected
from lower. This solution was evaluated by SDS-PAGE and Hemagglutination assay (HA). Ion gelation method with Na-
Tripolyphosphate (Tpp) anions as cross linker was used to prepare the antigen-loaded nanoparticles. Influenza A/H9N2 ether
treated and un-treated was incorporated separately in the Na-Tpp solution. After antigen encapsulation, physicochemical
properties of nanoparticles such as: Morphology, particle size and zeta potential were investigatedwith photon correlation
spectroscopy (PCS) and Laser Doppler Anemometry (LDA) using a Zetasizer 3000-HS (MalvernIns., UK) respectively. Finally,
the loading efficacy, loading capacity and Ag- releasing efficacy of them were evaluated by HA and Nano drop.
Results: The SDS-PAGE results show that Albumin was eliminated from virus solution. These results also reveal that treatment
of Influenza virus by ether were take place with proper quality. So, the efficiency of virus purification and ether treated was
confirmed by SDS-PAGE. The particle size and zeta potential of Cs nanoparticles were similar for treated and untreated viruses.
The loading efficacy of treated and un-treated virus loaded nanoparticles was 15 and 10HAU respectively and the Nano drop
results of in-vitro releasing for treated virus loaded nanoparticles was more than the untreated.
Conclusions: In this study it was found that ether treatment is a successful method for influenza spikes purification. The ethertreated
antigen was far superior to the untreated antigen in loading efficacy and antigen releasing yield; although there was
no significant difference in morphological and physicochemical properties of both. Therefore, ether treatment method could
be proposed as a suitable and affordable manner to encapsulation improvement of enveloped virus in chitosan nano particles,
such as influenza virus.