Evaluation of N-phosphonium chitosan as a novel vaccine carrier for intramuscular immunization
- PMID: 28992775
- DOI: 10.1177/0885328217735221
Evaluation of N-phosphonium chitosan as a novel vaccine carrier for intramuscular immunization
Abstract
Chitosan, as a potential vaccine delivery material, has obtained much attention for immunization prevention and therapy. However, its poor water solubility brings inconvenience for the practical applications. To address this issue, researchers have carried out many chemical modifications to prepare water-soluble chitosan derivatives for vaccine delivery. In this work, we prepared a chitosan derivative N-phosphonium chitosan with excellent water solubility and explored its potential as an intramuscular vaccine delivery system by using ovalbumin as a model antigen. Different vaccine formulations were intramuscularly injected into test mice. Through an immunohistochemistry assay, N-phosphonium chitosan-based antigen formulation could promote antigen arrival from injection site to the secondary lymph organ spleen. Further immunization results showed that 1 mg/ml N-phosphonium chitosan-based vaccine formulation could contribute to significantly higher level of antigen-specific immune responses, including higher antigen-specific IgG antibody titer, splenocyte proliferation, and cytokines secretion (interferon-γ, interleukin-10, and interleukin-4) by the splenocytes of the immunized mice. From the results, the water-soluble chitosan derivative N-phosphonium chitosan could be developed as a potential antigen carrier for immunization prevention and therapy.
Keywords: N-phosphonium chitosan; intramuscular immunization; vaccine delivery system.
Similar articles
-
pH Sensitive phosphorylated chitosan hydrogel as vaccine delivery system for intramuscular immunization.J Biomater Appl. 2017 May;31(10):1358-1369. doi: 10.1177/0885328217704139. Epub 2017 Apr 7. J Biomater Appl. 2017. PMID: 28387574
-
Administration routes affect the quality of immune responses: A cross-sectional evaluation of particulate antigen-delivery systems.J Control Release. 2010 Nov 1;147(3):342-9. doi: 10.1016/j.jconrel.2010.08.012. Epub 2010 Aug 18. J Control Release. 2010. PMID: 20727926
-
Chitosan modified squalene nanostructured lipid carriers as a promising adjuvant for freeze-dried ovalbumin vaccine.Int J Biol Macromol. 2021 Oct 1;188:855-862. doi: 10.1016/j.ijbiomac.2021.08.074. Epub 2021 Aug 16. Int J Biol Macromol. 2021. PMID: 34411614
-
Advances and Potential Applications of Chitosan Nanoparticles as a Delivery Carrier for the Mucosal Immunity of Vaccine.Curr Drug Deliv. 2017;14(1):27-35. doi: 10.2174/1567201813666160804121123. Curr Drug Deliv. 2017. PMID: 27494157 Review.
-
Chemical Modification of Chitosan for Efficient Vaccine Delivery.Molecules. 2018 Jan 25;23(2):229. doi: 10.3390/molecules23020229. Molecules. 2018. PMID: 29370100 Free PMC article. Review.
Cited by
-
Chitosan-Based Nanomaterial as Immune Adjuvant and Delivery Carrier for Vaccines.Vaccines (Basel). 2022 Nov 11;10(11):1906. doi: 10.3390/vaccines10111906. Vaccines (Basel). 2022. PMID: 36423002 Free PMC article. Review.
-
Blood-repellent and anti-corrosive surface by spin-coated SWCNT layer on intravascular stent materials.Phys Eng Sci Med. 2023 Mar;46(1):227-243. doi: 10.1007/s13246-022-01212-5. Epub 2023 Jan 2. Phys Eng Sci Med. 2023. PMID: 36592282
-
An Overview of Current Knowledge on the Properties, Synthesis and Applications of Quaternary Chitosan Derivatives.Polymers (Basel). 2020 Nov 30;12(12):2878. doi: 10.3390/polym12122878. Polymers (Basel). 2020. PMID: 33266285 Free PMC article. Review.
-
Theoretical and Experimental Optimization of the Graft Density of Functionalized Anti-Biofouling Surfaces by Cationic Brushes.Membranes (Basel). 2020 Dec 17;10(12):431. doi: 10.3390/membranes10120431. Membranes (Basel). 2020. PMID: 33348625 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical