4.7 Article

Chitosan-coated poly(lactic-co-glycolic) acid nanoparticles as an efficient delivery system for Newcastle disease virus DNA vaccine

期刊

INTERNATIONAL JOURNAL OF NANOMEDICINE
卷 9, 期 -, 页码 4609-4619

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJN.S70633

关键词

mucosal immune delivery system; immune effect

资金

  1. National Natural Science Foundation of the People's Republic of China [31072119]
  2. Chinese Ministry of Education [212048]
  3. Program for New Century Excellent Talents in University [NCET-12-0707]
  4. Innovative Research Team for Agricultural Microbiology Fermentation Technology at Heilongjiang Provincial University [2012td009]
  5. Changjiang Scholar Candidates Program for Provincial Universities in Heilongjiang [2014CJHB005]
  6. Scientific and Technological Key Project of Heilongjiang Province [GC13B403]
  7. Early Research and Development Cultivation Project of Scientific and Technological Achievements Industrialization for Provincial Universities in Heilongjiang [1253CGZH10]
  8. Innovation Foundation of Harbin [2013RFQXJ030]

向作者/读者索取更多资源

We determined the efficacy and safety of chitosan (CS)-coated poly(lactic-co-glycolic) acid (PLGA) nanoparticles (NPs) as a delivery system for a vaccine to protect chickens against Newcastle disease virus (NDV). The newly constructed vaccine contained DNA (the F gene) of NDV. The Newcastle disease virus (NDV) F gene deoxyribonucleic acid (DNA) plasmid (pFDNA)-CS/PLGA-NPs were spherical (diameter =699.1 +/- 5.21 nm [mean +/- standard deviation]) and smooth, with an encapsulation efficiency of 98.1% and a Zeta potential of +6.35 mV. An in vitro release assay indicated that CS controlled the burst release of plasmid DNA, such that up to 67.4% of the entire quantity of plasmid DNA was steadily released from the pFDNA-CS/PLGA-NPs. An in vitro expression assay indicated that the expression of nanoparticles (NPs) was maintained in the NPs. In an immunization test with specific pathogen-free chickens, the pFDNA-CS/PLGA-NPs induced stronger cellular, humoral, and mucosal immune responses than the plasmid DNA vaccine alone. The pFDNA-CS/PLGA-NPs did not harm 293T cells in an in vitro assay and did not harm chickens in an in vivo assay. Overall, the results indicated that CS-coated PLGA NPs can serve as an efficient and safe mucosal immune delivery system for NDV DNA vaccine.

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