Ghent University Academic Bibliography

Advanced

Spray-dried powders of starch and crosslinked poly(acrylic acid) as carriers for nasal delivery of inactivated influenza vaccine

Delphine Coucke UGent, Michael Schotsaert, Claude Libert UGent, Eveline Pringels, Chris Vervaet UGent, P Foreman, Xavier Saelens UGent and Jean Paul Remon UGent (2009) Vaccine. 27(8). p.1279-1286
abstract
mucosal vaccination has several advantages over parenteral vaccination. In this study,viscosity-enhancing mucosal delivery systems for the induction of an adaptive immune response against viral antigen were investigated. Powder formulations based on spray-dried mixtures of starch (Amioca (R))/poly(acrylic acid) (Carbopol (R) 974P) in different ratios were used as carriers of the viral antigen. A comparison of these formulations for intranasal delivery of heat-inactivated influenza virus combined with LTR 192G adjuvant was made in vivo in a rabbit model. Individual rabbit sera were tested for seroconversion against hemagglutinin (HA), the major surface antigen of influenza. The powder vaccine formulations were able to induce systemic anti-HA IgG responses. The presence of Carbopol (R) 974P improved the kinetics of the immune responses and the level of IgG titers in a dose-dependent way which was correlated with moderately irritating capacities of the formulation. In contrast, mucosal IgA responses were not detected. In conclusion, it was demonstrated that the use of bioadhesive carriers based on Amioca (R) starch and poly(acrylic acid) facilitates the induction of a systemic anti-HA antibody response after intranasal vaccination with a whole virus influenza vaccine.
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
INTRANASAL IMMUNIZATION, ANTIBODY-RESPONSES, TRACE AMOUNT, B-SUBUNIT, MUCOSAL IMMUNE-RESPONSES, HEAT-LABILE ENTEROTOXIN, Muco-adhesion, Nasal delivery, Nasal vaccination, Powder formulation, SYSTEMIC ANTIBODY, IN-VITRO, CHITOSAN, VIRUS
journal title
Vaccine
volume
27
issue
8
pages
1279 - 1286
publisher
Elsevier
Web of Science type
Article
Web of Science id
000263712200018
JCR category
MEDICINE, RESEARCH & EXPERIMENTAL
JCR impact factor
3.616 (2009)
JCR rank
20/90 (2009)
JCR quartile
1 (2009)
ISSN
0264-410X
DOI
10.1016/j.vaccine.2008.12.013
language
English
UGent publication?
yes
classification
A1
copyright statement
I don't know the status of the copyright for this publication
id
537104
handle
http://hdl.handle.net/1854/LU-537104
date created
2009-04-02 12:44:33
date last changed
2016-12-19 15:46:20
@article{537104,
  abstract     = {mucosal vaccination has several advantages over parenteral vaccination. In this study,viscosity-enhancing mucosal delivery systems for the induction of an adaptive immune response against viral antigen were investigated. Powder formulations based on spray-dried mixtures of starch (Amioca (R))/poly(acrylic acid) (Carbopol (R) 974P) in different ratios were used as carriers of the viral antigen. A comparison of these formulations for intranasal delivery of heat-inactivated influenza virus combined with LTR 192G adjuvant was made in vivo in a rabbit model. Individual rabbit sera were tested for seroconversion against hemagglutinin (HA), the major surface antigen of influenza. The powder vaccine formulations were able to induce systemic anti-HA IgG responses. The presence of Carbopol (R) 974P improved the kinetics of the immune responses and the level of IgG titers in a dose-dependent way which was correlated with moderately irritating capacities of the formulation. In contrast, mucosal IgA responses were not detected. In conclusion, it was demonstrated that the use of bioadhesive carriers based on Amioca (R) starch and poly(acrylic acid) facilitates the induction of a systemic anti-HA antibody response after intranasal vaccination with a whole virus influenza vaccine.},
  author       = {Coucke, Delphine and Schotsaert, Michael and Libert, Claude and Pringels, Eveline and Vervaet, Chris and Foreman, P and Saelens, Xavier and Remon, Jean Paul},
  issn         = {0264-410X},
  journal      = {Vaccine},
  keyword      = {INTRANASAL IMMUNIZATION,ANTIBODY-RESPONSES,TRACE AMOUNT,B-SUBUNIT,MUCOSAL IMMUNE-RESPONSES,HEAT-LABILE ENTEROTOXIN,Muco-adhesion,Nasal delivery,Nasal vaccination,Powder formulation,SYSTEMIC ANTIBODY,IN-VITRO,CHITOSAN,VIRUS},
  language     = {eng},
  number       = {8},
  pages        = {1279--1286},
  publisher    = {Elsevier},
  title        = {Spray-dried powders of starch and crosslinked poly(acrylic acid) as carriers for nasal delivery of inactivated influenza vaccine},
  url          = {http://dx.doi.org/10.1016/j.vaccine.2008.12.013},
  volume       = {27},
  year         = {2009},
}

Chicago
Coucke, Delphine, Michael Schotsaert, Claude Libert, Eveline Pringels, Chris Vervaet, P Foreman, Xavier Saelens, and Jean Paul Remon. 2009. “Spray-dried Powders of Starch and Crosslinked Poly(acrylic Acid) as Carriers for Nasal Delivery of Inactivated Influenza Vaccine.” Vaccine 27 (8): 1279–1286.
APA
Coucke, D., Schotsaert, M., Libert, C., Pringels, E., Vervaet, C., Foreman, P., Saelens, X., et al. (2009). Spray-dried powders of starch and crosslinked poly(acrylic acid) as carriers for nasal delivery of inactivated influenza vaccine. Vaccine, 27(8), 1279–1286.
Vancouver
1.
Coucke D, Schotsaert M, Libert C, Pringels E, Vervaet C, Foreman P, et al. Spray-dried powders of starch and crosslinked poly(acrylic acid) as carriers for nasal delivery of inactivated influenza vaccine. Vaccine. Elsevier; 2009;27(8):1279–86.
MLA
Coucke, Delphine, Michael Schotsaert, Claude Libert, et al. “Spray-dried Powders of Starch and Crosslinked Poly(acrylic Acid) as Carriers for Nasal Delivery of Inactivated Influenza Vaccine.” Vaccine 27.8 (2009): 1279–1286. Print.