Chitosan derived formulations and EmzaloidTM technology for mucosal vaccination against diphtheria : oral efficacy in mice / Elaine van der Westhuizen

Vaccination plays a very important part in daily life. It is essential to get vaccinated at an early age. The conventional parented method used is not always effective and not cost efficient. It requires qualified personnel and sterile conditions for administration of the vaccines. The aim of this s...

Full description

Bibliographic Details
Main Author: Van der Westhuizen, Elaine
Published: North-West University 2009
Subjects:
Online Access:http://hdl.handle.net/10394/633
id ndltd-NWUBOLOKA1-oai-dspace.nwu.ac.za-10394-633
record_format oai_dc
spelling ndltd-NWUBOLOKA1-oai-dspace.nwu.ac.za-10394-6332014-04-16T03:55:04ZChitosan derived formulations and EmzaloidTM technology for mucosal vaccination against diphtheria : oral efficacy in mice / Elaine van der WesthuizenVan der Westhuizen, ElaineOral vaccinationChitosan microparticlesChitosan nanoparticlesN-trimethyl chitosan chloride (TMC) microparticlesEmzaloid microparticlesEmzaloid nanoparticlesDiphtheria toxoidELISA assay.Vaccination plays a very important part in daily life. It is essential to get vaccinated at an early age. The conventional parented method used is not always effective and not cost efficient. It requires qualified personnel and sterile conditions for administration of the vaccines. The aim of this study was to investigate the effect of chitosan, N-trimethyl chitosan chloride (TMC) and Emzaloid™ particles on the local and systemic immune response of mice after oral vaccination with Diphtheria toxoid (DT). The different formulations used were chitosan microparticles (± 10 µm), chitosan nanoparticles (± 400 nm), TMC microparticles (± 5 µm), Emzaloid microparticles (± 4 µm) and Emzaloid nanoparticles (± 500 nm). All of these formulations proved to be very good delivery systems and can entrap large amounts of the antigen. Balb/c mice were used to determine the local and systemic immune response of these formulations. The mice were vaccinated orally on three consecutive days in week 1 and 3 with 40 Lf DT per week with a total volume of 300 µl. Blood samples were taken from the mice and analysed for a systemic immune response (IgG). The same mice were used to determine the local immune response (IgA). Faeces were collected from each mouse on day 1, 3, 4, 6, 14 and 20 for analysis. An enzyme-linked immunosorbent assay (ELISA) was used to determine IgG and IgA titers. It can be concluded that chitosan nanoparticles was the only formulation with a higher response than that of the currently used vaccine. Emzaloid nanoparticles showed no significant difference in response when compared to the currently used vaccine. All the other formulations showed a much smaller response than that of the conventional method of vaccination.Thesis (M.Sc. (Pharmaceutics))--North-West University, Potchefstroom Campus, 2005.North-West University2009-02-11T14:13:00Z2009-02-11T14:13:00Z2004Thesishttp://hdl.handle.net/10394/633
collection NDLTD
sources NDLTD
topic Oral vaccination
Chitosan microparticles
Chitosan nanoparticles
N-trimethyl chitosan chloride (TMC) microparticles
Emzaloid microparticles
Emzaloid nanoparticles
Diphtheria toxoid
ELISA assay.
spellingShingle Oral vaccination
Chitosan microparticles
Chitosan nanoparticles
N-trimethyl chitosan chloride (TMC) microparticles
Emzaloid microparticles
Emzaloid nanoparticles
Diphtheria toxoid
ELISA assay.
Van der Westhuizen, Elaine
Chitosan derived formulations and EmzaloidTM technology for mucosal vaccination against diphtheria : oral efficacy in mice / Elaine van der Westhuizen
description Vaccination plays a very important part in daily life. It is essential to get vaccinated at an early age. The conventional parented method used is not always effective and not cost efficient. It requires qualified personnel and sterile conditions for administration of the vaccines. The aim of this study was to investigate the effect of chitosan, N-trimethyl chitosan chloride (TMC) and Emzaloid™ particles on the local and systemic immune response of mice after oral vaccination with Diphtheria toxoid (DT). The different formulations used were chitosan microparticles (± 10 µm), chitosan nanoparticles (± 400 nm), TMC microparticles (± 5 µm), Emzaloid microparticles (± 4 µm) and Emzaloid nanoparticles (± 500 nm). All of these formulations proved to be very good delivery systems and can entrap large amounts of the antigen. Balb/c mice were used to determine the local and systemic immune response of these formulations. The mice were vaccinated orally on three consecutive days in week 1 and 3 with 40 Lf DT per week with a total volume of 300 µl. Blood samples were taken from the mice and analysed for a systemic immune response (IgG). The same mice were used to determine the local immune response (IgA). Faeces were collected from each mouse on day 1, 3, 4, 6, 14 and 20 for analysis. An enzyme-linked immunosorbent assay (ELISA) was used to determine IgG and IgA titers. It can be concluded that chitosan nanoparticles was the only formulation with a higher response than that of the currently used vaccine. Emzaloid nanoparticles showed no significant difference in response when compared to the currently used vaccine. All the other formulations showed a much smaller response than that of the conventional method of vaccination. === Thesis (M.Sc. (Pharmaceutics))--North-West University, Potchefstroom Campus, 2005.
author Van der Westhuizen, Elaine
author_facet Van der Westhuizen, Elaine
author_sort Van der Westhuizen, Elaine
title Chitosan derived formulations and EmzaloidTM technology for mucosal vaccination against diphtheria : oral efficacy in mice / Elaine van der Westhuizen
title_short Chitosan derived formulations and EmzaloidTM technology for mucosal vaccination against diphtheria : oral efficacy in mice / Elaine van der Westhuizen
title_full Chitosan derived formulations and EmzaloidTM technology for mucosal vaccination against diphtheria : oral efficacy in mice / Elaine van der Westhuizen
title_fullStr Chitosan derived formulations and EmzaloidTM technology for mucosal vaccination against diphtheria : oral efficacy in mice / Elaine van der Westhuizen
title_full_unstemmed Chitosan derived formulations and EmzaloidTM technology for mucosal vaccination against diphtheria : oral efficacy in mice / Elaine van der Westhuizen
title_sort chitosan derived formulations and emzaloidtm technology for mucosal vaccination against diphtheria : oral efficacy in mice / elaine van der westhuizen
publisher North-West University
publishDate 2009
url http://hdl.handle.net/10394/633
work_keys_str_mv AT vanderwesthuizenelaine chitosanderivedformulationsandemzaloidtmtechnologyformucosalvaccinationagainstdiphtheriaoralefficacyinmiceelainevanderwesthuizen
_version_ 1716664630440361984