Literature DB >> 12234249

Stable biocompatible adjuvants--a new type of adjuvant based on solid lipid nanoparticles: a study on cytotoxicity, compatibility and efficacy in chicken.

Carsten Olbrich1, Rainer Helmut Müller, Kerstin Tabatt, Oliver Kayser, Christoph Schulze, Rüdiger Schade.   

Abstract

A new type of adjuvant was tested for its ability to initiate antibody production in chickens, and its cellular and tissue compatibility were assessed. The stable biocompatible adjuvants tested are based on surface-modified solid lipid nanoparticles (SLNs), made from paraffin or biodegradable glycerides, and are simply admixed to the antigens before administration. The tissue-damaging potency of four formulations of the new adjuvants (H1, H2, H3 and H4) were first tested in vitro by using human foreskin fibroblasts and RAW 264.7 macrophages. The adjuvants were well tolerated by both cell types. Immunisation studies in chickens were performed by using a Mycoplasma bovis antigen and mouse immunoglobulin G (IgG). The resulting antibodies were non-invasively extracted from egg yolk. The use of the various adjuvant formulations resulted in a significant production of specific antibodies after the first and second booster immunisations. Freund's complete adjuvant (FCA), considered until now to be the "gold standard" among the adjuvants, revealed the highest antibody titre against mouse IgG. SLNs with a particle size of more than 100 nm exhibited a clear adjuvant activity, whereas SLNs with a particle size below 100 nm, in various concentrations, revealed a lower adjuvant activity. Immunisation of chickens with the mouse IgG alone, dissolved in phosphate-buffered saline, resulted in a slow antibody titre development. At the end of the experiment, the chickens were examined for vaccination-associated tissue damage. In contrast to FCA, the SLN formulations caused only minor tissue irritation at the injection sites. In conclusion, SLNs seem to be a promising alternative to FCA for antibody production in chickens, and potentially in other animals.

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Year:  2002        PMID: 12234249     DOI: 10.1177/026119290203000407

Source DB:  PubMed          Journal:  Altern Lab Anim        ISSN: 0261-1929            Impact factor:   1.303


  6 in total

1.  Isostatic ultra-high-pressure effects on supercooled melts in colloidal triglyceride dispersions.

Authors:  Christoph Blümer; Karsten Mäder
Journal:  Pharm Res       Date:  2005-09-22       Impact factor: 4.200

2.  Immunogenicity of peanut proteins containing poly(anhydride) nanoparticles.

Authors:  Juliana De S Rebouças; Juan M Irache; Ana I Camacho; Gabriel Gastaminza; María L Sanz; Marta Ferrer; Carlos Gamazo
Journal:  Clin Vaccine Immunol       Date:  2014-06-04

3.  Strong antibody responses induced by protein antigens conjugated onto the surface of lecithin-based nanoparticles.

Authors:  Brian R Sloat; Michael A Sandoval; Andrew M Hau; Yongqun He; Zhengrong Cui
Journal:  J Control Release       Date:  2009-09-01       Impact factor: 9.776

Review 4.  Egg yolk antibodies (IgY) and their applications in human and veterinary health: A review.

Authors:  E P V Pereira; M F van Tilburg; E O P T Florean; M I F Guedes
Journal:  Int Immunopharmacol       Date:  2019-05-22       Impact factor: 4.932

5.  Tacrolimus-Loaded Solid Lipid Nanoparticle Gel: Formulation Development and In Vitro Assessment for Topical Applications.

Authors:  Abdul Shakur Khan; Kifayat Ullah Shah; Mohammed Al Mohaini; Abdulkhaliq J Alsalman; Maitham A Al Hawaj; Yousef N Alhashem; Shakira Ghazanfar; Kamran Ahmad Khan; Zahid Rasul Niazi; Arshad Farid
Journal:  Gels       Date:  2022-02-18

Review 6.  Lipid-based colloidal carriers for peptide and protein delivery--liposomes versus lipid nanoparticles.

Authors:  Susana Martins; Bruno Sarmento; Domingos C Ferreira; Eliana B Souto
Journal:  Int J Nanomedicine       Date:  2007
  6 in total

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