Immunoevaluation and Characterization of Tetanus Toxoid by using Natural polymer as an adjuvant

Immunoevaluation and Characterization of Tetanus Toxoid

Authors

  • L Nirmala,
  • Vijayashree Nayak
  • Dr. Deecaraman
  • Dr. Subhadeep

Keywords:

Natural polymer, Tetanus antigen, Immunological evaluation, Antibody

Abstract

Natural polymer like potato starch is a mixture of amylose and amylopectin, . Extraction of Potato starch was performed by rasping, centrifugation, refining and drying method. In our research method, we employed potato starch as a biodegradable polymer; It has a great impact on pharmaceutical applications due to its bioavailability, non toxic, high change density and biodegradability. In our research work, we have selected Potato starch polymer as a model of immunomodulatory effect of vaccine of tetanus antigen. According to WHO, Tetanus is a systemic infectious disease caused by genus Cl Tetanii. It has been estimated that the tetanus fever endemicity among large populations and global emergence of multidrug resistant strains to impose greater urgency on the evaluation of existing and new vaccines to prevent mortality of neonates and in pregnancy. Recently available recombinant vaccine was seems to be side effect and cost effective. The starch polymer in the form of microspheres was preferred in order to replace the alum to elicit sustained immune response because alum induces local granuloma and hypersensitivity reaction to some individual. We have employed microencapsulation technique by using 0.5% ml glutaraldehyde as a crosslinking agent. The particle size was analyzed as 40.23μm. Invitro studies was analyzed by SEM, stabilities studies Immunogenicity studies was carried out by incubating the sample, centrifuged and tested for an antigen and the Compatibility study was performed by Infrared Spectroscopy, the antigen integrity was studied by SDS PAGE and ELISA. Immunoglobulin titer values was found out ( IgG, IgA,IgM, IgE) to show the increase level of antibody response.

References

1. Davis SS Polymeric system for vaccine delivery
Res Immuol, 1998, 149: 49-52.
2. Fiegel J, Fu J, Hanes J Journals of Control.
Release, 2004, 96: 411-423.
3. Hans J, Hagan D, Preparation and
Characterization of polymeric antigen delivery,
1997, Adv. Drug Del. Rev. 28, 97-119.
4. Lewis, DH, Chasin M, Langer R Biodegradable
Polymers as antigen Delivery Systems. Adv Drug
Del Rev, 1998, 27: 91-116.& Microparticulate as
a carriers for vaccines International journal of
Controlled delivery system ,1998,1(2) 69-75.
5. Morein B, Villacrks EM, Sjblander A Novel
adjuvants and vaccine delivery systems.
Veterinary Immunology and Immunopathology,
1996, 54: 373-384.
6. Sacchez A, Villamayor B, Guo Y, McIver J, Alonso
MJ Formulation strategies for the stabilization
of tetanus toxoid in. Poly (D, L-lactatide-coglycolide) microspheres. International journal of pharmaceutics, 1999, 185: 255-266.
7. Seong SY, Cho NH, Chun KH, Kim YH Novel mucosal immunization with polysaccharide protein conjugates entrapped in alginate microspheres. Journal of Controlled Release,1998, 53: 215–224.
8. Singh M, O’Hagan D, Julia R, Briones M, Ugozzoli M, Kazzaz J, Barackman JA combination of biodegradable micro particles and MF59 as systemic adjuents for recombinant IgD from HSV-2. Vaccine, 1998, 19: 16.
9. Singh M, O’Hagan D The preparation and characterization of polymeric antigen delivery systems for oral administration Advanced Drug Delivery Reviews, 1998, 34: 285–304.
10. Yadav AV, Montae HH. Development of Biodegradable Starch Microsphere for intra nasal Indian journal of pharmaceutical sciences,2008, 70: 170-174
11. Dubey RC Quantitative protein estimation. In: Textbook of Biotechnology, 2006,.S.Chand & Company LTD, Ram Nagar, New Delhi, 110055 pp: 634-635.

Downloads

Published

2011-03-31

How to Cite

Nirmala, L., Nayak, V., Deecaraman, D., & Subhadeep, D. (2011). Immunoevaluation and Characterization of Tetanus Toxoid by using Natural polymer as an adjuvant: Immunoevaluation and Characterization of Tetanus Toxoid. National Journal of Integrated Research in Medicine, 2(1), 42–48. Retrieved from http://www.nicpd.ac.in/ojs-/index.php/njirm/article/view/1896

Issue

Section

Original Articles