Sistema de administración oral del toxoide tetánico

Autores/as

  • VJ AHIRE Center of Relevance and Excellence in New Drug Delivery Systems (TIFAC-CORE in NDDS), Department of Pharmacy, The Maharaja Sayajirao University of Baroda, Vadodara, India.
  • JB DOSHI Toxoid Purifi cation Department, Serum Institute of India Pvt Ltd., 212/2, Soli Poonawala Road, Hadapsar, Pune, India
  • SD RAVETKAR Toxoid Purifi cation Department, Serum Institute of India Pvt Ltd., 212/2, Soli Poonawala Road, Hadapsar, Pune, India
  • KK SAWANT Center of Relevance and Excellence in New Drug Delivery Systems (TIFAC-CORE in NDDS), Department of Pharmacy, The Maharaja Sayajirao University of Baroda, Vadodara, India.

Palabras clave:

Quitosano, Inmunidad mucosal, Inmunidad sistémica, Toxoide tetánico

Resumen

Se ha estudiado la respuesta sistémica e inmune local frente al toxoide tetánico (TT) encapsulado en micropartículasde quitosano (CS), (CS-TT) preparado mediante reticulación iónica con tripolifosfato de sodio (STPP). Se administrarona ratones micropartículas CS-TT, TT en tampón de fosfato salino (PBS) y micropartículas CS simples, y seadministró TT (adsorbido) por vía intramuscular. Se analizó el suero para determinar los niveles de IgG anti-TTy se realizó un lavado intestinal para determinar los niveles de IgA anti-TT mediante la técnica ELISA. El estudiodemuestra la efi cacia del sistema de suspensión de micropartículas de quitosano, con TT, para inducir IgA en elintestino e IgC en la circulación sistémica.

Descargas

Los datos de descargas todavía no están disponibles.

Citas

O’Hagan DT. Microparticles and polymers for the mucosal delivery of vaccines. Adv Drug Deliv Rev 1998; 34: 305-320.

Van der Lubben IM, Kersten G, Fretz MM, Beuvery C, Verhoef JC, Junginger HE. Chitosan microparticles for Mucosal vaccination against diphtheria: oral and nasal efficacy studies in mice. Vaccine 2003; 21: 1400-1408.

Tabata Y, Inoue Y, Ikada Y. Size effect on systemic and mucosal immune responses induced by oral administration of biodegradable microspheres. Vaccine 1996; 14(17/18): 1677-1685.

Damge C, Aprahamian M, Humbert W, Pinget M. Ileal uptake of polyalkylcyanoacrylate nanocapsules in the rat. J Pharm Pharmacol 2000; 52: 1049-1056.

Eldridge JH, Hammond CJ, Meulbroek JA, Staas JK, Gilley RM, Tice TR. Controlled release in the gut associated lymphoid tissues. I. Orally administered biodegradable microspheres target the Peyer’s patches. J Contr Rel 1990;11: 205-214.

Ahire VJ, Sawant KK. Development of Rocket Electrophoresis Technique as an Analytical Tool in Preformulation Study of Tetanus Vaccine Formulation. Drug Dev Ind Pharm 2006; 32(7): 799-808.

Radi H, Mansoor A. Chitosan based gastrointestinal delivery systems. J Contr Rel 2003; 89: 151-165.

Singla AK, Chawla Chitosan M: Some pharmaceutical and biological aspects- An update. J Pharm Pharmacol 2001; 53:1047-1067.

Coppi G, Iannuccelli V, Leo E, Bernabei MT, Cameroni R. Protein immobilization in crosslinked alginate microparticles. J Microencap 2002; 19(1): 37-44.

Wassilak SGF, Roper MH, Murphy TV, Orenstein WA. Tetanus toxoid. In Vaccines; Plotkin SA, Mortimer EA, Ed., Saunders: Philadelphia: 4th ed., 2002: 745-781.

Esparaza I, Kissel T. Parameters affecting the immunogenicity of microencapsulated tetanus toxoid. Vaccine 1992; 10(10): 714-720.

Chang AC, Gupta RK. Stabilization of Tetanus Toxoid in Poly(DL-lactic-co-glycolic acid) Microspheres for the Controlled Release of Antigen. J Pharm Sci 1996; 85(2):129-132.

Grewal HMS, Karlsen TH, Vetvik H, Ahren C, Gjessing HK, Sommerfelt H, Haneberg B. Measurement of specific IgA in fecal Extracts and intestinal lavage fluid for monitoring of mucosal immune responses. J Immun Methods 2000; 239: 53-62.

Forrest BD. Effects of sample processing on the measurement of specific intestinal IgA immune response. Vaccine 1992; 10(11): 802-805.

Xing DKL, McLellan K, Corbel MJ, Sesardic D. Estimation of Antigenic Tetanus Toxoid Extracted from Biodegradable Microspheres. Biologicals 1996; 24: 57-65.

Xu Y, Du Y. Effect of molecular structure of chitosan on protein delivery properties of chitosan nanoparticles. Int J Pharm 2003; 250: 215-226.

Berger J, Resist M, Mayer JM, Felt O, Peppas NA, Gurny R. Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications. Eur J Pharm Biopharm 2004; 57: 19-34.

Liu WG, Kang DY. Chitosan and Its derivatives – a promising non viral vector for gene transfection. J Contr Rel 2002; 83:1-11.

Calvo P, Renuman-Lopez C, Vila-Jato JL, Alonso MJ. Novel hydrophilic chitosan-polyethylene oxide nanoparticles as protein carriers. J Appl Polym Sci 1997; 63: 125-132.

Elgersma AV, Zsom RLJ, Norde W, Lyklema J. The adsorption of bovine serum albumin on positively and negatively charged polystyrene lattices. J Colloid Int Sci 1990; 138: 145-156.

Barichello JM, Moriko M, Takayama K, Nagai T. Encapuslation of hydrophilic and lipophilic drugs in PLGA nanoparticles by the nanoprecipitation method. Drug Dev Ind Pharm 1999; 25: 471-476.

Roberts GAF. Chitin Chemistry, MacMillan Press: London, 1992: 203-206.

Mi FL, Shyu SS, Wong TB, Jang SF, Lee ST, Lu KT. Chitosan polyelectrolyte complexation for the preparation of gel beads and controlled release of anti-cancer drug. II Effect of pH-dependent ionic crosslinking or interpolymer complex using tripolyphosphate or polyphosphate as reagent. J Apl Polym Sci 1999; 74:1093-1107.

Brange J, Langkjaer L. Chemical stability of insulin, 3. Influence of excipients, formulation and pH. Act Pharm Nord 1992; 4: 149-158.

Ma Z, Yeoh HH, Lim LY. Formulation pH modulates the interaction of Insulin with chitosan nanoparticles. J Pharm Sci 2002; 91(6): 1396-1404.

Descargas

Publicado

2007-09-20

Cómo citar

1.
AHIRE V, DOSHI J, RAVETKAR S, SAWANT K. Sistema de administración oral del toxoide tetánico. Ars Pharm [Internet]. 20 de septiembre de 2007 [citado 8 de mayo de 2024];48(3):275-96. Disponible en: https://revistaseug.ugr.es/index.php/ars/article/view/4991

Número

Sección

Artículos Originales