Oral immunogenicity of the inactivated Vibrio cholerae whole-cell vaccine encapsulated in biodegradable microparticles

作者: Ming-Kung Yeh , Yu-Tien Liu , Jiin-Long Chen , Chiao-Hsi Chiang

DOI: 10.1016/S0168-3659(02)00140-2

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摘要: Abstract Vibrio cholerae (VC)-loaded microparticles as an oral vaccine delivery system were prepared with 6% w/v poly( dl -lactide-co-glycolide)(PLG) in the oil phase well 10% PVP and 5% NaCl aqueous phase, by water-in-oil-in-water emulsion/solvent extraction technique. VC was successfully entrapped trapping efficiencies up to 97.8% a loading level of 55.4±6.9 μg/mg. The microparticle particle size 3.8 μm had different distribution content core region (25.7±1.9 μg/mg) surface (6.2±0.9 μg/mg). immunogenic potential VC-loaded comparison PLG or solution evaluated adult mice immunization, which received one dose 20 mg physical mixed amphotericin B. control group solution. Serum samples collected from all tested on day immunization at 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 weeks postimmunization. Sera examined for vibriocidal antibodies microtitration Vibrio-specific serum IgG IgM assessed ELISA method. intact detected sera animals immunized VC. response specific high magnitude. Significantly higher antibody responses obtained when both B titrated against immunogenicity evoking than that only. These results demonstrate orally administered evoke activity mice. incorporation, physicochemical characterization data, animal this study may be relevant optimizing incorporation properties these targeting carriers.

参考文章(21)
Manmohan Singh, Amarjit Singh, Gursharan Prasad Talwar, Controlled Delivery of Diphtheria Toxoid Using Biodegradable Poly(D,L-Lactide) Microcapsules Pharmaceutical Research. ,vol. 8, pp. 958- 961 ,(1991) , 10.1023/A:1015832302605
M.-K. Yeh, J.-L. Chen, C.-H. Chiang, Vibrio cholerae-loaded poly(DL lactide co-glycolide) microparticles. Journal of Microencapsulation. ,vol. 19, pp. 203- 212 ,(2002) , 10.1080/02652040110081334
Ming-Kung Yeh, P.G. Jenkins, S.S. Davis, A.G.A. Coombes, Improving the delivery capacity of microparticle systems using blends of poly(DL-lactide co-glycolide) and poly(ethylene glycol) Journal of Controlled Release. ,vol. 37, pp. 1- 9 ,(1995) , 10.1016/0168-3659(95)00039-B
N. Kofler, C. Ruedl, C. Rieser, G. Wick, H. Wolf, Oral Immunization with Poly-(D,L-Lactide-Co-Glycolide) and Poly-(L-Lactic Acid) Microspheres Containing Pneumotropic Bacterial Antigens International Archives of Allergy and Immunology. ,vol. 113, pp. 424- 431 ,(1997) , 10.1159/000237618
Thomas J. Blanke, J.Russell Little, Sandi F. Shirley, Richard G. Lynch, Augmentation of murine immune responses by amphotericin B Cellular Immunology. ,vol. 33, pp. 180- 190 ,(1977) , 10.1016/0008-8749(77)90145-9
Sophie Kernéis, Anna Bogdanova, Jean-Pierre Kraehenbuhl, Eric Pringault, Conversion by Peyer's Patch Lymphocytes of Human Enterocytes into M Cells that Transport Bacteria Science. ,vol. 277, pp. 949- 952 ,(1997) , 10.1126/SCIENCE.277.5328.949
T Okutomi, T Ubukata, K Yamaoka, S Abe, H Yamaguchi, Augmentation of production of TNF-alpha and anti-tumour activity by an amphotericin B preparation for clinical use in mice. British Journal of Cancer. ,vol. 75, pp. 1613- 1616 ,(1997) , 10.1038/BJC.1997.275
David J.M. Lewis, Luiz R.R. Castello-Branco, Pavel Novotny, Gordon Dougan, Terence A. Poulton, George E. Griffin, Circulating cellular immune response to oral immunization of humans with cholera toxin B-subunit Vaccine. ,vol. 11, pp. 119- 121 ,(1993) , 10.1016/0264-410X(93)90005-I