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ORIGINAL ARTICLE

Chitosan–HPMC-blended microspheres as a vaccine carrier for the delivery of tetanus toxoid

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Pages 517-523 | Received 06 Aug 2014, Accepted 12 Sep 2014, Published online: 04 Dec 2014

Figures & data

Table I. Grouping and combinations used for in vivo immunogenicity study (n = 9).

Figure 1. Effect of morphology on SEM image of chitosan-HPMC blended empty microspheres. (A) 7/3, (B) 9/1, (C) 8/2.

Figure 1. Effect of morphology on SEM image of chitosan-HPMC blended empty microspheres. (A) 7/3, (B) 9/1, (C) 8/2.

Figure 2. SEM image of TT-encapsulated chitosan–HPMC microspheres.

Figure 2. SEM image of TT-encapsulated chitosan–HPMC microspheres.

Figure 3. SDS-PAGE analysis of TT. Lane 1: standard TT, Lane 2: TT extracted from chitosan–HPMC microspheres without heparin, Lane 3: TT extracted from chitosan–HPMC microspheres.

Figure 3. SDS-PAGE analysis of TT. Lane 1: standard TT, Lane 2: TT extracted from chitosan–HPMC microspheres without heparin, Lane 3: TT extracted from chitosan–HPMC microspheres.

Figure 4. Cumulative percentage release profiles of TT encapsulated in to chitosan–HPMC microspheres with or without heparin.

Figure 4. Cumulative percentage release profiles of TT encapsulated in to chitosan–HPMC microspheres with or without heparin.

Table II. The antibody levels of immune guinea pig sera after first bleeding at 6 months.

Table III. Antibody levels of immune guinea pig sera 9 months after primary immunization.

Table IV. Antibody levels of immune guinea pig sera 1 year after primary immunization with second booster dose.

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