the mucosal adjuvant potential of cross-linked dextran microspheres as dry powder
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abstract
objective(s) the immunoadjuvant potential of cross-linked dextran microspheres (cdm) as absorption enhancer and quillaja saponins (qs) as immunomodulator adjuvant was evaluated. materials and methods cdm loaded or tetanus-mixed toxoid (tt) or quillaja saponin (qs) were nasally administered to rabbits in dry powder form, three times in 2 weeks interval and serum igg and nasal lavage siga titers were determined by elisa. results the highest serum igg titer was induced by parenteral immunization through alum adsorbed tt (p< 0.001). among nasally immunized groups, the highest serum igg titer was induced by (tt+qs)cdm (p< 0.01). mixing of cdm with tt+qs powders (cdm+tt+qs), could not induce the high serum igg titers as (tt+qs)cdm (p< 0.01). cdm loaded with tt+qs induced higher igg titers than cdm loaded with tt alone (p< 0.01). no significant difference was observed in nasal lavage siga titers of various groups. conclusion cdm microspheres loaded with tt+qs significantly increased serum anti-tt igg titers, but mixing of cdm with tt+qs powder could not increase igg titers. both qs and cdm adjuvant could not significantly increase the lavage anti-tt iga titers.
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The Mucosal Adjuvant Potential of Cross-Linked Dextran Microspheres as Dry Powder
Objective(s) The immunoadjuvant potential of cross-linked dextran microspheres (CDM) as absorption enhancer and Quillaja saponins (QS) as immunomodulator adjuvant was evaluated. Materials and Methods CDM loaded or tetanus-mixed toxoid (TT) or Quillaja saponin (QS) were nasally administered to rabbits in dry powder form, three times in 2 weeks interval and serum IgG and nasal lavage sIgA tite...
full textThe Mucosal Adjuvant Potential of Cross-Linked Dextran Microspheres as Dry Powder
OBJECTIVES The immunoadjuvant potential of cross-linked dextran microspheres (CDM) as absorption enhancer and Quillaja saponins (QS) as immunomodulator adjuvant was evaluated. MATERIALS AND METHODS CDM loaded or tetanus-mixed toxoid (TT) or Quillaja saponin (QS) were nasally administered to rabbits in dry powder form, three times in 2 weeks interval and serum IgG and nasal lavage sIgA titers ...
full textMucosal Adjuvant Potential of Quillaja saponins and Cross-linked Dextran Microspheres, Co-administered with Liposomes Encapsulated with Tetanus Toxoid
Intranasal vaccination is particularly a striking route for mucosal immunization, due to the ease of administration and the induction of both mucosal and humoral immunity. However, soluble antigens (Ag) are not sufficiently taken up after the nasal administration and need to be co-administered with adjuvants, penetration enhancers or encapsulated in particles. So, in this study, tetanus toxoid ...
full textMucosal Adjuvant Potential of Quillaja saponins and Cross-linked Dextran Microspheres, Co-administered with Liposomes Encapsulated with Tetanus Toxoid
Intranasal vaccination is particularly a striking route for mucosal immunization, due to the ease of administration and the induction of both mucosal and humoral immunity. However, soluble antigens (Ag) are not sufficiently taken up after the nasal administration and need to be co-administered with adjuvants, penetration enhancers or encapsulated in particles. So, in this study, tetanus toxoid ...
full textmucosal adjuvant potential of quillaja saponins and cross-linked dextran microspheres, co-administered with liposomes encapsulated with tetanus toxoid
intranasal vaccination is particularly a striking route for mucosal immunization, due to the ease of administration and the induction of both mucosal and humoral immunity. however, soluble antigens (ag) are not sufficiently taken up after the nasal administration and need to be co-administered with adjuvants, penetration enhancers or encapsulated in particles. so, in this study, tetanus toxoid ...
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Intranasal vaccination is particularly a striking route for mucosal immunization, due to the ease of administration and the induction of both mucosal and humoral immunity. However, soluble antigens (Ag) are not sufficiently taken up after the nasal administration and need to be co-administered with adjuvants, penetration enhancers or encapsulated in particles. So, in this study, tetanus toxoid ...
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Journal title:
iranian journal of basic medical sciencesجلد ۱۵، شماره ۳، صفحات ۸۷۳-۸۷۹
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