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Fabrication of Pulsatile Polymeric Microparticles Encapsulating Rabies Antigen
Published on: May 12, 2023
[Development of microencapsulating measles live vaccine]
Abstract:
Designing of non-injection methods of immunization against measles has recently turned into a topical issue. Development of mucosal vaccines ensuring the "entry gate" immunity, which is highly effective in airborne infection, is in the focus of attention. The authors developed a method of microencapsulating the viral particles into the matrix of pH-dependent polymers. Microencapsulated live measles vaccine shaped as 0.6-2.0 microm particles was obtained. The specific activity of measles virus in the drug was 3.36-4.31 log TCD50/0.5 ml. In subcutaneous immunization of guinea pigs with capsules, the best results were obtained in a single administration of vaccine based on ethylcrylate, sodium alginate/ chitosan and sodium slaginate/HMDA. In the intranasal administration of vaccine based on sodium alginate/spermin and sodium alginate/HMDA, there was a need in 2 and 3 stages of immunization.
Insights
Developing non-injection measles vaccines is crucial. Microencapsulating measles virus in pH-dependent polymers created a novel vaccine, showing promise for effective immunization.
Area of Science:
- Immunology
- Vaccinology
- Biotechnology
Background:
- Non-injection immunization methods are increasingly important for measles prevention.
- Mucosal vaccines offer potential for effective "entry gate" immunity against airborne infections like measles.
Purpose of the Study:
- To develop and evaluate microencapsulated measles vaccines for non-invasive administration.
- To investigate the efficacy of pH-dependent polymer-based microcapsules for measles virus delivery.
Main Methods:
- Microencapsulation of live measles virus particles within pH-dependent polymer matrices.
- Characterization of microcapsule particle size (0.6-2.0 microm) and viral activity (3.36-4.31 log TCD50/0.5 ml).
- Subcutaneous and intranasal immunization studies in guinea pigs using various polymer formulations.
Main Results:
- Single subcutaneous administration of ethylcrylate, sodium alginate/chitosan, or sodium alginate/HMDA microcapsules showed promising results.
- Intranasal administration required multiple immunizations (2-3 stages) for sodium alginate/spermin and sodium alginate/HMDA formulations.
- Successful creation of microencapsulated live measles vaccine with preserved viral activity.
Conclusions:
- Microencapsulation in pH-dependent polymers is a viable strategy for developing non-injection measles vaccines.
- Specific polymer formulations demonstrate differential efficacy depending on the administration route (subcutaneous vs. intranasal).
- Further research into optimized formulations and administration protocols is warranted for intranasal delivery.
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