In situ gels as a modern method of intranasal vaccine delivery
- Authors: Bakhrushina E.O.1, Mikhel J.B.1, Kondratieva V.M.2, Demina N.B.1, Grebennikova T.V.2
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Affiliations:
- I.M. Sechenov First Moscow State Medical University of the Ministry of Health of Russia
- National Research Center of Epidemiology and Microbiology named after Honorary Academician N.F. Gamaleya of the Ministry of Health of Russia
- Issue: Vol 67, No 5 (2022)
- Pages: 395-402
- Section: REVIEWS
- URL: https://journals.rcsi.science/0507-4088/article/view/118234
- DOI: https://doi.org/10.36233/0507-4088-139
- ID: 118234
Cite item
Abstract
The continuous emergence of new pathogens and the evolution of microbial drug resistance make it absolutely necessary to develop innovative, effective vaccination strategies. Use of nasal vaccination can increase convenience, safety, cause both local and systemic immune reactions. Intranasal administration nevertheless has a number of shortcomings that can be overcome by using the latest achievements of pharmaceutical science. One of the aspects of such solution may be the use of systems for the production of intranasal vaccines in situ – polymer compositions that provide a directed sol-gel transition controlled by the physiological conditions of the nasal cavity. At the same time, the gelation of the administered dose in contact with the nasal mucosa involves prolonged exposure of the drug at the injection site, greater mucoadhesion, counteraction to mucociliary clearance, modified and more complete release. A number of both foreign and domestic manufacturers produces polymers such as chitosan, gums, polyoxyethylene and polyoxypropylene block copolymers (poloxamers, proxanols), carbomers. For effective pharmaceutical development of new intranasal IBD delivery systems corresponding to the QbD concept, not only the knowledge of the range of excipients is necessary, but also simple, accessible, and reproducible methods for determining indicators that define the critical parameters of such delivery systems. In accordance with the conducted scientific search, the main indicators of standardization of in situ intranasal systems were identified: temperature and time of gel formation, gel strength, rheological characteristics, mucoadhesion, release, nasal mucociliary clearance time.
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##article.viewOnOriginalSite##About the authors
Elena O. Bakhrushina
I.M. Sechenov First Moscow State Medical University of the Ministry of Health of Russia
Author for correspondence.
Email: bakhrushina_e_o@staff.sechenov.ru
ORCID iD: 0000-0001-8695-0346
PhD, Associate Professor, Associate Professor of the department of Pharmaceutical Technologies
Russian Federation, 119048, MoscowJoseph B. Mikhel
I.M. Sechenov First Moscow State Medical University of the Ministry of Health of Russia
Email: mikheliosif@gmail.com
ORCID iD: 0000-0002-2866-0049
Student of the 5th year of the OD of the Institute of Pharmacy. A.P. Nelyubina
Russian Federation, 119048, MoscowValeria M. Kondratieva
National Research Center of Epidemiology and Microbiology named after Honorary Academician N.F. Gamaleya of the Ministry of Health of Russia
Email: 1999valeriak@mail.ru
ORCID iD: 0000-0001-9163-4516
Graduate student
Russian Federation, 123098, MoscowNatalia B. Demina
I.M. Sechenov First Moscow State Medical University of the Ministry of Health of Russia
Email: demina_n_b@staff.sechenov.ru
ORCID iD: 0000-0003-4307-8791
Doctor of Pharmaceutical Sciences, Professor, Professor at the department of Pharmaceutical and Biomedical Technology
Russian Federation, 119048, MoscowTatyana V. Grebennikova
National Research Center of Epidemiology and Microbiology named after Honorary Academician N.F. Gamaleya of the Ministry of Health of Russia
Email: t_grebennikova@mail.ru
ORCID iD: 0000-0002-6141-9361
Doctor of Biological Sciences, Professor, Corresponding Member RAS, Head Laboratory of Molecular Diagnostics, Head of department of Molecular Vaccinology and Immunodiagnostics
Russian Federation, 123098, MoscowReferences
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