Main Aspects of Pharmaceutical Development of In situ Immunobiological Drugs for Intranasal Administration
- Authors: Bakhrushina E.1, Mikhel I.1, Kondratieva V.2, Demina N.1, Grebennikova T.3, Krasnyuk Jr I.1, Krasnyuk I.1
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Affiliations:
- Institute of Pharmacy, Sechenov First Moscow State Medical University
- Centre of Epidemiology and Microbiology, The Gamaleya National Centre of Epidemiology and Microbiology
- Centre of Epidemiology and Microbiology, The Gamaleya National Centre of epidemiology and microbiology
- Issue: Vol 25, No 11 (2024)
- Pages: 1394-1405
- Section: Biotechnology
- URL: https://rjsocmed.com/1389-2010/article/view/644417
- DOI: https://doi.org/10.2174/0113892010260017231002075152
- ID: 644417
Cite item
Full Text
Abstract
Introduction:The review presents the latest developments in the area of intranasal in situ delivery systems of immunobiological drugs (IBDs). Interest in intranasal administration for IBDs has increased significantly due to the COVID-19 pandemic. However, not only intranasal delivery of vaccines is developing, but also bacteriophages, interferons, etc. In situ systems that make a selective phase transition can be a modern solution to intranasal delivery problems caused by mucociliary clearance. In addition, smart-polymers used as the main excipients in in situ systems can be used as specific adjuvants.
Methods:A scientific search was conducted on the PubMed database of medical publications for the period from 2000 to 2022, using the keywords \"intranasal in situ vaccine\"; \"intranasal in situ immunization\". There were analyzed in detail more than 70 scientific studies on intranasal in situ delivery of IBDs.
Results and Conclusions:Despite the large number of new studies, the potential of possibilities of intranasal in situ systems is not being realized. Based on the results of the literature review an algorithm was created for the development of in situ systems for intranasal delivery of IBDs. Such algorithms and the methods of study design organization described in the review will help to facilitate the R&D process and bring the drug to commercial market, which will help to improve the quality of medical care.
About the authors
Elena Bakhrushina
Institute of Pharmacy, Sechenov First Moscow State Medical University
Email: info@benthamscience.net
Iosif Mikhel
Institute of Pharmacy, Sechenov First Moscow State Medical University
Author for correspondence.
Email: info@benthamscience.net
Valeriya Kondratieva
Centre of Epidemiology and Microbiology, The Gamaleya National Centre of Epidemiology and Microbiology
Email: info@benthamscience.net
Natalia Demina
Institute of Pharmacy, Sechenov First Moscow State Medical University
Email: info@benthamscience.net
Tatyana Grebennikova
Centre of Epidemiology and Microbiology, The Gamaleya National Centre of epidemiology and microbiology
Email: info@benthamscience.net
Ivan Krasnyuk Jr
Institute of Pharmacy, Sechenov First Moscow State Medical University
Email: info@benthamscience.net
Ivan Krasnyuk
Institute of Pharmacy, Sechenov First Moscow State Medical University
Email: info@benthamscience.net
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Supplementary files
