Development of an Intranasal In Situ System for Ribavirin Delivery: In Vitro and In Vivo Evaluation

Author:

Mikhel Iosif B.1ORCID,Bakhrushina Elena O.1ORCID,Petrusevich Danila A.1,Nedorubov Andrey A.2,Appolonova Svetlana A.3ORCID,Moskaleva Natalia E.3ORCID,Demina Natalia B.1,Kosenkova Svetlana I.1ORCID,Parshenkov Mikhail A.1ORCID,Krasnyuk Ivan I.1ORCID,Krasnyuk Ivan I.1

Affiliation:

1. A.P. Nelyubin Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow 119048, Russia

2. Institute of Translational Medicine and Biotechnology, I.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow 119048, Russia

3. Centre of Biopharmaceutical Analysis and Metabolomics, I.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow 119048, Russia

Abstract

Recently, ribavirin has demonstrated effectiveness in treating glioblastoma through intranasal administration utilizing the nose-to-brain delivery route. Enhancing ribavirin’s bioavailability can be achieved by utilizing intranasal stimuli-responsive systems that create a gel on the nasal mucosa. The research examined thermosensitive, pH-sensitive, and ion-selective polymers in various combinations and concentrations, chosen in line with the current Quality by Design (QbD) approach in pharmaceutical development. Following a thorough assessment of key parameters, the optimal composition of gellan gum at 0.5%, Poloxamer 124 at 2%, and purified water with ribavirin concentration at 100 mg/mL was formulated and subjected to in vivo testing. Through experiments on male rats, the nose-to-brain penetration mechanism of the active pharmaceutical ingredient (API) was elucidated, showcasing drug accumulation in the olfactory bulbs and brain.

Publisher

MDPI AG

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