Brain targeted rivastigmine mucoadhesive thermosensitive In situ gel: Optimization, in vitro evaluation, radiolabeling, in vivo pharmacokinetics and biodistribution
Date
2018
Journal Title
Journal ISSN
Volume Title
Type
Article
Publisher
Editions de Sante
Series Info
Journal of Drug Delivery Science and Technology
43
43
Scientific Journal Rankings
Abstract
The purpose of our investigation was to promote the bioavailability and the brain delivery of rivastigmine tartarate (RV) through optimization of mucoadhesive thermosensitive in situ gel via intranasal (IN) route. The mucoadhesive in situ gels were developed using pluronic F127 (PF127) as thermogelling agent and different mucoadhesive polymers. A full factorial design was implemented to study the influence of three factors; pluronic type at two levels (PF127, PF127/PF68), mucoadhesive polymer type at four levels (HPMC, Chitosan, Carbopol 934 and NaCMC) and mucoadhesive polymer concentration at two levels (0.5 and 1%w/v). The studied responses were sol-gel temperature, consistency, gel strength, adhesion work and T50% of drug release. In vivo pharmacokinetic and biodistribution studies of the selected formula were investigated using radiolabeling approach using normal albino mice. The optimal RV in situ gel (PF127 and 1% Carbopol 934) showed significant transnasal permeation (84%) which was reflected in better distribution to the brain (0.54 %ID/g), when compared to RV IN solution (0.16 %ID/g) and RV IV intravenous solution (0.15 %ID/g). In conclusion, the investigated results showed the potential use of mucoadhesive in situ gel as a promising system for brain targeting of RV via the transnasal delivery system. � 2017 Elsevier B.V.
Description
Scopus
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MSA Google Scholar
Keywords
Brain targeting, Intranasal, Pluronic, Radiolabeling, Rivastigmine, Thermosensitive in situ gel, carbopol 934, chitosan, gelling agent, poloxamer, rivastigmine, albino mouse, animal experiment, area under the curve, Article, drug absorption, drug bioavailability, drug brain level, drug delivery system, drug release, factorial design, flow kinetics, gelation, in vitro study, in vivo study, isotope labeling, maximum plasma concentration, mouse, mucoadhesion, mucoadhesive thermosensitive in situ gel, nonhuman, pharmacokinetic parameters, radiochemistry, synthesis, time to maximum plasma concentration