4.7 Article

Improved Bioavailability of Montelukast through a Novel Oral Mucoadhesive Film in Humans and Mice

期刊

PHARMACEUTICS
卷 13, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/pharmaceutics13010012

关键词

montelukast; drug delivery; Alzheimer’ s disease; dementia

资金

  1. Austrian Science Funds (FWF) [P 31362-B34]
  2. IntelGenx

向作者/读者索取更多资源

The study reformulated the leukotriene receptor antagonist Montelukast (MTK) into a mucoadhesive film, which demonstrated significantly improved bioavailability in clinical studies. The oral film may reduce the non-responder rate in asthma patients and offer potential repurposing of MTK in other diseases. Additionally, the film showed promising penetration of the blood-brain barrier, suggesting potential therapeutic use in neurodegenerative diseases like dementias and stroke.
The leukotriene receptor antagonist Montelukast (MTK) is an approved medication for the treatment of asthma and allergic rhinitis. The existing marketed tablet forms of MTK exhibit inconsistent uptake and bioavailability, which partially explains the presence of a significant proportion of MTK low- and non-responders in the population. Besides that, tablets are suboptimal formulations for patients suffering from dysphagia, for example, seen in patients with neurodegenerative diseases such as Alzheimer's disease, a disease with increasing interest in repurposing of MTK. This, and the need for an improved bioavailability, triggered us to reformulate MTK. Our aim was to develop a mucoadhesive MTK film with good safety and improved pharmacological features, i.e., an improved bioavailability profile in humans as well as in a mouse model of Alzheimer's disease. We tested dissolution of the MTK mucoadhesive film and assessed pharmacoexposure and kinetics after acute and chronic oral application in mice. Furthermore, we performed a Phase I analysis in humans, which included a comparison with the marketed tablet form as well as a quantitative analysis of the MTK levels in the cerebrospinal fluid. The novel MTK film demonstrated significantly improved bioavailability compared to the marketed tablet in the clinical Phase 1a study. Furthermore, there were measurable amounts of MTK present in the cerebrospinal fluid (CSF). In mice, MTK was detected in serum and CSF after acute and chronic exposure in a dose-dependent manner. The mucoadhesive film of MTK represents a promising alternative for the tablet delivery. The oral film might lower the non-responder rate in patients with asthma and might be an interesting product for repurposing of MTK in other diseases. As we demonstrate Blood-Brain-Barrier (BBB) penetrance in a preclinical model, as well as in a clinical study, the oral film of MTK might find its use as a therapeutic for acute and chronic neurodegenerative diseases such as dementias and stroke.

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