Development of meloxicam potassium-containing co-spray-dried inhalation powder with sodium stearate

Pulmonary drug delivery (PDD) has potential for both local and systemic therapy. Our research group is focus- ing on the development of dry powder inhalation (DPI) systems for PDD due to their beneficial properties. Although there is not yet a marketed inhalation product for non-steroidal anti-infla...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Benke Edit
Révész Piroska
Ambrus Rita
Dokumentumtípus: Cikk
Megjelent: 2021
Sorozat:ACTA PHARMACEUTICA HUNGARICA 91 No. 2
Tárgyszavak:
doi:10.33892/aph.2021.91.75-82

mtmt:32530842
Online Access:http://publicatio.bibl.u-szeged.hu/24595
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520 3 |a Pulmonary drug delivery (PDD) has potential for both local and systemic therapy. Our research group is focus- ing on the development of dry powder inhalation (DPI) systems for PDD due to their beneficial properties. Although there is not yet a marketed inhalation product for non-steroidal anti-inflammatory drugs (NSAIDs), their therapeutic use in sev- eral lung diseases is well established and successful DPI developments have been performed with them. Sodium stearate (NaSt) is a promising excipient for DPI development, but its role in NSAIDs has not yet been investigated. Thus, the aim was to study DPI samples produced by co-spray-drying, applying meloxicam potassium (MXP) as an NSAID drug, and different concentrations (0-2 w/w%) of NaSt. Physicochemical investigations, in vitro lung deposition, and in vitro drug release measurements were performed. It can be stated that co-spray-drying of MXP with NaSt resulted in remarkable morphological differences by increasing the concentration of NaSt, which had a positive effect on cohesive work. Further- more, applying of NaSt accelerates the dissolution in simulated lung fluid (SLF). NaSt as excipient has a future for the formulation of the DPI systems because there are in the development focus the attaintment of the higher FPF values and improvement of dissolution in SLF. 
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700 0 1 |a Ambrus Rita  |e aut 
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