Quality by Design Based Formulation Study of Meloxicam-Loaded Polymeric Micelles for Intranasal Administration

Our study aimed to develop an "ex tempore" reconstitutable, viscosity enhancer- and preservative-free meloxicam (MEL)-loaded polymeric micelle formulation, via Quality by Design (QbD) approach, exploiting the nose-to-brain pathway, as a suitable tool in the treatment of neuroinflammation....

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Main Authors: Bence Sipos (Author), Piroska Szabó-Révész (Author), Ildikó Csóka (Author), Edina Pallagi (Author), Dorina Gabriella Dobó (Author), Péter Bélteky (Author), Zoltán Kónya (Author), Ágota Deák (Author), László Janovák (Author), Gábor Katona (Author)
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Published: MDPI AG, 2020-07-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Bence Sipos  |e author 
700 1 0 |a Piroska Szabó-Révész  |e author 
700 1 0 |a Ildikó Csóka  |e author 
700 1 0 |a Edina Pallagi  |e author 
700 1 0 |a Dorina Gabriella Dobó  |e author 
700 1 0 |a Péter Bélteky  |e author 
700 1 0 |a Zoltán Kónya  |e author 
700 1 0 |a Ágota Deák  |e author 
700 1 0 |a László Janovák  |e author 
700 1 0 |a Gábor Katona  |e author 
245 0 0 |a Quality by Design Based Formulation Study of Meloxicam-Loaded Polymeric Micelles for Intranasal Administration 
260 |b MDPI AG,   |c 2020-07-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics12080697 
500 |a 1999-4923 
520 |a Our study aimed to develop an "ex tempore" reconstitutable, viscosity enhancer- and preservative-free meloxicam (MEL)-loaded polymeric micelle formulation, via Quality by Design (QbD) approach, exploiting the nose-to-brain pathway, as a suitable tool in the treatment of neuroinflammation. The anti-neuroinflammatory effect of nose-to-brain NSAID polymeric micelles was not studied previously, therefore its investigation is promising. Critical product parameters, encapsulation efficiency (89.4%), Z-average (101.22 ± 2.8 nm) and polydispersity index (0.149 ± 0.7) and zeta potential (−25.2 ± 0.4 mV) met the requirements of the intranasal drug delivery system (nanoDDS) and the targeted profile liquid formulation was transformed into a solid preservative-free product by freeze-drying. The viscosity (32.5 ± 0.28 mPas) and hypotonic osmolality (240 mOsmol/L) of the reconstituted formulation provides proper and enhanced absorption and probably guarantees the administration of the liquid dosage form (nasal drop and spray). The developed formulation resulted in more than 20 times faster MEL dissolution rate and five-fold higher nasal permeability compared to starting MEL. The prediction of IVIVC confirmed the great potential for in vivo brain distribution of MEL. The nose-to-brain delivery of NSAIDs such as MEL by means of nanoDDS as polymeric micelles offers an innovative opportunity to treat neuroinflammation more effectively. 
546 |a EN 
690 |a NSAID 
690 |a nanoDDS 
690 |a polymeric micelle 
690 |a quality by design 
690 |a preformulation study 
690 |a freeze-drying 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 12, Iss 8, p 697 (2020) 
787 0 |n https://www.mdpi.com/1999-4923/12/8/697 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/708a73b60fc44a44b9d31b018a3fd8c0  |z Connect to this object online.