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Freeze-dried nanocrystal dispersion of novel deuterated pyrazoloquinolinone ligand (DK-I-56-1) : process parameters and lyoprotectant selection through the stability study
ID
Mitrović, Jelena R.
(
Author
),
ID
Bjelošević Žiberna, Maja
(
Author
),
ID
Ahlin Grabnar, Pegi
(
Author
),
ID
Planinšek, Odon
(
Author
),
ID
Savić, Snežana D.
(
Author
), et al.
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https://www.sciencedirect.com/science/article/pii/S0928098723001872
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Abstract
Recently, nanocrystal dispersions have been considered as a promising formulation strategy to improve the bioavailability of the deuterated pyrazoloquinolinone ligand DK-I-56-1 (7-methoxy-2-(4-methoxy-d3-phenyl)-2,5-dihydro-3H-pyrazolo[4,3-c]quinolin-3-one). In the current study, the freeze-drying process (formulation and process parameters) was investigated to improve the storage stability of the previously developed formulation. Different combinations of lyoprotectant (sucrose or trehalose) and bulking agent (mannitol) were varied while formulations were freeze-dried under two conditions (primary drying at -10°C or -45°C). The obtained lyophilizates were characterized in terms of particle size, solid state properties and morphology, while the interactions within the samples were analyzed by Fourier transform infrared spectroscopy. In the preliminary study, three formulations were selected based on the high redispersibility index values (around 95%). The temperature of primary drying had no significant effect on particle size, but stability during storage was impaired for samples dried at -10°C. Samples dried at lower temperature were more homogeneous and remained stable for three months. It was found that the optimal ratio of sucrose or trehalose to mannitol was 3:2 at a total concentration of 10% to achieve the best stability (particle size < 1.0 μm, polydispersity index < 0.250). The amorphous state of lyoprotectants probably provided a high degree of interaction with nanocrystals, while the crystalline mannitol provided an elegant cake structure. Sucrose was superior to trehalose in maintaining particle size during freeze-drying, while trehalose was more effective in keeping particle size within limits during storage. In conclusion, results demonstrated that the appropriate combination of sucrose/trehalose and mannitol together with the appropriate selection of lyophilization process parameters could yield nanocrystals with satisfactory stability.
Language:
English
Keywords:
pyrazoloquinolinone
,
nanocrystals
,
freeze-drying
,
sucrose
,
trehalose
,
mannitol
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
FFA - Faculty of Pharmacy
Publication status:
Published
Publication version:
Version of Record
Year:
2023
Number of pages:
12 str.
Numbering:
Vol. 189, art. 106557
PID:
20.500.12556/RUL-148364
UDC:
66.017-022.513.2:620.3
ISSN on article:
0928-0987
DOI:
10.1016/j.ejps.2023.106557
COBISS.SI-ID:
161164291
Publication date in RUL:
18.08.2023
Views:
1096
Downloads:
50
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Record is a part of a journal
Title:
European Journal of Pharmaceutical Sciences
Shortened title:
Eur. j. pharm. sci.
Publisher:
Elsevier
ISSN:
0928-0987
COBISS.SI-ID:
17553413
Licences
License:
CC BY-NC-ND 4.0, Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
Link:
http://creativecommons.org/licenses/by-nc-nd/4.0/
Description:
The most restrictive Creative Commons license. This only allows people to download and share the work for no commercial gain and for no other purposes.
Secondary language
Language:
Slovenian
Keywords:
pirazolokinolinon
,
nanokristali
,
liofilizacija
,
saharoza
,
trehaloza
,
manitol
,
farmacevtske oblike
,
nanomateriali
Projects
Funder:
Other - Other funder or multiple funders
Funding programme:
Science Fund of the Republic of Serbia
Project number:
7749108
Name:
Neuroimmune aspects of mood, anxiety and cognitive effects of leads/drug candidates acting at GABAA and/or sigma-2 receptors: in vitro/in vivo delineation by nano- and hiPSC-based platforms
Acronym:
NanoCellEmoCog
Funder:
NIH - National Institutes of Health
Project number:
R01 NS076517
Funder:
NIH - National Institutes of Health
Project number:
R01 MH096463
Funder:
NSF - National Science Foundation
Funding programme:
Division of Chemistry
Project number:
CHE-1625735
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