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Oral lyophilizates obtained using aggressive drying conditions : effect of excipients
ID Bjelošević Žiberna, Maja (Avtor), ID Planinšek, Odon (Avtor), ID Ahlin Grabnar, Pegi (Avtor)

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Izvleček
Orodispersible drug formulations are a current trend in the pharmaceutical industry, mostly intended for pediatric and geriatric patients. Oral lyophilizates are solid forms, intended either to be placed in the mouth or to be dispersed (or dissolved) in water before administration. The correct excipient composition is a prerequisite to provide lyophilizates with the appropriate visual appearance and disintegration time. Typically, they are composed of binders, such as gelatin and polyvinylpyrrolidone, fillers such as sucrose, mannitol, or sorbitol, taste modifiers, colorants, sweeteners, and preservatives. The main purpose of this study was to determine the optimal excipient scaffold to ensure the proper appearance of lyophilizates that have undergone aggressive drying conditions and a disintegration time of less than 3 min. In addition to mannitol and gelatin, the most frequently used binders, PVP K25, PVP K90, glycine, croscarmellose, and hydrolyzed gelatin were investigated. The results obtained revealed that lyophilizates with only mannitol and gelatin have a disintegration time that is too long, and that replacement of gelatin with PVP K25 led to friable and cracked lyophilizates. Considering disintegration time and visual appearance, lyophilizates with a mixture of gelatin, PVP K25, and mannitol (1:2:5) formed from liquid formulations with 6% (w/w) excipients were determined to be the most suitable. As a binder, PVP K25 expresses more appropriate characteristics relating to PVP K90. Addition of croscarmellose provided lyophilizates with a shorter disintegration time, whereas glycine only had a positive effect on the elegant appearance of lyophilizate cakes. Hydrolyzed gelatin was introduced with the aim of obtaining an even shorter disintegration time and at the same time an acceptable visual appearance of lyophilizates. This was achieved by lyophilization of solutions with 15% (w/w) of excipients with a hydrolyzed gelatin:PVP K25:glycine/croscarmellose:mannitol ratio of 4:2:0.5:4.5. Such lyophilizates show the highest potential for incorporation of poorly soluble and low-dose drugs.

Jezik:Angleški jezik
Ključne besede:patient-friendly dosage forms, orodispersible dosage forms, oral lyophilizates, excipient selection, hydrolyzed gelatin, aggressive drying
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:FFA - Fakulteta za farmacijo
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2023
Št. strani:8 str.
Številčenje:Vol. 82, art. 104379
PID:20.500.12556/RUL-144903 Povezava se odpre v novem oknu
UDK:661.12
ISSN pri članku:1773-2247
DOI:10.1016/j.jddst.2023.104379 Povezava se odpre v novem oknu
COBISS.SI-ID:146036995 Povezava se odpre v novem oknu
Datum objave v RUL:22.03.2023
Število ogledov:395
Število prenosov:70
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Gradivo je del revije

Naslov:Journal of drug delivery science and technology
Skrajšan naslov:J. drug deliv. sci. technol.
Založnik:Elsevier
ISSN:1773-2247
COBISS.SI-ID:2045297 Povezava se odpre v novem oknu

Licence

Licenca:CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
Opis:Najbolj omejujoča licenca Creative Commons. Uporabniki lahko prenesejo in delijo delo v nekomercialne namene in ga ne smejo uporabiti za nobene druge namene.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:pacientom prijazne dozirne oblike, orodisperzibilne dozirne oblike, peroralni liofilizati, izbor pomožnih snovi, hidrolizirana želatina, agresivno sušenje, farmacevtska industrija

Projekti

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P1-0189
Naslov:Farmacevtska tehnologija: od dostavnih sistemov učinkovin do terapijskih izidov zdravil pri otrocih in starostnikih

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:L1-3160
Naslov:Razvoj visokokoncentriranih proteinskih formulacij in vrednotenje kinetike absorpcije po subkutani aplikaciji

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