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The advancement of in vitro lipolysis : two-step flow-through method for the evaluation of lipid-based drug delivery systems
ID
Rede, Katarina
(
Avtor
),
ID
Gašperlin, Mirjana
(
Avtor
),
ID
Bogataj, Marija
(
Avtor
),
ID
Bolko Seljak, Katarina
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(2,07 MB)
MD5: CD7FB05FDDA89CCB0C85A8AFA156A393
URL - Izvorni URL, za dostop obiščite
https://www.mdpi.com/1999-4923/17/5/545
Galerija slik
Izvleček
Objectives: A novel two-step flow-through in vitro lipolysis model was developed for the evaluation of drug release from a self-microemulsifying drug delivery system (SMEDDS). Methods: Firstly, the SMEDDS was dispersed in an acidic medium. Subsequently, the pH was increased, and a lipolytic reaction was immediately initiated, accompanied by medium flow onset. The latter enabled increase of the initial low pH of the medium, improving the physiological relevance of the method by simulating dosage form retainment in the stomach and transfer to the duodenum, which is very important for a weakly basic active pharmaceutical ingredient (API) incorporated in an SMEDDS. Results: Conversely to the traditional pH-stat in vitro lipolysis, the developed method is not established on titration, as the reaction vessel pH is regulated by a medium flow and buffer capacity. Individual parameters, such as pancreatin activity, buffer capacity, and medium shift, were researched using traditional pH-stat in vitro lipolysis prior to their implementation in the flow-through setup. Conclusions: The concentration of the solubilized model API, carvedilol, was increased as pancreatin activity decreased and as buffer capacity increased. The ratios between release profiles obtained under different conditions utilizing the pH-stat and novel two-step flow-through in vitro lipolysis were comparable; however, the differences were more pronounced in the flow-through method.
Jezik:
Angleški jezik
Ključne besede:
in vitro lipolysis
,
flow-through dissolution system
,
drug release
,
self-microemulsifying drug delivery systems
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:
2025
Št. strani:
21 str.
Številčenje:
Vol. 17, iss. 5, art. 545
PID:
20.500.12556/RUL-168758
UDK:
615.015.14+544.351.3
ISSN pri članku:
1999-4923
DOI:
10.3390/pharmaceutics17050545
COBISS.SI-ID:
234023939
Datum objave v RUL:
23.04.2025
Število ogledov:
411
Število prenosov:
92
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Pharmaceutics
Skrajšan naslov:
Pharmaceutics
Založnik:
MDPI
ISSN:
1999-4923
COBISS.SI-ID:
517949977
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
in vitro lipoliza
,
pretočni sistem raztapljanja
,
sproščanje zdravila
,
samomikroemulgirajoči sistemi za dostavo zdravil
,
dostavni sistemi
,
topnost
Projekti
Financer:
ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:
P1-0189
Naslov:
Farmacevtska tehnologija: od dostavnih sistemov učinkovin do terapijskih izidov zdravil pri otrocih in starostnikih
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