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Application of a novel dissolution medium with lipids for In vitro simulation of the postprandial gastric content
ID
Felicijan, Tjaša
(
Avtor
),
ID
Rakoše, Iva
(
Avtor
),
ID
Prislan, Manca
(
Avtor
),
ID
Locatelli, Igor
(
Avtor
),
ID
Bogataj, Marija
(
Avtor
),
ID
Trontelj, Jurij
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(3,10 MB)
MD5: D21F2D1A09444972E106D10000912C6A
URL - Izvorni URL, za dostop obiščite
https://www.mdpi.com/1999-4923/16/8/1040
Galerija slik
Izvleček
Food can change various physiological parameters along the gastrointestinal tract, potentially impacting postprandial drug absorption. It is thus important to consider different in vivo conditions during in vitro studies. Therefore, a novel dissolution medium simulating variable postprandial pH values and lipid concentrations was developed and used in this study. Additionally, by establishing and validating a suitable analytical method, the effects of these parameters on the dissolution of a model drug, cinnarizine, and on its distribution between the lipid and aqueous phases of the medium were studied. Both parameters, pH value and lipid concentration, were shown to influence cinnarizine behavior in the in vitro dissolution studies. The amount of dissolved drug decreased with increasing pH due to cinnarizine’s decreasing solubility. At pH values 5 and 7, the higher concentration of lipids in the medium increased drug dissolution, and most of the dissolved drug was distributed in the lipid phase. In all media with a lower pH of 3, dissolution was fast and complete, with a significant amount of drug distributed in the lipid phase. These results are in accordance with the in vivo observed positive food effect on cinnarizine bioavailability described in the literature. The developed medium, with its ability to easily adjust the pH level and lipid concentration, thus offers a promising tool for assessing the effect of co-ingested food on the dissolution kinetics of poorly soluble drugs.
Jezik:
Angleški jezik
Ključne besede:
fed-state medium
,
dissolution
,
SMOFlipid®
,
cinnarizine
,
HPLC analysis
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:
2024
Št. strani:
18 str.
Številčenje:
Vol. 16, iss. 8, art. 1040
PID:
20.500.12556/RUL-161043-70c21a22-8736-b676-19aa-b62e9db35e6b
UDK:
544.351.3:615
ISSN pri članku:
1999-4923
DOI:
10.3390/pharmaceutics16081040
COBISS.SI-ID:
204238339
Datum objave v RUL:
06.09.2024
Število ogledov:
182
Število prenosov:
52
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:
medij napolnjenega stanja
,
raztapljanje
,
SMOFlipid®
,
cinarizin
,
HPLC analiza
,
topnost
,
zdravila
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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