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Matrixing designs for shelf-life determination of parenteral drug product : a comparative analysis of full and reduced stability testing design
ID
Pavčnik, Lara
(
Avtor
),
ID
Locatelli, Igor
(
Avtor
),
ID
Trdan Lušin, Tina
(
Avtor
),
ID
Roškar, Robert
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(697,77 KB)
MD5: 81394D5CDAE888046F11CA003BBBB5AD
URL - Izvorni URL, za dostop obiščite
https://www.mdpi.com/1999-4923/16/9/1117
Galerija slik
Izvleček
This article highlights the applicability of matrixing designs in stability studies for parenteral medications. The traditional approach involves extensive testing over the product’s shelf-life. However, matrixing designs offer an alternative approach where only a fraction of samples is tested at each time point. The study conducted in this article focused on three parenteral medications and examined stability data under long-term condition. Degradation products were identified as critical parameter, and kinetics of degradation varied among the selected products. A systematic methodology was adopted to evaluate the data using different matrixing designs. The regression models obtained were assessed using statistical parameters S and R$^2$. Also, each of the 28 matrixing designs were compared to the full design with statistical parameter RMSE and the shelf-life. The results confirmed that each of the evaluated matrixing designs can be applied, whether degradation product shows a linear or non-linear increase, and demonstrated that a reduction of two time points per batch is the most appropriate. In conclusion, this research contributes to the understanding of utilizing reduced matrixing designs in stability studies for parenteral medications and can be an effective strategy to reduce costs and time of stability testing while maintaining the necessary level of precision and reliability.
Jezik:
Angleški jezik
Ključne besede:
shelf-life
,
matrixing design
,
ICH Q1D
,
stability study
,
degradation kinetics
,
parenteral dosage forms
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:
12 str.
Številčenje:
Vol. 16, iss. 9, art. 1117
PID:
20.500.12556/RUL-162173
UDK:
615
ISSN pri članku:
1999-4923
DOI:
10.3390/pharmaceutics16091117
COBISS.SI-ID:
206005507
Datum objave v RUL:
19.09.2024
Število ogledov:
127
Število prenosov:
31
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:
rok uporabnosti
,
matrično oblikovanje
,
ICH Q1D
,
študija stabilnosti
,
kinetika razgradnje
,
parenteralne dozirne oblike
,
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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