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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
(
Author
),
ID
Locatelli, Igor
(
Author
),
ID
Trdan Lušin, Tina
(
Author
),
ID
Roškar, Robert
(
Author
)
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MD5: 81394D5CDAE888046F11CA003BBBB5AD
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https://www.mdpi.com/1999-4923/16/9/1117
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Abstract
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.
Language:
English
Keywords:
shelf-life
,
matrixing design
,
ICH Q1D
,
stability study
,
degradation kinetics
,
parenteral dosage forms
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
FFA - Faculty of Pharmacy
Publication status:
Published
Publication version:
Version of Record
Year:
2024
Number of pages:
12 str.
Numbering:
Vol. 16, iss. 9, art. 1117
PID:
20.500.12556/RUL-162173
UDC:
615
ISSN on article:
1999-4923
DOI:
10.3390/pharmaceutics16091117
COBISS.SI-ID:
206005507
Publication date in RUL:
19.09.2024
Views:
129
Downloads:
31
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Record is a part of a journal
Title:
Pharmaceutics
Shortened title:
Pharmaceutics
Publisher:
MDPI
ISSN:
1999-4923
COBISS.SI-ID:
517949977
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Secondary language
Language:
Slovenian
Keywords:
rok uporabnosti
,
matrično oblikovanje
,
ICH Q1D
,
študija stabilnosti
,
kinetika razgradnje
,
parenteralne dozirne oblike
,
zdravila
Projects
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P1-0189
Name:
Farmacevtska tehnologija: od dostavnih sistemov učinkovin do terapijskih izidov zdravil pri otrocih in starostnikih
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