» Articles » PMID: 31540243

A Novel Framework to Aid the Development of Design Space Across Multi-Unit Operation Pharmaceutical Processes-A Case Study of Saponins Immediate Release Tablet

Overview
Journal Pharmaceutics
Publisher MDPI
Date 2019 Sep 22
PMID 31540243
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

The fundamental principle of Quality by Design (QbD) is that the product quality should be designed into the process through an upstream approach, rather than be tested in the downstream. The keystone of QbD is process modeling, and thus, to develop a process control strategy based on the development of design space. Multivariate statistical analysis is a very useful tool to support the implementation of QbD in pharmaceutical process development and manufacturing. Nowadays, pharmaceutical process modeling is mainly focused on one-unit operations and system modeling for the development of design space across multi-unit operations is still limited. In this study, a general procedure that gives a holistic view for understanding and controlling the process settings for the entire manufacturing process was investigated. The proposed framework was tested on the Saponins immediate release tablet (PNS IRT) production process. The critical variables and the critical units acting on the process were identified according to the importance of explaining the variability in the multi-block partial least squares path model. This improved understanding of the process by illustrating how the properties of the raw materials, the process parameters in the wet granulation and the compaction and the intermediate properties affect the tablet properties. Furthermore, the design space was developed to compensate for the variability source from the upstream. The results demonstrated that the proposed framework was an important tool to gain understanding and control the multi-unit operation process.

Citing Articles

Understanding of Wetting Mechanism Toward the Sticky Powder and Machine Learning in Predicting Granule Size Distribution Under High Shear Wet Granulation.

Jiang Y, Zhou K, He H, Zhou Y, Tang J, Guan T AAPS PharmSciTech. 2024; 25(8):253.

PMID: 39443400 DOI: 10.1208/s12249-024-02973-w.


Pharmaceutical application of multivariate modelling techniques: a review on the manufacturing of tablets.

Shi G, Lin L, Liu Y, Chen G, Luo Y, Wu Y RSC Adv. 2022; 11(14):8323-8345.

PMID: 35423324 PMC: 8695199. DOI: 10.1039/d0ra08030f.


In-Depth Understanding of Granule Compression Behavior under Variable Raw Material and Processing Conditions.

Casian T, Iurian S, Gavan A, Porfire A, Pop A, Crisan S Pharmaceutics. 2022; 14(1).

PMID: 35057072 PMC: 8780340. DOI: 10.3390/pharmaceutics14010177.


Effect of Spray Drying Conditions on Physical Properties of Saponin (PNS) Powder and the Intra-Batch Dissolution Variability of PNS Hydrophilic Matrix Tablet.

Yang M, Xu B, Wang X, Li W, Cao J, Li W Drug Des Devel Ther. 2021; 15:1425-1440.

PMID: 33833502 PMC: 8019609. DOI: 10.2147/DDDT.S295825.


Quality Assessment of Different Species and Differently Prepared Slices of Zedoray Rhizome by High-Performance Liquid Chromatography and Colorimeter with the Aid of Chemometrics.

Sun F, Yang X, Liu F, Zhang Y, Wang S, Cao H J Anal Methods Chem. 2020; 2020:8866250.

PMID: 33062375 PMC: 7542477. DOI: 10.1155/2020/8866250.


References
1.
Yu L . Pharmaceutical quality by design: product and process development, understanding, and control. Pharm Res. 2008; 25(4):781-91. DOI: 10.1007/s11095-007-9511-1. View

2.
Mortier S, Van Bockstal P, Corver J, Nopens I, Gernaey K, Beer T . Uncertainty analysis as essential step in the establishment of the dynamic Design Space of primary drying during freeze-drying. Eur J Pharm Biopharm. 2016; 103:71-83. DOI: 10.1016/j.ejpb.2016.03.015. View

3.
Jiang C, Flansburg L, Ghose S, Jorjorian P, Shukla A . Defining process design space for a hydrophobic interaction chromatography (HIC) purification step: application of quality by design (QbD) principles. Biotechnol Bioeng. 2010; 107(6):985-97. DOI: 10.1002/bit.22894. View

4.
Djuris J, Djuric Z . Modeling in the quality by design environment: Regulatory requirements and recommendations for design space and control strategy appointment. Int J Pharm. 2017; 533(2):346-356. DOI: 10.1016/j.ijpharm.2017.05.070. View

5.
Harms J, Wang X, Kim T, Yang X, Rathore A . Defining process design space for biotech products: case study of Pichia pastoris fermentation. Biotechnol Prog. 2008; 24(3):655-62. DOI: 10.1021/bp070338y. View