2023
DOI: 10.3390/pharmaceutics15061587
|View full text |Cite
|
Sign up to set email alerts
|

Reviewing the Impact of Powder Cohesion on Continuous Direct Compression (CDC) Performance

Abstract: The pharmaceutical industry is undergoing a paradigm shift towards continuous processing from batch, where continuous direct compression (CDC) is considered to offer the most straightforward implementation amongst powder processes due to the relatively low number of unit operations or handling steps. Due to the nature of continuous processing, the bulk properties of the formulation will require sufficient flowability and tabletability in order to be processed and transported effectively to and from each unit o… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
0
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 9 publications
(3 citation statements)
references
References 156 publications
0
0
0
Order By: Relevance
“…Malfunctioning of any kind may lead to unstable products and batches with significant variability. 209 Regulatory agencies regulate a therapeutic product's safety and desired response while eliminating its harmful and undesired effects. CS, which comes from animal sources, should undergo rigorous microbial tests to remove animal-borne contamination.…”
Section: Regulatory Landscape and Challenges Associated With Translat...mentioning
confidence: 99%
“…Malfunctioning of any kind may lead to unstable products and batches with significant variability. 209 Regulatory agencies regulate a therapeutic product's safety and desired response while eliminating its harmful and undesired effects. CS, which comes from animal sources, should undergo rigorous microbial tests to remove animal-borne contamination.…”
Section: Regulatory Landscape and Challenges Associated With Translat...mentioning
confidence: 99%
“…For a tablet formulation to have adequate compressibility and compactability, the flow must not negatively impact the process. In this sense, a critical attribute is the cohesion of the formulation, which is significant in the manufacturing process of any solid pharmaceutical form [36,39]. When the flow of a material is considered suitable for formulation development, it means that in the compressibility stage, the particles will have an affinity to adhere to each other, mainly due to the size and shape of the particles [36,40].…”
Section: Granule Flow and True Densitymentioning
confidence: 99%
“…For a tablet formulation to have adequate compressibility and compactability, the flow mustn't negatively impact the process. In this sense, an essential critical attribute is the cohesion of the formulation, considered significant in the manufacturing process of any solid pharmaceutical form [30,33]). When the flow of a material is considered suitable for formulation development, it means that in the compressibility stage, the particles will have an affinity to adhere to each other, mainly due to the size and shape of the particles being one of the factors that most contribute to this behavior [30,34].…”
Section: Granule Flow and True Densitymentioning
confidence: 99%