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Startseite » News » A Quality by Design (QbD) study in direct compression using highly compactible and flowing microcrystalline cellulose CEOLUS™ UF-711

A Quality by Design (QbD) study in direct compression using highly compactible and flowing microcrystalline cellulose CEOLUS™ UF-711

28. April 2022
Analysis-1 with fixed Tableting speed (40 rpm)

A Quality by Design (QbD) study in direct compression using highly compactible and flowing microcrystalline cellulose CEOLUS™ UF-711

OBJECTIVE

CEOLUSTM UF-711 is highly compactible and flowing microcrystalline cellulose (MCC). While UF-711 has over 1.5 times the compactibility of standard grade PH-102, it has the same flow characteristics as PH-102. This is because the UF-711 particle has a round shape and has many pores inside its particle.

The purpose of this QbD study is to demonstrate that UF-711 has higher robustness than PH-102 by analyzing the impact of formulation and process variables on tablet’s critical quality attributes (CQA) in direct compression of poorly compactible drug.

What is CeolusTM UF-711?

CEOLUSTM UF-711 is an NF/EP/JP compatible MCC.


Powder properties

Tab.1 Powder properties of CEOLUSTM grades:

Bulk density (g/cm3) Av.particle diameter (µm) Repose Angle (o)
UF-711 0.22 50 42
UF-702 0.29 90 34
KG 1000 0.12 50 57
KG 802 0.21 50 49
PH 101 0.29 50 45
PH 102 0.30 90 42

Particle morphology

Fig.2 Particle morphology of CEOLUSTM grades:

Fig.2 Particle morphology of CEOLUS grades

Fig.3 Relationship between compactibility and flowability of MCC grade:

Fig.3 Relationship between compactibility and flowability of MCC grade


METHOD

METHOD Ceolus UF-711


Formulation and Process variables

1) Drug Loading,      2) Lubricant level,    3) Tableting speed.

Formulation and Process variables

Asahi Kasei compared the robustness between UF-711 and PH-102 by measuring design space, where tablet hardness was over 110 N.


RESULTS

Analysis-1 with fixed Tableting speed (40 rpm):

Analysis-1 with fixed Tableting speed (40 rpm)

UF-711:  At 50% drug loading, hardness of UF-711 formulations exceeded 110 N even at 2.25% lubricant.

PH-102:  Hardness was strongly influenced by lubricant level. Even in case of 30% drug loading, hardness could not reach 110 N at 2.25% lubricant.

Analysis-2 with fixed drug loading level

Analysis-2 with fixed drug loading level

UF-711/VC50%: Hardness stayed high (over 110 N) at high lubricant level.

PH-102/VC30%: Hardness decreased with increasing lubricant level.

 

UF-711 had wider design space in spite of drug loading level 20% higher than PH-102.

UF-711 has lower lubricant sensitivity than PH-102.


CONCLUSION

This QbD Study demonstrated that CEOLUSTM UF-711 formulation may contain a larger amount of ascorbic acid and furthermore had higher robustness than PH-102 in direct compression. Highly compactible and flowable MCC CEOLUSTM UF-711 is suitable for direct compression at high drug loading (over 50%) formulation.


REFERENCE

The data of this page is a property of Asahi Kasei Corporation.


Request a sample or more information:

Tags: excipientsformulation

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