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      • Calcium Carbonate
      • Calcium Phosphates
      • Calcium Sulfate
      • Halites
      • Metallic Oxides
      • Silica
    • Organic Chemicals
      • Actual Sugars
      • Artificial Sweeteners
      • Carbohydrates
      • Cellulose
      • Cellulose Esters
      • Cellulose Ethers
      • CMC and Croscarmellose Sodium
      • Converted Starch
      • Dried Starch
      • Microcrystalline Cellulose
      • Modified Starch
      • Starch
      • Sugars
      • Sugar Alcohols
    • Petrochemicals
      • Acrylic Polymers
      • Glycols
      • Mineral Hydrocarbons
      • Mineral Oils
      • Mineral Waxes
      • Petrolatum
      • Polyethylene Glycol (PEG)
      • Povidones
      • Propylene Glycol
      • Other Petrochemical Excipients
    • Oleochemicals
      • Fatty Alcohols
      • Glycerin
      • Mineral Stearates
      • Pharmaceutical Oils
      • Other Oleochemical Excipients
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  • Applications
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Startseite » News » Particle Size-independent Variation of Bulk Excipients

Particle Size-independent Variation of Bulk Excipients

28. May 2019
Diagram of an aeration test

Particle Size-independent Variation of Bulk Excipients

Microcrystalline Cellulose (MCC) has been used as a pharmaceutical excipient for many years, due to its abundance, ease of production and resistance to degradation.  As with any excipient, however, variability between batches of supplied material can in turn lead to similar variability in processing, resulting in product that is out of specification, and needs to be reworked or even scrapped.  Recent Quality by Design (QbD) initiatives have made it necessary to optimise production processes to ensure the consistency and reliability of final products.

A robust method of quantifying the variations in batches of excipients that contribute to differences in downstream process behaviour enables a design space of acceptable raw material properties to be established. This approach is an essential part of QbD.  However, even well-established techniques for material characterisation (such as particle size analysis) do not always provide the required differentiation, as they only evaluate of one physical property of the particles.

 

Multivariate Analysis of Powder Batches

Three grades of MCC were used as an excipient in the production of pharmaceutical tablets by direct compression. Particle size analysis of the three grades generated almost identical D50 values (100 µm) for each grade, and it was determined that three samples were indistinguishable from each other.

All three samples were further analysed using an FT4 Powder Rheometer®, to evaluate whether differences existed that weren’t identified by the D50 value and consequently whether particle size alone is sufficient as a tool predicting in-process performance.

Test Results:

Dynamic Testing: Aeration

Diagram of an aeration test
Particle Size-independent Variation of Bulk Excipients

 

Sample C generated a significantly higher Aeration Ratio (AR) than the other samples, demonstrating that its packing structure changes to a greater extent when air is introduced into the sample. This typically indicates a lower degree of cohesive strength between particles.  Sample A and Sample B exhibited different responses, with the lower sensitivity to the introduction of air suggesting greater cohesivity compared to Sample C.

 

Bulk Testing: Permeability

Diagram of bulk testing
Bulk Testing: Permeability

Sample C generated a considerably higher Pressure Drop across the Powder Bed than the other two samples, indicating that it is the least permeable of the three.  Low permeability means that any air that becomes entrained in the bulk is less able to escape. Considering the example of a tabletting process, greater air content within the dose would typically lead to capping and lamination as well as weight variation in the final product.

 

 

Shear Cell Testing

Diagram of shear cell testing
Shear Cell Testing

Sample A showed considerably different behaviour to the other two samples, generating the highest Shear Stress values at low normal stress levels, but the lowest values at higher levels. This suggests that the way the powders perform in a given process would be heavily influenced by stress levels they are subjected to, and illustrates the need to characterise powders using process relevant techniques.  Considering the results for Sample B, the Yield Locus, generated by a best-fit line through the data points, is so steep that it intercepts the y-axis below the origin.  This leads to a negative value for Cohesion, and generates no result for Flow Function (as the minor Mohr circle cannot be constructed in order to produce a value for Unconfined Yield Strength). This illustrates the importance of recording actual measured Shear Stress values alongside parameters derived from Mohr’s circle analysis, as the mathematical model used to obtain these parameters may not always provide data for comparison.

 

Conclusions

The FT4 has demonstrated clear and repeatable differences between three grades of MCC, suggesting a likely difference in their process performance which is not identified by the single physical property of particle size alone.  Of the three samples, Sample A displayed the highest Permeability and the lowest sensitivity to Aeration, as well as being less sensitive to changes in applied stress during Shear Cell tests. This suggests that it is the most efficiently packed of the three samples and is to exhibit more free-flowing behaviour across a range of conditions.  Sample C generated the highest Shear Stress values, was most sensitive to Aeration and exhibited the lowest Permeability, suggesting a greater sensitivity to the process conditions than the other samples and illustrating the need to understand the relationship between the process environment and the material properties.

Powder flowability is not an inherent material property, but is more about the ability of powder to flow in a desired manner in a specific piece of equipment. Successful processing demands that the powder and the process are well-matched and it is not uncommon for the same powder to perform well in one process but poorly in another. This means that several characterisation methodologies are required, the results from which can be correlated with process ranking to produce a design space of parameters that correspond to acceptable process behaviour.  Rather than relying on single number characterisation to describe behaviour across all processes, the FT4’s multivariate approach simulates a range of unit operations, allowing for the direct investigation of a powder’s response to various process and environmental conditions.

 

For more information about Freeman Technology please go to the Freemantech website.

 

Author Information

Tim Freeman

Managing Director, Freeman Technology (a Micromeritics company)

Tim Freeman is Managing Director of powder characterisation company Freeman Technology for whom he has worked since the late 1990s. He was instrumental in the design and continuing development of the FT4 Powder Rheometer® and the Uniaxial Powder Tester. Through his work with various professional bodies, and involvement in industry initiatives, Tim is an established contributor to wider developments in powder processing.

Tim has a degree in Mechatronics from the University of Sussex in the UK. He is a mentor on a number of project groups for the Engineering Research Center for Structured Organic Particulate Systems in the US and a frequent contributor to industry conferences in the area of powder characterisation and processing. A past Chair of the American Association of Pharmaceutical Scientists (AAPS) Process Analytical Technology Focus Group Tim is a member of the Editorial Advisory Board of Pharmaceutical Technology and features on the Industry Expert Panel in European Pharmaceutical Review magazine.  Tim is also a committee member of the Particle Technology Special Interest Group at the Institute of Chemical Engineers, Vice-Chair of the D18.24 sub-committee on the Characterisation and Handling of Powders and Bulk Solids at ASTM and a member of the United States Pharmacopeial (USP) General Chapters Physical Analysis Expert Committee (GC-PA EC).

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      • Emulsifier
      • Excipient for Inhalation
      • Filler
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      • Glidant
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      • Lubricant
      • Nanotechnology
      • Orally Dissolving Technology Excipient
      • Pellet
      • Plasticizer
      • Preservative
    • Solubilizer – Viscocity Agent
      • Solubilizer
      • Speciality Excipient
      • Surfactants
      • Suspension Agent
      • Sustained Release Agent
      • Sweeteners
      • Taste Masking
      • Topical Excipient
      • Viscosity Agent
  • Sources
    • Handbook of Pharmaceutical Excipients – 9th Edition
    • EINECS Numbers
    • Excipient DMF List
    • Excipient cGMP Certification Organisations
    • FDA Inactive Ingredient List
    • FDA GRAS Substances (SCOGS) Database
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  • Suppliers
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      • ADM
      • ARMOR PHARMA
      • Ceolus™ & Celphere™
      • Ashland
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      • Beneo – galenIQ
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      • Budenheim
    • C-G
      • Captisol
      • Croda
      • Cyclolab
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      • Evonik
      • Fuji Chemical Industries
      • Gattefossé
      • Gangwal Healthcare
    • I-O
      • ingredientpharm
      • IOI Oleochemical
      • JRS Pharma
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      • KLK Oleo Life Science
      • Lactalis Ingredients Pharma
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      • Dr. Paul Lohmann
      • Lubrizol
      • Magnesia
      • MEGGLE Excipients
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      • Pfanstiehl
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