Single-particle geometries of pharmaceutical powders from X-ray tomography; a simple and reliable sample preparation method

The size and shape of the particles within a powder are critical quality-control attributes in the pharmaceutical industry. These microscopic attributes significantly affect the macroscopic properties of the powder, such as the bulk density and flowability. Methods for determining the particle size distribution (PSD) and characterisation of particle shape are therefore essential but can be extremely challenging, particularly when looking at individual particle shapes. This work introduces a new sample preparation method for X-ray micro-computed tomography (μCT) that is convenient, fast, and produces well-dispersed samples, allowing the identification of individual particles. The resulting contrast is excellent even for organic pharmaceutical powders, which are often challenging to image due to the low attenuation coefficient of their components. Simultaneously, an analysis method is proposed that reliably applies to all tested powders, automatically filtering out artefacts such as bubbles. The combined method unambiguously identifies individual particles, allowing the determination of PSD, particle shape classification, and analysis of the internal morphology of particles. Validation is provided through comparisons with laser diffraction, sieve analysis, and optical microscopy. While this new standardised μCT method is slightly more labour intensive than other characterisation methods, it requires only a minimal amount of material (∼15 mg) and provides superior morphological information, which can be used to help explain or predict bulk properties. This is particularly beneficial in early-phase development, where access to large quantities of powder is limited. • New sample preparation method for X-ray microtomography (μCT) of fragile powders. • Works for organic, inorganic, and temperature-sensitive powders. • Accurate particle size distributions (PSDs) from just ∼15 mg of powder. • Identifies single grains for size, shape, and morphology analysis. • Links single-grain traits to bulk powder properties.

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Publication Details

Journal
Tomography of Materials and Structures
Published
2025-04-26
DOI
https://doi.org/10.1016/j.tmater.2025.100067
Primary Topic
X-ray Diffraction in Crystallography
Type
article
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article

Single-particle geometries of pharmaceutical powders from X-ray tomography; a simple and reliable sample preparation method

James A. Elliott, Umair Zafar, Dingeman L.H. van der Haven, Ioannis S. Fragkopoulos et al.
Tomography of Materials and Structures
X-ray Diffraction in Crystallography
article

Single-particle geometries of pharmaceutical powders from X-ray tomography; a simple and reliable sample preparation method

James A. Elliott, Umair Zafar, Dingeman L.H. van der Haven, Ioannis S. Fragkopoulos, Jan Lasson Andreasen
article en

Abstract

The size and shape of the particles within a powder are critical quality-control attributes in the pharmaceutical industry. These microscopic attributes significantly affect the macroscopic properties of the powder, such as the bulk density and flowability. Methods for determining the particle size distribution (PSD) and characterisation of particle shape are therefore essential but can be extremely challenging, particularly when looking at individual particle shapes. This work introduces a new sample preparation method for X-ray micro-computed tomography (μCT) that is convenient, fast, and produces well-dispersed samples, allowing the identification of individual particles. The resulting contrast is excellent even for organic pharmaceutical powders, which are often challenging to image due to the low attenuation coefficient of their components. Simultaneously, an analysis method is proposed that reliably applies to all tested powders, automatically filtering out artefacts such as bubbles. The combined method unambiguously identifies individual particles, allowing the determination of PSD, particle shape classification, and analysis of the internal morphology of particles. Validation is provided through comparisons with laser diffraction, sieve analysis, and optical microscopy. While this new standardised μCT method is slightly more labour intensive than other characterisation methods, it requires only a minimal amount of material (∼15 mg) and provides superior morphological information, which can be used to help explain or predict bulk properties. This is particularly beneficial in early-phase development, where access to large quantities of powder is limited. • New sample preparation method for X-ray microtomography (μCT) of fragile powders. • Works for organic, inorganic, and temperature-sensitive powders. • Accurate particle size distributions (PSDs) from just ∼15 mg of powder. • Identifies single grains for size, shape, and morphology analysis. • Links single-grain traits to bulk powder properties.

Tomography of Materials and StructuresVol. 8
Novo Nordisk (Denmark) (DK), University of Cambridge (GB)
Openalex Percentile: Top 94%
X-ray Diffraction in Crystallography
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