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Selecting a stable solid form of remdesivir using microcrystal electron diffraction and crystal structure prediction

Academic source · RSC Advances

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Site published: 2026-11-03 · Updated: 2026-11-03

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What the paper reports

This study combined MicroED with crystal structure prediction to support solid-form selection for remdesivir. Experimentally determined structural information was evaluated alongside computational crystal-energy analysis, demonstrating a joint experimental and modeling approach when conventional large-crystal growth is difficult. The work concerns solid-state characterization and selection, not a new assessment of antiviral efficacy or clinical performance.

Why this paper is included

Shows how measured structures can inform CSP-based decisions; experimental stability and process suitability still require independent evaluation.

The interpretation above is analysis, not a conclusion attributed to the original source.

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Prepared through Biotech Assistant’s automated research workflow. Editorial standards and corrections

MicroED structure determination Pharmaceutical solid state

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