First published 10/3/2026, 7:42:15 PM · Last updated 10/3/2026, 7:42:15 PM

Development and validation of high performance liquid chromatographic method for the determination of esomeprazole in tablets

A 2020 journal article published by The Journal of Food and Drug Analysis (JFDA) and the Taiwan Food and Drug Administration describes development and validation of an HPLC method to quantify esomeprazole in tablet formulations. The supplied source content did not include further experimental details or results.

Categories: science-and-space, public-health

Generated scores

Scores are based on the cited reporting and use a 1–10 scale. Read the methodology.

Confidence: 6/10How certain the assessment is based on the clarity and evidence in the cited reporting.
Geographic reach: 4/10How widely the event reaches, from a local area (1) to worldwide impact (10).
Global importance: 2/10The event's broader significance, from limited importance (1) to major global importance (10).
Impact magnitude: 2/10The scale or severity of the real-world impact, from minor (1) to extreme (10).
Positivity: 7/10How harmful or beneficial the event is, from strongly harmful (1) to strongly positive (10).
Urgency: 1/10How time-sensitive the event is, from low urgency (1) to immediate attention needed (10).

Why it matters

A validated analytical method for measuring a pharmaceutical active ingredient is relevant to drug quality testing and regulatory analysis.

Sources

Development and validation of high performance liquid chromatographic method for the determination of esomeprazole in tabletsMetadata provided by Crossref. Usage terms

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