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Updated: Aug 6, 2026

An Intestine/Liver Microphysiological System for Drug Pharmacokinetic and Toxicological Assessment
Published on: December 3, 2020
Establishing a robust, versatile second-order calibration model for accurate acetylsalicylic acid measurement across
Somaye Vali Zade1, Sajedeh Alavi2, Marzieh Ranjbar1
1Halal Research Center of IRI, Food and Drug Administration, Ministry of Health and Medical Ducation, Tehran, Iran.
Background:
Accurate quantification of acetylsalicylic acid (ASA) in pharmaceutical formulations is critical due to its widespread therapeutic use. However, excipient variability and uncalibrated interfering species often compromise the reliability of conventional methods. This study aims to address these challenges by developing a robust and versatile calibration model for ASA determination that ensures consistency across different formulations while maintaining precision and efficiency.
Results:
A second-order calibration model was developed using UV-Vis pH-spectrophotometric data, processed via the RAFA model, to quantify ASA accurately across diverse formulations. By exploiting the second-order advantage, this model accurately quantified ASA even in the presence of uncalibrated interferences. Key parameters such as wavelength range (231-290 nm) and pH (3-7) were optimized to improve robustness. Validation with seven pharmaceutical formulations yielded low prediction errors (<8 %), demonstrating the model's versatility and adaptability to varying excipient compositions and conditions, including temperature variations.
Significance:
This study presents a versatile calibration model for ASA quantification that is robust, adaptable, and cost-effective. Its ability to perform under diverse conditions underscores its potential for broader applications in pharmaceutical quality control and analysis.
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