Assessment of phenprocoumon stability and excipient compatibility using thermoanalytical techniques and FT-IR spectroscopy

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Authors: Iulia Gallo, Ion Fratilescu, Camelia Epuran, Alexandru Pahomi, Maria Dumitrescu, Mihaela Maria Budiul, Mădălina Grădinaru, Titus Vlase, Gabriela Vlase
Cited by: 1
References: 45

Abstract

Abstract Phenprocoumon, a widely used anticoagulant in Europe, was assessed for solid-state compatibility with common tablet excipients by FT-IR over time and by thermogravimetric analysis. The excipients investigated included starch, hydroxypropyl methylcellulose, magnesium stearate, lactose, mannitol, talc, silicon dioxide, and polyvinylpyrrolidone, as they are frequently employed in tablet manufacturing as fillers, binders, disintegrants, or lubricants. All excipients proved compatible except magnesium stearate, which showed clear signs of interaction in both FT-IR and thermal analysis, indicating a specific incompatibility that requires caution in formulation. Such compatibility studies are essential in pharmaceutical development, as drug–excipient interactions may compromise stability, bioavailability, and overall therapeutic efficacy.

Fields of Study & Subjects

Drug Solubulity and Delivery Systems Microencapsulation and Drying Processes Inhalation and Respiratory Drug Delivery

Publication details

Journal / source
Journal of Thermal Analysis and Calorimetry
Publisher
Springer Science and Business Media LLC
Volume
151
Issue
20
Pages
16825-16838
Publication date
22 June 2026
Language
EN