Compatibility study of the acetylsalicylic acid with different solid dosage forms excipients

Journal of Thermal Analysis - Tập 112 - Trang 407-419 - 2013
Dumitru Tita1, Tunde Jurca2, Adriana Fulias1, Eleonora Marian2, Bogdan Tita1
1Faculty of Pharmacy, University of Medicine and Pharmacy “Victor Babeş”, Timisoara, Romania
2Speciality of Pharmacy, Faculty of Medicine and Pharmacy, University of Oradea, Oradea, Romania

Tóm tắt

This study is part of a research project aimed to find and optimize methods by which drug-excipient compatibility can be reliably and quickly assessed. The objective of the present study was to evaluate the compatibility of the acetylsalicylic acid (ASA), an non-steroidal anti-inflammatory drug, with pharmaceutical excipients of common use including diluents, binders, disintegrants, lubricants and solubilising agents. In order to investigate the possible interactions between ASA and eleven excipients differential scanning calorimetry (DSC) and thermogravimetry/derivative thermogravimetry analysis completed by Fourier transform infrared spectroscopy (FT-IR) and X-ray powder diffraction were used for compatibility study. The DSC has proven to be, among the selected analytical techniques, the most sensitive and specific in assessing the compatibility. The samples, as physical mixtures, were prepared by mixing the analyte and excipients in a proportion of 1:1 (w:w). On the basis of thermal results (especially DSC), confirmed by FT-IR and X-ray analysis, a possible chemical interaction was found between the ASA with polyvinylpyrrolidone K30 (PVP) and magnesium stearate, respectively a possible physical interaction with colloidal silicon dioxide and stearic acid (Ac. St.).

Tài liệu tham khảo