Review article
https://doi.org/10.15255/KUI.2022.014
Determination of Physicochemical Compatibility of Drugs Using Analytical Techniques: A Review of 5-aminosalicylate and Folic Acid Fixed-dose Combination Development
Mario-Livio Jeličić
; Faculty of Pharmacy and Biochemistry, University of Zagreb, Ante Kovačića 1, 10 000 Zagreb, Croatia
Abstract
With the use of fixed-dose drug combinations, the potential risk of non-adherence needs to be minimised, which is particularly important in patients with chronic diseases. The development of such dosage form is a complex process in which an important role is played by testing the physicochemical compatibility of the components intended for the manufacture of the desired product. Various analytical techniques, such as thermoanalytical (DSC, DTA), spectroscopic (FTIR, XRPD) and chromatographic (HPLC), in combination with certain degradation studies, such as forced degradation and isothermal degradation, are often used. In this review, on the example of the development of a fixed-dose combination of 5-aminosalicylate and folic acid, procedures suitable for testing the compatibility of drug components, as well as analytical techniques and various ways of interpretation of results are described.
Keywords
physicochemical compatibility; analytical techniques; 5-aminosalicylates; folic acid; fixed-dose combinations
Hrčak ID:
285547
URI
Publication date:
14.11.2022.
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