Advances in ATR-FTIR Spectroscopic Imaging for the Analysis of Tablet Dissolution and Drug Release

• Published in: Molecules (Basel, Switzerland) Switzerland), 2023-06, Vol.28 (12), p.4705
• Main Authors: van Haaren, Céline, De Bock, Marieke, Kazarian, Sergei G
• Format: Article
• Language: English
• Subjects: chemical imaging; Diagnostic Imaging; Dissolution; Dosage; Drug dosages; Drug Liberation; drug release; Formulations; FTIR spectroscopic imaging; Imaging techniques; Infrared spectroscopy; Magnetic resonance imaging; Mandatory drug testing; Molecular structure; Optimization; Oral administration; Pharmaceutical industry; Pharmaceuticals; Review; solid oral dosage forms; Solubility; Spectroscopy, Fourier Transform Infrared - methods; Spectrum analysis; Tablets - chemistry
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules28124705

One of the major challenges in the development of effective pharmaceutical formulations for oral administration is the poor solubility of active pharmaceutical ingredients. For this reason, the dissolution process and drug release from solid oral dosage forms, such as tablets, is usually thoroughly studied in order to understand the dissolution behaviour under various conditions and optimize the formulation accordingly. Standard dissolution tests used in the pharmaceutical industry provide information on the amount of drug released over time; however, these do not allow for a detailed analysis of the underlying chemical and physical mechanisms of tablet dissolution. FTIR spectroscopic imaging, by contrast, does offer the ability to study these processes with high spatial and chemical specificity. As such, the method allows us to see the chemical and physical processes which occur inside the tablet as it dissolves. In this review, the power of ATR-FTIR spectroscopic imaging is demonstrated by presenting a number of successful applications of this chemical imaging technique to dissolution and drug release studies for a range of different pharmaceutical formulations and study conditions. Understanding these processes is essential for the development of effective oral dosage forms and optimization of pharmaceutical formulations.