UV–vis Imaging of Piroxicam Supersaturation, Precipitation, and Dissolution in a Flow-Through Setup

• Published in: Analytical chemistry (Washington) Vol. 90; no. 11; pp. 6413 - 6418
• Main Authors: Sun, Yu, Chapman, Alex, Larsen, Susan W, Jensen, Henrik, Petersen, Nickolaj J, Goodall, David M, Østergaard, Jesper
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 05.06.2018
• Subjects: Analytical chemistry; Anti-Inflammatory Agents, Non-Steroidal - chemistry; Aqueous environments; Aqueous solutions; Bioavailability; Chemical Precipitation; Chemistry; Dissolution; Drug delivery systems; Drugs; Imaging; Microscopy; Microscopy - methods; Optical Imaging - instrumentation; Optical Imaging - methods; Piroxicam - chemistry; Pyrrolidinones - chemistry; Raman spectroscopy; Solid phases; Solubility; Spectrophotometry, Ultraviolet - instrumentation; Spectrophotometry, Ultraviolet - methods; Spectrum Analysis, Raman - methods; Supersaturation; Ultrasonic imaging; Ultraviolet Rays
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/acs.analchem.8b00587

Evaluation of drug precipitation is important in order to address challenges regarding low and variable bioavailability of poorly water-soluble drugs, to assess potential risk of patient safety with infusion therapy, and to explore injectable in situ suspension-forming drug delivery systems. Generally, drug precipitation is assessed in vitro through solution concentration analysis methods. Dual-wavelength UV–vis imaging is a novel imaging technique that may provide an opportunity for simultaneously monitoring changes in both solution and solid phases during precipitation. In the present study, a multimodal approach integrating UV–vis imaging, light microscopy, and Raman spectroscopy was developed for characterization of piroxicam supersaturation, precipitation, and dissolution in a flow-through setup. A solution of piroxicam dissolved in 1-methyl-2-pyrrolidinone was injected into a flowing aqueous environment (pH 7.4), causing piroxicam to precipitate. Imaging at 405 and 280 nm monitored piroxicam concentration distributions during precipitation and revealed different supersaturation levels dependent on the initial concentration of the piroxicam solution. The combination with imaging at 525 nm, light microscopy, and Raman spectroscopy measurements demonstrated concentration-dependent precipitation and the formation, growth, and dissolution of individual particles. Results emphasize the importance of the specific hydrodynamic conditions on the piroxicam precipitation. The approach used may facilitate comprehensive understanding of drug precipitation and dissolution processes and may be developed further into a basic tool for formulation screening and development.