Parts per Million Powder X‑ray Diffraction

• Published in: Analytical chemistry (Washington) Vol. 87; no. 21; pp. 10950 - 10955
• Main Authors: Newman, Justin A, Schmitt, Paul D, Toth, Scott J, Deng, Fengyuan, Zhang, Shijie, Simpson, Garth J
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 03.11.2015; American Chemical Society (ACS)
• Subjects: Amorphous materials; Analytical chemistry; Bioavailability; Crystal structure; Diffraction; Dispersions; Ingredients; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; Limit of Detection; Pharmaceuticals; Polymer blends; Powder Diffraction - methods; Signal to noise ratio; Synchrotrons; X-rays
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/acs.analchem.5b02758

Here we demonstrate the use of second harmonic generation (SHG) microscopy-guided synchrotron powder X-ray diffraction (PXRD) for the detection of trace crystalline active pharmaceutical ingredients in a common polymer blend. The combined instrument is capable of detecting 100 ppm crystalline ritonavir in an amorphous hydroxypropyl methylcellulose matrix with a high signal-to-noise ratio (>5000). The high spatial resolution afforded by SHG microscopy allows for the use of a minibeam collimator to reduce the total volume of material probed by synchrotron PXRD. The reduction in probed volume results in reduced background from amorphous material. The ability to detect low crystalline loading has the potential to improve measurements in the formulation pipeline for pharmaceutical solid dispersions, for which even trace quantities of crystalline active ingredients can negatively impact the stability and bioavailability of the final drug product.